Skip to main content
Bioresources and Bioprocessing logoLink to Bioresources and Bioprocessing
. 2023 Nov 28;10(1):85. doi: 10.1186/s40643-023-00702-y

An overview of fermentation in the food industry - looking back from a new perspective

Shahida Anusha Siddiqui 1,2,, Zeki Erol 3, Jerina Rugji 3, Fulya Taşçı 3, Hatice Ahu Kahraman 3, Valeria Toppi 4, Laura Musa 5, Giacomo Di Giacinto 4, Nur Alim Bahmid 6, Mohammad Mehdizadeh 7,8, Roberto Castro-Muñoz 9,10,
PMCID: PMC10991178  PMID: 38647968

Abstract

Fermentation is thought to be born in the Fertile Crescent, and since then, almost every culture has integrated fermented foods into their dietary habits. Originally used to preserve foods, fermentation is now applied to improve their physicochemical, sensory, nutritional, and safety attributes. Fermented dairy, alcoholic beverages like wine and beer, fermented vegetables, fruits, and meats are all highly valuable due to their increased storage stability, reduced risk of food poisoning, and enhanced flavor. Over the years, scientific research has associated the consumption of fermented products with improved health status. The fermentation process helps to break down compounds into more easily digestible forms. It also helps to reduce the amount of toxins and pathogens in food. Additionally, fermented foods contain probiotics, which are beneficial bacteria that help the body to digest food and absorb nutrients. In today’s world, non-communicable diseases such as cardiovascular disease, type 2 diabetes, cancer, and allergies have increased. In this regard, scientific investigations have demonstrated that shifting to a diet that contains fermented foods can reduce the risk of non-communicable diseases. Moreover, in the last decade, there has been a growing interest in fermentation technology to valorize food waste into valuable by-products. Fermentation of various food wastes has resulted in the successful production of valuable by-products, including enzymes, pigments, and biofuels.

Keywords: Fermentation, Non-communicable disease, Waste valorization, Fermented dairy, Fermented meat, Fermented plant-based foods

Introduction

The growing concern about the availability of safe and sustainable natural food supplies is a direct result of a rapidly expanding global population (Knorr and Augustin 2022). For the production of the next generation of food components and products, fermentation stands out among other approaches like cellular or acellular products, edible biomass, and edible insects. Compared to conventional farming, the production of fermented products requires reduced land, generates fewer greenhouse gas emissions, and consumes less water. Additionally, fermented foods have been linked with health benefits such as lowering cholesterol levels, boosting the immune system, protecting against infections, cancer, osteoporosis, obesity, diabetes, allergies, atherosclerosis, and reducing lactose sensitivity (Tamang and Thapa 2022). The beneficial effects of fermented foods are mostly credited to bioactive peptide fractions produced during fermentation through microbial protein breakdown (Şanlier et al. 2019).

Fermentation is a time-honored method used for ages to prolong the shelf life of food and augment its nutritional quality (Augustin et al. 2023). It has been used to preserve various animal-derived, seafood, and plant-originated foods. Middle Eastern, European, and Indian cultures developed cheese, cultured milk, and fermentation-based milk products. On the contrary, animal husbandry was more restricted to Eastern countries including Japan, Korea, and China. A wide range of ingredients used to produce alcoholic beverages and fermented foods was also influenced by cultural, social, religious, and economic variables. Therefore, fermented foods that originated in Asia tended to be based on rice and grains, vegetables, fish, and soybeans, while in Africa, native cereal grains such as millet, sorghum, maize, and wheat represent popular fermenting substrates (Tamang et al. 2020). The regulated action of microorganisms on a food substrate is at the root of fermentation. Fermentation may be spontaneously induced by microorganisms commonly found in raw ingredients. Traditional sauerkraut, sourdough bread, and kimchi result from fermented foods rendered through spontaneous fermentation. Advances in biotechnology have made fermentation into an established process. Using starting cultures allow for acquiring a standardized food product (Bourdichon et al. 2021). For food applications, strain engineering often involves harmless microorganisms like Bacillus spp., yeast like Saccharomyces cerevisiaeKomagataella phaffiiKluyveromyces spp., or filamentous fungi (Augustin et al. 2023; Chai et al. 2022a, b; Vieira Gomes et al. 2018). Specific food components like antioxidants, colorants, flavors, enzymes, and vitamins can also be manufactured through fermentation (Santiago‐Díaz et al. 2022). Antioxidants, bacteriocins, pigments, enzymes, and other food components are increasingly being manufactured utilizing food waste as a fermentation substrate. A direct connection exists between eliminating food waste and developing creative, high-value assets generated by applying an under- or untapped resource (Yang et al. 2022). In the bargain, scientific investigations have ensured insights into using fermentation technology to produce fermented edible insects to promote food security. There are already available fermented insect-containing edible preparations such as sauces, powder, paste, and fermented dishes containing insects with the possibility of extension (Kewuyemi et al. 2020). Examples of such fermented sauces include those made using Locusta migratoria and Galleria mellonella. These sauces were very satisfactory compared with conventional seafood sauces (Mouritsen et al. 2017).

Fermentation further improves compound extraction efficiency, alters the antioxidant profile, and generates novel bioactive compounds from the food matrix. Lately, there is an emerging understanding that precision fermentation represents a key innovation in the food industry’s impending fourth industrial revolution. Modernizing food production with precision fermentation is becoming increasingly popular. Because of its potential to reduce waste and increase the efficiency of protein, lipid, and carbohydrate production (Augustin et al. 2023). This overview will discuss fermentation’s cultural significance and ecological importance, technological advancements of fermented beverage and food worldwide, health benefits, nutritional value, and microbiological insights into various fermented foods. We will examine distinct types of fermented foods of animal, plant, microalgae, and edible insect origin. For every kind of product, bacteria involved in fermentation, consumers’ acceptance, place of origin, and consumption will be discussed. There is also a discussion of how the industrial revolution has impacted the process of fermented foods and how fermentation is used to value food waste.

Technology advancements in fermentation

The process of fermentation encompasses the biochemical activity of organisms throughout their life cycle, from growth to death. Industrial-scale production of food, pharmaceuticals, and alcoholic beverages utilizes fermentation technology powered by these organisms. Industrial fermentation technology relies on the fundamental principle of cultivating organisms in optimal conditions. This is achieved by providing the required raw materials, including carbon, nitrogen, salts, trace elements, and vitamins, essential for their growth (Sharma et al. 2020). Additionally, the temperature, pH, and oxygen concentrations must be controlled in order to ensure the highest possible yield of the desired product. The fermentation process is also closely monitored to ensure that the organisms are not exposed to any toxins or pathogens that could potentially affect the outcome. The mounting focus on environmental conservation and renewable energy has sparked a surge of interest in the retrieval of fermentation products, including industrial chemicals, organic acids, and feed or food additives. This upswing has caused a proliferation of products beyond the customary high-value, low-volume pharmaceuticals, with fermentation now rivaling the synthesis of commodity chemicals itself. Companies must optimize efficiency and reduce waste by-products to remain competitive in producing low-cost, high-volume chemicals. Currently, scientific communities are keenly exploring the biotechnological potential of agro-industrial remnants.

Emerging fermentation-based technologies have revolutionized the food industry in various ways. Cai et al. (2020) reported that sulforaphane yields were increased by 16 times when broccoli florets were pre-heated at 65 °C for 3 min followed by maceration and lactic acid bacteria fermentation in a laboratory scale. Additionally, these technologies have paved the way for producing a pea protein hydrolysate component that enhances the saltiness of food. In a study by Xu et al. (2020), fermentation of carrot juice was found to enhance the nutritional profile of carrot juice by using probiotic Lactobacillus gasseri. Fermented straight carrot juice was found to have a reduction in sugar (27%) according to their results. It is possible to improve fermentation processes and tweak fermented foods’ nutritional and sensory attributes using these methods. To enhance fermentation, the following factors at each stage need to be addressed: selecting and designing of targets, strain optimization, bioprocess development, feedstock improvement, and final product formulation and production. One fermentation technique utilized by various industries, including food, pharmaceuticals, and textiles, is solid-state fermentation (SSF), which involves utilizing solid support rather than a liquid to produce microorganism metabolites. SSF boasts several benefits: minimal waste production and a reduced environmental impact, natural solids as a medium with low energy costs and capital investments, no sterilization requirement, improved downstream processes and reduced microbial contaminants (Sun et al. 2022).

Acidogenic fermentation (AF) is crucial in producing valuable chemicals like C1–C6 carboxylic acids and alcohol. However, low product titers have been a persistent challenge due to thermodynamic limitations. Recent research shows that boosting the redox potential in AF can enhance metabolic pathways, enabling a smoother flow of electrons and lowering activation energy barriers. This improves substrate utilization rates, product yields, and speciation. This augmented system, known as electro-fermentation (EF), has tremendous potential to revolutionize fermentation technology by offering an exogenous electricity supply (Chandrasekhar and Venkata Mohan 2014; Luo et al. 2022; Nagarajan et al. 2022).

Ultrasound waves that exceed 20 kHz have emerged as an eco-friendly option for processing agri-foods. This sound technology applies a cavitation process, during the formation of bubbles and their burst, leading to a sterilization effect on food and drink products. Ultrasonication aids in the deactivation of enzymes and microorganisms by disrupting the cell membrane (Gavahian et al. 2022). Ultrasonic systems are easily applicable on an industrial scale as they do not require immersion of the product into a liquid medium. This allows hydrophilic nutritional compounds to be maintained, enabling these systems to be employed on a large scale. Wineries have successfully employed this emerging technology to enhance wine aroma, flavor, color, and phenolic profile. Research has uncovered the benefits of ultrasonic technology on wine fermentation and aging. This innovative approach improves wine quality by increasing the key aging indicators including phenolic substances and color intensities and deactivates microbes. Furthermore, ultrasound application results in enhanced physiological, phytochemical, biochemical, and organoleptic characteristics of alcoholic drinks. Celotti et al. (2020) investigated the influence of high power ultrasound on anthocyanins and phenolic levels in red young wines. Following 15 and 30 days of storage, the tannin content of the treated wine decreased by 15% and 40%, respectively, due to the higher ultrasound amplitude (81%). This suggests that high power ultrasound can be used to significantly reduce the tannin content of red young wines, making them less bitter and more palatable. Moreover, Zhang et al. (2016) studied the physicochemical characteristics of red wine after ultrasound treatment. 240 W of power ultrasound, a frequency of 80 kHz, and a temperature of 20 °C are considered optimal conditions for ultrasound application in red wine processing. A significant change was observed in total phenolic compounds, electrical conductivity, and chromatic characteristics of the samples. However, pH or acidity titratable did not differ significantly. These studies provide evidence that ultrasound treatment can be used as an effective tool to manipulate the physicochemical characteristics of red wine.

The benefits of producing lactic acid from renewable sources have sparked much interest across different fields. The petrochemical industry has embraced this approach for its high yield and cost-effective productivity using readily available substrates (Zhao et al. 2016). However, the disposal of biomass and waste materials from various sources poses a significant environmental challenge (RedCorn and Engelberth 2016). The ideal solution is an integrated biorefinery platform that produces high-value bioproducts while addressing waste management. The potential applications of fermentation-produced optical pure lactic acid in the food, pharmaceutical, cosmetic, and the textile industry have made it a highly promising option for packaging materials. Polylactic acid, derived from natural resources, is a green substitute for petrochemical-based bioplastics. While biodegradability is a significant advantage, lactic acid's high price production has hindered the widespread application of this material (Bastidas-Oyanedel et al. 2015; Kumar et al. 2019).

In developing countries, small-scale food fermentation technologies have been refined through practical wisdom rather than scientific innovation. As a result, many manufacturers need more certainty about modernizing and altering their fermentation processes. However, it is crucial to enhance the safety and quality of fermented foods while preserving their distinctiveness and keeping production costs low. One practical approach is the consortium method, which has successfully improved Thailand's small-scale soy sauce fermentation (O’toole 2019). This approach facilitates ongoing collaboration between industry and scientists, providing the latter with the necessary research focus to help the industry thrive. While the small-scale fermentation industry has hesitated to embrace starter cultures due to concerns over the loss of unique flavor, modern molecular biology techniques have ushered in a new era of tailored starter culture development. In recent studies, microflora from distinct product origins exhibited variations in sensory quality and composition, highlighting the potential for customization. To support this trend, a cell bank is currently in the works as a resource for Thai fermented pork sausage, intending to ease the implementation of starter cultures in production (Østergaard et al. 1998; Mongkolwai et al. 1997; Valyasevi and Rolle 2002).

Fermentation in the food industry as an environmentally friendly alternative to improve nutritional value

Global population growth often correlates with increased demand for food and energy. Large amounts of food waste have been generated by industrialization and lack of proper waste management strategies (Ng et al. 2020). By 2030, 2.1 billion tons of food waste will be generated annually, according to a Boston Consulting Group report (Martin-Rios et al. 2021). The agricultural and food processing industries face two major challenges. On the one hand, it is critical to limit their impact on the environment to minimize climate change effects. Conversely, the insufficiency of superior alternatives to health-promoting diets (Rastogi et al. 2022). Food shortages and environmental consequences result from lost and wasted agricultural output during processing and distribution (Read et al. 2020). A high proportion of nutrients are found in plant-based food processing waste, including pulp, peels, and silage, but these materials are typically disposed of in landfills or washed into water bodies, causing the fast depletion of dissolved oxygen (Ishangulyyev et al. 2019). A high sugar, refined carb, processed meat, artificial additive, and trans-fat diet is also linked to obesity, Type 2 diabetes (T2D), hormonal imbalances, and cardiovascular disease (Tandon et al. 2022). Food fermentation technology has a number of advantages, including environmental and health benefits (Paramithiotis et al. 2022; Rastogi et al. 2022). In fermented foods, microorganisms and enzymes are involved in the enzymatic transformation of food substances, emphasizing microbial changes as the distinguishing feature.

A wide range of fermented products make up FFs, including fermented meat, fish, dairy products, fermented fruits, and alcoholic drinks. Furthermore, they include vinegar, cocoa, soy sauce, fish sauce, and coffee (Gänzle 2022). Industrial FF production has evolved from household techniques. Fermented beverages are uncontrolled at household levels due to ubiquitous microorganisms. Traditional fermentation, despite being economical, also preserves food (Adesulu and Awojobi 2014). A functional microorganism provides the health benefits of antibacterial, antioxidant, and peptide synthesis in FFs. Additionally, fermentation can produce nutritious foods and sustainable food supplies. Compared to traditional chemical synthesis methods, fermentation is more flexible, cost-effective, and environmentally friendly (Fig. 1). There has been more investigation into fermentation-based synthesis, optimization, and downstream of medicines, biofuels, biofertilizers, and biodegradable polymers (Rastogi et al. 2022). Microbiological fermentation converts green waste into valuable products. Food waste is considered edible or inedible fractions originating from animals or plants generated before or after consumption (Torres-León et al. 2021). Fermentation technique for bioconversion is significantly influenced by the type of food waste used. Solid-state fermentation is often performed on solid substrates to improve nutrient efficiency, while submerged fermentation is generally used on liquid substrates (Sadh et al. 2018). Due to its low cost, high productivity, and simplicity, submerged fermentation is more commonly used in industrial-scale fermentation. Food waste is considered an excellent input for microbial fermentation due to its abundance of phenolics, proteins, fatty acids, minerals, and several bioactive ingredients. Therefore, the biotransformation of these rich sources allows value-added outputs without waste treatment (Dursun and Dalgıç, 2016; Ng et al. 2020). Food processing wastes can be used to produce enzymes, biofuels, oligosaccharides, growth-promoting agents, polysaccharides, bioplastics, proteins, and bioactive compounds (Sadh et al. 2018; Torres-León et al. 2021).

Fig. 1.

Fig. 1

Fermentation’s primary benefits. “Created with BioRender.com”

Lipids extracted from waste materials can also be precursors to bioethanol synthesis (96%) through fermentation (Ashokkumar et al. 2022). Reducing waste, increasing energy production, and developing other healthcare products are all enhanced by transforming organic waste into value-added bioproducts. Bioproducts such as protease enzyme have been produced by microbial fermentation of food waste (De Castro et al. 2015; Mathias et al. 2017), β-glucosidase enzyme using brewer´s spent grain (BSG) as substrate (Leite et al. 2019), antioxidant peptides using microorganism fermentation (Aspergillus oryzae) and turbot skin as substrate (Fang et al. 2017). Sepúlveda et al. (2020) conducted a study to develop ellagic acid using polyphenols from orange peel wastes through submerged fermentation. This study demonstrated the effectiveness of this method for converting molecules present in orange waste to produce high-value products like ellagic acid. A combined submerged and solid-state fermentation method using Neurospora intermedia was successfully used by Gmoser et al. (2019) for the conversion of waste bread into protein and carotenoids. By using wheat waste as a substrate, Dursun and Dalgıç (2016) achieved astaxanthin pigment production by four different yeast species. It is difficult to estimate the bioproducts produced through bioconversion processes due to the unidentified exact amounts of bioactive content of food waste. Thus, innovative biotechnology techniques must be employed to optimize the reutilization and recycling of food-processing and agricultural wastes (Ng et al. 2020).

Consumers' desire for healthier foods drives manufacturers to seek out new methods of preparing food (Adebo et al. 2018). While FFs were initially developed to prolong foods’ shelf-life, they are now commonly used to enhance food safety, sensory quality, and nutritional value (Macori and Cotter 2018). Lately, there has been a surge in awareness of FFs as possible sources of functional foods (Adebo et al. 2018). The fermentation process alters substrates and generates biologically active or biologically available final products, improving nutritional and functional properties. Fermentation by-products such as organic acids, ethanol, and bacteriocins minimize contamination risk (Marco et al. 2017). Beneficial microorganisms, or derivatives obtained from fermentation may contribute to the health benefits of FF consumption (Adebo et al. 2018; Macori and Cotter 2018; Marco et al. 2017).

Fermentation changes the nutritional and bioactive qualities of food matrices. This is due to the combined effects of the raw material's enzymatic activity and microorganism metabolism (Savaiano 2014). In plant-based fermented foods, lactic acid bacteria produce glycosyl hydrolase, esterase, decarboxylase, and phenolic acid reductase to convert phenolic substances into physiologically active metabolites (Filannino et al. 2015). The fermented dairy products contain biologically active peptides such as yogurt, cheese, fermented milk, kefir, dahi, etc. These peptides have anti-thrombotic, anti-hypertensive, immune-modulatory, osteogenic, and antioxidant properties. LABs generate biological peptides by breaking down dairy proteins (Pihlanto and Korhonen 2015). Fermentation metabolites vary by strain, but lactic acid (LA) is the primary product. Lactic acid can reach 1% in several LAB fermentations. Pro-inflammatory cytokines, bone marrow-derived macrophages, and dendritic cells are diminished by LA in a dose-dependent manner (Iraporda et al. 2015; Marco et al. 2017). Despite the enhanced availability of trace minerals and vitamins, fermentation of plant and dairy matrices amplifies the production of vitamins, particularly folate, riboflavin, and B12 (Macori and Cotter 2018; Marco et al. 2017). Fermentation quality depends strongly on the activity of the microorganisms involved in the process and the substrate used in fermentation. As prebiotics, fibers enhance fermentation bacteria's microbial population, while also influencing the biochemical profile of the final products with health benefits (Adebo et al. 2018). Intestinal health can be positively impacted by short-chain fatty acids including butyric acid, propionic acid, and acetic acid derived from dietary fiber fermentation (Hati et al. 2019; Kang et al. 2021). Fermentates may also provide some health benefits of FFs. A fermentate is a powdered preparation incorporating beneficial bacteria, metabolites, and bioactive components derived from fermentation and substrates (Mathur et al. 2020). A range of fermentates containing different ingredients have been shown to have beneficial outcomes, including effects on gut health due to the production of lactose-hydrolyzed products for lactose intolerant individuals and the production of glycosylated products using β-galactosidases enzyme (Saqib et al. 2017), regulates food intake and prevents weight loss using glucagon-like peptide-1 (GLP-1) (Cho et al. 2014; van Bloemendaal et al. 2014), the anti-inflammatory activity of paraprobiotic CP2305 (Lactobacillus gasseri CP2305) by affecting the growth of fecal Bacteroides vulgatus and Dorea longicatena, which are involved in intestinal infection (Nishida et al. 2017), as well as the potential benefits of heat-killed bacteria in treating dermatological disorders (Piqué et al. 2019). Heat-killed Lactobacillus kunkeei YB38 increased bowel movements and improved the intestinal environment in humans, according to Asama et al. (2016). Warda et al. (2019) found that long-term intake of an ADR-159 diet containing inactivated lactobacilli had no negative effects on health outcomes of male mice.

Fermented foods and non-communicable diseases

Dietary habits are significant in the hierarchy of essential factors triggering non-communicable diseases (NCD). High saturated fatty acids, sodium, a sedentary lifestyle, and a diet poor in fruits and vegetables are some risk factors for developing NCD (Angeles-Agdeppa et al. 2020). From a health stance, integrating FFs into the daily diet has been in the spotlight of several investigations. The presence of beneficial microorganisms such as LABs concomitantly with their biologically active metabolites has been associated with several positive effects concerning NCD (Mathur et al. 2020). LAB fermentation technologies provide various bioactive substances with potential health benefits (Mathur et al. 2020).

The health benefits generated from fermented products are mainly regarded as the metabolic activities of the fermenting microbial community or their biologically active metabolites (Table 1). As an example, various LABs have been found to produce exopolysaccharides (EPSs) during fermentation. The produced EPSs have been related to different health benefits, including antidiabetic, cholesterol-reducing, antioxidant, and immunomodulatory effects (Nampoothiri et al. 2017; Patel and Prajapat 2013). EPSs derived from LABs exhibit their anti-cholesterol activity by alleviating cholesterol assimilation in the intestine and inducing the release of bile acids (Nampoothiri et al. 2017). Among FFs, fermented dairy products have been linked to a variety of health benefits. Dairy products represent a rich source of proteins, fat, and lactose which generate different bioactive molecules due to their enzymatic activities. During fermentation, several different LAB strains may secrete enzymes that help break down complicated inedible substrates into more easily digestible ones. These enzymes include β-galactosidase, amylase, protease, lipase, and glucoamylase (Macori and Cotter 2018; Marco et al. 2017). The secretion of the β-galactosidase enzyme facilitates the breakdown of lactose, thus addressing lactose intolerance. Despite facilitating nutrient absorption, particularly in fermented cereals, LABs contribute to removing toxic compounds such as phytic acid by enhancing phytase activity (Marco et al. 2017).

Table 1.

Fermented products and health relationship

Category Food matrix Microorganisms Influential compound Health benefits References
Fermented dairy Milk Lactobacillus plantarum PU11 ACE-inhibitory peptides and GABA Anti-hypertensive Nejati et al. (2013)
Fermented dairy Milk L. lactis NRRL B-50 571, L. lactis NRRL B-50 572 ACE-inhibitory peptides Hypotensive and heart rate-lowering Rodríguez-Figueroa et al. (2013)
Fermented dairy Kefir Mixed flora Not specified Antifungal effect Gamba et al. (2016)
Fermented plant-based foods Dosa batter, curd, handva batter, soycurd and fermented cabbage L. fermentum PH5, PD2 Not specified Hypocholesterolemic effect Thakkar et al. (2020)
Fermented dairy Kule naoto L. rhamnosus BFE5264 and L. plantarum NR74 Not specified Reduction in cholesterol absorption in Caco-2 cells Yoon et al. (2013)
Fermented edible insects Mealworm and Grasshopper flour L. lactis (NRRL B-50571, NRRL B-50572 Polyphenolic compounds Antioxidant and antihypertensive activity Mendoza-Salazar et al. (2021)
Fermented plant-derived milk Soy milk L. rhamnosus C2, C6 and L. casei NCDC 17, 297 Polyphenolic compounds Antioxidative activity Subrota et al. (2013)
Fermented dairy Fermented goat milk with passion fruit by-product Lactobacillus casei Lc-1, Streptococcus thermophilus TA040 Short chain fatty acids, polyphenolic compounds Modulation of gut microbiota Neves Casarotti et al. (2020)
Fermented plant-based foods Pag-sian-dorng L. plantarum BCC 47723 Complex glycopolymers and proteins, teichoic acids found in cell surface Zearalenone removal Adunphatcharaphon et al. (2021)
Fermented dairy Cow, Buffalo and goat milk Lactobacillus helveticus, Lactobacillus delbrueckii subsp. bulgaricus, and Streptococcus thermophilus Proteolytic enzymes Casein allergy Anggraini et al. (2018)
Fermented dairy Bovine milk Enterococcus faecalis VB63F Proteolytic enzymes Hypoallergenic Biscola et al. (2016)
Fermented plant-based foods Peanut pulp Bacillus natto Proteolytic enzymes Hypoallergenic Jiang et al. (2020)
Fermented plant-based foods Soybeans Bacillus subtilis Proteolytic enzymes Hypoallergenic Yang et al. (2020)
Fermented plant-based foods Myriciaria dubia Mc. Vaugh L. helveticus (ATCC 12046) and L. plantarum (NCDO 1193) α-Amylaseα-Glucosidase Anti-diabetes, hypertension Fujita et al. (2017)
Fermented plant-based foods Moringa oleifera LAB Not specified

Decreases hepatic adiposity and ameliorates

Glucose intolerance

Joung et al. (2017)
Fermented plant-based foods Carica papaya, L Not specified Papain protection from the oxidative damage associated with diabetes Raffaelli et al. (2015)

Intake of fermented dairy was correlated with a lower incidence of cardiovascular diseases. Furthermore, additional research quantifying the functional impact and side effects may give a more understandable mechanism (Zhang et al. 2020a). Moreover, anti-hypertensive angiotensin-converting-enzyme (ACE) inhibitor peptides in fermented dairy products are particularly interesting (Fekete et al. 2015). The anti-hypertensive effect is also induced by several bioactive compounds in fermented dairy, including valyl-prolyl-proline and isoleucyl-prolyl-proline (Nongonierma and FitzGerald 2015). Among NCDs, cancer has been regarded as one of the most critical diseases closely related to dietary habits. It is predicted that 30–40% of cancer cases may be averted by modifying risk factors and behavioral modifications, the most important of which is food. There is evidence that suggests that consuming FFs may lower cancer risk due to the presence of specific nutrients (Tasdemir and Sanlier 2020). The occurrence of diverse reactive oxygen species and other free radicals due to various metabolic reactions beyond the tolerance levels disrupts body homeostasis. The presence of disorders at the cellular level advances the appearance of cancer. Antioxidants are assumed to impair carcinogenesis by preventing DNA from free radicals, slowing cell proliferation in response to oxidants, and triggering apoptosis (Khurana et al. 2018; Tasdemir and Sanlier 2020). Fermentation is finalized by producing specific products with robust antioxidant properties, including phenolic compounds, anthocyanins, EPSs, and bioactive peptides (Kok and Hutkins 2018; Marco et al. 2017; Tasdemir and Sanlier 2020). Gao et al. (2013) have outlined the anti-tumor effects of bioactive substances generated from FFs on the gastric cancer cell line SGC7901. Conversely, T2D significantly contributes to an individual’s reduced life expectancy (Sivamaruthi et al. 2018). Several in vitro, in vivo, and clinical investigations have reported the antidiabetic impacts of FFs. (Fujita et al. 2017) have noted that camu-camu fermented with LABs can support T2D and hypertension. Furthermore, Raffaelli et al. (2015) outlined that fermented papaya fruit can mitigate diabetes-related oxidative damage. By increasing membrane permeability, fermented papaya fruit improves platelet function. Fermented Moringa oleifera could ameliorate glucose intolerance in high-fat diet obese mice (Joung et al. 2017).

Fermented foods have been reported to have an antidiabetic effect in numerous scientific studies. Algonaiman et al. (2022) investigated the antidiabetic and hypolipidemic properties of fermented oat extract in rats. The study found that the fermented oat extract had a significant effect on blood glucose levels and lipid profile of the rats. It also improved body weight and decreased oxidative stress in the rats. The results suggest that fermented oat extract may be a potential alternative for the management of diabetes. The antidiabetic properties of lactic acid bacteria isolated from traditional fermented foods were evaluated by Cai et al. (2019). The results showed that the lactic acid bacteria were effective in reducing blood glucose levels and had a protective effect against oxidative stress. This suggests that lactic acid bacteria could be used to develop functional food products for the management of diabetes. Two Lactobacillus species were used in the study by Feng et al. (2018a, b) to assess fermented buckwheat's antidiabetic effects. They reported that tartary buckwheat fermented with L. plantarum TK9 and L. paracasei TK1501 has the potential to regulate blood glucose in diabetics. Antidiabetic effects of fermented lettuce extracts were studied by Jeong et al. (2021). This study indicates fermented lettuce extract could be considered an effective additive to diabetic foods to balance blood glucose levels and improve insulin resistance. The antibacterial and antidiabetic properties of synbiotic fermented milk have been studied by Shafi et al. (2019). In diabetic rabbits, the product was found to reduce blood glucose levels, urea levels, and creatinine levels. Antioxidant, antimicrobial, and antidiabetic activities of probiotic-fermented blueberry juices were significantly improved compared to non-fermented juices (Zhong et al. 2021).

Additionally, bioactive metabolites of fermentation are well-known for their immune-modulatory properties. Consumption of FFs has been associated with increased IgA-producing cells and enhanced macrophage activity (Park and Bae 2016). Immunomodulation is related to the generation of cytokines such as IL-12, tumor necrosis factor-gamma (TNF-y), and interferon-y (IFN-y) as a consequence of increased T cell and dendritic cell activity (Jones et al. 2014). Irritable bowel syndrome (IBS), for example, may also be controlled with fermented foods like kimchi, Crohn’s disease, and infections caused by external invasions or poor eating habits (Han et al. 2020; Kim and Park 2018; Seong et al. 2021). Glucagon-like peptide-1 (GLP-1) is a significant hormone linked to suppressed appetite, and it has been hypothesized that inducing GLP-1 reduces appetite and food consumption (Cho et al. 2014; van Bloemendaal et al. 2014). (Chaudhari et al. 2017) have reported that fermentates of Lactobacillus helveticus induce the proglucagon and secretion of GLP-1 in STC-1 (pGIP/Neo) cells.

Food allergies

Allergy is one of the most severe NCD associated with food intake. Although food-related allergies are estimated to affect 1–10% of the population, the prevalence of the condition is reported to be higher in children, reaching 5–12.6% (Pi et al. 2022). Foods like milk, egg, shellfish, peanut, soy, wheat, and fish are most commonly associated with allergies (Ricci et al. 2019). Food allergies typically appear within two hours of exposure because there is no immunological and clinical tolerance to the food allergen (Barni et al. 2020). Because it is almost impossible to exclude allergens from dietary patterns, processing these items has received greater significance (Fu et al. 2019). Physical, chemical, and biological processes may reduce allergens in food. Compared to other existing procedures, fermentation is also convenient and safe, besides improving the physicochemical and nutritional value of the foods (Pi et al. 2019). Fermentation alleviates food allergies in several ways. High molecular substances, including proteins, may be broken down through fermentation into more tolerable low molecular entities like small molecule polypeptides and amino acids, causing an alteration in structure and altered characteristics (Fu et al. 2019).

A number of pathways occur during fermentation that reduce the allergenicity of food allergens, such as proteolytic enzymes, denaturation by acidic environments, glycosylation, and the Maillard reaction (Pi et al. 2019). Several metabolites formed from fermentation can regulate the immune system by adjusting the proliferation and cytokine release from T cells, Th 17 cells, and Treg cells (Dargahi et al. 2019). For instance, propionic acid produced from fermentation induces dendritic cells to generate TGF-b and retinoic acid. TGF-b and retinoic acid cause a switch of naive T cells to Tregs and inhibit Th2 generation. Additionally, fermentation metabolites such as 10-hydroxy cis-12-octadecenoic acid and linoleic acid escalate intestinal barrier function and lower systemic food allergen levels (Hirata and Kunisawa 2017). Moreover, the soy-derived acidic polysaccharide APS-I has also been shown to stimulate IgA synthesis in the intestines (Cao et al. 2019). pH, temperature, and substrate are among the processing parameters in the allergenicity reduction is microbial strain utilized in fermentation. Fermentation's influence on dietary allergies is most visible in some foods, such as peanuts, soybeans, milk, etc. (Fu et al. 2019). For instance, allergenicity in fermented cow, buffalo, and goat milk was reduced after co-cultivation of Lactobacillus helveticusLactobacillus delbrueckii subsp. bulgaricus, and Streptococcus thermophilus (Anggraini et al. 2018). Likewise, the proteolytic activity of Enterococcus faecalis VB63F decreased the allergenicity of fermented bovine milk by degrading the protein fraction (Bos d 9–11) responsible for the allergic reaction (Biscola et al. 2016). Bacillus spp. has been reported to exhibit anti-allergic effects when used in several plant-based foods' fermentation. For instance, results showed that the allergenicity of peanut protein could be reduced by using Bacillus natto in a fermentation process using peanut pulp (Jiang et al. 2020). Moreover, according to Yang et al. (2020), Bacillus subtilis showed the most significant hypoallergenic impact (44.5%) in the allergenicity of soybean when compared to other fermenting bacteria. Mecherfi et al. (2019) reported that Lactococcus lactis reduced gluten-related sensitization. The primary epitopes responsible for wheat allergy were found in the gliadin repeating domain hydrolyzed by L. lactis. Multiple bacterial strains used in fermentation are more effective in alleviating food allergenicity. Nevertheless, it should not be underestimated that some strains can produce bitter peptides that negatively affect the taste of the fermented product. Consequently, fermenting food offers a new approach to lowering the allergenicity of diverse foods when combined with other processing methods, such as heat treatment, pulsed light, and ultrasonication (Pi et al. 2019).

Fermentation microbiology

Fermentation is an ancient activity dating back to the earliest human civilizations when scientific principles were not yet recognized and studied (El-Mansi et al. 2019). According to the International Scientific Association for Probiotics and Prebiotics (ISSAP), foods that have undergone microbial growth and enzymatic conversion are defined as fermented foods (Marco et al. 2021). Fermentation helps to preserve foods, making them last longer and making them easier to digest. It also adds flavor, texture, and nutrition to foods, making them more appealing to consumers. Additionally, fermentation helps to break down complex compounds into simpler forms that can be more easily absorbed by the body. During food fermentation, complex components are broken down into simpler parts, many of which may be biologically active, using microorganisms (Macori and Cotter 2018). Available scientific data indicate that many fermented foods contain both nutritive and non-nutritional components that can control particular target processes in vivo related to consumer well-being and health (Tamang et al. 2016). The presence of microorganisms in fermented foods can provide consumers with numerous health benefits, such as probiotic properties, antibacterial properties, antioxidant properties, and peptide synthesis (Tamang et al. 2016). Therefore, regular consumption of fermented foods may significantly contribute to improved human health.

Fermentation is a widely used process in the food industry, and its products are diverse and beneficial to our health. Different types of fermentation can be categorized based on the microorganisms involved in the fermentation process, the primary metabolites produced by these microorganisms, the raw materials used, the fermentation method, oxygen demand, pH level, and nutritional metabolism (Vilela et al. 2019). The most common category, based on the microorganisms responsible for the fermentation and its product, is acetic acid (vinegar), lactic acid (dairy products, vegetables, cereals, meat), ethanol/alcohol (baking, brewing, winemaking), alkaline (Japanese natto) (Vilela et al. 2019). Fermentation typically involves the utilization of compounds from the feedstock by microorganisms such as yeast and lactic acid bacteria (LAB) like Lactobacillus, Lactococcus, Pediococcus, Enterococcus, and Streptococcus, commonly found in fermented milk products. These microorganisms produce a variety of compounds, including alcohols, acids, and gases, during the fermentation process. These compounds can be used to produce a variety of products, such as fermented dairy products and alcoholic beverages. As a subfield of bioengineering, fermentation has gained increasing attention from a variety of fields, including microbiology, chemical engineering, genetic engineering, cell engineering, mechanical engineering, software, and computer hardware (Feng et al. 2018b). There is no doubt that fermentation is a significant field of research and that its potential applications are still expanding. Fermentation can be applied to manufacture pharmaceuticals, chemicals, and biofuels, and produce food, beverages, and animal feed. It is an efficient and cost-effective process, and can also be used to produce renewable energy. Multiple microbe interactions lead to fermented foods, primarily traditional fermented foods. During food fermentation, flavor-active compounds form due to proteolysis and hydrolysis of peptides, with the conversion of amino acids and the formation of flavor-enhancing amino acid compounds (Zhao et al. 2016). Many fermented filtrates or extracts have potential health benefits, including high nutritional value, antioxidant activity, gut microbiome balance, and immune enhancement (Kim et al. 2019). Highly selective biocatalytic processes regulate complex systems of biochemical reactions. It should be noted, however, that not all enzymes are 100% selective. Proteases, for instance, can freely bind to many substrates with similar chemical structures, reducing their efficiency. Thus, it is essential to consider these potential limitations when attempting to develop biocatalytic processes. To address this issue, enzymes can be engineered to be more selective by altering the active site of the enzyme or by introducing allosteric regulation. Additionally, enzymes can be used in combination with substrate-binding proteins to increase their selectivity. Biocatalysis selectivity is enhanced by localizing the enzyme reaction to a specific compartment or environment (Zakharchenko et al. 2018). Gene expression regulates enzyme concentration chemically. For example, the composition and sugar content of the fruit varies according to species, stage of development, and variety. Genetic control of sugar metabolism to improve fruit quality is essential (Desnoues et al. 2016). Therefore, biocatalysis selectivity can be improved by regulating gene expression according to the environment, resulting in improved fruit quality.

Potential probiotics and starters

A probiotic is a live microorganism that provides health benefits to its host when administered in sufficient amounts. In order to grow and form colonies in the digestive tract, probiotics must be resistant to stomach acid and bile (Saad et al. 2013). It is generally understood that probiotics are derived from a heterogeneous group of LAB (Lactobacillus, Enterococcus) and Bifidobacterium genera, such as lactic acid bacteria and those commercially available for human consumption. Although yeasts play a major role in food and are widely distributed, they have not yet been well investigated as potential probiotic candidates. As probiotics, yeasts and other microbes are also being developed (Kim et al. 2019; Suez et al. 2019). Foods containing such bacteria belong to the functional foods category, which describes foods that have a health benefit. In the 1980s, Japan first used the term "functional food" to describe foods enriched with ingredients that have physiologically beneficial effects (Topolska et al. 2021). As well as producing proteinaceous antimicrobial agents, LABs also produce bacteriocins. Bacteriocins are peptides that exhibit antibacterial activity against food spoilage organisms and foodborne pathogens but do not affect producer organisms (Moradi et al. 2020). Clinical relevance of probiotics was first reported in the literature for the treatment of diarrhea, ulcerative colitis, and pouchitis. There are two critical factors when choosing a probiotic candidate regarding potential health benefits. Viability and quantity upon ingestion, survival and stability in the digestive system (Di Cagno et al. 2020). Vera-Pingitore et al. (2016) identified strain L. plantarum Q823 as a viable probiotic candidate for use during fermentation of quinoa-based beverages. Despite growing in quinoa-based products, this strain survives and colonizes the human GI tract. Akkermansia muciniphila has attracted excessive attention recently and is considered a potential probiotic because other studies demonstrated a causal relationship with obesity, inflammation, cancer, and metabolic abnormalities (Dao et al. 2016). As integral commercial starter cultures, LABs play an essential part in food fermentation by breaking down carbohydrates into more minor metabolites, including lactic acid, acetic acid, or carbon dioxide. Fermented food manufacturers can get starter cultures readily available in a highly concentrated form or create a custom culture. Selecting the proper factory is determined by the quantity of products that need to be produced. Factors such as the level of automation, microbiological expertise, production costs, and economic considerations all come into play.

Additionally, microbial starter cultures play a crucial role in maintaining a product's quality and functionality, including taste, texture, pH, and alcohol content (Bachmann et al. 2015). Industrial food fermentation uses lactic acid yeast, and ongoing research is focused on improving them (Table 2). A starter medium should have desirable properties such as durability in process, rapid growth, high biomass and yield, and specific organoleptic characteristics (Smid and Kleerebezem 2014).

Table 2.

Fermentation starter microorganisms in various products

Fermented products’ name Bacteria involved in fermentation Type of fermentation Place/origin consumption References
Kefir Lactic acid bacteria (LAB) Starter culture Caucasus Lopitz-Otsoa et al. (2006)
Sucuk Lactic acid bacteria (LAB) Starter culture Türkiye Bingol et al. (2014)
Kimchi Lactic acid bacteria (LAB), Leuconostoc, Weissella, and Lactobacillus Spontaneous, added commercially Korea Noh et al. (2016)
Sourdough bread Yeasts, lactic acid bacteria (LAB), and acetic acid bacteria (AAB) Spontaneous, starter, added commercially Middle East and Europe Landis et al. (2021)
Nham P. pentosaceus and L. Namurensis, Lactic acid bacteria (LAB) and nitrate-reducing bacteria Starter culture Thailand Kantachote et al. (2015)
Tempeh R. oligosporus Starter culture, backslopping Indonesia Ahnan‐Winarno et al. (2021)

Utilization of extremophiles in fermentation

The term “extremophile” describes organisms that survive under challenging environmental circumstances (temperature, pH, salinity, and pressure) and is receiving significant interest due to their capacity for catalyzing reactions and the possibility of practical utilization in extreme environments (Gupta et al. 2014). Among the substrates they address are acidophilic, alkaliphilic, halophilic, xerophilic, thermophilic, psychrophilic, methylotrophs, and gaseous substrates (Adebo et al. 2017). It is imperative that a practical approach to controlling aflatoxin B1 (AFB1) is developed, as its presence in food can be a serious health concern. Thermophiles can also contaminate food. Powdered milk products can be contaminated by Anoxybacillus flavithermus and Geobacillus spp. (Irwin 2020). Lactase activity is lacking in Geobacillus thermoglucosidasius and it grows slowly in fat-free milk, dependent on A. flavithermus presence to provide them with glucose and galactose for growth (Zhao et al. 2018). They deliver appropriate nutrients and other substances, such as beta-carotene, which can be used as a pigment or to provide vitamin A, as do Halophiles.

Furthermore, they can spoil highly acidic foods with low water activity, such as Debaryomyces hansenii, an extremophilic yeast. As D. hansenii outcompetes unwanted microorganisms for nutrients and produces antimicrobial metabolites, both extracellularly and intracellularly, it inhibits the germination of Clostridium butyricum and C. tyrobutyricum in cheese brines. The ability of D. hansenii to multiply in cheese and its ability to consume lactate, citrate, lactose, and galactose make it an excellent starter culture for producing cheese.

Furthermore, several reports indicate that D hansenii enzymes may be active in meat fermentation, but they had minimal influence on the formation of volatile substances essential for aroma production in garlic-flavored fermented sausages and model mince (Krüger et al. 2018). In fermented foods, extremophilic lipases and esterases hydrolyze glycerols and fatty acids to produce polyunsaturated fatty acids. Additionally, piezophilic extremozymes are also useful for fermented food products that require high pressure (Zhang et al. 2015).

Fermented dairy products

Fermented foods, especially dairy, represent a rapidly expanding sector of the global food market, making it imperative to recognize and understand dairy fermented foods in the past and present (Kaur et al. 2022). The word “ferment” derives from Latin “fervere”, which means to boil, and is defined as “the chemical breakdown of a substance by bacteria, yeast or other microorganisms, typically by foaming and releasing heat”. Fermented foods are the products of controlled microbiological growth and enzyme transformations of food ingredients, and fermentation is a deliberate and controlled method of achieving desired qualities (Marco et al. 2021). Fermentation is the breakdown of organic molecules into simpler forms by microorganisms (Sharma et al. 2020). By introducing certain microorganisms, fermentation can produce desired flavors and aromas, as well as enhance the nutritional value and shelf-life of foods. In addition, fermentation can help preserve foods by producing antimicrobial compounds, such as lactic acid, which can prevent spoilage.

Fermented dairy products fall into two categories: traditional and non-traditional (Kroger et al. 1992). Conventional fermented dairy products were first produced approximately 10,000–15,000 years ago, when human lifestyle changed from gathering food to producing it (Bintsis and Papademas 2022). This change was due to the domestication of animals and the use of their milk as a food source. The fermentation process was used to preserve the milk and make it more palatable. This allowed for the production of a variety of dairy products such as cheese, yogurt, and kefir. Societies during the Neolithic period consciously preferred to consume different animals' milk for cultural and taste reasons and processed this milk in various ways (Charlton et al. 2019; Salque et al. 2013). Traditional fermentation has been employed for centuries in raw milk processing. The process is spontaneous, and part of the fermented product is used to inoculate the new batch (Galli et al. 2022). In contrast, non-traditional fermented milk products have recently been developed. These products are produced with known microbial cultures based on scientific principles, and their quality can be optimized (Galli et al. 2022; Kroger et al. 1992). Non-traditional fermented milk products are more consistent in quality as the addition of known microbial cultures creates a more controlled fermentation process. This process also ensures that the products are standardized and free of any potential health risks associated with raw milk. It has been reported that probiotic-based fermented functional foods are becoming increasingly popular since the early 2000s (Kaur et al. 2022). From the past to the present, fermentation practices have been influenced by various factors such as raw materials, climatic conditions, production area, social, cultural, religious, and economic aspects (Galimberti et al. 2021). These factors have helped to shape the diversity of fermented products, and have also helped to influence the consumption of probiotic-based fermented functional foods. The popularity of these foods has been further strengthened by the health benefits associated with them, such as improved digestion, increased nutrient absorption, and enhanced immunity. Milk and dairy products are now consumed worldwide, primarily in pasteurized and fermented forms. However, variations in consumption rates are caused by per capita income and the impact of regional preferences (Muunda et al. 2023). This is due to the fact that those with higher incomes can afford to purchase more nutrient-rich foods and have access to a variety of different ingredients to choose from. Additionally, regional preferences play a significant role in the demand for certain food items, as people’s taste and cultural preferences vary from one region to another.

Fermented foods with live microorganisms include yogurt, kefir, cheeses, miso, natto, tempeh, kimchi, kombucha, and some beers (Voidarou et al. 2021). Some foods are subjected to pasteurization, smoking, baking, or filtering after fermentation, causing live microorganisms to die or be removed. Sourdough bread (baked), shelf-stable pickles (heated), sausages (heated), soy sauce (heated), vinegar (heated), most beers, distilled spirits (filtered), coffee and chocolate beans (roasted) are fermented products (Li et al. 2022). Still, microorganisms have died or been eliminated from fermentation. Foods such as fresh sausages, vegetables preserved in brine or vinegar, processed soy sauce, non-fermented dried meats and fish, and acidified cottage cheese are not considered fermented, as live microorganisms are not involved in production. Fermented foods are sometimes called “probiotic foods” or “probiotics” and are used interchangeably. However, using these definitions interchangeably is incorrect (Marco et al. 2021). Probiotics contribute to their beneficial effects when administered in sufficient quantities. They do not have to take a specific form to have a positive effect on the host. Probiotics are live microorganisms that have a beneficial effect on the host, while fermented foods are simply foods that have gone through a process of fermentation (Dahiya and Nigam 2022). The probiotic benefits of fermented foods come from the live microorganisms present in the food, which are not always present in sufficient quantities to have a positive effect on the host. Molecular components of probiotic-containing foods show prophylactic or therapeutic effects against disease-causing agents. These foods are generally known as nutraceuticals, foodiceuticals, functional foods, or medifoods (Kaur et al. 2022). These foods interest consumers based on their nutritional and organoleptic properties and beneficial effects on human health (Luz et al. 2021). The effects of these foods are attributed to the presence of bioactive compounds, which can be of plant or microbial origin. These compounds, such as antioxidants, polyphenols, vitamins, and minerals, have protective effects against disease-causing agents like bacteria and viruses.

The fermentation process produces large quantities of lactic acid, alcohol, or acetic acid that inhibit other microorganisms. They also continue to reproduce unaffected by these generated substances, a process known as “amensalism” (Teng et al. 2021). These by-products generated by the fermentation process are toxic to other microorganisms, making them unable to reproduce. This gives the fermenting microorganisms a competitive advantage, allowing them to outcompete other microorganisms in the environment. Fermented products are usually thicker than milk because acid precipitates milk proteins. Pathogens are inhibited by high acidity and low pH (Kumar 2017). Fermented dairy products have a unique, desirable flavor, texture, aroma, and improved digestibility compared to the raw materials they produce (Bintsis and Papademas 2022). However, the wrong fermentation process poses a health hazard. Unhygienic conditions or improper food production lead to contamination and spoilage. Foodborne disorders are brought on by spontaneous fermentation by unidentified microbes, which promotes the growth of undesired and even hazardous microorganisms (Teng et al. 2021). This can cause food to be unsafe to eat, leading to food poisoning. Symptoms of food poisoning can range from mild to severe, and can even be life-threatening. Therefore, it is important for food producers to take proper steps to prevent contamination and spoilage.

Propionic acid bacteria (PAB) and lactic acid bacteria (LAB) are microorganisms utilized to make cheese and other fermented dairy products. LAB is used to acidify milk, and PAB is used for its aromatizing properties (Thierry et al. 2015). Propionic acid bacteria are microorganisms that produce propionic acid and are involved in producing fermented propionic cheeses, such as Swiss cheese, with exceptional adaptability to technological and physiological stress conditions. The propionic acid fermentation in cheese causes characteristic pores, cracks, and a slightly sweet flavor (Antone et al. 2022; Bücher et al. 2021). Propionic acid bacteria are also responsible for the formation of carbon dioxide during the fermentation process, which gives cheese its airy, spongy texture. This also contributes to the flavor of the cheese, as the carbon dioxide imparts a slightly sour taste. Propionic acid bacteria metabolism differs significantly from lactic acid microorganisms. It is characterized by the production of carbohydrates during fermentation, except for lactic acid, propionic acid, and acetic acid (Vakhrusheva et al. 2022). As a result of PAB's metabolic activities, the product is enriched with organic acids, vitamins (B2, B12, K, and folate), and other nutrients, increasing the stability and nutritional value of food products (Antone et al. 2022). Fermented dairy products provide an ideal environment for probiotic bacteria to grow in the human gut. LAB include Lactobacillus, Streptococcus, Lactococcus, Bifidobacterium, Leuconostoc, Enterococcus, and Pediococcus, which are among the most common strains of probiotic bacteria found in fermented dairy products (García-Cano et al. 2019; Kaur et al. 2022). In addition, yeasts and molds such as Debaryomyces, Kluyveromyces, SaccharomycesGeotrichum, Mucor, Penicillium, and Rhizopus species are employed as fermenting microorganisms (Sharma et al. 2020). Fermented milk products are prepared using different starter cultures, and the types of microorganisms used in production are specified in the regulations (Table 3). Fermentation preserves probiotic properties while maintaining microbial viability and production (García-Cano et al. 2019; Kaur et al. 2022). This helps to ensure that the fermented milk products are safe to consume and that they have the desired probiotic properties. This is because the starter cultures help to control the growth of unwanted microorganisms while promoting the growth of beneficial ones.

Table 3.

Microorganisms used as starter cultures in fermented milk products (CAC 2003)

Fermented dairy products Microorganisms used fermented milk products
Yoghurt

Streptococcus thermophilus

Lactobacillus delbrueckii subsp. bulgaricus

Alternate culture yoghurt

Streptococcus thermophilus

Lactobacillus spp.

Acidophilus milk Lactobacillus acidophilus
Kefir

Starter culture prepared from kefir grains

Lactobacillus kefiri

Lactobacillus kefiranofaciens

Lactobacillus kefirgranum

Kluyveromyces marxianus

Saccharomyces spp.

Lactobacillus spp.

Leuconostoc spp.

Lactococcus spp.

Acetobacter spp.

Kumys

Lactobacillus delbrueckii subsp. bulgaricus

Kluyveromyces marxianus

Due to their resistance to low pH, adaptability to milk and other foods, and GRAS (generally recognized as safe) status, Lactobacillus species are also widely used (Galli et al. 2022). LAB are intentionally added to the product as starter cultures to reduce the ripening period and improve sensory characteristics such as color, flavor, aroma, and texture (García-Cano et al. 2019). Furthermore, food digestibility and product safety are enhanced by LAB fermentation due to the inhibition of spoilage and pathogenic bacteria. Certain LAB strains are considered probiotics because of their positive effects on the gastrointestinal system and human health and their significant roles (García-Cano et al. 2019). Lactic acid bacteria regulate the release of fatty acids. These properties of LAB involve metabolic processes involving enzymes such as lipases, proteases, and antibacterial proteins (Galli et al. 2022). Fermentation of yogurt and cheese results in a pH decrease due to the synthesis of metabolites such as organic acids, lactic acid, hydrogen peroxide, bacteriocin, diacetyl, acetaldehyde, and reuterin (Akbar et al. 2019).

Lactic fermentation and alcoholic fermentation are the two main types of fermentation carried out by microorganisms in fermented milk products, respectively (Galli et al. 2022). In lactic fermentation, lactic acid bacteria are the dominant species. Lactic fermentation products are classified according to LAB characteristics as mesophilic fermented milk, such as buttermilk, thermophilic products, such as yogurt, acidophilic milk, and probiotic products. Alcoholic fermentation occurs in products such as kefir, kumys, and Viili by yeasts and lactic acid bacteria (Galli et al. 2022). Microbial cultures, particularly those having proteolytic activity, are frequently employed in the dairy industry to produce cheese, yogurt, kefir, and other so-called fermented milk products. In manufacturing cheese, proteolytic enzymes are used to coagulate milk proteins and hydrolyze proteins. Proteolytic enzymes extract protein hydrolysates from milk to produce easily digestible dairy products (Kieliszek et al. 2021). Proteases produced by lactic acid bacteria used in lactic fermentation are capable of reducing milk protein allergens, depending on the strain and the proteolysis process. Lactic acid bacteria are a good source of hydrolyzing allergenic proteins in milk, and one isolate (Enterococcus faecalis VB43) was reported to be an excellent potential agent for the production of hypoallergenic dairy products (Biscola et al. 2018). Lactic acid bacteria use β-galactosidase to hydrolyze lactose into glucose and galactose. The hydrolysis of lactose lowers the intestinal pH and promotes the production of lactic acid, which inhibits the growth of microorganisms that cause putrification (Gholamhosseinpour and Hashemi 2019; Sharma et al. 2020). Furthermore, lactic acid is essential for calcium absorption and developing organoleptic properties (Sharma et al. 2020). The bioavailability of minerals such as calcium, potassium, zinc, magnesium, magnesium, potassium iodide, and phosphorus is increased due to the fermentation process of lactic acid bacteria and acidity (García-Burgos et al. 2020).

Several studies are currently being carried out that may be useful for isolating new probiotics and developing fermented milk products with probiotic properties. Luz et al. (2021) examined seven LAB strains isolated from breast milk for their probiotic properties and used Lactobacillus plantarum 5H1 and Lactobacillus plantarum 5L1 strains in the production of probiotic fermented milk. LAB strains have a wide range of antimicrobial activity against pathogenic bacteria and toxicogenic fungi. During the milk fermentation process, an increase in lactic acid content, a decrease in milk pH, and an increase in total bacterial count were observed. During storage, LAB viability in fermented milk remained at 8-log10 CFU/mL. Lactobacillus plantarum 5H1 and Lactobacillus plantarum 5L1 exhibited significant antimicrobial activity, sensitivity to antimicrobials, a broad spectrum of enzymatic activity, adhesion to Caco-2 cells, and reduction of Salmonella enterica adhesion. Furthermore, these selected strains remained viable during fermented milk storage and fermentation at 4 °C. This indicates that these strains are extremely hardy and have the potential to be used as probiotics that can survive through the fermentation and storage process.

The ability of microorganisms in fermented milk products to benefit the host is dependent on the presence of sufficient numbers of probiotic microorganisms in various products as well as the ability of adequate numbers of live microorganisms to reach the human intestine (Farahmand et al. 2021; Ranadheera et al. 2012). Thus, the legislation specifies the minimum number of live microorganisms that must be present in fermented milk products. The total number of microorganisms forming the starter culture used in products named fermented milk, yogurt, alternate culture yogurt, acidophilus milk, kefir, and kumys should be at least 107 CFU/g, the number of yeasts should be at least 104 CFU/g, and the label should be at least 106 CFU/g (Mukherjee et al. 2022). The number of live probiotics during the shelf life of fermented dairy products varies depending on many factors. These factors include the temperature of storage conditions, hydrogen peroxide (H2O2) produced by other bacteria present, dissolved oxygen content due to processing conditions, pH of the end product, acidity, and strain variation. In particular, the decrease in pH during storage, the presence of dissolved oxygen, and the presence of preservatives in the final products are the major factors contributing to the loss of cell viability (Farahmand et al. 2021; Terpou et al. 2017). At the end of their shelf life, 22 of 36 commercial probiotic fermented milk products sourced from the UK and European markets (61.1%) contained more than 106 CFU/g of Lactobacillus strains in accordance with the minimum recommended therapeutic level for probiotics. Rep-PCR was used to differentiate the isolated strains using the GTG-5 primer, and the isolated Lactobacillus species were identified as Lactobacillus acidophilus, Lactobacillus casei, and Lactobacillus paracasei (Farahmand et al. 2021). Another study found many areas for improvement in the number of cultures and accuracy of label information in commercial kefir products. More qualified controls of fermented foods are needed to demonstrate and understand their potential health benefits for humans. Consumers should demand higher levels of accuracy and quality, and regulatory bodies should conduct regular checks on these products (Metras et al. 2021). The antibacterial activity of LAB in fermented milk samples against Salmonella typhimurium, Staphylococcus aureus, Escherichia coli, and Listeria monocytogenes was determined. L. lactis subsp. lactis had a broader antimicrobial spectrum than the other isolates, and the probiotic evaluation of L. lactis showed that it could survive at low pH (pH 3) and 0.3–3% bile salts. It was concluded that LAB with antimicrobial activity is promising against food spoilage and pathogenic microorganisms in foods (Akbar et al. 2019). Hikmetoglu et al. (2020) reported that the microbial content (Lactobacillus spp., Lactococcus spp., Lactobacillus acidophilusBifidobacterium spp., and yeasts) of traditional kefir increased during fermentation and did not change significantly during cold storage of 7 days. Lactose content decreased during fermentation, while lactic acid gradually increased and remained constant during storage. Galactooligosaccharides in kefir samples were found to be stable during storage. The major LAB species isolated and identified from traditional fermented milk in Ghana based on 16S rRNA gene sequencing were Ent. faecium, Lb. fermentum, Lb. plantarum, and Pd. acidilactici (Motey et al. 2021).

Consumers can choose from a variety of fermented milk products. There are a few homemade products among them, but most are manufactured industrially. A variety of fermented milks and derivatives have been developed around the world, each with its own history. The type of milk used, the pre-treatment of the milk, temperature, fermentation conditions, and subsequent technological processes greatly influence their nature. The type of milk used can affect the flavor, texture, and overall characteristics of the fermented milk product. Pre-treatment of the milk can also influence the flavor, such as pasteurization or homogenization. Temperature and fermentation conditions can also have an effect, such as the length of fermentation and the type of starter culture used. Finally, the post-treatment processes, such as packaging and storage, can influence the shelf life and other characteristics of the product. Curd, yogurt, cheese, and kefir are among the most popular dairy foods (Kumar 2017).

Curd is a dairy product obtained by souring milk or decomposing it after adding any acidic substance. In some cases, it can also be made by mixing milk with acidic substances like lemon juice or vinegar. The liquid part is whey, and the solid part is curd. Whey contains the whey proteins of milk, while curd comprises milk proteins or casein (Kumar 2017). Traditionally, the curd is prepared from raw milk or boiled milk. Raw milk can undergo natural fermentation without adding any microorganisms, while boiled curd is prepared by inoculating boiled milk from the previous batch for fermentation (Joishy et al. 2019). It was determined that the main bacterial genera in the curd obtained from boiled milk were Lactobacillus, Leuconostoc, Lactococcus, and Acetobacter. In contrast, the leading bacterial genera in the curd obtained from raw milk were Chryseobacterium, Enterococcus, Lactobacillus, Leuconostoc, Lactococcus, Streptococcus, Klebsiella, Acinetobacter, Pseudomonas, and Enhidrobacter. Lactococcuslactis subsp. cremoris dominated the curd obtained from both raw and boiled milk. Moreover, several metabolites such as 10-methyl dodecanoic-5-olide, ascorbic acid, and 2,2,4-trimethyl-1,3-pentanediol diisobutyrate were significantly higher in curd produced from raw milk, while dodecanoic acid and glycerol 2-acetate were substantially higher in curd produced from boiled milk. Lactobacillus strain and metabolites detected in curd samples were farm-specific (Joishy et al. 2019).

Yogurt is milk's lactic fermentation product. Lactic acid fermentation is the process by which lactic acid bacteria convert milk sugar, lactose, into lactic acid, lowering the pH. Acidification is a key mechanism responsible for coagulation during yogurt fermentation (Muncan et al. 2020). The casein proteins that make up the gel matrix are responsible for the thick structure of the yogurt after it has been coagulated. Casein micelles in milk exist as a colloidal calcium caseinate phosphate complex. The acidification of the milk, i.e., the lowering of the pH, leads to the dissolution of the colloidal calcium phosphate and the release of the casein content from the milk. First, at the beginning of acidification, when the pH value is reduced from 6.7 to 6, only a small amount of colloidal calcium phosphate is dissolved, so structural changes in micelles are limited. When the pH is reduced to 5, the colloidal calcium phosphate is completely dissolved, and when the pH drops to the isoelectric point of casein (pH 4.6), casein micelles aggregate and form the yogurt gel matrix (Muncan et al. 2020). The yogurt cultures Lactobacillus delbrueckii subsp. bulgaricus and S. thermophilus have a symbiotic relationship and produce yogurt with an excellent taste, acidity, and viscosity. L. delbrueckii subsp. bulgaricus can readily utilize pyruvic acid, formic acid, folic acid, and long-chain fatty acids produced by S. thermophilus, while L. delbrueckii subsp. bulgaricus contributes to S. thermophilus growth (Dan et al. 2017). Furthermore, the volatile compounds produced by lactic acid bacteria significantly influence the flavor of the products. The flavor comprises a variety of volatile compounds, including acids, aldehydes, alcohols, ketones, esters, and aromatic hydrocarbons, and each class has its organoleptic properties (Dan et al. 2017; Farag et al. 2022). Yogurt is not a probiotic food, but it contains non-probiotic bacteria from milk fermentation. However, probiotic yogurt can be obtained by adding probiotic bacteria. Also, yogurt products obtained from a mixture of probiotics (L. rhamnosus GG) and prebiotics (dietary fiber) can be received (Kaur et al. 2022). The probiotic bacteria in yogurt contain beneficial bacteria that can help to support the good bacteria already present in the body. They can help to restore the balance of bacteria in the gut, which can help improve digestion and overall health. Prebiotics, on the other hand, are dietary fibers that act as food for the beneficial bacteria, helping them to thrive and grow in the gut. Therefore, combining probiotic bacteria with prebiotics can help to create a more beneficial environment in the gut.

Kefir is acidic-alcoholic fermented milk formed by the fermentation of milk by cauliflower-like kefir grains or starter microorganisms containing lactic acid bacteria, acetic acid bacteria, and yeasts, and is different from other fermented products due to the specificity of starter microorganisms (Al-Mohammadi et al. 2021; Bengoa et al. 2019; Fatahi et al. 2021). Kefir grains are white or light yellow in color, elastic in consistency, 0.3 to 3.5 cm in diameter, and composed of protein and polysaccharides (Al-Mohammadi et al. 2021; Bengoa et al. 2019). Kefir grains comprise approximately 83% water, 4 ± 5% protein, and 9 ± 10% a polysaccharide called kefiran (Bengoa et al. 2019). During fermentation, lactic acid, acetic acid, ethanol, carbon dioxide, organic acids, amino acids, vitamins (E, B3, B6, and B12), minerals (Se, Fe, Zu, and Mn), and enzymes (glutathione peroxidase, catalase, and superoxide dismutase) are formed (Fatahi et al. 2021). The pH of kefir ranges between 4.2 and 4.6, the ratio of ethanol between 0.5 and 2.0%, the ratio of lactic acid between 0.8 and 1%, and the ratio of CO2 between 0.02 and 0.2% (Rosa et al. 2017). Kefir inhibits pathogenic bacteria and fungi, and the inhibitory activity is more robust against bacteria (Al-Mohammadi et al. 2021). The antimicrobial activity of kefir and probiotic yogurt samples produced from cow, camel, sheep, and goat milk was investigated. It was determined that kefir samples had more substantial antifungal and antibacterial effects than probiotic yogurt samples, and kefir and yogurt samples produced from sheep and cow milk showed the highest and lowest antimicrobial activity against S. aureus, E. coli, S. enterica, and L. monocytogenes, respectively. A. niger, S. aureus, and L. monocytogenes were the most susceptible microorganisms, while Penicillium sppand E. coli were the most resistant. Bioactive substances, organic acids, ethyl alcohol, hydrogen peroxide, diacetyl, peptides, possibly bacteriocins, and other inhibitory compounds have been suggested to be responsible for inhibiting the growth of pathogenic bacteria (Azizkhani et al. 2021).

Kumys is a fermented milk product made by fermenting mare's milk in two stages with bacteria and yeasts: lactic fermentation and alcoholic fermentation. The mare’s milk to be used in kumys production should have an acidity of ≤ 0.06% lactic acid, a density of 1029–1033 g/mL, and a fat content of at least 1% (Kondybayev et al. 2021). Fermentation is 1–3 days at about 20 °C (Liu et al. 2019). The consistency of kumys is a liquid, homogeneous, carbonated, slightly foaming drink without any fat particles (Kondybayev et al. 2021). The products of kumys fermentation are lactic acid, ethyl alcohol (0.6–3%), carbon dioxide, and other by-products such as volatile acids, alcohols, and other compounds with strong and distinctive aroma and taste (Afzaal et al. 2021; Kondybayev et al. 2021). According to the lactic acid content, three types of kumys are defined: strong, medium, and light (Afzaal et al. 2021). The fermentation time of kumys does not affect its quality. Milk from fresh mares and mature kumys had the highest chemical and nutritional content, while immature kumys (fermentation time less than 9 h) was not good quality (Liu et al. 2019). The microbiota of raw mare’s milk has a higher microbial diversity than that of kumys. Raw mare's milk is rich in LAB, such as Lactobacillus helveticus, Lactobacillus plantarum, Lactococcus lactis, and Lactococcus kefiranofaciens. In contrast, raw mare's milk contains pathogenic bacteria such as Staphylococcus succinus, Acinetobacter lwoffii, Klebsiella oxytoca, and Klebsiella pneumoniae. The change in microbiota composition and structure could be attributed to the transition from a slightly alkaline environment in raw mare's milk to a highly acidic kumys environment. The acidic environment in kumys inhibited the growth of most environmental pathogens, increased food hygiene, and minimized the risk of infection by endogenous pathogens found in raw mare’s milk (Zhang et al. 2020b).

Fermented foods are also valued for their improved shelf life, safety, nutritional value, and other properties, and are the most widely consumed by humans (Walhe et al. 2021). Fermented dairy products have several health benefits when consumed regularly and in a balanced and appropriate proportion (Kaur et al. 2022). The various health benefits of yogurt, cheese, kefir, and other traditional fermented milk products have been extensively researched. Probiotic strains of bacteria present in fermented dairy products are beneficial for gut health and can reduce the risk of certain diseases (Okoniewski et al. 2023). Additionally, fermented dairy products are a rich source of vitamins and minerals, including calcium, potassium, phosphorus, and B vitamins. Fermented dairy products are an effective treatment method that contains natural ingredients with high nutritional and digestibility, anti-hypertensive, hypo-cholesterolemic, antioxidant, immunomodulatory, and anti-inflammatory properties and fewer adverse side effects (García-Burgos et al. 2020). Probiotic consumption has been shown to positively affect the reduction of ailments from diarrhea to cancer (Akbar et al. 2019). Regular kefir consumption has been linked to benefits for lactose intolerance and the digestive system, as well as antibacterial, antihypertensive, anti-inflammatory, hypo-cholesterolemic effects, plasma glucose control, antioxidant, anticarcinogenic, antiallergenic activity, and wound healing (Rosa et al. 2017). Koskinen et al. (2018) found that low-fat fermented dairy consumption was inversely correlated with cardiovascular disease risk. However, cardiovascular disease risk has been reported with very high consumption of unfermented dairy products and milk. Zhang et al. (2020a) stated that fermented dairy products reduce cardiovascular disease risk. (Lee et al. 2020) reported that Lactobacillus plantarum B719 can be used as an alternative in treating primary postmenopausal osteoporosis. (Fatahi et al. 2021) At 24 and 48 h, the interactions between different concentrations of kefir drink and U87 cancer cells (glioblastoma), the most severe form of brain tumor, were evaluated. As a result, it was discovered that kefir significantly reduced the growth rate of U87 cells at increasing concentrations and had a killing effect. It could be used as a complementary treatment.

Companys et al. (2021) reported that consuming fermented dairy products reduces the risk of stroke and cardiovascular diseases, and consuming yogurt reduces the risk of developing type 2 diabetes mellitus. However, there is insufficient evidence that fermented milk or cheese consumption protects against metabolic syndrome. It is stated that the available evidence on the effect of dietary cheese and yogurt on hypertension is limited and that consumption of smoked cheeses should be limited in hypertensive patients due to their high sodium content. Walhe et al. (2021) isolated three isolates with probiotic potential (Enterococcus faecium (EF), Enterococcus faecium (Chole1), and Lactobacillus pentosus (7MP) from yogurt and determined that among these three isolates, Enterococcus faecium (EF) and Enterococcus faecium (Chole1) produced vitamin B12 in a fair amount (1 ng/mL); whereas, Lactobacillus pentosus (7MP) had the highest cholesterol reduction potential (48%) compared to the others.

Fermented meat products

Meat fermentation is an ancient preservation method widely used to increase meat products’ taste, aroma, palatability, color, tenderness, and shelf life. Meat is exposed to microorganisms or enzyme activities during fermentation, so desirable changes occur in meat biochemistry. The process of fermentation causes proteins and fats to break down, resulting in a more tender meat product and a more intense flavor (Wang et al. 2022). The breakdown of proteins and fats also helps to protect the meat from spoilage, thus increasing its shelf life. Meat physicochemical, biochemical, and microbiological changes run the fermentation process and support the formation of desirable meat products (Kumar et al. 2017). The fermentation process is an essential metabolic process converting carbohydrates into acids, gases, and alcohol, resulting in the conversion of raw meat to fermented meat products through the activities of “cultured” or “native” microorganisms (Kumar et al. 2017). This is because the anaerobic environment formed during the fermentation procedure encourages the growth of some lactic acid bacteria strains (Ravyts et al. 2012). These bacteria strains produce lactic acid that gives fermentation products their distinctive flavor and texture. Lactic acid also acts as a natural preservative, extending the product's shelf life. Fermentation of meat products is performed by lactic acid bacteria on a “native culture” or “starter culture”. Using native flora for meat fermentation may cause many problems, including inconsistent quality. This problem was solved by cultivating a commercial starter culture in a controlled environment to maintain the same quality (Kumar et al. 2017). Pediococcus cerevisiae was the first starter culture for meat fermentation (Deibel et al. 1961). Then, the other species are Lactobacillus sakei and Lactobacillus curvatus among the LAB, Staphylococcus xylosus, and S. carnosus among the coagulase-negative staphylococci and Debaryomyces hansenii among yeasts were also used for meat product fermentation (Alessandria et al. 2014). LABs produce bacteriocins that improve meat quality and stability during fermentation. Bacteriocins are proteinaceous compounds that exhibit antibacterial activity against pathogens. Bacteriocins show bactericidal effects except for eukaryotic cells and are also tolerant of heat and salt (De Vuyst and Leroy 2007). This means that when these compounds are added to the fermentation process, they can help to inhibit the growth of harmful bacteria while also preserving the flavor of the meat. Furthermore, the heat and salt tolerance of bacteriocins ensures that the meat will remain safe for consumption for a longer period of time.

Sausages, dating back to 1500 BC, are the most popular and oldest meat products consumed globally because of their flavor and nutritional function. Generally, sausages are produced from salted minced or chopped meat. They are formed by filling seasoned raw meat with starter cultures into natural or artificial casings, then hanging them to ferment and ripen (Kumar et al. 2017). The starter culture is typically a single LAB species or a LAB mixed with other bacteria (Staphylococcus xylosus or S. carnosus) (Holck et al. 2017).

Microbial spoilage in fermented meats

Microorganisms found in the meat microbiota interact with each other and meat substrate during processing and storage. A small percentage of these microorganisms growing on meat can deteriorate foods through their metabolic activities. For instance, lactic acid bacteria (LAB) produce lactic acid from meat carbon sources. Lactic acid produced by LAB has various positive and negative effects based on the kind of meat product (Lahiri et al. 2022). It also helps to form desirable changes in fermented meats, such as an acidic taste and decreased pH. However, it may cause undesirable changes in other products. Thus, microbial spoilage is a highly complex structure with varying properties depending on the microorganism, substrate, and the nature of the fermented product. Although several microbial metabolic pathways are known that lead to changes in the taste, color, odor, or texture of meat products and stimulate the generation of defined spoilage compounds, the primary mechanism that leads to spoilage still needs to be fully resolved. Therefore, to understand this mechanism that leads to meat spoilage, it is essential to initially comprehend the microbial factors of meat, their interactions, and metabolic activities (Zagorec and Champomier-Vergès 2023). To understand the primary mechanism that leads to meat spoilage, it is important to analyze the microbial components of meat, their interactions, and their metabolic activities. This will help to identify the pathways and mechanisms that lead to spoilage and can help improve food safety and quality.

Mycotoxins in fermented meat

Meat and meat products can be contaminated with toxic compounds, such as mycotoxins, during production, storage, and distribution (Pleadin et al. 2021). Mycotoxins contamination in the final product can be related to raw materials, spices, additives used in production, or hazardous environmental components. Therefore, these toxic components that cause contamination can adversely affect human health (Pleadin et al. 2016). Mycotoxins are produced by certain types of fungi and can be found in crops, grains, and even in animal feed. When these contaminated raw materials are used in the production of meat and meat products, mycotoxins can be passed on to the final product.

Mycotoxins are secondary metabolites produced by molds, responsible for acute and chronic toxicity of humans and animals. Mycotoxin contamination can occur in meat products in these ways; due to meats supplied from animals fed with contaminated feed, the components such as contaminated spices added to the meat products, and can arise as a consequence of the activity of molds growing on the surface of fermented meat (Alapont et al. 2014; Bertuzzi et al. 2013). Ochratoxin A (OTA) and aflatoxin B1 (AFB1) are the most common mycotoxins contaminating fermented meat products. AFB1 is the most common liver carcinogen categorized in group 1 by the International Agency for Research of Cancer (IARC). Aspergillus flavus and Aspergillus parasiticus are known as responsible species for the production of AFB1. OTA is a group 2B carcinogen, and the genus of Aspergillus and Penicillium are responsible for its production (Pleadin et al. 2021). Mycotoxigenic molds isolated from fermented meat products can produce mycotoxins under various conditions, such as environmental temperature, humidity, and water activity during the ripening period of meat products (Pleadin et al. 2015). Several studies have pointed out the possibility of the presence of mycotoxin contamination in fermented meat products as a result of inadequate control of production and storage conditions, indicating the necessity of prevention of contamination that can adversely affect human health (Alapont et al. 2014; Pleadin et al. 2016). Pleadin et al. (2016) observed significant AFB1 and OTA levels in “Slavonski Kulen” fermented sausages as 11.79 ± 2.34 µg kg–1, 16.13 ± 3.32 µg kg–1, respectively. OTA levels in Istrian, Slavonian, and Kulenova Seka fermented sausages were determined as 0.25 ± 0.01 µg kg–1, 0.27 µg kg–1 and 0.26 ± 0.14 µg kg–1, respectively (Kudumija et al. 2020). In another study, OTA levels in İberian ham were noticed as 3.20 µg kg–1 (Rodríguez et al. 2015).

Biogenic amines in fermented meat

Biogenic amines are organic compounds found naturally in many foodstuffs with an aliphatic, aromatic, or heterocyclic structure formed due to microbial decarboxylation of amino acids or the amination of aldehydes and ketones (Santos 1996). These compounds are formed by the action of microbial enzymes on amino acids, and they can contribute to the flavor, aroma, and texture of foods. They are also important as they can act as toxins, leading to food spoilage and safety issues.

It has been known that high-concentration exposure to biogenic amines can lead to toxic effects on respiratory and cardiovascular systems (Tsafack and Tsopmo 2022). Biogenic amines are more frequently found in fermented meat and meat products because of their predisposition to amine decarboxylation by the natural microbial flora. They may be produced during the fermentation stage by the activity of microorganisms while the meat proteolysis. Insufficient hygienic quality of raw material, re-contamination, and deficiencies in production and storage steps significantly impact the formation of biogenic amines (Gernah et al. 2011). In such circumstances, they are also used as a spoilage indicator and poor hygiene conditions for meat products. Lactic acid bacteria that have grown and displayed their metabolic activity on these fermented meat products have a crucial function in forming biogenic amines such as putrescine, cadaverine, histamine, and tyramine (EFSA 2011).

Biogenic amines have been reported numerous times in fermented meat products (Alves et al. 2017; Rabie et al. 2014; Sun et al. 2016). Alves et al. (2017) evaluated the biogenic amine levels of Portuguese and Serbian fermented dry sausages. While histamine was not detected in both sausages, cadaverine, putrescin, and tyramine were found significantly in these samples. Another study assessed biogenic amines in dry-ripened sausages made from different meats (horse, beef, and turkey). The study concluded that the total biogenic amine contents, from highest to lowest, were ranked for turkey, beef, and horse sausages, respectively. The high levels of total biogenic amines originated from the elevated histamine, putrescine, and tyramine content in turkey sausages (Rabie et al. 2014). Sun et al. (2016) observed the high histamine, tyramine, and cadaverine levels in traditional Chinese Sichuan-Style sausages (mean value of 196 mg/kg, 164.6 mg/kg, 141.6 mg/kg, respectively). Researchers indicated that these results were linked to poor hygiene of raw materials and insufficient hygiene conditions during processing steps. Due to the activity of microorganisms, fermented meat products contain higher levels of biogenic amines. Insufficient hygienic conditions were found to increase the amount of free amino acids present in the raw materials. These free amino acids are then available to be used by microorganisms during the fermentation process, leading to the increased biogenic amine contents of the final product.

Fermented meat products worldwide

Raw meat is a highly perishable food, and preservation of meat is a significant problem. In early civilizations, preservation techniques such as salting and drying under the sun were used for long-term meat preservation. These preservation strategies resulted in lower water activity levels, which protected the meat from spoilage and pathogenic microorganisms (Zeuthen 2007). Many traditional fermented meat products are consumed by different cultures worldwide because of differences in raw materials, formulations, or manufacturing processes. The low water activity levels of the salted and dried meat provided a hostile environment for microorganisms, thereby preventing the growth of spoilage and pathogenic microorganisms. This allowed the meat to be stored for a longer period of time without it spoiling. Additionally, traditional fermented meats are processed differently in various cultures, resulting in different flavors, textures, and shelf lives. These products are an essential source of information about society's consumption habits. The quality and quantity of fermented meat products produced vary by country (Kumar et al. 2017). Table 4 lists some common fermented meat products.

Table 4.

Some of the common fermented meat products worldwide

Origin/region Product name Substrate/raw materials Fermented meat group Microorganisms involved in fermentation References
Germany Teewurst Pork, beef Fermented sausage LAB Austin-Watson et al. (2013)
India Kargyong Satchu Pork or beef Fermented sausage LAB Bhutia et al. (2021)
Italy Piacentino, Crespone, Mortadella Pork Salami LB Baldin et al. (2018), Połka et al. (2015)
Italy Prosciutto, Pancetta Pork Fermented meat LAB Parlindungan et al. (2021)
Portugal Alheira Pork or beef Fermented sausage LAB Fernandes et al. (2022)
Spain Androlla Pork Dry cured sausage LAB and Staphylococcus spp. Landeta et al. (2013)
Chorizzo Pork Dry sausage Lactobacillus and Streptococcus spp. Juárez-Castelán et al. (2019), Prado et al. (2019)
Serbia Sremska, Petrovská klobása Pork and beef fermented sausage LAB Milicevic et al. (2021), Vasilev et al. (2015)
Thailand Nham, Goon chiang, Sai-krok e-san mu Pork Fermented sausage LAB Botthoulath et al. (2018), Wanangkarn et al. (2014)
Turkey Sucuk, Pastırma Beef Fermented sausage dry-cured meat LAB Kamiloğlu (2022), Öz et al. (2017)

Fermentation role in alternative proteins

Fermentation of plant-based products

Fermentation of plant-derived products was used for many decades. From a historical perspective, during the Neolithic period in 8500–400 BC, fermentation accidentally started with plant-derived products, such as grain, to produce wine-like beverages, which can preserve plant-based products longer (Lavefve et al. 2019). Two thousand five hundred years ago, fermented beans were discovered to produce soy sauce Asian. The list of fermented plant-based products is found in multiple countries, as shown in Table 5. Last few decades, fermented plant-related food has become a novel food trend, although its popularity has decreased due to food industrialization, especially in European countries (Giacalone et al. 2022; Michel et al. 2021; Profeta et al. 2021). The interest in the last decades is due to the demand for healthy food products with healthy properties found in plant-based products (Anusha Siddiqui et al. 2022; Bryant and Sanctorum 2021; Schiano et al. 2020). For example, kombucha is produced from lactic acid bacteria, and acetic acid bacteria generate the product without alcohol, which is more acceptable for consumers in European countries.

Table 5.

Fermented plant-based products

Fermented plant products Plant-based source Bacteria involved Consumers attitude Origin References
Anishi Taro (Yam) leaves B. subtilis and B. licheniformis Acted as a main ingredient in different food products Nagaland, India Jamir and Deb (2021), Mir et al. (2018)
Burong mustala Mustard Pediococcus sp., L. brevis Consumed directly as pickles Philippines Di Cagno et al. (2013)
Cucumber Cucumber L. pentosus, L. Plantarum, L. Brevis, Weissella spp., P. ethanolidurans, Leuconostoc spp., and Lactococcus spp. Consumed directly as pickles United states, Asia Moore et al. (2021), Pérez-Díaz et al. (2017)
Dakguadong / Pak-Gardong Mustard leaves L. plantarum Consumed directly as pickles Thailand Di Cagno et al. (2013)
Dhamuoi Cabbage Lc. Mesenteroides, L. plantarum consumed as a pickle Vietnam Di Cagno et al. (2013)
Ekung/Hirring Bamboo tender shoots Lactobacillus plantarum, L. lactis, L. brevis, L. casei and T. halophilus Eaten raw and also by cooking with fish, meat and vegetables Arunachal Pradesh Sharma and Yaiphathoi (2020)
Fermented garlic Garlic B. subtilis, B. methylotrophicus and B. amyloliquefaciens As condiment prepared with dressed olive oils Spain Chua et al. (2022)
Fermented peppers Peppers Lactobacillus spp., Lc. citreum, Weissella cibaria, L. plantarum, L. paraplantarum, H. pseudoguilliermondii, K. ohmeri No effects of fermentation on the quality of the fermented peppers Latin America and Caribbean González-Quijano et al. (2014)
Goyang Leaves of magane-saag (Cardamine macrophylla Willd.) L. plantarum, L. brevis, L. lactis, E. faecium, P. pentosus and candida spp. Consumed as a dish or with boiled noodles, meat and yak Sikkim and Nepal Mir et al. (2018)
Gundruk Rayo-sag’, mustard leaves, and cabbages Pediococcus and Lactobacillus spp., L. cellobiosus and L. plantarum Consumed as a side dish and as an appetizer Nepal Tamang et al. (2005)
Inziangsang Leaves of mustard L. plantarum, L. brevis and Pediococcus Consumed as a soup Nagaland and Manipur Tamang et al. (2005)
Khalpi Cucumber L. plantarum, L. brevis and Leuconostoc fallax Eaten as pickle after mixing with mustard oil, salt and powdered chilies Nepal Tamang et al. (2005)
Kimchi / Sauerkraut Cabbage, hot pepper, green onion, and ginger Lc. mesenteroides, L. brevis, P. cerevisiae, L. plantarum, Weissella spp. Consumed as a as pickle or soup Korea, Europe, USA Di Cagno et al. (2013), Kwak et al. (2014), Xiong et al. (2012)
Kombucha Tea leaves Lactic acid-producing bacteria, acetic acid-producing bacteria, and yeasts Consumed as beverage and functional drink, related health Eastern Asia De Noronha et al. (2022), Lavefve et al. (2019)
Lung-Siej Bamboo shoots Lc. fallax, L. mesenteroides, L. brevis, L. curvatus, and Lt. lactis Consumed as curry mixed with fish and meat Meghalaya, North-eastern India Nongdam (2015)
Mesu Tender bamboo shoot L. plantarum, L. brevis, L. curvatus, Lc. citreum, P. pentosaceus Consumed as a pickle mixed with edible oil chillies Darjeeling hills and Sikkim, North-eastern India Tamang et al. (2005)
Olives Olive L. plantarum Consumed as a pickle USA, Spain, and middle-east countries Hamid abadi Sherahi et al. (2018)
Oncom hitam By products from tofu C. mesenterica, C. parapsilosis, C. parapsilosis var. intermedia, C. pelliculosa, C. reukaufii, C. solani, Mucor sp., M. javanicus, R. oligosporus, and R. oryzae,· C. mesenterica, and C. llarapsilosis As main dish consumed with rice Indonesia Ho (1986)
Salgam Carrots L. plantarum, L. paracasei, L. fermentum, L. brevis Consumed as a pickle Turkey Di Cagno et al. (2013)
Sinki/Paocai Radish-tap-root L. fermentum, L. brevis and L. plantarum Act as an effective appetizer India, Nepal, and Bhutan Yan et al. (2008)
Soibum Bamboo shouts P. pentosaceus, L. brevis, L. plantarum, Lc. fallax, Lc. lactic Consumed as a side dish Manipur, India Mir et al. (2018)
Soidon Bamboo shoots tips L. brevis, Lc. fallax and Lc. lactis Used as a curry by mixing with potato, green chillies, salt and fermented fish Manipur, India Jeyaram et al. (2010)
Soy sauce/miso/kecap Soybean Bacillus, Aspergillus, Klebsiella, Cladosporium, Shimwellia, Aspergillus soyaeZygosaccharomyces rouxiiTetragenococcus halophilus Consumed as seasoning for food products China, Indonesia and eastern Asia Apriyantono et al. (1996), Cao et al. (2019), Fibri and Frøst (2019), Lee et al. (2017), Marco et al. (2017), Yang et al. (2017)
Tofu and tempeh Soybean Bacillus or LAB species, Lactic Acid Bacteria Consumed with rice and other Indonesia Cao et al. (2019), Fibri and Frøst (2019), Ho et al. (2018)

Note: B.: Bacillus, L.: Lactobacillus, P.: Pediococcus, Lc.: Leuconostoc, H.: Hanseniaspora, K.: Kodamaea, E.: Enterococcus, P.: Pediococcus, T.: Tetragenococcus. LAB: Lactic acid bacteria, Lt.: Lactococcus, C.: Candida

Many fermented foods, as shown in Table 5are a type of traditional foods which can raise the popularity of traditional food exposure to global consumers (Anusha Siddiqui et al. 2022). For example, pickling is fermented by immersing vegetables in vinegar into various foods to prolong their shelf life. The pickling system process looks like the fermentation of sauerkraut using lactic acid bacteria and salted brin performed at acidic fermentation (Di Cagno et al. 2013; Vitali et al. 2012). The world's most popular pickling is the small cucumber pickled vegetable, made with lactic acid bacteria, such as lactobacillus spp, Weissella spp, Pediococcus spp, Pediococcus sp, Leuconostoc spp, and Lactococcus spp. The fermentation in pickling can improve the taste of the pickling products. The pickling can be produced from other plant-based products, like olives (Hamid Abadi Sherahi et al. 2018) and carrots (Di Cagno et al. 2013). Other fermented plant-based products, such as fermented peppers and soybeans, have been reported. Peppers can be fermented with high levels of acetic acid, while soybean is fermented to produce various products, including soy sauce, tofu, and tempeh. Those fermented plant-based products involve different types of microorganisms.

Lactic acid bacteria, such as lactobacillus spp. play an essential role in the fermentation of food products (Di Cagno et al. 2013; Marco et al. 2017). Fermentation of vegetables typically happens accidentally, called spontaneous fermentation, where fermentation occurs due to lactic acid bacteria in the cabbage. Lactic acid bacteria initiated fermentation. Other species responsible for vegetable fermentation are lactobacillus brevis, Leuconostoc mesenteroides, pediococcus, etc. (Di Cagno et al. 2013; Xiong et al. 2012). For this species, culture-based methods are applied to initiate fermentation. The microorganisms involved during product fermentation determine the types of products. As an example, soibum and soidon are fermented products made from bamboo shoots in Manipur, India. Soibum involves the P. pentosaceous and L. plantarum, which are not used for fermenting Soidon products (Jeyaram et al. 2010; Yan et al. 2008). This also affects consumers' use of products. Soibum is typically served as a side dish, while Soidon is used as a curry mixed with potato and green chilies (Jeyaram et al. 2010; Mir et al. 2018). This difference in fermentation process and use of different ingredients results in a distinct flavor, texture, and aroma of Soibum and Soidon. As a result, consumers have different preferences for these two products, and they use them for different cooking preparations.

Fermentation of fruits

Compared to plant-based food products, fermentation fruits are generally used as a beverage. Table 6 shows a list of fermented fruits with responsible bacteria. Fermented fruit products relate to a valuable and large beneficial microorganism. The majority of the time, different native microorganisms present in the raw components spontaneously ferment diverse plant-based substances to produce fermented products. The fermentation of fruits involves lactic acid bacteria, a small part of the microbiota of raw fruits (Di Cagno et al. 2013). Depending on the kind of vegetable, hetero- and homo-fermentative organisms from the genera Pediococcus, Enterococcus, Weissella, Lactobacillus, and Leuconostoc, were variably detected. The most prevalent species were Weissella cibaria/Weissella confusa and Lactobacillus plantarum. Fermented sweet cherries, for example, represent the alternative source of indigenous microorganisms (Di Cagno et al. 2011). The microbiota from the fruits is adapted to the fermented brine solution making the microorganisms isolated from an ecosystem typically having technological properties, such as resistance to salt, high acidification rates, pH, temperature, and phenolics (Di Cagno et al. 2013; Marco et al. 2017).

Table 6.

Fermented fruits

Fermented fruits Fruit source Bacteria involved Consumers attitude Origin References
Fermented cashew apple Cashew apple L. mesenteroides Consumed as beverage Brazil Gupta and Abu-Ghannam (2011)
Pickled juice Fruits L. buchneri Consumed as a pickle China Zeng et al. (2010)
Topache/Fermented pineapple pulp Pineapple Meyerozyma caribbica Consumed as fresh Mexico Vitali et al. (2012)
Hardaliye Grape L. paracasei, L. casei, L. pontis, L. brevis, L. acetotolerans, L. sanfrancisco, and L. vaccinostercus Stored in suitable containers at 4ºC and consumed either fresh or following aging Turkey Kabak and Dobson, (2011)
Fermented sweet cherry puree Sweet cherry P. pentosaceus, L. plantarum Processed as brined, canned and frozen, dried or used for juices or syrups Italy Di Cagno et al. (2011)
Wine Grape S. cerevisiae and S. bayanus Consumed as beverage Georgia Sahay (2019)
Cider Apple L. brevis, L. paracollinoides, L. casei, L. diolivorans Consumed as beverage UK Di Cagno et al. (2013)

L.: Lactobacillus, P.: Pediococcus, S.: Saccharomyces

Other fermented fruits in Table 6 are also found in other countries with different fruit sources. Fermented cashew apples contain oligosaccharides, which can be evaluated with Lactobacillus johnsonii to determine the degree of polymerization. However, the fermented cashew apple is still considered to have an unpleasant taste to be consumed by humans (Vergara et al. 2010). The fermentation of fruit with L. johnsonii happens due to the focus on enzymatic synthesis, where glucose and fructose are used as enzyme acceptors. UK consumers drink cider, another beverage product from apples. This beverage is fermented by L. brevis, L. paracollinoides, L. casei, Ldiolivorans. It is also under the same conditions as wine from grapes (Di Cagno et al. 2013). In general, fruit fermentation research is limited, whereas the fruits contain beneficial microorganisms to explore deeply to understand the importance of microorganisms isolated for the generated food products. Cider is produced by fermenting apples with certain species of lactic acid bacteria, which help to break down the fructose and glucose in the apples into ethanol. This fermentation process is similar to the process used to produce wine from grapes, although the microorganisms used are slightly different. As a result, more research is needed to better understand the role of microorganisms in fruit fermentation and their potential to generate beneficial food products.

Fermentation of cereals

The majority of fermented foods manufactured from grains are found in Africa. The natural microbiota is employed to ferment grains like maize, millet, rice, or sorghum. The grains are frequently cooked, crushed, malted, and occasionally filtered. Many well-known cereal-based products have distinctive regional variations in content and preparation (Achi and Asamudo 2019; Tsafrakidou et al. 2020). African cereal products may be divided into a few main types; liquids, porridges, (semi)solid prepared doughs, and liquid drinks, such as nonalcoholic gruels (Achi and Asamudo 2019).

Table 7 lists fermented cereals and microorganisms responsible for fermentation. The Burkinabe dish of ben-saalga, a thin porridge made from fermented pearl millet (Pennisetum glaucum) sediment cooked in water, is well-known in Ghana (Achi and Asamudo 2019; Nout et al. 1995). Natural fermentation is often dominated by L. fermentum, L. plantarum, and P. pentosaceus, requiring the energy density of fermented gruels derived from cereal; some L. plantarum strains can hydrolyze starch, which can be advantageous. Another product is Ogi, a well-known morning gruel traditionally made by naturally fermented maize grains to create a supplementary diet for kids (Achi and Asamudo 2019; Gupta and Abu-Ghannam 2011; Nout et al. 1995). The precise composition will impact the end product's viscosity, fermentability, and content. It can also be prepared from sorghum or millet grains. Ogi is often ingested following heat treatment, eliminating the probiotic properties of lactic acid bacteria (Gupta and Abu-Ghannam 2011). It must be noted that these foods’ functional properties are connected not only to how bioactive live cells interact with the host but also indirectly by ingesting bioactive chemicals generated during fermentation. Thus, natural fermentation is a viable way to promote a healthy lifestyle through the consumption of plant-based foods with antimicrobial properties.

Table 7.

Fermented cereals

Fermented cereals Cereal source Bacteria involved Consumers attitude Origin Reference
Bensaalga, koko Corn, pearl millet and red sorghum L. fermentum, L. plantarum, and Ped. pentosaceus Consumed as gruel Burkina Faso, Ghana Achi and Asamudo (2019)
Borde Maize, barley, wheat, finger millet, sorghum Lactic acid bacteria, such as Lactobacillus spp Consumed as brown cultured beverage, with a dark consistency and a sweet–sour taste and consumed by adults and children often as a low-cost meal replacement Ethiopia Achi and Asamudo (2019), Hotessa and Robe (2020)
Boza Wheat, millet, corn Lactic acid bacteria, like Lactobacillus spp., and yeasts including Saccharomyces spp, Candida spp Consumed as beverage for consumers of all ages and is generally during winter months Turkey and Balkan countries Hancioǧlu and Karapinar (1997), Kabak and Dobson (2011)
Burukutu Guinea corn Acetobacter spp., Candida spp., Enterobacter spp., Lactobacillus spp., S. cerevisiae, S. chavelieri, Lc. mesenteroides Consumed as an alcoholic beverage West Africa Adebo (2020), Bala et al. (2017)
Bushera Sorghum Lactobacillus spp., Lactococcus spp., Leuconostoc spp., Enterococcus spp., and Streptococcus spp. Consumed by all ages and used as a weaning food and a thirst-quenching drink in the households Uganda Achi and Asamudo (2019), Adebo (2020), Muyanja et al. (2003)
Chibuku Maize and sorghum Lactobacillus spp. and S. cereviseae Consumed as alcoholic beverage Zimbabwe Adebo (2020), Mawonike et al. (2018)
Dolo Red sorghum grains L. delbrueckii, L. fermentum, L. lactis, P. acidilactici, S. cerevisae Consumed as alcoholic beverage Burkina Faso/Togo Adebo (2020)
Dosa (fermented paste fried as pan-cake) Rice and lentils Leuconostoc spp., mesenteroides spp., Streptococcus spp., Lactobacillus spp. Consumed during breakfast India Gupta and Abu-Ghannam (2011), Sawadogo-Lingani et al. (2021)
Enturire Sorghum L. plantarumS. cerevisaeWeissela confusa Consumed as alcoholic beverage Uganda Adebo (2020)
Gowe (sifanu) Sorghum and maize flours Lactic acid bacteria, such as Lactobacillus spp. and yeasts Consumed as beverage by people living in urban areas Benin Achi and Asamudo (2019)
Humulur Sorghum Bacillus spp., Lactobacillus spp., yeasts Used as a gruel Sudan Adams (1998), Adebo (2020)
Idli (steam cooked fermented paste) Rice flour Lc. mesenteroides, S. faecalis, L. delbrueckii, L. fermenti, L. lactis, and P. cerevisiae Consumed during breakfast India Gupta and Abu-Ghannam (2011)
Ikigage Sorghum Issatchenkia orientalisL. buchneri, L. fermentumLactobacillus spp., S. cerevisiae Consumed as alcoholic beverage Rwanda Lyumugabe et al. (2010)
Injera Teff C. guillermondiiLactobacillus spp, yeasts Consumed as flat bread Ethiopia Achi and Asamudo (2019)
Khambir Wheat L. brevis, L. plantarum, L. Casei, Bacillus, mold, yeast, and lactic acid bacterial Consumed as flat bread Middle east countries Tsafrakidou et al. (2020)
Kenkey Corn Lactic acid bacteria, Enterobacter spp. and yeasts Consumed as cooked/steamed dough Ghana Achi and Asamudo (2019), Gupta and Abu-Ghannam (2011), Nout et al. (1995), Wesolowska et al. (2018)
Kisra Sorghum flour C. intermedia, C. kruseiDebrayomyces hansenii, Enterococcus faeciumL. amylovorusL. brevisL. confususL. fermentumPichia kudriavzevii Consumed as flat bread Sudah, south Africa Achi and Asamudo (2019)
Kunun-zaki Millet grains Lactobacillus plantarum, Lb. fermentum, and Lactococcus lactis Consumed as a refreshing drink, an appetizer, a food complement, and to quench thirst Nigeria Achi and Asamudo (2019)
Kwete Sorghum, millet or maize Lactobacillus and Lactococcus Light brown in color, with a thick consistency and a sweet–sour taste Uganda Achi and Asamudo (2019)
Mahewu Corn meal Lc. lactis Consumed as beverage, prepared from the maize porridge Africa and some arabian arabian gulf Achi and Asamudo (2019), Gupta and Abu-Ghannam (2011)
Mbege Black/ white glutinous rice L. plantarum, Leuc. mesenteroidesS. cerevisiae, Schizosaccharomyces pombe Consumed as beverage Tanzania Achi and Asamudo (2019)
Merissa Dates, millet and sorghum Saccharomyces spp. Consumed as alcoholic drink Sudan Achi and Asamudo (2019)
Obiolor Sorghum and millet malts lactic acid bacteria and yeasts

Consumed as beverage, served as functional foods

Daily consumption and associated with a good health

Nigeria Achi and Asamudo (2019)
Ogi Corn L. acidophilusL. agilisL. cellobiosusL. confususL. murinusL. plantarum Popular breakfast gruel and a complementary food for children Sub-Saharan Africa Achi and Asamudo (2019), Gupta and Abu-Ghannam (2011)
Ori-ese Sorghum Bacillus subtilisC. tropicalisL. acidophilusL. fermentumL. plantarumMucor spp., Pediococcus spp., Penicillium spp., Spombe Consumed as porridge Nigeria Achi and Asamudo (2019)
Otika/Pito Sorghum B. cereus, B. subtilis, C. krusei, C. tropicalis, Enterobacter clocae, L. brevis,L. fermentumL. plantarumLeuconostoc mesenteroides, S. cerevisae Consumed as alcoholic beverage Nigeria Achi and Asamudo (2019)
Pozol Maize Lc. mesenteroides, L. plantarum, L. confusus, Lt. lactis and Lt. raffinolactis Used for making dough Mexico Gupta and Abu-Ghannam (2011)
Tarhana Wheat flour L. delbrueckii and S. cerevisiae, Lc. lactis, Lc. diacetylactis, Lb. acidophilus, Lb. casei, and Leuconostoc cremoris Consumed as a snack the Middle East and Turkey Kabak and Dobson (2011)
Tchapalo Sorghum LbrevisLcellobiosusLcoprophilusLfermentumL. hilgardiiLplantarum Consumed as alcoholic beverage Ivory Coast Achi and Asamudo (2019)
Tchoukoutou Sorghum and millet L. divergens, L. fermentum, L. fructivorans, S. cerevisae, S. pastorianus, Torulasposa delbrueckii Consumed as alcoholic beverage Benin Kayodé et al. (2007)
Tella Wheat, maize, sorghum, and teff L. pastorianumiS. cerevisae Consumed as beverage Ethiopia Wedajo Lemi (2020)
Ting Sorghum L. caseiL. coryniformisL. curvatusL. fermentum, L. harbinensisL. parabuchneriL. plantarumL. reuteriL. rhamnosus Consumed as porridge Botswana, South Africa Sekwati-Monang et al. (2011)
Toddy Palm trees Bacillus subtilis Used for sap from coconut Sri Lanka, Nepal, Bangladesh Gupta and Abu-Ghannam (2011)
Togwa Sorghum, maize, millet and maize–sorghum Lactobacillus spp, P. pentosaceus, Weissella confusa, Issatchenkia orientalis, S. cerevisiae, C. pelliculosa, and C. tropicalis Consumed by the working people and also used as refreshment and a weaning food, with sweet taste and sour nonalcoholic beverage Tanzania Achi and Asamudo (2019)

B.: Bacillus, L.: Lactobacillus, P.: Pediococcus, Lc.: Leuconostoc, H.: Hanseniaspora, K.: Kodamaea, E.: Enterococcus, P.: Pediococcus, T.: Tetragenococcus. LAB: Lactic acid bacteria, Lt.: Lactococcus, C.: Candida

In several African nations, alcoholic and non-alcoholic beverages are made from fermented sorghum and millet (Achi and Asamudo 2019). They serve as the base grains for the non-alcoholic beverage bushera and the traditional alcoholic beverage muramba. Lactococcus, Leuconostoc, Lactobacillus, Weissella, and Enterococcus are responsible for bushera production (Muyanja et al. 2003). While Ethiopian customers are well-versed with barley meals and beverages, including Kunun-zaki, shorba, kinche, tihlo, shamet, chuko, beso, etc., is another millet-fermented beverage that is frequently enjoyed in Northern Nigeria. Lactic acid fermentation is a typical, simple, and affordable method for processing foods, including starch, to ferment cereal products. Cereal food products’ nutritional and organoleptic value is improved through lactic acid bacteria fermentation. The sensory qualities represent the first significant advancement. Bread, loaves, confectionary, pastes, noodles, gruels, semi-digested drinks, and supplemental meals for infants and children are produced by lactic acid fermentation of cereal substrate (Tsafrakidou et al. 2020).

Fermentation of insects

In many civilizations worldwide, eating insects has long been a widespread practice (Anusha Siddiqui et al. 2022; Caparros Megido et al. 2016). Because of their better feed-conversion efficiency, reproductive potential, and environmental sustainability, insect-based products have gained favor as trendy new food items in addition to their excellent nutritional value (Niva and Vainio 2021). To enhance the sensory, nutritious, and shelf-life properties of new components and products and their availability and customer acceptance/receptivity, scientists and technologists have adopted both conventional and cutting-edge processing techniques (Caparros Megido et al. 2014; Mancini et al. 2019). With its ability to enhance fermented meals’ flavor, rheology, and texture and alter people’s perceptions of processed insect products, fermentation has attracted considerable study. Fermented sauces created with wax moth grasshoppers (Locusta migratoria) and larvae (Galleria mellonella) exhibited substantial acceptance for several sensory descriptors such as “sour”, “bitter”, “sweet”, and “umami”, when compared to a commercial fish sauce (Mouritsen et al. 2017). This behavior was due to increased fermentation-derived substances such as lactic acid, free amino acids, and fatty acids. There is much work to be done in order to harness the benefits of fermentation in order to enhance the sensory quality of insect-based food products and improve their availability in the marketplace. Moreover, this process may transform raw materials into biomass, fuels, and chemicals, all with a wide range of commercial uses. To treat edible insects, fermentation technology can potentially increase insect components' functioning and their use. The fermentation products of insects and bacteria are listed in Table 8.

Table 8.

Fermented insects

Fermented insects Insect source Bacteria involved Consumers attitude References
Fermented cricket flour Cricket Lactiplantibacillus plantarum Overally accepted remarked with “happiness” Bartkiene et al. (2023)
Fermented Tenebrio molitor larvae Larvae Cordyceps militaris mycelia Increased to healthy food products Ha et al. (2022)
Fermented Tenebrio molitor larvae larvae Aspergillus oryzae and Bacillus licheniformis Used as seasoning sauces Cho et al. (2018)
Fermented silkworm larvae Larvae Aspergillus kawachii Consumed as a food and traditional medicine Cho et al. (2019)
Fermented yellow mealworm larvae Larvae Pediococcus acidilactici, Lactobacillus curvatus, and Staphylococcus xylosus No consumer study observed, but expected to have shelf-life extension Borremans et al. (2018)
Fermented mealworms Larvae Pediococcus acidilactici, Lactobacillus curvatus, and Staphylococcus xylosus Used to extend the shelf life of the insect food De Smet et al. (2019)

Compared to the fermentation of the previously mentioned items, the fermentation of insect feeds is relatively new. Cho et al. (2019) used an Aspergillus kawachii solid-state fermentation to treat the flour made by mulberry silkworm larvae (Bombyx mori). The scientists examined how fermented silkworms produced free amino acids, fatty acids, minerals, and alcoholic chemicals. In a study by Jang et al. (2018), several microorganisms were used to ferment yellow mealworm larvae (Tenebrio molitorLactobacillus plantarum, Lactobacillus gasseri, Aspergillus kawachii, Saccharomyces cerevisiae, and Bacillus subtilis). Following fermentation with each strain separately, extracts of water, ethanol, and methanol were made and used to evaluate the biological characteristics of the products.

According to the facts above, fermentation is a workable alternative to other methods of preparing active insect metabolites. These naturally occurring substances, produced by fermentation, might be utilized as components in functional foods and nutraceuticals. Due to the bioactive substances insects have produced through fermentation, they will one day provide consumers with health benefits. However, further study is needed to benefit from their future uses and numerous health benefits in the future. Indeed, fermentation offers a unique method of obtaining active compounds from insects that may be used in a variety of applications. These compounds can be used to produce medicines, vitamins, and cosmetics, among other things. They can also be used to create sustainable food products, such as protein bars, that can provide essential nutrients to those with limited access to a balanced diet.

Fermentation of seaweed

Seaweed fermentation has been previously observed in food or medicine (Gullón et al. 2020, 2021; Wendin and Undeland 2020). The demand for seaweed in the Asian market, which has resulted in sharp increases in aquaculture yields, has been a significant factor in the continuous rise in seaweed consumption over the past few decades. Global seaweed harvesting was 29 million tonnes in 2016. Their primary uses were synthesizing hydrocolloids for food and pharmaceuticals, animal feed, and human consumption (Zhang et al. 2022). While early investigations indicated excellent yields, seaweeds are particularly ideal for this purpose because their development systems do not compete with crops and do not require fresh water.

Seaweed fermentation products are most pertinent because the primary structural polysaccharides undergo hydrolysis, producing a high quantity of glucose (Monteiro et al. 2021). Laminarin, alginate, and fucoidan are found in brown seaweeds, agar and carrageenans in red seaweeds, starch and ulvan in green seaweeds, and laminarin, alginate, and fucoidan are found in brown seaweeds (Milinovic et al. 2021; Pérez-Alva et al. 2022). Brown seaweeds provide extra fermentable sugars in the form of mannitol and glucuronic acid that, provided mannitol-fermented cultures have been used, can further enrich the fermentable mash. These sugars and the hydrolyzed polysaccharides undergo glycolysis to produce pyruvate, which is subsequently fermented to produce either lactic acid or ethanol and CO2, as shown in Fig. 2. Most microbial cultures cannot use several seaweed sugars, including mannuronic and uronic acids, fucose, rhamnose, and xylose, making ethanol fermentation of seaweed difficult, so genetically modified cultures have been created to convert seaweed sugars well (Monteiro et al. 2021). Seaweed has an intact protein complex, hydrolyzed after fermentation. The fermentation also physically disrupts seaweed cells and consequently breakdown the protein–phenolic blends to release the Fermentation of various seaweeds depending on the sugar content in seaweeds to select the bacteria involved in the fermentation process, shown in Table 9. Seaweed Gracilaria verrucosa can be fermented with Hortaea werneckii, Lactobacillus spp., and Staphylococcus. The fermentation of seaweeds increased antioxidant and antimicrobial activity (Fatmawati et al. 2022). The increase in antimicrobial activity implicated the protection of seaweeds from pathogenic and spoilage bacteria and improved the seaweeds' nutritional value by reducing the insoluble and indigestible fractions (Maiorano et al. 2022). Figure 2 shows the fermentation process. The fermentation process activates the seaweeds' antimicrobial activity which helps to protect them from bacteria and other contaminants. This process also aids in the breakdown of indigestible components, making the seaweeds more bioavailable and easier to digest. This makes them ideal for use in a variety of applications, such as biofuels, nutritional supplements, and pharmaceuticals.

Fig. 2.

Fig. 2

a Chemical fermentation path of the seaweeds, and b physical appearance of the fermentation of process in seaweeds. “Created with BioRender.com”

Table 9.

Fermented seaweed

Seaweed Bacteria involved Consumers attitude References
Fermented Gracilaria verrrucosa Marine yeast Hortaea werneckii No consumer concern was observed, the fermented seaweeds had increasing antibacterial and antioxidant activity Fatmawati et al. (2022)
Fermented Gracilaria gracilis Lactobacillus sakei, Staphylococcus carnosus and Staphylococcus xylosus Improving the nutritional value of the seaweeds Maiorano et al. (2022)
Edible red seaweed Bangia fusco-purpurea Lactobacillus delbrueckii and Lactobacillus plantarum Consumed as special dietary food to improve hyperlipidemia and obesity Li et al. (2023)
Kappaphycus spp Aspergillus oryzae As a food ingredient to improve the nutritional, taste and textural properties of food products Norakma et al. (2022)
Green seaweed Ulva spp. Paradendryphiella salina (marine fungus) As a promising source of functional and sustainable ingredients for food Landeta-Salgado et al. (2021)
Edible Irish brown seaweeds Himanthalia elongata, Laminaria digitata and Laminaria saccharina Lactobacillus plantarum As functional foods Gupta et al. (2011)

Furthermore, bacteria involving the fermentation process can also utilize fungi found in the marine area. Landeta-Salgado et al. (2021) reported the fermentation of green seaweeds Ulva spp. hydrolyzed by the marine fungi Paradendryphiella salina. The results showed an increase in yield, protein, and amino acids. However, the research on the fermentation of seaweeds for functional foods still needs to be completed. Further analysis of fermented seaweeds’ effects on food processing is essential.

Coffee fermentation

Coffee is a widely consumed beverage prepared from coffee beans. Despite fermentation being necessary to remove the mucilage layer, subsequent heat-intensive processes (roasting and brewing) produce a drink that is close, as shown in Fig. 3. During coffee fermentation, parchment coffee's mucilage must be removed. Coffee mucilage contains starch, cellulose, and pectin. The mucilage may make it difficult to dry coffee beans and, in rare cases, may also promote mold growth, lowering the final coffee quality (Haile and Kang 2019a). Spontaneous fermentation is often employed since it is explicitly done to remove mucilage (Haile and Kang 2019b).

Fig. 3.

Fig. 3

Coffee fermentation from wet processing. Created with BioRender.com

Furthermore, coffee beans already contain all the ingredients needed to produce coffee flavor and fragrance during roasting (Joët et al. 2010). Yet, fermentation can broaden the variety of chemicals that give coffee flavor and fragrance, including more than 700 volatile and nonvolatile chemicals. According to reports, yeast, LAB, and Enterobacteriaceae are predominantly responsible for wet fermentation, whereas acetic acid bacteria and Pichia yeasts are responsible for dry fermentation (Lavefve et al. 2019), as shown in Table 6. Since the mid-1900s, numerous microorganisms have been isolated from wet processing fermentation. Since aromatic chemicals are created when the mucilage layer in wet processing is removed, wet-processed coffee has better scent attributes than dry-processed coffee (Haile and Kang 2019a). Current research on coffee fermentation during dry, semi-dry, and wet processing focuses on using aromatic yeasts to create flavor (De Melo Pereira et al. 2015; Evangelista et al. 2014). A wide range of microbial species (Table 10) are present during coffee fermentation; however, only a small number of these native microorganisms were chosen because of their potential effects on the coffee’s flavor and fragrance. Fermentation should be regulated to achieve this favorable outcome. The choice of suitable microorganisms that positively impact coffee flavor and fragrance during fermentation is crucial. Thus, it is important to properly regulate fermentation in order to achieve desired flavor and aroma in coffee. The choice of the right microorganisms is important because it is these microorganisms that produce the compounds responsible for the flavor and aroma of coffee. Therefore, by regulating the fermentation process, the desired flavor and aroma can be achieved.

Table 10.

Fermentation of coffee

Fermented coffee Bacteria involved Consumers attitude References
Wet fermented coffee LAB, Enterobacteriaceae, and Yeast Consumed for refreshment drink De Melo Pereira et al. (2015), Lavefve et al. (2019)
Dry fermented coffee Acetic acid bacteria and Pichia yeasts Consumed for refreshment drink Evangelista et al. (2014), Lavefve et al. (2019)

Precision fermentation

Producing edible microbes has the potential to bypass many of the environmental constraints of food production and reduce its environmental footprint at a time when climate change threatens the global food production system (Linder 2019). The use of fermentation has been a useful method of food preservation in the past. The microbial populations involved made the resulting products typical concerning where processing occurred (Campbell-Platt 1994). Precision fermentation uses synthetic biology, especially genetic engineering, to insert specific genes into the DNA backbone of single-celled organisms and microorganisms to produce desired fermentation properties and products (Augustin et al. 2023). One way to reduce by-product formation is to create synthetic cellular factories in which all available resources are diverted to produce the compounds needed and nothing more. Known as precision fermentation or synthetic biology, the technique is now being touted as a potential alternative to traditional fermentation (Fig. 4). The focus is designing optimized metabolic pathways and assembling the genes involved in the microbial chassis. In order to analyze and characterize microbial genomes and metabolic functions, this technology relies heavily on artificial intelligence, bioinformatics, systems biology, and computational biology (Teng et al. 2021).

Fig. 4.

Fig. 4

Precision fermentation. “Created with BioRender.com”

Recent advances based on genomics and synthetic biology include precision fermentation and biomass fermentation to produce specific compounds for food and chemical industrial or pharmaceutical purposes (Teng et al. 2021). A variety of vitamins are found in microbial biomass, including biotin, folic acid, niacin, pantothenic acid, pyridoxine, riboflavin, and thiamine (Ritala et al. 2017). Rapid advances in precision biology enable microbial programming to produce complex organic molecules (Augustin et al. 2023). Sugars, alcohols, organic acids, and hydrocarbons are simple organic feedstocks that can be used to culture microorganisms. In the field of carbohydrates, precision fermentation for the production of oligosaccharides has received the most attention. Several patents describe the construction of genetically engineered microbial cells to enhance oligosaccharide production. The primary targets are human milk and its associated oligosaccharides applied to infant formula and supplements. These oligosaccharides provide non-nutritional biological properties to infants, such as promoting gut health and the growth of beneficial microflora in the gut (Ambrogi et al. 2023; Barile and Rastall 2013). Microbial biomass producers often prefer low-cost organic by-products from the food industry, such as molasses, vegetable starch, and whey (Linder 2019). Microbial biomass production costs are also strongly influenced by choice of organic substrate for microbial growth (often called feedstock) (Linder 2019). The use of fermentation has been a useful method of food preservation in the past. the microbial populations involved made the resulting products typical concerning where processing occurred (Campbell-Platt 1994).

Large-scale production of fermented food products involves the use of starter cultures. defined aliquots of selected microbial cultures are added to the substrate to be fermented. depending on the selected starter culture, the fermentation process can be directed. for example, lactic acid bacteria (LAB) ferment lactose present in the substrate by lowering the pH; they inhibit the growth of undesirable bacteria but also contribute to the flavor and texture of the food (Parente et al. 2017). There are still inherent risks, especially when using traditional or spontaneous fermentation. Pathogenic microorganisms or harmful metabolites can spoil the final product and pose a health risk to consumers. Therefore, applying genomic analysis will help improve safety through the early detection of harmful microorganisms. Finally, combining genomics and synthetic biology to design desirable traits rationally holds promise for using non-food biomass to create new foods that are safe, healthy, and appealing to consumers (Teng et al. 2021). Genomic studies of food microbiomes have made great strides as rapid advances in sequencing technologies have greatly reduced sequencing costs and led to an increasing number of genomes published in public databases. Metagenomic analysis using HTS helps to reveal metabolic functions and parameters that affect fermentation processes, such as B. Substrate consumption, enzyme production, or metabolic output. Metabolic modeling combined with flux balance analysis to simulate microbial growth and metabolite production in response to changes in the culture environment (Alkema et al. 2016). Altogether, metabolic analysis and modeling would not only help to improve yield, taste, or texture in industrial-scale fermentation based on starter cultures but could also benefit smaller, artisanal producers to avoid contamination or spoilage by suppressing the growth of unwanted microbes or metabolic functions(Teng et al. 2021) By pushing the limits of precision fermentation; we can envision future food production systems in which fermentation plays a central role in producing a variety of food products.

In precision fermentation, microorganisms are programmed using synthetic biology techniques to produce food and pharmaceutical ingredients as cell factories (Pham 2018). Selection of recombinant host microorganisms and strain engineering is the first task to determine the possibility of constructing a microorganism that expresses and produces target molecules in sufficient quantities using appropriate fermentation conditions to increase production efficiency. Microbial hosts are preferred because they are easily manipulated genetically, and standardized fermentation equipment can be used. For food applications, strain engineering often utilizes benign bacteria (e.g., Bacillus spp.) and yeasts because microorganisms that are generally considered safe (GRAS) or harmless are preferred for food applications and so strain engineering often utilizes benign bacteria (such as Bacillus spp.), yeasts (such as Saccharomyces cerevisiae, Pichia pastoris (now Komagataella phaffii), Kluyveromyces spp.), or filamentous fungi (such as Trichoderma spp., notably the popular T. reesei strains) (Chai et al. 2022a, b).

Innovation can occur through novel species and strains or by leveraging genetic engineering and synthetic biology techniques to optimize the yield of desired products, for example, by improving expression, secretion, substrate conversion, and product titer. The untapped potential of natural microbial biodiversity to provide efficient microbial cell factories for novel and safe fermented foods is revealed by “omics” tools and recent advances in synthetic biology. These tools can be utilized to develop products that match desired characteristics and precisely control the fermentation process rather than randomly (Teng et al. 2021). Precision fermentation is easily suited for producing selected proteins, lipids, and carbohydrates due to its ability to produce molecules that mimic comparable compositions derived from conventional agriculture. For example, the oleaginous red yeast Rhodosporidium toruloideshas has been genetically engineered to improve the natural synthesis of lipids, carotenoids, and novel compounds of industrial importance. A thorough understanding of the metabolism of microbial communities can also facilitate the development of new substrates, especially by-products and wastes of the food industry, for the production of value-added products. The research team has demonstrated the value of fermenting food waste with the probiotic Bacillus subtilis to create new foods with higher nutritional value (Mok et al. 2019). A more sustainable strategy is biomass fermentation for protein production, based on the ability of microorganisms to reproduce rapidly under optimal conditions and produce favorably high protein contents exceeding 50% dry weight. Examples of such products are Marmite made from yeast extract, fermented bean paste, and fungal protein from the filamentous fungus Fusarium venenatum, which has recently been used as a raw material for artificial meat (Berka et al. 2004).

From a genomics point of view, single-cell protein production could be comparatively easily explored by high-throughput strain screening, adaptation, and engineering to engineering microbial strains and cell factories for protein production (Teng et al. 2021) Fungi are eukaryotic and saprophytic microorganisms with solid environmental adaptability, making them suitable microbial hosts for precision fermentation. The natural tendency of many fungal species to accumulate high levels of commercially valuable food compounds (organic acids, carotenoids, polyketides, and fungal pigments) makes them conveniently efficient hosts for the industrial-scale production of these products. From a metabolic engineering perspective, a key strength of using fungi compared to bacteria is that their eukaryotic nature makes them tolerant and able to functionally express heterologous eukaryotic proteins and enzymes, achieving proper protein folding and post-translational modifications (Lyu et al. 2019). Many species of fungi are involved in food production, such as Saccharomyces cerevisiae whose genome has been sequenced and allowed to produce vanillin and other aromatic compounds (Nxumalo and Thimiri Govinda Raj 2020). Another fungus used in precision fermentation is Yarrowia lipolytica, a ubiquitous oleaginous fungus that tolerates wide variations in pH and salinity (Miller and Alper 2019). it has the unique metabolic ability to degrade hydrophobic and lipophilic substrates and accumulate more than 40 percent lipid by dry cell weight. It is an excellent source of lipid derivatives or fatty acids (Bilal et al. 2021). Other fungi, besides those mentioned above, can also produce valuable compounds. Kluyveromyces lactisin particular, is an established commercial lactase producer, and its commercial production of recombinant bovine chymosin could be considered a pioneering success in precision fermentation. Fungi play a significant role in traditional fermentations, including beer, wine, bread, cheese, sauces, vegetables, and meat.

In contrast to precision fermentation, most commercial traditional food fermentations are artisanal, natural, and largely undefined, as exemplified by the imprecise method of backing. In recent years, however, precise methods are increasingly being explored and applied to traditional fermentations to speed up the process, increase product yields, improve food quality, safety, nutrition, and flavor profiles, and reduce process costs. Such methods include high-throughput screening strategies, CRISPR-Cas9 genome editing tools, and multi-omics (Chai et al. 2022a, b).

Valorization of food waste by fermentation

Food waste (FW) comprises complex carbohydrates, proteins, lipids, organic acids, enzymes, and nutraceuticals (Carmona-Cabello et al. 2018; O’Connor et al. 2021; Ravindran and Jaiswal 2016). Although its definition has been widely debated, according to the Food and Agriculture Organization (FAO), it is defined as the “total occurred qualitative and quantitative food losses during the supply chain process, which happens at the different stages like production, post-harvesting and processing”. FW is usually considered a non-dangerous waste, except for animal-derived waste strictly controlled by the European regulation (EC) No 1069/2009. FW is becoming a growing and vital problem locally and globally. In fact, according to the FAO, one-third of all food production is lost or wasted globally every year. FW is traditionally disposed of in landfills or incinerated for energy production (Melikoglu et al. 2013). The disposal of FW in landfills is related to several adverse environmental effects (Pires et al. 2021).

In addition, FW is responsible for more than 20% of the total global production of greenhouse gases (GHC), including methane (CH4), nitrous oxide (N2O), and carbon dioxide (CO2) (Munesue et al. 2015). For this reason, the prevention of its products, together with its valorization, is of crucial importance. Indeed, due to the growing public awareness of the indiscriminate disposal of FW and its harmful ecological impact, there is an increasing interest in the recycling and bioconversion of FW, and for this, FW valorization is becoming an expanding industry. Valorization of FW refers to the processes for converting food waste materials into a range of more valuable products. The recycling and the bioconversion of FW significant opportunities to support sustainable development (Capson-Tojo et al. 2016). Fermentation is one of the oldest approaches used for product transformation into value-added products using microorganisms. In fact, by converting these by-products through the microbial fermentation process, different value-added products can be produced, including feed and food additives, single-cell protein (SPC), biofertilizers, bioplastics, chemicals, fuels, food grade pigments and nutraceuticals (Lin et al. 2019). Moreover, FW valorization will bring economic, environmental, and social benefits through, in addition to the manufacture of value-added products, the mitigation of environmental pollution, and overcoming the issues related to odor and the spread of pathogens (Bilo et al. 2018).

Intending to valorize food waste, several promising technologies using acidogenic fermentation (Fig. 5) with anaerobic microbial communities are taking hold to generate different value-added products from biowastes (Ortiz-Sanchez et al. 2023). These techniques are often alternative or supplementary to more conventional ones and employ anaerobic digestion (Palacios et al. 2017). The transformation of bioproducts via natural processes is one of the significant advantages. The resulting products are safe and healthy for human consumption (Pires et al. 2021). Several are the products that can be recovered from FW. For instance, the carbohydrates in the FW can be fermented to produce lactic acid, ethanol, volatile fatty acids (carboxylic acids with 1 to 4 carbon atoms, VFA), or hydrogen (De Groof et al. 2021; Im et al. 2020; Tang et al. 2017; Zhang et al. 2021) and these products can be then extracted to serve as renewable commodity chemicals or liquid fuels (Kannengiesser et al. 2016). Moreover, to mitigate the negative impact, an enhanced approach to the waste management of the fruits and vegetables processing industry is a critical step in the transition to the bioeconomy. It is now well known that agro-industrial activity creates multiple and different types of waste, which are susceptible to being spontaneously fermented by the microbiota present, of course, in these by-products (Sabater et al. 2020; Valenti et al. 2020).

Fig. 5.

Fig. 5

Valorization of food waste by fermentation. “Created with BioRender.com”

Many studies dealing with the fermentation of fruits and vegetable by-products as an alternative way of valorizing food waste using different microorganisms have been reported in the literature (Lu et al. 2022). Several examples are reported in the literature based on fermentation-based valorization strategies, including the anaerobic digestion of organic feedstock, date palm waste, cocoa by-products, and sourdough to produce lactic acid as an alternative for raw material, enzymes, polysaccharides, beverages, and nutraceuticals (Vasquez et al. 2019). The bacteria commonly used in controlled food manufacture are Streptococcus thermophilusLactococcus lactisLeuconostoc spp., and Lactobacillus spp., for dairy products and the genera Pediococcus, Oenococcus, and Weissella play a pivotal role in plant-based fermented products (Bachtarzi et al. 2019). These valorization strategies using these bacteria, which we can also refer to as lactic acid bacteria (LAB), counted the production of lactic acid that could be replenished in the food chain, as well as improving the digestibility of proteins and the sensory properties of these plant by-products that could be used for food ingredients. However, fermentation strategies and bioconversion processes have been described to increase digestibility, enhance nutritional value and decrease the levels of antinutritional factors in these substrates, also employing other bacterial species, yeast, and molds (Yue et al. 2014). Therefore, the fermentation of agro-feed residues by LAB, alone or in combination with other microorganisms, paves the way for developing new sustainable circular economy strategies. In addition to fermentation strategies using LAB, other fermentative bacteria are reported to have been applied to valorize vegetable by-products (Table 11) and other vegetable sources, including different Clostridium and Bacillus bacterial species. Most of these applications focused on producing functional ingredients, such as lactic acid, poly-γ-glutamic acid, bioactive peptides to be reintegrated into the food chain, and other compounds like glycosidases or caproate of industrial interest. Regarding the genus BacillusBacillus coagulansBacillus amyloliquefaciensBacillus licheniformis and B. subtilis have been used, alone or in combination with other bacterial species and with fungi, to ferment products derived from rice, soy, oak, fruit, sorghum (Tropea 2022). On the other hand, it should be noted that the Clostridium bacterial species is mainly used in the fermentation fruit waste. For example, in this regard, a successful fermentation strategy has been reported using both Clostridium cellulovorans and Clostridium beijerinckii strains to ferment mandarin orange waste. In this study, it has been demonstrated that, although normally, D-limonene included in citrus fruits inhibits yeast activity and makes ethanolic fermentation difficult; however, the physiological concentration of D-limonene does not inhibit the growth of the two Clostridium strains. Thus, starting from the isopropanol-butanol-ethanol fermenting ability of C. beijerinckii and the cellulosic biomass-degrading capacity of C. cellulovorans allows biofuels to be produced from this particular specific fruit waste (Yalemtesfa and Tenkegna 2010). Moreover, it has been highlighted the possibility of using vegetable and fruit waste to generate bioenergy in the form of biofuel. Fruit wastes, in particular, were used in the production of bioethanol. Instead, vegetable wastes, high in cellulose, hemicelluloses, and lignin, were employed to produce second-generation bioethanol (Thi et al. 2016). Moreover, Soya by-products were mostly subjected to solid-state fermentation at 30–47 °C using Aspergillus niger and Bacillus species or yeast employing lower temperatures (20–28 °C) (Wang et al. 2019). Instead, Barley bran and brewing waste were mostly inoculated with Aspergillus Trichoderma and LAB species. Another example of the use of fermentation to valorize FW is reported by Brancoli et al. (2021). The authors reported a solid-state fermentation process carried out by the edible fungus Neurospora intermedia using bread waste as feedstock for producing a protein-rich food product. In this research, which can contribute to highlighting how it is possible to manage wasted bread more sustainably, it has been proposed that solid-state fermentation could be used to recover the otherwise discarded surplus bread (Brancoli et al. 2021; Tropea 2022). Another opportunity is the possibility of using food industry waste as animal feed. This possibility appears to be very interesting, as it would bring both environmental and public benefits besides reducing animal production costs. As reported by Tropea et al. (Tropea et al. 2021), among the microbial cultures used in the biotechnological methods to recover food waste, lactic bacteria have several advantages over other bacterial species, especially in animal/fish processing wastes. They are, in fact, generally recognized as safe (GRAS).

Table 11.

Food waste valorization

Food waste Microorganism Fermentation process References
Sweet potato waste, banana skin, orange peel and mango waste Saccharomyces sp., Saccharomyces cerevisiae, Candida tropicalis, Lactobacillus acidophilus Solid fermentation; liquid fermentation; Dulf et al. (2016)
Pineapple waste, banana waste Saccharomyces cerevisiae Solid fermentation Verotta et al. (2018)
Rice bran, Brewery waste Lactobacillus delbuieckii spp., Bacillus licheniformis, Aspergillus niger Liquid fermentation, solid-state fermentation Mathias et al. (2017)
Dairy waste (whey) Cryptococcus albidus sp. Aerius Liquid fermentation Nemeth and Kaleta (2015)
Potato peel Xanthomonas citri Solid-state fermentation Vidhyalakshmi et al. (2012)
Orange peel Chaetomium spp. (KC-06) and Aspergillus niger Solid-state fermentation Yalemtesfa and Tenkegna (2010)
Peanut waste, pomaces and brandy distillery wastes, pomegranate wastes Rhizopus oligosporus: Aspergillus awamori, Rhizopus oryzae; Aspergillus niger and Rhizopus oligosporus, Punica granatum Solid-state fermentation Sadh et al. (2018)
Apricot pomace, apple pomace Aspergillus awamori, Aspergillus niger (ATCC-6275) and Rhizopus oligosporus (ATCC-22959); Phanerocheate chrysosporium Solid-state fermentation Sadh et al. (2018)
Olive pomace, bakery waste Yamadazyma guilliermondii, Yarrowia lipolytica; Xantophylomyces dendrorhous, Sporidiobolus salmonicolor; Monascus purpureus Solid-state fermentation Dursun and Dalgıç (2016)
Tomato waste Aspergillus niger Solid-state fermentation Jamal and Akbar, (2016)
Cotton seed meal, soy bean powder and wheat bran Streptomyces fradiae NCIM 2418 Solid-state fermentation Dulf et al. (2016)
Pulp and paper solid waste Rhizopus oryzae 1526 Solid-state fermentation Das et al. (2016)
Rice bran Aspergillus oryzae and Rhizopus oryzae Solid-state fermentation Das et al. (2016)

Moreover, it has been shown that the products obtained upon the fermentation with Lactobacillus are also reported to have other beneficial effects on aquatic animal intestines, such as antimicrobial and antioxidative properties (Hoseinifar et al. 2014). Fermented fish waste appears as a liquid product, obtained from the liquefaction of tissues carried out by the enzymes already present in the fish and expedited by an acid pH (Tropea et al. 2021). It has been observed that these fish-derived products can rapidly adapt to the intestines of both aquatic and domestic animals, thus making it possible for them to be used in probiotic aquaculture feeds. For instance, studies are reported in the literature in which fish by-products (non-edible parts such as head, viscera, skin, and bones) of Dicentrarchus labrax are fermented by the microorganisms S. cerevisiae strains and Lactobacillus reuteri strains (Tropea et al. 2021). It has also been shown a fermentation process using non-sterilized fish wastes, supplemented with lemon peel as a filler and prebiotic source, carried on by two combined starter cultures of Saccharomyces cerevisiae and Lactobacillus reuteri. In this process, fish waster was bio-converted into a high protein content supplement used for aquaculture feeds. The final fermented product was found to be poor in spoilage microorganisms and rich in healthy microorganisms by displaying a lipid and protein content that makes it suitable for aquaculture feed. These results encourage fish waste and lemon peel conversion into animal feed (Tropea et al. 2021). Munesue et al. (2015) showed another use of food waste valorization through fermentation. Their study used pomaces, i.e., the waste generated from pressing fruits and olives to obtain juices and olive oil, as a feed supplement for animal production. The authors reported that the food obtained from animals fed with fermented pomaces was free from negative effects and with an improvement in nutritional quality.

Fermentation processes for valorizing food waste can also be an attractive opportunity to obtain new value-added products in other fields besides food, such as the cosmetic and pharmaceutical fields. A study conducted by Ferracane et al. (2021) was intended to evaluate the production and characteristics of soaps made from non-edible fermented olive oil (NEFOO soap) by assessing the pH, color, and solubility. Moreover, the glucan and pectin contents found in the green husks of walnuts grown in two different soil and climate areas of Southern Italy were also evaluated for their potential use after fermentation in food, cosmetic, and pharmaceuticals fields in a study carried out by La Torre et al. (La Torre et al. 2020). To date, few studies focus on the possibility of producing biogas from fermented FW. This biogas could then be used for heat or electricity production. In particular, there are several biotechnological processes, like one or two-stage fermentation, dark fermentation combined with aerobic digestion, and photo fermentation combined with aerobic digestion, which can be used to convert the plenty of organic fraction present in the FW to hydrogen. A study has shown that the higher the carbohydrate content of food waste, the better it will be valorized and converted into H2. Studies also show that food waste is suitable for methane production thanks to its physical and chemical characteristics (Thi et al. 2016). Finally, Panyawoot et al. (2022) conducted a study to evaluate the effects of the feed obtained via fermentation on final consumers. In this study, the authors assessed the impact of fermented discarded durian peel with Lactobacillus casei, cellulase, and molasses alone or combined in total mixed rations on feed utilization, digestibility, ruminal fermentation, and nitrogen utilization in growing crossbreed Thai Native-Anglo-Nubians goats. The research highlighted that the discarded durian peel fermented with molasses and L. casei had a much more excellent digestibility and propionate concentration. On the other hand, this product led to less methane and urinary nitrogen production.

A future perspective on fermentation

Fermentation methods have produced many products for many years, including chemicals, materials, food, and medicines. In general, and excluding medicines, industrials fermentations are less competitive compared to the chemical industries or agriculture. More and more products can be obtained by fermentation through a safe, green, and sustainable process. However, for this technology to be increasingly competitive in the future, some issues must be solved. Some of them are freshwater shortage, heavy energy consumption, microbial contamination, the complexity of sterile operations, poor oxygen utilization in the cultures, food-related ingredients as substrates et al. For these reasons, future fermentation processes should be more effective and better from the point of view of the issues just mentioned (Chen and Jiang 2018). First, new fermentation methodologies should avoid the problems of bacterial contamination. Indeed, the microorganisms currently used are very susceptible to contamination by other microorganisms. For example, bacterial strains commonly used for fermentation methods, such as E. coli and Bacillus spp., Corynebacterium glutamicum, and Pseudomonas spp., and also yeast is grown in mild conditions, which also allow the growth of most microorganisms present in the air, in the water or the soil (Chen and Jiang 2018). For this, production facilities must be sterilized entirely to prevent microbiological contamination. This makes processes extremely complex, which also impacts the cost of production, which becomes higher. Therefore, the use of more resistant microorganisms and the implementation of measures to prevent contamination are two main requirements for the future improvement of fermentation processes. A study conducted on two bacteria Halomonas spp. and Xerophiles demonstrated that using these bacterial strains could answer the challenge of bacterial contamination. These microorganisms, extremophilic or unique substrate-selected bacteria, can grow under conditions that, at the same time, prevent the development of other microorganisms. As a result, since sterilization can be avoided, fermentation procedures can be more straightforward, and the presence of highly trained microbial fermentation engineers may be avoided.

Moreover, as these extremophile bacteria are more robust, they are also more stable under changing growth conditions, allowing the automation of the procedures (Chen and Jiang 2018). In future fermentation techniques, the problem of freshwater shortage could be solved by recycling the fermentation broth or using seawater rather than fresh water. The fermentation broth is rich in substances such as quorum-sensing molecules, proteins, polysaccharides, genetic materials, and lipids that could be used in cellular metabolic processes and thus become nutrients for the cells still (Yue et al. 2014). Another step in the prospects of fermentation processes will be favoring anaerobic or microaerobic microorganisms. Indeed, today’s fermentation processes use aerobic bacteria that need a lot of oxygen to grow and to convert substrates into products, especially in large-scale bioreactors, in which air compressors provide oxygen. However, since oxygen solubility in water is low, most of these molecules escape into the air, passing through the bioreactors. One solution adopted is the overexpression of bacterial hemoglobin to improve the oxygen uptake, but the use of anaerobic/microaerophilic bacteria would really help and would also minimize energy consumption, especially during product formation. Furthermore, using microorganisms growing in a wide range of temperatures will save even more energy (Ouyang et al. 2018).

Currently, glucose derived from hydrolysate starch is mainly used to produce several products. In future fermentation, waste substrates, such as molasses, activated sludge, cellulose, hydrolyzed sugars, methane, CO, and H2, should be used as nutrients for cellular growth, avoiding waste production. Future fermentation will rely on modifying and controlling bacterial cell morphology and self-aggregation cell ability to more simply separate cells and fermented broth only by gravity, thus without using centrifugation and filtration techniques. These two expensive and time-consuming methods are currently used to separate smaller cells and heavily fermented broth (Wang et al. 2019). Fermentation industries also create a lot of waste water composed mainly of organic cell debris and inorganic salts. Waste products could be treated to become nutritive molecules for the cell to grow again. In this way, the treated fermented broth could return to the bioreactors as food for cell growth and avoid wastewater generation (Tang et al. 2017). Moreover, new fermentation approaches will focus on using bacteria resistant to extreme conditions. For instance, it was reported that the bacterium Halomonas campaniensis sp. LS21 was able under non-sterilization conditions continuously for several days without contamination (Yue et al. 2014). Most of the current fermentation processes are run batch or fed-batch and require a lot of heavy manual controls (Chen and Jiang 2018).

Moreover, using plastic materials will reduce bioreactors’ weight and enhance structures’ transparency. Using cement instead will allow the building of larger bioreactors like building skyscrapers. Future fermentations will be conducted under sterilization conditions. The fact that future fermentations will be done under non-sterile and in continuous conditions controlled by artificial intelligence (AI) will reduce even more water and energy consumption (Chen and Liu 2021). All fermentation processes generate supernatants and solid biomass as wastes. Both these two products need to be treated. For this, future fermentations can be designed to produce small molecular extracellular products and insoluble intracellular inclusion bodies, i.e., polyhydroxyalkanoates (PHA), polyphosphates, and so on. In this way, there would be a more significant recovery of products, otherwise eliminated, starting from a single process, improving the process economy (Ma et al. 2020).

Conclusion

The scientific investigations have provided deep insight into fermentation technology’s benefits regarding human health, food properties, and ecological well-being. Intriguingly, fermented functional foods have emerged as a critical subsector of the functional food industry, which has grown steadily over the past few years. Using various microbial species, particularly yeasts and various LAB strains, has significant industrial uses and even more promising future benefits in developing healthy cultured food and beverages. Fermentation has many potential health benefits, including producing beneficial lactic acid bacteria, ease of metabolism, increased nutritional availability, improved state of mind and behavior, and cardiovascular health benefits. Dairy and meat are the most popular fermented products widely consumed. On the other side, along with dairy and meat, fermented fruit and vegetables are well known for their worldwide consumption and health benefits. Increased awareness of alternative proteins has recently expanded fermented products with core ingredients of insects and seaweed. Moreover, to maximize the bioconversion efficiency of food waste, it is necessary to optimize the food-derived waste and use cutting-edge biotechnology methods. Innovative techniques like precision fermentation are well-suited to manufacture desired proteins, lipids, and carbohydrates because they enable the generation of molecules with similar constitutions as their conventionally farmed counterparts. In the future, fermentation industries will operate continuously, automation can be installed, and this will lead to a reduction in human involvement and the prevention of mistakes. In future fermentation, low-cost materials such as plastics, cement, or ceramic can be used instead of steel. In the bargain, Artificial Intelligence will be in charge of controlling fermentation, thus providing more efficient, sterile, and less energy, water, and workforce processes.

Author contributions

SAS: conceptualization, methodology, validation, formal analysis, resources, writing-original draft, writing- review and editing, visualization, data curation, project administration, investigation, supervision. ZE: writing-original draft. JR: conceptualization, methodology, investigation, writing-original draft. FT: writing-original draft. HAK: writing-original draft. VT: writing-original draft. LM: writing-original draft. GDG: writing-original draft. NAB: writing-original draft. MM: writing-review and editing. RC-M: reviewing and editing, Funding.

Funding

Financial support from Nobelium Joining Gdańsk Tech Research Community (contract number DEC 33/2022/IDUB/l.1; NOBELIUM nr 036236) is gratefully acknowledged. R. Castro-Muñoz also acknowledges the School of Engineering and Science and the FEMSA-Biotechnology Center at Tecnológico de Monterrey for their support through the Bioprocess (0020209I13) Focus Group.

Data availability

The data that support the findings of this study are available from the corresponding author, [Shahida Anusha Siddiqui], upon reasonable request.

Declarations

Ethics approval and consent to participate

Not applicable.

Consent for publication

Not applicable.

Competing interests

The authors report there are no competing interests to declare.

Footnotes

Publisher's Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Contributor Information

Shahida Anusha Siddiqui, Email: s.siddiqui@dil-ev.de.

Roberto Castro-Muñoz, Email: food.biotechnology88@gmail.com.

References

  1. Achi OK, Asamudo NU. Cereal-based fermented foods of africa as functional foods. In: Mérillon JM, Ramawat K, editors. Bioactive molecules in food. Reference series in phytochemistry. Cham: Springer; 2019. [Google Scholar]
  2. Adams MR. Fermented weaning foods. In: Wood BJB, editor. Microbiology of Fermented Foods. Boston: Springer; 1998. [Google Scholar]
  3. Adebo OA. African sorghum-based fermented foods: past. Curr Future Prospects Nutr. 2020;12:1111. doi: 10.3390/nu12041111. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Adebo OA, Njobeh PB, Sidu S, Adebiyi JA, Mavumengwana V. Aflatoxin B1 degradation by culture and lysate of a Pontibacter specie. Food Control. 2017;80:99–103. doi: 10.1016/j.foodcont.2017.04.042. [DOI] [Google Scholar]
  5. Adebo OA, Njobeh PB, Adeboye AS, Adebiyi JA, Sobowale SS, Ogundele OM, Kayitesi E. Innovations in technologies for fermented food and beverage ındustries. In: Panda S, Shetty P, editors. Food microbiology and food safety. Cham: Springer; 2018. [Google Scholar]
  6. Adesulu AT, Awojobi KO. Enhancing sustainable development through indigenous fermented food products in Nigeria. Afr J Microbiol Res. 2014;8(12):1338–1343. doi: 10.5897/ajmr2013.5439. [DOI] [Google Scholar]
  7. Adunphatcharaphon S, Petchkongkaew A, Visessanguan W. In vitro mechanism assessment of zearalenone removal by plant-derived Lactobacillus plantarum BCC 47723. Toxins. 2021;13(4):286. doi: 10.3390/toxins13040286. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Afzaal M, Saeed F, Anjum F, Waris N, Husaain M, Ikram A, Ateeq H, Muhammad Anjum F, Suleria H. Nutritional and ethnomedicinal scenario of koumiss: a concurrent review. Food Sci Nutr. 2021;9(11):6421–6428. doi: 10.1002/fsn3.2595. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Ahnan-Winarno AD, Cordeiro L, Winarno FG, Gibbons J, Xiao H. Tempeh: a semicentennial review on its health benefits, fermentation, safety, processing, sustainability, and affordability. Compr Rev Food Sci Food Saf. 2021;20(2):1717–1767. doi: 10.1111/1541-4337.12710. [DOI] [PubMed] [Google Scholar]
  10. Akbar A, Sadiq MB, Ali I, Anwar M, Muhammad N, Muhammad J, Shafee M, Ullah S, Gul Z, Qasim S, Ahmad S, Anal AK. Lactococcus lactis subsp. lactis isolated from fermented milk products and its antimicrobial potential. CyTA J Food. 2019;17(1):214–220. doi: 10.1080/19476337.2019.1575474. [DOI] [Google Scholar]
  11. Alapont C, López-Mendoza MC, Gil JV, Martínez-Culebras PV. Mycobiota and toxigenic Penicillium species on two Spanish dry-cured ham manufacturing plants. Food Addit Contam Part A. 2014;31(1):93–104. doi: 10.1080/19440049.2013.849007. [DOI] [PubMed] [Google Scholar]
  12. Alessandria V, Rantsiou K, Dolci P, Cocolin L. Methodologies for the study of microbial ecology in fermented sausages. In: Toldrá F, Hui YH, Astiasarán I, Sebranek JG, Talon R, editors. Handbook of fermented meat and poultry. Wiley; 2014. pp. 177–188. [Google Scholar]
  13. Algonaiman R, Alharbi HF, Barakat H. Antidiabetic and hypolipidemic efficiency of Lactobacillus plantarum fermented oat (Avena sativa) extract in streptozotocin-induced diabetes in rats. Fermentation. 2022;8(6):267. doi: 10.3390/fermentation8060267. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Alkema W, Boekhorst J, Wels M, van Hijum SAFT. Microbial bioinformatics for food safety and production. Brief Bioinform. 2016;17(2):283–292. doi: 10.1093/bib/bbv034. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Al-Mohammadi A-R, Ibrahim RA, Moustafa AH, Ismaiel AA, Abou Zeid A, Enan G. Chemical constitution and antimicrobial activity of kefir fermented beverage. Molecules. 2021;26(9):2635. doi: 10.3390/molecules26092635. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Alves SP, Alfaia CM, Škrbić BD, Živančev JR, Fernandes MJ, Bessa RJB, Fraqueza MJ. Screening chemical hazards of dry fermented sausages from distinct origins: Biogenic amines, polycyclic aromatic hydrocarbons and heavy elements. J Food Compos Anal. 2017;59:124–131. doi: 10.1016/j.jfca.2017.02.020. [DOI] [Google Scholar]
  17. Ambrogi V, Bottacini F, Cao L, Kuipers B, Schoterman M, van Sinderen D. Galacto-oligosaccharides as infant prebiotics: production, application, bioactive activities and future perspectives. Crit Rev Food Sci Nutr. 2023;63(6):753–766. doi: 10.1080/10408398.2021.1953437. [DOI] [PubMed] [Google Scholar]
  18. Angeles-Agdeppa I, Sun Y, Tanda KV. Dietary pattern and nutrient intakes in association with non-communicable disease risk factors among Filipino adults: a cross-sectional study. Nutr J. 2020;19(1):79. doi: 10.1186/s12937-020-00597-x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Anggraini, H., Tongkhao, K., and Chanput, W. 2018. Reducing milk allergenicity of cow, buffalo, and goat milk using lactic acid bacteria fermentation. 070010. 10.1063/1.5062808
  20. Antone U, Ciprovica I, Zolovs M, Scerbaka R, Liepins J. Propionic acid fermentation-study of substrates, strains, and antimicrobial properties. Fermentation. 2022;9(1):26. doi: 10.3390/fermentation9010026. [DOI] [Google Scholar]
  21. Anusha Siddiqui S, Bahmid NA, Mahmud CMM, Boukid F, Lamri M, Gagaoua M. Consumer acceptability of plant-, seaweed-, and insect-based foods as alternatives to meat: a critical compilation of a decade of research. Crit Rev Food Sci Nutr. 2022 doi: 10.1080/10408398.2022.2036096. [DOI] [PubMed] [Google Scholar]
  22. Apriyantono A, Wiratma E, Nurhayati HH, Lie L, Judoamidjojo M, Puspitasari-Nienaber NL, Budiyanto S, Sumaryanto H. Analysis of volatiles of Kecap Manis (a typical ındonesian soy sauce) Flav Sci. 1996 doi: 10.1533/9781845698232.1.62. [DOI] [Google Scholar]
  23. Asama T, Kimura Y, Kono T, Tatefuji T, Hashimoto K, Benno Y. Effects of heat-killed Lactobacillus kunkeei YB38 on human intestinal environment and bowel movement: a pilot study. Benef Microb. 2016;7(3):337–344. doi: 10.3920/BM2015.0132. [DOI] [PubMed] [Google Scholar]
  24. Ashokkumar V, Flora G, Venkatkarthick R, SenthilKannan K, Kuppam C, Mary Stephy G, Kamyab H, Chen W-H, Thomas J, Ngamcharussrivichai C. Advanced technologies on the sustainable approaches for conversion of organic waste to valuable bioproducts: emerging circular bioeconomy perspective. Fuel. 2022;324:124313. doi: 10.1016/j.fuel.2022.124313. [DOI] [Google Scholar]
  25. Augustin MA, Hartley CJ, Maloney G, Tyndall S. Innovation in precision fermentation for food ingredients. Crit Rev Food Sci Nutr. 2023 doi: 10.1080/10408398.2023.2166014. [DOI] [PubMed] [Google Scholar]
  26. Austin-Watson C, Grant A, Brice M. Suppression of Listeria monocytogenes by the native micro-flora in teewurst sausage. Foods. 2013;2(4):478–487. doi: 10.3390/foods2040478. [DOI] [PMC free article] [PubMed] [Google Scholar]
  27. Azizkhani M, Saris PEJ, Baniasadi M. An in-vitro assessment of antifungal and antibacterial activity of cow, camel, ewe, and goat milk kefir and probiotic yogurt. J Food Meas Charact. 2021;15(1):406–415. doi: 10.1007/s11694-020-00645-4. [DOI] [Google Scholar]
  28. Bachmann H, Pronk JT, Kleerebezem M, Teusink B. Evolutionary engineering to enhance starter culture performance in food fermentations. Curr Opin Biotechnol. 2015;32:1–7. doi: 10.1016/j.copbio.2014.09.003. [DOI] [PubMed] [Google Scholar]
  29. Bachtarzi N, Kharroub K, Ruas-Madiedo P. Exopolysaccharide-producing lactic acid bacteria isolated from traditional Algerian dairy products and their application for skim-milk fermentations. LWT. 2019;107:117–124. doi: 10.1016/j.lwt.2019.03.005. [DOI] [Google Scholar]
  30. Bala JD, Kuta FA, Abioye OP, Adabara NU, Adelere IA, Abdulsalam R, Al-Gheethi AAS, Kaizar H, Onovughakpor C. Microbiology and quality assessment of burukutu: a Nigerian fermented alcoholic beverage. Niger J Technol Res. 2017;12(1):103–108. doi: 10.4314/njtr.v12i1.15. [DOI] [Google Scholar]
  31. Baldin JC, Munekata PES, Michelin EC, Polizer YJ, Silva PM, Canan TM, Pires MA, Godoy SHS, Fávaro-Trindade CS, Lima CG, Fernandes AM, Trindade MA. Effect of microencapsulated Jabuticaba (Myrciaria cauliflora) extract on quality and storage stability of mortadella sausage. Food Res Int. 2018;108:551–557. doi: 10.1016/j.foodres.2018.03.076. [DOI] [PubMed] [Google Scholar]
  32. Barile D, Rastall RA. Human milk and related oligosaccharides as prebiotics. Curr Opin Biotechnol. 2013;24(2):214–219. doi: 10.1016/j.copbio.2013.01.008. [DOI] [PubMed] [Google Scholar]
  33. Barni S, Liccioli G, Sarti L, Giovannini M, Novembre E, Mori F. Immunoglobulin E (IgE)-mediated food allergy in children: epidemiology, pathogenesis, diagnosis, prevention, and management. Medicina. 2020;56(3):111. doi: 10.3390/medicina56030111. [DOI] [PMC free article] [PubMed] [Google Scholar]
  34. Bartkiene E, Zokaityte E, Starkute V, Zokaityte G, Kaminskaite A, Mockus E, Klupsaite D, Cernauskas D, Rocha JM, Özogul F, Guiné RPF. Crickets (Acheta domesticus) as wheat bread ingredient: influence on bread quality and safety characteristics. Foods. 2023;12(2):325. doi: 10.3390/FOODS12020325/S1. [DOI] [PMC free article] [PubMed] [Google Scholar]
  35. Bastidas-Oyanedel J-R, Bonk F, Thomsen MH, Schmidt JE. Dark fermentation biorefinery in the present and future (bio)chemical industry. Rev Environ Sci Bio/technol. 2015;14(3):473–498. doi: 10.1007/s11157-015-9369-3. [DOI] [Google Scholar]
  36. Bengoa AA, Iraporda C, Garrote GL, Abraham AG. Kefir micro-organisms: their role in grain assembly and health properties of fermented milk. J Appl Microbiol. 2019;126(3):686–700. doi: 10.1111/jam.14107. [DOI] [PubMed] [Google Scholar]
  37. Berka RM, Nelson BA, Zaretsky EJ, Yoder WT, Rey MW. Genomics of Fusarium venenatum: An alternative fungal host for making enzymes. Appl Mycol Biotechnol. 2004;4:191–203. doi: 10.1016/S1874-5334(04)80010-8. [DOI] [Google Scholar]
  38. Bertuzzi T, Gualla A, Morlacchini M, Pietri A. Direct and indirect contamination with ochratoxin A of ripened pork products. Food Control. 2013;34(1):79–83. doi: 10.1016/j.foodcont.2013.04.011. [DOI] [Google Scholar]
  39. Bhutia MO, Thapa N, Tamang JP. Molecular characterization of bacteria, detection of enterotoxin genes, and screening of antibiotic susceptibility patterns in traditionally processed meat products of Sikkim, India. Front Microbiol. 2021 doi: 10.3389/fmicb.2020.599606. [DOI] [PMC free article] [PubMed] [Google Scholar]
  40. Bilal M, Xu S, Iqbal HMN, Cheng H. Yarrowia lipolytica as an emerging biotechnological chassis for functional sugars biosynthesis. Crit Rev Food Sci Nutr. 2021;61(4):535–552. doi: 10.1080/10408398.2020.1739000. [DOI] [PubMed] [Google Scholar]
  41. Bilo F, Pandini S, Sartore L, Depero LE, Gargiulo G, Bonassi A, Federici S, Bontempi E. A sustainable bioplastic obtained from rice straw. J Clean Prod. 2018;200:357–368. doi: 10.1016/j.jclepro.2018.07.252. [DOI] [Google Scholar]
  42. Bingol EB, Ciftcioglu G, Yilmaz Eker F, Yardibi H, Yesil O, Bayrakal G, Demirel G. Effect of starter cultures combinations on lipolytic activity and ripening of dry fermented sausages. Ital J Anim Sci. 2014 doi: 10.4081/ijas.2014.3422. [DOI] [Google Scholar]
  43. Bintsis T, Papademas P. The evolution of fermented milks, from artisanal to industrial products: a critical review. Fermentation. 2022;8(12):679. doi: 10.3390/fermentation8120679. [DOI] [Google Scholar]
  44. Biscola V, Tulini FL, Choiset Y, Rabesona H, Ivanova I, Chobert J-M, Todorov SD, Haertlé T, Franco BDGM. Proteolytic activity of Enterococcus faecalis VB63F for reduction of allergenicity of bovine milk proteins. J Dairy Sci. 2016;99(7):5144–5154. doi: 10.3168/jds.2016-11036. [DOI] [PubMed] [Google Scholar]
  45. Biscola V, Choiset Y, Rabesona H, Chobert JM, Haertlé T, Franco BDGM. Brazilian artisanal ripened cheeses as sources of proteolytic lactic acid bacteria capable of reducing cow milk allergy. J Appl Microbiol. 2018;125(2):564–574. doi: 10.1111/jam.13779. [DOI] [PubMed] [Google Scholar]
  46. Borremans A, Lenaerts S, Crauwels S, Lievens B, Van Campenhout L. Marination and fermentation of yellow mealworm larvae (Tenebrio molitor) Food Control. 2018;92:47–52. doi: 10.1016/J.FOODCONT.2018.04.036. [DOI] [Google Scholar]
  47. Botthoulath V, Upaichit A, Thumarat U. Characterization of Listeria-active bacteriocin produced by a new strain Lactobacillus plantarum subsp. plantarum SKI19 isolated from “sai krok e-san mu”. Int Food Res J. 2018;25(6):2362–2371. [Google Scholar]
  48. Bourdichon F, Arias E, Babuchowski A, Bückle A, Bello FD, Dubois A, Fontana A, Fritz D, Kemperman R, Laulund S, McAuliffe O, Miks MH, Papademas P, Patrone V, Sharma DK, Sliwinski E, Stanton C, Von Ah U, Yao S, Morelli L. The forgotten role of food cultures. FEMS Microbiol Lett. 2021 doi: 10.1093/femsle/fnab085. [DOI] [PMC free article] [PubMed] [Google Scholar]
  49. Brancoli P, Gmoser R, Taherzadeh MJ, Bolton K. The use of life cycle assessment in the support of the development of fungal food products from surplus bread. Fermentation. 2021;7(3):173. doi: 10.3390/fermentation7030173. [DOI] [Google Scholar]
  50. Bryant C, Sanctorum H. Alternative proteins, evolving attitudes: Comparing consumer attitudes to plant-based and cultured meat in Belgium in two consecutive years. Appetite. 2021;161:105161. doi: 10.1016/J.APPET.2021.105161. [DOI] [PubMed] [Google Scholar]
  51. Bücher C, Burtscher J, Domig KJ. Propionic acid bacteria in the food industry: An update on essential traits and detection methods. Compr Rev Food Sci Food Saf. 2021;20(5):4299–4323. doi: 10.1111/1541-4337.12804. [DOI] [PubMed] [Google Scholar]
  52. CAC (2003) Standard for fermented milks. https://www.fao.org/fao-who-codexalimentarius/sh-proxy/en/?lnk=1&url=https%253A%252F%252Fworkspace.fao.org%252Fsites%252Fcodex%252FStandards%252FCXS%2B243-2003%252FCXS_243e.pdf
  53. Cai T, Wu H, Qin J, Qiao J, Yang Y, Wu Y, Qiao D, Xu H, Cao Y. In vitro evaluation by PCA and AHP of potential antidiabetic properties of lactic acid bacteria isolated from traditional fermented food. LWT. 2019;115:108455. doi: 10.1016/j.lwt.2019.108455. [DOI] [Google Scholar]
  54. Cai YX, Augustin MA, Jegasothy H, Wang JH, Terefe NS. Mild heat combined with lactic acid fermentation: a novel approach for enhancing sulforaphane yield in broccoli puree. Food Funct. 2020;11(1):779–786. doi: 10.1039/c9fo02089f. [DOI] [PubMed] [Google Scholar]
  55. Campbell-Platt G. Fermented foods-a world perspective. Food Res Int. 1994;27(3):253–257. doi: 10.1016/0963-9969(94)90093-0. [DOI] [Google Scholar]
  56. Cao ZH, Green-Johnson JM, Buckley ND, Lin QY. Bioactivity of soy-based fermented foods: a review. Biotechnol Adv. 2019;37(1):223–238. doi: 10.1016/J.BIOTECHADV.2018.12.001. [DOI] [PubMed] [Google Scholar]
  57. Caparros Megido R, Sablon L, Geuens M, Brostaux Y, Alabi T, Blecker C, Drugmand D, Haubruge É, Francis F. Edible ınsects acceptance by belgian consumers: promising attitude for entomophagy development. J Sens Stud. 2014;29(1):14–20. doi: 10.1111/joss.12077. [DOI] [Google Scholar]
  58. Caparros Megido R, Gierts C, Blecker C, Brostaux Y, Haubruge É, Alabi T, Francis F. Consumer acceptance of insect-based alternative meat products in Western countries. Food Qual Prefer. 2016;52:237–243. doi: 10.1016/j.foodqual.2016.05.004. [DOI] [Google Scholar]
  59. Capson-Tojo G, Rouez M, Crest M, Steyer JP, Delgenès JP, Escudié R. Food waste valorization via anaerobic processes: a review. Rev Environ Sci Bio/technol. 2016;15(3):499–547. doi: 10.1007/s11157-016-9405-y. [DOI] [Google Scholar]
  60. Carmona-Cabello M, Garcia IL, Leiva-Candia D, Dorado MP. Valorization of food waste based on its composition through the concept of biorefinery. Curr Opin Green Sustain Chem. 2018;14:67–79. doi: 10.1016/j.cogsc.2018.06.011. [DOI] [Google Scholar]
  61. Celotti E, Stante S, Ferraretto P, Román T, Nicolini G, Natolino A. High power ultrasound treatments of red young wines: effect on anthocyanins and phenolic stability indices. Foods. 2020;9(10):10. doi: 10.3390/foods9101344. [DOI] [PMC free article] [PubMed] [Google Scholar]
  62. Chai KF, Ng KR, Samarasiri M, Chen WN. Precision fermentation to advance fungal food fermentations. Curr Opin Food Sci. 2022;47:100881. doi: 10.1016/j.cofs.2022.100881. [DOI] [Google Scholar]
  63. Chai S, Zhu Z, Tian E, Xiao M, Wang Y, Zou G, Zhou Z. Building a versatile protein production platform using engineered Trichoderma reesei. ACS Synth Biol. 2022;11(1):486–496. doi: 10.1021/acssynbio.1c00570. [DOI] [PubMed] [Google Scholar]
  64. Chandrasekhar K, Venkata Mohan S. Induced catabolic bio-electrohydrolysis of complex food waste by regulating external resistance for enhancing acidogenic biohydrogen production. Biores Technol. 2014;165:372–382. doi: 10.1016/j.biortech.2014.02.073. [DOI] [PubMed] [Google Scholar]
  65. Charlton S, Ramsøe A, Collins M, Craig OE, Fischer R, Alexander M, Speller CF. New insights into Neolithic milk consumption through proteomic analysis of dental calculus. Archaeol Anthropol Sci. 2019;11(11):6183–6196. doi: 10.1007/s12520-019-00911-7. [DOI] [Google Scholar]
  66. Chaudhari DD, Singh R, Mallappa RH, Rokana N, Kaushik JK, Bajaj R, Batish VK, Grover S. Evaluation of casein and whey protein hydrolysates as well as milk fermentates from Lactobacillus helveticus for expression of gut hormones. Indian J Med Res. 2017;146:409–419. doi: 10.4103/ijmr.IJMR_802_15. [DOI] [PMC free article] [PubMed] [Google Scholar]
  67. Chen GQ, Jiang XR. Next generation industrial biotechnology based on extremophilic bacteria. Curr Opin Biotechnol. 2018;50:94–100. doi: 10.1016/j.copbio.2017.11.016. [DOI] [PubMed] [Google Scholar]
  68. Chen G, Liu X. On the future fermentation. Microb Biotechnol. 2021;14(1):18–21. doi: 10.1111/1751-7915.13674. [DOI] [PMC free article] [PubMed] [Google Scholar]
  69. Cho YM, Fujita Y, Kieffer TJ. Glucagon-like peptide-1: glucose homeostasis and beyond. Annu Rev Physiol. 2014;76(1):535–559. doi: 10.1146/annurev-physiol-021113-170315. [DOI] [PubMed] [Google Scholar]
  70. Cho JH, Zhao HL, Kim JS, Kim SH, Chung CH. Characteristics of fermented seasoning sauces using Tenebrio molitor larvae. Innov Food Sci Emerg Technol. 2018;45:186–195. doi: 10.1016/J.IFSET.2017.10.010. [DOI] [Google Scholar]
  71. Cho HD, Min HJ, Won YS, Ahn HY, Cho YS, Seo K. Solid state fermentation process with Aspergillus kawachii enhances the cancer-suppressive potential of silkworm larva in hepatocellular carcinoma cells. BMC Complement Altern Med. 2019;19(1):241. doi: 10.1186/S12906-019-2649-7/TABLES/3. [DOI] [PMC free article] [PubMed] [Google Scholar]
  72. Chua LS, Abdullah FI, Lim SH. Physiochemical changes and nutritional content of black garlic during fermentation. Appl Food Res. 2022;2(2):100216. doi: 10.1016/J.AFRES.2022.100216. [DOI] [Google Scholar]
  73. Companys J, Pedret A, Valls RM, Solà R, Pascual V. Fermented dairy foods rich in probiotics and cardiometabolic risk factors: a narrative review from prospective cohort studies. Crit Rev Food Sci Nutr. 2021;61(12):1966–1975. doi: 10.1080/10408398.2020.1768045. [DOI] [PubMed] [Google Scholar]
  74. Dahiya D, Nigam PS. Probiotics, prebiotics, synbiotics, and fermented foods as potential biotics in nutrition improving health via microbiome-gut-brain axis. Fermentation. 2022;8:303. doi: 10.3390/fermentation8070303. [DOI] [Google Scholar]
  75. Dan T, Wang D, Wu S, Jin R, Ren W, Sun T. Profiles of volatile flavor compounds in milk fermented with different proportional combinations of Lactobacillus delbrueckii subsp. bulgaricus and Streptococcus thermophilus. Molecules. 2017;22(10):1633. doi: 10.3390/molecules22101633. [DOI] [PMC free article] [PubMed] [Google Scholar]
  76. Dao MC, Everard A, Aron-Wisnewsky J, Sokolovska N, Prifti E, Verger EO, Kayser BD, Levenez F, Chilloux J, Hoyles L, Dumas M-E, Rizkalla SW, Doré J, Cani PD, Clément K, Consortium, M.-O Akkermansia muciniphila and improved metabolic health during a dietary intervention in obesity: Relationship with gut microbiome richness and ecology. Gut Microb. 2016;65(3):426–436. doi: 10.1136/gutjnl-2014-308778. [DOI] [PubMed] [Google Scholar]
  77. Dargahi N, Johnson J, Donkor O, Vasiljevic T, Apostolopoulos V. Immunomodulatory effects of probiotics: can they be used to treat allergies and autoimmune diseases? Maturitas. 2019;119:25–38. doi: 10.1016/j.maturitas.2018.11.002. [DOI] [PubMed] [Google Scholar]
  78. Das RK, Brar SK, Verma M. Potential use of pulp and paper solid waste for the bio-production of fumaric acid through submerged and solid state fermentation. J Clean Prod. 2016;5(112):4435–4444. doi: 10.1016/j.jclepro.2015.08.108. [DOI] [Google Scholar]
  79. De Castro RJS, Ohara A, Nishide TG, Bagagli MP, Gonçalves Dias FF, Sato HH. A versatile system based on substrate formulation using agroindustrial wastes for protease production by Aspergillus niger under solid state fermentation. Biocatal Agric Biotechnol. 2015;4(4):678–684. doi: 10.1016/j.bcab.2015.08.010. [DOI] [Google Scholar]
  80. De Groof V, Coma M, Arnot T, Leak DJ, Lanham AB. Selecting fermentation products for food waste valorisation with HRT and OLR as the key operational parameters. Waste Manage. 2021;127:80–89. doi: 10.1016/j.wasman.2021.04.023. [DOI] [PubMed] [Google Scholar]
  81. De Melo Pereira GV, Neto E, Soccol VT, Medeiros ABP, Woiciechowski AL, Soccol CR. Conducting starter culture-controlled fermentations of coffee beans during on-farm wet processing: growth, metabolic analyses and sensorial effects. Food Res Int. 2015;75:348–356. doi: 10.1016/J.FOODRES.2015.06.027. [DOI] [PubMed] [Google Scholar]
  82. De Noronha MC, Cardoso RR, dos Santos Dalmeida CT, Vieira do Carmo MA, Azevedo L, Maltarollo VG, Júnior JIR, Eller MR, Cameron LC, Ferreira MSL, Barros FAR. Black tea kombucha: Physicochemical, microbiological and comprehensive phenolic profile changes during fermentation, and antimalarial activity. Food Chem. 2022;384:132515. doi: 10.1016/J.FOODCHEM.2022.132515. [DOI] [PubMed] [Google Scholar]
  83. De Smet J, Lenaerts S, Borremans A, Scholliers J, Van Der Borght M, Van Campenhout L. Stability assessment and laboratory scale fermentation of pastes produced on a pilot scale from mealworms (Tenebrio molitor) LWT. 2019;102:113–121. doi: 10.1016/J.LWT.2018.12.017. [DOI] [Google Scholar]
  84. de Vergara CMAC, Honorato TL, Maia GA, Rodrigues S. Prebiotic effect of fermented cashew apple (Anacardium occidentale L.) juice. LWT Food Sci Technol. 2010;43(1):141–145. doi: 10.1016/J.LWT.2009.06.009. [DOI] [Google Scholar]
  85. De Vuyst L, Leroy F. Bacteriocins from lactic acid bacteria: production, purification, and food applications. Microb Physiol. 2007;13(4):194–199. doi: 10.1159/000104752. [DOI] [PubMed] [Google Scholar]
  86. Deibel RH, Wilson GD, Niven CF. Microbiology of meat curing IV. A lyophilized pediococcus cerevisiae starter culture for fermented sausage. Appl Microbiol. 1961;9(3):239–243. doi: 10.1128/am.9.3.239-243.1961. [DOI] [PMC free article] [PubMed] [Google Scholar]
  87. Desnoues E, Baldazzi V, Génard M, Mauroux J-B, Lambert P, Confolent C, Quilot-Turion B. Dynamic QTLs for sugars and enzyme activities provide an overview of genetic control of sugar metabolism during peach fruit development. J Exp Bot. 2016;67(11):3419–3431. doi: 10.1093/jxb/erw169. [DOI] [PMC free article] [PubMed] [Google Scholar]
  88. Di Cagno R, Surico RF, Minervini G, Rizzello CG, Lovino R, Servili M, Taticchi A, Urbani S, Gobbetti M. Exploitation of sweet cherry (Prunus avium L.) puree added of stem infusion through fermentation by selected autochthonous lactic acid bacteria. Food Microbiol. 2011;28(5):900–909. doi: 10.1016/J.FM.2010.12.008. [DOI] [PubMed] [Google Scholar]
  89. Di Cagno R, Coda R, De Angelis M, Gobbetti M. Exploitation of vegetables and fruits through lactic acid fermentation. Food Microbiol. 2013;33(1):1–10. doi: 10.1016/J.FM.2012.09.003. [DOI] [PubMed] [Google Scholar]
  90. Di Cagno R, Filannino P, Cantatore V, Polo A, Celano G, Martinovic A, Cavoski I, Gobbetti M. Design of potential probiotic yeast starters tailored for making a cornelian cherry (Cornus mas L.) functional beverage. Int J Food Microbiol. 2020;323:108591. doi: 10.1016/j.ijfoodmicro.2020.108591. [DOI] [PubMed] [Google Scholar]
  91. dos Mathias TRS, de Aguiar PF, de Silva JBA, de Mello PPM, Sérvulo EFC. Brewery wastes reuse for protease production by lactic acid bacteria fermentation. Food Technol Biotechnol. 2017 doi: 10.17113/ftb.55.02.17.4378. [DOI] [PMC free article] [PubMed] [Google Scholar]
  92. Dulf FV, Vodnar DC, Socaciu C. Effects of solid-state fermentation with two filamentous fungi on the total phenolic contents, flavonoids, antioxidant activities and lipid fractions of plum fruit (Prunus domestica L.) by-products. Food Chem. 2016;209:27–36. doi: 10.1016/j.foodchem.2016.04.016. [DOI] [PubMed] [Google Scholar]
  93. Dursun D, Dalgıç AC. Optimization of astaxanthin pigment bioprocessing by four different yeast species using wheat wastes. Biocatal Agric Biotechnol. 2016;7:1–6. doi: 10.1016/j.bcab.2016.04.006. [DOI] [Google Scholar]
  94. EFSA Scientific opinion on risk based control of biogenic amine formation in fermented foods. EFSA J. 2011 doi: 10.2903/j.efsa.2011.2393. [DOI] [Google Scholar]
  95. El Mecherfi K, Lupi R, Albuquerque M, De Albuquerque C, Haertlé T (2019) Gluten fermentation with selected lactic acid bacteria strains induces its proteolysis and decreases its antigenicity. Conference: Allergy, 74: (S106). 10.13140/RG.2.2.25651.78886
  96. El-Mansi EMT, Nielsen J, Mousdale D, Carlson RP. Fermentation microbiology and biotechnology. 4. CRC Press; 2019. [Google Scholar]
  97. Evangelista SR, da Cruz Pedrozo Miguel MG, de Souza Cordeiro C, Silva CF, Marques Pinheiro AC, Schwan RF. Inoculation of starter cultures in a semi-dry coffee (Coffea arabica) fermentation process. Food Microbiol. 2014;44:87–95. doi: 10.1016/J.FM.2014.05.013. [DOI] [PubMed] [Google Scholar]
  98. Fang B, Sun J, Dong P, Xue C, Mao X. Conversion of turbot skin wastes into valuable functional substances with an eco-friendly fermentation technology. J Clean Prod. 2017;156:367–377. doi: 10.1016/j.jclepro.2017.04.055. [DOI] [Google Scholar]
  99. Farag MA, Saleh HA, El Ahmady S, Elmassry MM. Dissecting yogurt: the impact of milk types, probiotics, and selected additives on yogurt quality. Food Rev Intl. 2022;38:634–650. doi: 10.1080/87559129.2021.1877301. [DOI] [Google Scholar]
  100. Farahmand N, Ouoba LII, Naghizadeh Raeisi S, Sutherland J, Ghoddusi HB. Probiotic Lactobacilli in fermented dairy products: selective detection. Enumer Identification Scheme Microorg. 2021;9(8):1600. doi: 10.3390/microorganisms9081600. [DOI] [PMC free article] [PubMed] [Google Scholar]
  101. Fatahi A, Soleimani N, Afrough P. Anticancer activity of kefir on glioblastoma cancer cell as a new treatment. Int J Food Sci. 2021;2021:1–5. doi: 10.1155/2021/8180742. [DOI] [PMC free article] [PubMed] [Google Scholar]
  102. Fatmawati F, Sibero MT, Trianto A, Wijayanti DP, Sabdono A, Pringgenies D, Radjasa OK. The influence of fermentation using marine yeast Hortaea werneckii SUCCY001 on antibacterial and antioxidant activity of Gracilaria verrucosa. Biodiversitas. 2022;23(10):5258–5266. doi: 10.13057/BIODIV/D231035. [DOI] [Google Scholar]
  103. Fekete Á, Givens D, Lovegrove J. Casein-derived lactotripeptides reduce systolic and diastolic blood pressure in a meta-analysis of randomised clinical trials. Nutrients. 2015;7(1):659–681. doi: 10.3390/nu7010659. [DOI] [PMC free article] [PubMed] [Google Scholar]
  104. Feng L, Xie Y, Peng C, Liu Y, Wang H. A novel antidiabetic food produced via solid-state fermentation of tartary buckwheat using L. plantarum TK9 and L. paracasei TK1501. Food Technol Biotechnol. 2018 doi: 10.17113/ftb.56.03.18.5540. [DOI] [PMC free article] [PubMed] [Google Scholar]
  105. Feng R, Chen L, Chen K. Fermentation trip: Amazing microbes, amazing metabolisms. Ann Microbiol. 2018;68(11):Articolo 11. doi: 10.1007/s13213-018-1384-5. [DOI] [Google Scholar]
  106. Fernandes N, Faria AS, Carvalho L, Choupina A, Rodrigues C, Cadavez V, Gonzales-Barron U. Molecular identification of lactic acid producing bacteria isolated from alheira, a traditional portuguese fermented sausage. Foods. 2022;18(1):73. doi: 10.3390/Foods2022-13035. [DOI] [PMC free article] [PubMed] [Google Scholar]
  107. Ferracane A, Tropea A, Salafia F. Production and maturation of soaps with non-edible fermented olive oil and comparison with classic olive oil soaps. Fermentation. 2021;7(4):Articolo 4. doi: 10.3390/fermentation7040245. [DOI] [Google Scholar]
  108. Fibri DLN, Frøst MB. Consumer perception of original and modernised traditional foods of Indonesia. Appetite. 2019;133:61–69. doi: 10.1016/J.APPET.2018.10.026. [DOI] [PubMed] [Google Scholar]
  109. Filannino P, Bai Y, Di Cagno R, Gobbetti M, Gänzle MG. Metabolism of phenolic compounds by Lactobacillus spp. during fermentation of cherry juice and broccoli puree. Food Microbiol. 2015;46:272–279. doi: 10.1016/j.fm.2014.08.018. [DOI] [PubMed] [Google Scholar]
  110. Fu L, Cherayil BJ, Shi H, Wang Y, Zhu Y. Food allergy. Singapore: Springer; 2019. Food processing to eliminate food allergens and development of hypoallergenic foods; pp. 123–146. [Google Scholar]
  111. Fujita A, Sarkar D, Genovese MI, Shetty K. Improving anti-hyperglycemic and anti-hypertensive properties of camu-camu (Myriciaria dubia Mc. Vaugh) using lactic acid bacterial fermentation. Process Biochem. 2017;59:133–140. doi: 10.1016/j.procbio.2017.05.017. [DOI] [Google Scholar]
  112. Galimberti A, Bruno A, Agostinetto G, Casiraghi M, Guzzetti L, Labra M. Fermented food products in the era of globalization: tradition meets biotechnology innovations. Curr Opin Biotechnol. 2021;70:36–41. doi: 10.1016/j.copbio.2020.10.006. [DOI] [PubMed] [Google Scholar]
  113. Galli V, Venturi M, Mari E, Guerrini S, Granchi L. Selection of yeast and lactic acid bacteria strains, isolated from spontaneous raw milk fermentation, for the production of a potential probiotic fermented milk. Fermentation. 2022;8(8):407. doi: 10.3390/fermentation8080407. [DOI] [Google Scholar]
  114. Gamba RR, Caro CA, Martínez OL, Moretti AF, Giannuzzi L, De Antoni GL, León Peláez A. Antifungal effect of kefir fermented milk and shelf life improvement of corn arepas. Int J Food Microbiol. 2016;235:85–92. doi: 10.1016/j.ijfoodmicro.2016.06.038. [DOI] [PubMed] [Google Scholar]
  115. Gänzle M. The periodic table of fermented foods: limitations and opportunities. Appl Microbiol Biotechnol. 2022;106(8):2815–2826. doi: 10.1007/s00253-022-11909-y. [DOI] [PubMed] [Google Scholar]
  116. Gao J, Gu F, Ruan H, Chen Q, He J, He G. Induction of apoptosis of gastric cancer cells SGC7901 in vitro by a cell-free fraction of Tibetan kefir. Int Dairy J. 2013;30(1):14–18. doi: 10.1016/j.idairyj.2012.11.011. [DOI] [Google Scholar]
  117. García-Burgos M, Moreno-Fernández J, Alférez MJM, Díaz-Castro J, López-Aliaga I. New perspectives in fermented dairy products and their health relevance. J Funct Foods. 2020;72:104059. doi: 10.1016/j.jff.2020.104059. [DOI] [Google Scholar]
  118. García-Cano I, Rocha-Mendoza D, Ortega-Anaya J, Wang K, Kosmerl E, Jiménez-Flores R. Lactic acid bacteria isolated from dairy products as potential producers of lipolytic, proteolytic and antibacterial proteins. Appl Microbiol Biotechnol. 2019;103(13):5243–5257. doi: 10.1007/s00253-019-09844-6. [DOI] [PMC free article] [PubMed] [Google Scholar]
  119. Gavahian M, Manyatsi TS, Morata A, Tiwari BK. Ultrasound-assisted production of alcoholic beverages: from fermentation and sterilization to extraction and aging. Compr Rev Food Sci Food Saf. 2022;21(6):5243–5271. doi: 10.1111/1541-4337.13043. [DOI] [PubMed] [Google Scholar]
  120. Gernah DI, Ariahu CC, Ingbian IK. Effects of malting and lactic fermentation on some chemical and functional properties of maize (Zea mays) Am J Food Technol. 2011;6(5):404–412. doi: 10.3923/ajft.2011.404.412. [DOI] [Google Scholar]
  121. Gholamhosseinpour A, Hashemi SMB. Ultrasound pretreatment of fermented milk containing probiotic Lactobacillus plantarum AF1: carbohydrate metabolism and antioxidant activity. J Food Process Eng. 2019;42(1):e12930. doi: 10.1111/jfpe.12930. [DOI] [Google Scholar]
  122. Giacalone D, Clausen MP, Jaeger SR. Understanding barriers to consumption of plant-based foods and beverages: insights from sensory and consumer science. Curr Opin Food Sci. 2022;48:100919. doi: 10.1016/J.COFS.2022.100919. [DOI] [Google Scholar]
  123. Gmoser R, Sintca C, Taherzadeh MJ, Lennartsson PR. Combining submerged and solid state fermentation to convert waste bread into protein and pigment using the edible filamentous fungus N. intermedia. Waste Manage. 2019;97:63–70. doi: 10.1016/j.wasman.2019.07.039. [DOI] [PubMed] [Google Scholar]
  124. González-Quijano GK, Dorantes-Alvarez L, Hernández-Sánchez H, Jaramillo-Flores ME, de Jesús Perea-Flores M, Vera-Ponce de León A, Hernández-Rodríguez C. Halotolerance and survival kinetics of lactic acid bacteria isolated from Jalapeño pepper (Capsicum annuum L.) Fermentation. J Food Sci. 2014;79(8):M1545–M1553. doi: 10.1111/1750-3841.12498. [DOI] [PubMed] [Google Scholar]
  125. Gullón B, Gagaoua M, Barba FJ, Gullón P, Zhang W, Lorenzo JM. Seaweeds as promising resource of bioactive compounds: overview of novel extraction strategies and design of tailored meat products. Trends Food Sci Technol. 2020;100:1–18. doi: 10.1016/J.TIFS.2020.03.039. [DOI] [Google Scholar]
  126. Gullón P, Astray G, Gullón B, Franco D, Campagnol PCB, Lorenzo JM. Inclusion of seaweeds as healthy approach to formulate new low-salt meat products. Curr Opin Food Sci. 2021;40:20–25. doi: 10.1016/J.COFS.2020.05.005. [DOI] [Google Scholar]
  127. Gupta S, Abu-Ghannam N. Probiotic fermentation of plant based products: possibilities and opportunities. Crit Rev Food Sci Nutr. 2011;52(2):183–199. doi: 10.1080/10408398.2010.499779. [DOI] [PubMed] [Google Scholar]
  128. Gupta GN, Srivastava S, Khare SK, Prakash V. Extremophiles: an overview of microorganism from extreme environment. Int J Agric Environ Biotechnol. 2014;7(2):371–380. doi: 10.5958/2230-732X.2014.00258.7. [DOI] [Google Scholar]
  129. Ha NI, Mun SK, Im SB, Jang HY, Jeong HG, Kang KY, Park KW, Seo KS, Ban SE, Kim KJ, Yee ST. 2022. Changes in functionality of tenebrio molitor larvae fermented by Cordyceps militaris mycelia. Foods. [DOI] [PMC free article] [PubMed]
  130. Haile M, Kang WH. Antioxidant activity, total polyphenol, flavonoid and tannin contents of fermented green coffee beans with selected yeasts. Fermentation. 2019;5:29. doi: 10.3390/FERMENTATION5010029. [DOI] [Google Scholar]
  131. Haile M, Kang WH. The role of microbes in coffee fermentation and their ımpact on coffee quality. J Food Qual. 2019 doi: 10.1155/2019/4836709. [DOI] [Google Scholar]
  132. Hamid Abadi Sherahi M, Shahidi F, Yazdi FT, Hashemi SMB. Effect of Lactobacillus plantarum on olive and olive oil quality during fermentation process. LWT. 2018;89:572–580. doi: 10.1016/J.LWT.2017.10.025. [DOI] [Google Scholar]
  133. Han YM, Kang EA, Min Park J, Young Oh J, Yoon Lee D, Hye Choi S, Baik HK. Dietary intake of fermented kimchi prevented colitis-associated cancer. J Clin Biochem Nutr. 2020;67(3):263–273. doi: 10.3164/jcbn.20-77. [DOI] [PMC free article] [PubMed] [Google Scholar]
  134. Hancioǧlu Ö, Karapinar M. Microflora of Boza, a traditional fermented Turkish beverage. Int J Food Microbiol. 1997;35(3):271–274. doi: 10.1016/S0168-1605(96)01230-5. [DOI] [PubMed] [Google Scholar]
  135. Hati S, Patel M, Mishra BK, Das S. Short-chain fatty acid and vitamin production potentials of Lactobacillus isolated from fermented foods of Khasi Tribes, Meghalaya, India. Ann Microbiol. 2019;69(11):1191–1199. doi: 10.1007/s13213-019-01500-8. [DOI] [Google Scholar]
  136. Hikmetoglu M, Sogut E, Sogut O, Gokirmakli C, Guzel-Seydim ZB. Changes in carbohydrate profile in kefir fermentation. Bioactive Carbohydr Diet Fibre. 2020;23:100220. doi: 10.1016/j.bcdf.2020.100220. [DOI] [Google Scholar]
  137. Hirata S, Kunisawa J. Gut microbiome, metabolome, and allergic diseases. Allergol Int. 2017;66(4):523–528. doi: 10.1016/j.alit.2017.06.008. [DOI] [PubMed] [Google Scholar]
  138. Ho CC. Identity and characteristics of Neurospora intermedia responsible for oncom fermentation in Indonesia. Food Microbiol. 1986;3(2):115–132. doi: 10.1016/S0740-0020(86)80035-1. [DOI] [Google Scholar]
  139. Ho VTT, Fleet GH, Zhao J. Unravelling the contribution of lactic acid bacteria and acetic acid bacteria to cocoa fermentation using inoculated organisms. Int J Food Microbiol. 2018;279:43–56. doi: 10.1016/J.IJFOODMICRO.2018.04.040. [DOI] [PubMed] [Google Scholar]
  140. Holck A, Axelsson L, McLeod A, Rode TM, Heir E. Health and safety considerations of fermented sausages. J Food Qual. 2017 doi: 10.1155/2017/9753894. [DOI] [Google Scholar]
  141. Hoseinifar SH, Sharifian M, Vesaghi MJ, Khalili M, Esteban MÁ. The effects of dietary xylooligosaccharide on mucosal parameters, intestinal microbiota and morphology and growth performance of Caspian white fish (Rutilus frisii kutum) fry. Fish Shellfish Immunol. 2014;39(2):231–236. doi: 10.1016/j.fsi.2014.05.009. [DOI] [PubMed] [Google Scholar]
  142. Hotessa N, Robe J. Ethiopian indigenous traditional fermented beverage: the role of the microorganisms toward nutritional and safety value of fermented beverage. Int J Microbiol. 2020 doi: 10.1155/2020/8891259. [DOI] [PMC free article] [PubMed] [Google Scholar]
  143. Im S, Lee MK, Yun YM, Cho SK, Kim DH. Effect of storage time and temperature on hydrogen fermentation of food waste. Int J Hydrogen Energy. 2020;45(6):3769–3775. doi: 10.1016/j.ijhydene.2019.06.215. [DOI] [Google Scholar]
  144. Iraporda C, Errea A, Romanin DE, Cayet D, Pereyra E, Pignataro O, Sirard JC, Garrote GL, Abraham AG, Rumbo M. Lactate and short chain fatty acids produced by microbial fermentation downregulate proinflammatory responses in intestinal epithelial cells and myeloid cells. Immunobiology. 2015;220(10):1161–1169. doi: 10.1016/j.imbio.2015.06.004. [DOI] [PubMed] [Google Scholar]
  145. Irwin JA. Overview of extremophiles and their food and medical applications. In: Salwan R, Sharma V, editors. Physiological and biotechnological aspects of extremophiles. Academic Press; 2020. pp. 65–87. [Google Scholar]
  146. Ishangulyyev R, Kim S, Lee S. Understanding food loss and waste-why are we losing and wasting food? Foods. 2019;8(8):297. doi: 10.3390/foods8080297. [DOI] [PMC free article] [PubMed] [Google Scholar]
  147. Jamal P, Akbar I. Process development for maximum lycopene production from selected fruit waste and its antioxidant and antiradical activity. J Food Process Technol. 2016 doi: 10.4172/2157-7110.1000576. [DOI] [Google Scholar]
  148. Jamir B, Deb CR. Nutritional and microbiological study of anishi: a traditional fermented food product of Nagaland, India. J Adv Food Sci Technol. 2021;4(3):113–121. [Google Scholar]
  149. Jang SH, Sim SY, Ahn HY, Seo KI, Cho YS. Physicochemical properties and biological activities of Tenebrio molitor fermented by several kinds of micro-organisms. J Life Sci. 2018;28(8):923–930. doi: 10.5352/JLS.2018.28.8.923. [DOI] [Google Scholar]
  150. Jeong SY, Kim E, Zhang M, Lee Y-S, Ji B, Lee S-H, Cheong YE, Yun S-I, Kim Y-S, Kim KH, Kim MS, Chun HS, Kim S. Antidiabetic effect of noodles containing fermented lettuce extracts. Metabolites. 2021;11(8):520. doi: 10.3390/metabo11080520. [DOI] [PMC free article] [PubMed] [Google Scholar]
  151. Jeyaram K, Romi W, Singh TA, Devi AR, Devi SS. Bacterial species associated with traditional starter cultures used for fermented bamboo shoot production in Manipur state of India. Int J Food Microbiol. 2010;143(1–2):1–8. doi: 10.1016/J.IJFOODMICRO.2010.07.008. [DOI] [PubMed] [Google Scholar]
  152. Jiang X, Ding H, Liu Q, Wei Y, Zhang Y, Wang Y, Lu Y, Ma A, Li Z, Hu Y. Effects of peanut meal extracts fermented by Bacillus natto on the growth performance, learning and memory skills and gut microbiota modulation in mice. Br J Nutr. 2020;123(4):383–393. doi: 10.1017/S0007114519002988. [DOI] [PubMed] [Google Scholar]
  153. Joët T, Laffargue A, Descroix F, Doulbeau S, Bertrand B, kochko, A. de, and Dussert, S. Influence of environmental factors, wet processing and their interactions on the biochemical composition of green Arabica coffee beans. Food Chem. 2010;118(3):693–701. doi: 10.1016/J.FOODCHEM.2009.05.048. [DOI] [Google Scholar]
  154. Joishy TK, Dehingia M, Khan MR. Bacterial diversity and metabolite profiles of curd prepared by natural fermentation of raw milk and back sloping of boiled milk. World J Microbiol Biotechnol. 2019;35(7):102. doi: 10.1007/s11274-019-2677-y. [DOI] [PubMed] [Google Scholar]
  155. Jones SE, Paynich ML, Kearns DB, Knight KL (2014) Protection from intestinal inflammation by bacterial exopolysaccharides. J Immunol 192(10):4813–4820. 10.4049/jimmunol.1303369 [DOI] [PMC free article] [PubMed]
  156. Joung H, Kim B, Park H, Lee K, Kim HH, Sim HC, Do HJ, Hyun CK, Do MS. Fermented Moringa oleifera decreases hepatic adiposity and ameliorates glucose intolerance in high-fat diet-induced obese mice. J Med Food. 2017;20(5):439–447. doi: 10.1089/jmf.2016.3860. [DOI] [PubMed] [Google Scholar]
  157. Juárez-Castelán C, García-Cano I, Escobar-Zepeda A, Azaola-Espinosa A, Álvarez-Cisneros Y, Ponce-Alquicira E. Evaluation of the bacterial diversity of Spanish-type chorizo during the ripening process using high-throughput sequencing and physicochemical characterization. Meat Sci. 2019;150:7–13. doi: 10.1016/j.meatsci.2018.09.001. [DOI] [PubMed] [Google Scholar]
  158. Kabak B, Dobson ADW. An introduction to the traditional fermented foods and beverages of Turkey. Crit Rev Food Sci Nutr. 2011;51(3):248–260. doi: 10.1080/10408390903569640. [DOI] [PubMed] [Google Scholar]
  159. Kamiloğlu A. Functional and technological characterization of lactic acid bacteria isolated from Turkish dry-fermented sausage (sucuk) Braz J Microbiol. 2022;53(2):959–968. doi: 10.1007/s42770-022-00708-2. [DOI] [PMC free article] [PubMed] [Google Scholar]
  160. Kang CH, Kim JS, Park HM, Kim S, Paek NS. Antioxidant activity and short-chain fatty acid production of lactic acid bacteria isolated from Korean individuals and fermented foods. 3 Biotech. 2021;11(5):217. doi: 10.1007/s13205-021-02767-y. [DOI] [PMC free article] [PubMed] [Google Scholar]
  161. Kannengiesser J, Sakaguchi-Söder K, Mrukwia T, Jager J, Schebek L. Extraction of medium chain fatty acids from organic municipal waste and subsequent production of bio-based fuels. Waste Manage. 2016;47:78–83. doi: 10.1016/j.wasman.2015.05.030. [DOI] [PubMed] [Google Scholar]
  162. Kantachote D, Ratanaburee A, Sukhoom A, Sumpradit T, Asavaroungpipop N. Use of -aminobutyric acid producing lactic acid bacteria as starters to reduce biogenic amines and cholesterol in Thai fermented pork sausage (Nham) and their distribution during fermentation. LWT. 2015;70:171–177. doi: 10.1016/j.lwt.2016.02.041. [DOI] [Google Scholar]
  163. Kaur H, Kaur G, Ali SA. Dairy-based probiotic-fermented functional foods: an update on their health-promoting properties. Fermentation. 2022;8(9):425. doi: 10.3390/fermentation8090425. [DOI] [Google Scholar]
  164. Kayodé AP, Hounhouigan DJ, Nout MJ, Niehof A. Household production of sorghum beer in Benin: technological and socio-economic aspects. Int J Consum Stud. 2007;31(3):258–264. doi: 10.1111/j.1470-6431.2006.00546.x. [DOI] [Google Scholar]
  165. Kewuyemi YO, Kesa H, Chinma CE, Adebo OA. Fermented edible insects for promoting food security in Africa. InSects. 2020;11(5):283. doi: 10.3390/insects11050283. [DOI] [PMC free article] [PubMed] [Google Scholar]
  166. Khurana RK, Jain A, Jain A, Sharma T, Singh B, Kesharwani P. Administration of antioxidants in cancer: debate of the decade. Drug Discov Today. 2018;23(4):763–770. doi: 10.1016/j.drudis.2018.01.021. [DOI] [PubMed] [Google Scholar]
  167. Kieliszek M, Pobiega K, Piwowarek K, Kot AM. Characteristics of the proteolytic enzymes produced by lactic acid bacteria. Molecules. 2021;26(7):1858. doi: 10.3390/molecules26071858. [DOI] [PMC free article] [PubMed] [Google Scholar]
  168. Kim HY, Park KY. Clinical trials of kimchi intakes on the regulation of metabolic parameters and colon health in healthy Korean young adults. J Funct Foods. 2018;47:325–333. doi: 10.1016/j.jff.2018.05.052. [DOI] [Google Scholar]
  169. Kim JA, Bayo J, Cha J, Choi YJ, Jung MY, Kim DH, Kim Y (2019) Investigating the probiotic characteristics of four microbial strains with potential application in feed industry. PloS one 14(6):e0218922. 10.1371/journal.pone.0218922 [DOI] [PMC free article] [PubMed]
  170. Knorr D, Augustin MA. Food systems at a watershed: Unlocking the benefits of technology and ecosystem symbioses. Crit Rev Food Sci Nutr. 2022 doi: 10.1080/10408398.2021.2023092. [DOI] [PubMed] [Google Scholar]
  171. Kok CR, Hutkins R. Yogurt and other fermented foods as sources of health-promoting bacteria. Nutr Rev. 2018;76:4–15. doi: 10.1093/nutrit/nuy056. [DOI] [PubMed] [Google Scholar]
  172. Kondybayev A, Loiseau G, Achir N, Mestres C, Konuspayeva G. Fermented mare milk product (Qymyz, Koumiss) Int Dairy J. 2021;119:105065. doi: 10.1016/j.idairyj.2021.105065. [DOI] [Google Scholar]
  173. Koskinen TT, Virtanen HEK, Voutilainen S, Tuomainen T-P, Mursu J, Virtanen JK. Intake of fermented and non-fermented dairy products and risk of incident CHD: the Kuopio Ischaemic Heart Disease Risk Factor Study. Br J Nutr. 2018;120(11):1288–1297. doi: 10.1017/S0007114518002830. [DOI] [PubMed] [Google Scholar]
  174. Kroger M, Kurmann J, Rasic J (1992) Fermented milks—Past, present, and future. In Applications of biotechnology to traditional fermented foods. National Academy Press, p 61
  175. Krüger A, Schäfers C, Schröder C, Antranikian G. Towards a sustainable biobased industry. Highlighting the impact of extremophiles. N Biotechnol. 2018;40:144–153. doi: 10.1016/j.nbt.2017.05.002. [DOI] [PubMed] [Google Scholar]
  176. Kudumija N, Vulić A, Lešić T, Vahčić N, Pleadin J. Aflatoxins and ochratoxin A in dry-fermented sausages in Croatia, by LC-MS/MS. Food Addit Contam Part B. 2020;13(4):225–232. doi: 10.1080/19393210.2020.1762760. [DOI] [PubMed] [Google Scholar]
  177. Kumar A. Role of microbes in dairy industry. Nutr Food Sci Int J. 2017 doi: 10.19080/nfsij.2017.03.555612. [DOI] [Google Scholar]
  178. Kumar P, Chatli MK, Verma AK, Mehta N, Malav OP, Kumar D, Sharma N. Quality, functionality, and shelf life of fermented meat and meat products: A review. Crit Rev Food Sci Nutr. 2017;57(13):2844–2856. doi: 10.1080/10408398.2015.1074533. [DOI] [PubMed] [Google Scholar]
  179. Kumar A, Thakur A, Panesar PS. Recent developments on sustainable solvents for emulsion liquid membrane processes. J Clean Prod. 2019;240:118250. doi: 10.1016/j.jclepro.2019.118250. [DOI] [Google Scholar]
  180. Kwak SH, Cho YM, Noh GM, Om AS. Cancer Preventive potential of kimchi lactic acid bacteria (Weissella cibaria, Lactobacillus plantarum) J Cancer Prev. 2014;19(4):253. doi: 10.15430/JCP.2014.19.4.253. [DOI] [PMC free article] [PubMed] [Google Scholar]
  181. La Torre GL, Cicero N, Bartolomeo G, Rando R, Vadalà R, Santini A, Durazzo A, Lucarini M, Dugo G, Salvo A. Assessment and monitoring of fish quality from a coastal ecosystem under high anthropic pressure: a case study in Southern Italy. Int J Environ Res Public Health. 2020;17(9):3285. doi: 10.3390/ijerph17093285. [DOI] [PMC free article] [PubMed] [Google Scholar]
  182. Lahiri D, Nag M, Sarkar T, Ray RR, Shariati MA, Rebezov M, Bangar SP, Lorenzo JM, Domínguez R. Lactic acid bacteria (LAB): autochthonous and probiotic microbes for meat preservation and fortification. Foods. 2022;11:2792. doi: 10.3390/foods11182792. [DOI] [PMC free article] [PubMed] [Google Scholar]
  183. Landeta G, Curiel JA, Carrascosa AV, Muñoz R, de las Rivas B. Technological and safety properties of lactic acid bacteria isolated from Spanish dry-cured sausages. Meat Sci. 2013;95(2):272–280. doi: 10.1016/j.meatsci.2013.05.019. [DOI] [PubMed] [Google Scholar]
  184. Landeta-Salgado C, Cicatiello P, Lienqueo ME. Mycoprotein and hydrophobin like protein produced from marine fungi Paradendryphiella salina in submerged fermentation with green seaweed Ulva spp. Algal Res. 2021;56:102314. doi: 10.1016/J.ALGAL.2021.102314. [DOI] [Google Scholar]
  185. Landis EA, Oliverio AM, McKenney EA, Nichols LM, Kfoury N, Biango-Daniels M, Shell LK, Madden AA, Shapiro L, Sakunala S, Drake K, Robbat A, Booker M, Dunn RR, Fierer N, Wolfe BE. The diversity and function of sourdough starter microbiomes. Elife. 2021;10:e61644. doi: 10.7554/eLife.61644. [DOI] [PMC free article] [PubMed] [Google Scholar]
  186. Lavefve L, Marasini D, Carbonero F. Microbial ecology of fermented vegetables and non-alcoholic drinks and current knowledge on their impact on human health. Adv Food Nutr Res. 2019;87:147–185. doi: 10.1016/BS.AFNR.2018.09.001. [DOI] [PubMed] [Google Scholar]
  187. Lee MH, Li FZ, Lee J, Kang J, Lim SI, Nam YD. Next-generation sequencing analyses of bacterial community structures in soybean pastes produced in Northeast China. J Food Sci. 2017;82(4):960–968. doi: 10.1111/1750-3841.13665. [DOI] [PubMed] [Google Scholar]
  188. Lee CS, Lee SH, Kim SH. Bone-protective effects of Lactobacillus plantarum B719-fermented milk product. Int J Dairy Technol. 2020;73(4):706–717. doi: 10.1111/1471-0307.12701. [DOI] [Google Scholar]
  189. Leite P, Silva C, Salgado JM, Belo I. Simultaneous production of lignocellulolytic enzymes and extraction of antioxidant compounds by solid-state fermentation of agro-industrial wastes. Ind Crops Prod. 2019;137:315–322. doi: 10.1016/j.indcrop.2019.04.044. [DOI] [Google Scholar]
  190. Li KJ, Burton-Pimentel KJ, Vergères G, Feskens EJM, Brouwer-Brolsma EM. Fermented foods and cardiometabolic health: definitions, current evidence, and future perspectives. Front Nutr. 2022;9:976020. doi: 10.3389/fnut.2022.976020. [DOI] [PMC free article] [PubMed] [Google Scholar]
  191. Li Z, Dong Y, Zhang Y, Zheng M, Jiang Z, Zhu Y, Deng S, Li Q, Ni H. Lactobacillus-fermentation enhances nutritional value and improves the inhibition on pancreatic lipase and oral pathogens of edible red seaweed Bangia fusco-purpurea. LWT. 2023 doi: 10.1016/J.LWT.2023.114643. [DOI] [Google Scholar]
  192. Lin W, Lin M, Zhou H, Wu H, Li Z, Lin W. The effects of chemical and organic fertilizer usage on rhizosphere soil in tea orchards. PLoS ONE. 2019;14(5):e0217018. doi: 10.1371/journal.pone.0217018. [DOI] [PMC free article] [PubMed] [Google Scholar]
  193. Linder T. Making the case for edible microorganisms as an integral part of a more sustainable and resilient food production system. Food Secur. 2019;11(2):265–278. doi: 10.1007/s12571-019-00912-3. [DOI] [Google Scholar]
  194. Liu W, Wang J, Zhang J, Mi Z, Gesudu Q, Sun T. Dynamic evaluation of the nutritional composition of homemade koumiss from Inner Mongolia during the fermentation process. J Food Process Preserv. 2019 doi: 10.1111/jfpp.14022. [DOI] [Google Scholar]
  195. Lopitz-Otsoa F, Rementeria A, Elguezabal N, Garaizar J. Kefir: A symbiotic yeasts-bacteria community with alleged healthy capabilities. Revista Iberoamericana De Micologia. 2006;23(2):67–74. doi: 10.1016/s1130-1406(06)70016-x. [DOI] [PubMed] [Google Scholar]
  196. Lu S, Chen S, Li H, Paengkoum S, Taethaisong N, Meethip W, Surakhunthod J, Sinpru B, Sroichak T, Archa P, Thongpea S, Paengkoum P. Sustainable valorization of tomato pomace (Lycopersicon esculentum) in animal nutrition: a review. Animals. 2022;12(23):3294. doi: 10.3390/ani12233294. [DOI] [PMC free article] [PubMed] [Google Scholar]
  197. Luo L, Sriram S, Johnravindar D, Martin LP, T., Wong, J. W. C., and Pradhan, N. Effect of inoculum pretreatment on the microbial and metabolic dynamics of food waste dark fermentation. Biores Technol. 2022;358:127404. doi: 10.1016/j.biortech.2022.127404. [DOI] [PubMed] [Google Scholar]
  198. Luz C, Calpe J, Manuel Quiles J, Torrijos R, Vento M, Gormaz M, Mañes J, Meca G. Probiotic characterization of Lactobacillus strains isolated from breast milk and employment for the elaboration of a fermented milk product. J Funct Foods. 2021;84:104599. doi: 10.1016/j.jff.2021.104599. [DOI] [Google Scholar]
  199. Lyu X, Lee J, Chen WN. Potential natural food preservatives and their sustainable production in yeast: terpenoids and polyphenols. J Agric Food Chem. 2019;67(16):4397–4417. doi: 10.1021/acs.jafc.8b07141. [DOI] [PubMed] [Google Scholar]
  200. Lyumugabe F, Kamaliza G, Bajyana E, Thonart P. Microbiological and physico-chemical characteristic of Rwandese traditional beer “Ikigage”. Afr J Biotech. 2010;9:4241–4246. [Google Scholar]
  201. Ma H, Zhao Y, Huang W, Zhang L, Wu F, Ye J, Chen GQ. Rational flux-tuning of Halomonas bluephagenesis for co-production of bioplastic PHB and ectoine. Nat Commun. 2020;11(1):3313. doi: 10.1038/s41467-020-17223-3. [DOI] [PMC free article] [PubMed] [Google Scholar]
  202. Macori G, Cotter PD. Novel insights into the microbiology of fermented dairy foods. Curr Opin Biotechnol. 2018;49:172–178. doi: 10.1016/j.copbio.2017.09.002. [DOI] [PubMed] [Google Scholar]
  203. Maiorano G, Ramires FA, Durante M, Palamà IE, Blando F, De Rinaldis G, Perbellini E, Patruno V, Gadaleta Caldarola C, Vitucci S, Mita G, Bleve G. 2022. The controlled semi-solid fermentation of seaweeds as a strategy for their stabilization and new food applications. Foods. [DOI] [PMC free article] [PubMed]
  204. Mancini S, Moruzzo R, Riccioli F, Paci G. European consumers’ readiness to adopt insects as food. A Review. Food Res Int. 2019;122:661–678. doi: 10.1016/j.foodres.2019.01.041. [DOI] [PubMed] [Google Scholar]
  205. Marco ML, Heeney D, Binda S, Cifelli CJ, Cotter PD, Foligné B, Gänzle M, Kort R, Pasin G, Pihlanto A, Smid EJ, Hutkins R. Health benefits of fermented foods: microbiota and beyond. Curr Opin Biotechnol. 2017;44:94–102. doi: 10.1016/J.COPBIO.2016.11.010. [DOI] [PubMed] [Google Scholar]
  206. Marco ML, Sanders ME, Gänzle M, Arrieta MC, Cotter PD, De Vuyst L, Hill C, Holzapfel W, Lebeer S, Merenstein D, Reid G, Wolfe BE, Hutkins R. The International Scientific Association for Probiotics and Prebiotics (ISAPP) consensus statement on fermented foods. Nat Rev Gastroenterol Hepatol. 2021;18(3):196–208. doi: 10.1038/s41575-020-00390-5. [DOI] [PMC free article] [PubMed] [Google Scholar]
  207. Martin-Rios C, Hofmann A, Mackenzie N. Sustainability-oriented innovations in food waste management technology. Sustainability. 2021;13:210. doi: 10.3390/su13010210. [DOI] [Google Scholar]
  208. Mathur H, Beresford TP, Cotter PD. Health benefits of lactic acid bacteria (LAB) fermentates. Nutrients. 2020;12(6):1679. doi: 10.3390/nu12061679. [DOI] [PMC free article] [PubMed] [Google Scholar]
  209. Mawonike R, Chigunyeni B, Chipumuro M. Process improvement of opaque beer (chibuku) based on multivariate cumulative sum control chart. J Inst Brew. 2018;124(1):16–22. doi: 10.1002/JIB.466. [DOI] [Google Scholar]
  210. Melikoglu M, Lin C, Webb C. Analysing global food waste problem: Pinpointing the facts and estimating the energy content. Open Engineering. 2013;3(2):157–164. doi: 10.2478/s13531-012-0058-5. [DOI] [Google Scholar]
  211. Mendoza-Salazar A, Santiago-López L, Torres-Llanez MJ, Hernández-Mendoza A, Vallejo-Cordoba B, Liceaga AM, González-Córdova AF. In vitro antioxidant and antihypertensive activity of edible insects flours (Mealworm and Grasshopper) fermented with Lactococcus lactis Strains. Fermentation. 2021;7(3):153. doi: 10.3390/fermentation7030153. [DOI] [Google Scholar]
  212. Metras BN, Holle MJ, Parker VJ, Miller MJ, Swanson KS. Commercial kefir products assessed for label accuracy of microbial composition and density. JDS Commun. 2021;2(3):87–91. doi: 10.3168/jdsc.2020-0056. [DOI] [PMC free article] [PubMed] [Google Scholar]
  213. Michel F, Hartmann C, Siegrist M. Consumers’ associations, perceptions and acceptance of meat and plant-based meat alternatives. Food Qual Prefer. 2021;87:104063. doi: 10.1016/J.FOODQUAL.2020.104063. [DOI] [Google Scholar]
  214. Milicevic B, Tomović V, Danilović B, Savić D. The influence of starter cultures on the lactic acid bacteria microbiota of Petrovac sausage. Ital J Food Sci. 2021;33(2):24–34. doi: 10.15586/ijfs.v33i2.1918. [DOI] [Google Scholar]
  215. Miller KK, Alper HS. Yarrowia lipolytica: more than an oleaginous workhorse. Appl Microbiol Biotechnol. 2019;103:9251–9262. doi: 10.1007/s00253-019-10200-x. [DOI] [PubMed] [Google Scholar]
  216. Mir SA, Raja J, Masoodi FA. Fermented vegetables, a rich repository of beneficial probiotics—a review. Ferment Technol. 2018;7(1):1–6. doi: 10.4172/2167-7972.1000150. [DOI] [Google Scholar]
  217. Mok WK, Tan YX, Lee J, Kim J, Chen WN. A metabolomic approach to understand the solid-state fermentation of okara using Bacillus subtilis WX-17 for enhanced nutritional profile. AMB Expr. 2019;9(1):60. doi: 10.1186/s13568-019-0786-5. [DOI] [PMC free article] [PubMed] [Google Scholar]
  218. Mongkolwai T, Assavanig A, Amnajsongsiri C, Flegel TW, Bhumiratana A. Technology transfer for small and medium soy sauce fermentation factories in Thailand: a consortium approach. Food Res Int. 1997;30(8):555–563. doi: 10.1016/S0963-9969(98)00033-7. [DOI] [Google Scholar]
  219. Monteiro P, Lomartire S, Cotas J, Pacheco D, Marques JC, Pereira L, Gonçalves AMM. Seaweeds as a fermentation substrate: a challenge for the food processing industry. Processes. 2021;9(11):1953. doi: 10.3390/PR9111953. [DOI] [Google Scholar]
  220. Moore JF, DuVivier R, Johanningsmeier SD. Formation of γ-aminobutyric acid (GABA) during the natural lactic acid fermentation of cucumber. J Food Compos Anal. 2021;96:103711. doi: 10.1016/J.JFCA.2020.103711. [DOI] [Google Scholar]
  221. Moradi M, Kousheh SA, Almasi H, Alizadeh A, Guimarães JT, Yılmaz N, Lotfi A. Postbiotics produced by lactic acid bacteria: the next frontier in food safety. Compr Rev Food Sci Food Saf. 2020;19(6):3390–3415. doi: 10.1111/1541-4337.12613. [DOI] [PubMed] [Google Scholar]
  222. Motey GA, Owusu-Kwarteng J, Obiri-Danso K, Ofori LA, Ellis WO, Jespersen L. In vitro properties of potential probiotic lactic acid bacteria originating from Ghanaian indigenous fermented milk products. World J Microbiol Biotechnol. 2021;37(3):52. doi: 10.1007/s11274-021-03013-6. [DOI] [PubMed] [Google Scholar]
  223. Mouritsen OG, Duelund L, Calleja G, Frøst MB. Flavour of fermented fish, insect, game, and pea sauces: garum revisited. Int J Gastronomy Food Sci. 2017;9:16–28. doi: 10.1016/j.ijgfs.2017.05.002. [DOI] [Google Scholar]
  224. Mukherjee A, Gómez-Sala B, O’Connor EM, Kenny JG, Cotter PD. Global regulatory frameworks for fermented foods: a review. Front Nutr. 2022;9:902642. doi: 10.3389/fnut.2022.902642. [DOI] [PMC free article] [PubMed] [Google Scholar]
  225. Muncan J, Tei K, Tsenkova R. Real-time monitoring of yogurt fermentation process by aquaphotomics near-infrared spectroscopy. Sensors. 2020;21(1):177. doi: 10.3390/s21010177. [DOI] [PMC free article] [PubMed] [Google Scholar]
  226. Munesue Y, Masui T, Fushima T. The effects of reducing food losses and food waste on global food insecurity, natural resources, and greenhouse gas emissions. Environ Econ Policy Stud. 2015;17(1):43–77. doi: 10.1007/s10018-014-0083-0. [DOI] [Google Scholar]
  227. Muunda E, Mtimet N, Bett E, Wanyoike F, Alonso S. Milk purchase and consumption patterns in peri-urban low-income households in Kenya. Front Sustain Food Syst. 2023;7:1084067. doi: 10.3389/fsufs.2023.1084067. [DOI] [Google Scholar]
  228. Muyanja C, Kikafunda J, Narvhus JA, Helgetun K, Langsrud T. Production methods and composition of bushera: a Ugandan traditional fermented cereal beverage. Afr J Food Agric Nutr Dev. 2003;3(1):10–19. doi: 10.4314/ajfand.v3i1.19108. [DOI] [Google Scholar]
  229. Milinovic J, Mata P, Diniz M, Noronha JP (2021) Umami taste in edible seaweeds: The current comprehension and perception. Int J Gastron Food Sci 23: 100301. 10.1016/j.ijgfs.2020.100301
  230. Nagarajan S, Jones RJ, Oram L, Massanet-Nicolau J, Guwy A. Intensification of acidogenic fermentation for the production of biohydrogen and volatile fatty acids-a perspective. Fermentation. 2022;8(7):7. doi: 10.3390/fermentation8070325. [DOI] [Google Scholar]
  231. Nampoothiri KM, Beena DJ, Vasanthakumari DS, Ismail B. Health benefits of exopolysaccharides in fermented foods. In: Frias J, Martinez-Villaluenga C, Peñas E, editors. Fermented foods in health and disease prevention. Elsevier; 2017. pp. 49–62. [Google Scholar]
  232. Nejati F, Rizzello CG, Di Cagno R, Sheikh-Zeinoddin M, Diviccaro A, Minervini F, Gobbetti M. Manufacture of a functional fermented milk enriched of Angiotensin-I Converting Enzyme (ACE)-inhibitory peptides and γ-amino butyric acid (GABA) LWT Food Sci Technol. 2013;51(1):183–189. doi: 10.1016/j.lwt.2012.09.017. [DOI] [Google Scholar]
  233. Nemeth A, Kaleta Z. Complex utilization of dairy waste (whey) in biorefinery. WSEAS Trans Environ Dev. 2015;11:80–88. [Google Scholar]
  234. Neves Casarotti S, Fernanda Borgonovi T, de Mello Tieghi T, Sivieri K, Penna LBA. Probiotic low-fat fermented goat milk with passion fruit by-product: In vitro effect on obese individuals’ microbiota and on metabolites production. Food Res Int. 2020;136:109453. doi: 10.1016/j.foodres.2020.109453. [DOI] [PubMed] [Google Scholar]
  235. Ng HS, Kee PE, Yim HS, Chen P-T, Wei Y-H, Chi-Wei Lan J. Recent advances on the sustainable approaches for conversion and reutilization of food wastes to valuable bioproducts. Biores Technol. 2020;302:122889. doi: 10.1016/j.biortech.2020.122889. [DOI] [PubMed] [Google Scholar]
  236. Nishida K, Sawada D, Kawai T, Kuwano Y, Fujiwara S, Rokutan K. Para-psychobiotic Lactobacillus gasseri 2305 ameliorates stress-related symptoms and sleep quality. J Appl Microbiol. 2017;123(6):1561–1570. doi: 10.1111/jam.13594. [DOI] [PubMed] [Google Scholar]
  237. Niva M, Vainio A. Towards more environmentally sustainable diets? Changes in the consumption of beef and plant- and insect-based protein products in consumer groups in Finland. Meat Sci. 2021 doi: 10.1016/J.MEATSCI.2021.108635. [DOI] [PubMed] [Google Scholar]
  238. Noh BS, Seo HY, Park WS, Oh S. Safety of Kimchi. In: Prakash V, Martín-Belloso O, Keener L, Astley S, Braun S, McMahon H, Lelieveld H, editors. Regulating safety of traditional and ethnic foods. Academic Press; 2016. pp. 369–380. [Google Scholar]
  239. Nongdam P (2015) Traditional fermented bamboo shoot foods of North-East India and their characteristic natural microbial flora. 10th World Bamboo Congress, Korea 2015
  240. Nongonierma AB, FitzGerald RJ. The scientific evidence for the role of milk protein-derived bioactive peptides in humans: a review. J Funct Foods. 2015;17:640–656. doi: 10.1016/j.jff.2015.06.021. [DOI] [Google Scholar]
  241. Norakma MN, Zaibunnisa AH, Razarinah WARW. The changes of phenolics profiles, amino acids and volatile compounds of fermented seaweed extracts obtained through microbial fermentation. Mater Today Proc. 2022;48:815–821. doi: 10.1016/J.MATPR.2021.02.366. [DOI] [Google Scholar]
  242. Nout MJR, Kok B, Vela E, Nche PF, Rombouts FM. Acceleration of the fermentation of kenkey, an indigenous fermented maize food of Ghana. Food Res Int. 1995;28(6):599–604. doi: 10.1016/0963-9969(95)00059-3. [DOI] [Google Scholar]
  243. Nxumalo Z, Thimiri Govinda Raj DB. Application and challenges of synthetic biology. In: Singh V, editor. Advances in synthetic biology. Singapore: Springer; 2020. [Google Scholar]
  244. O’Connor J, Hoang SA, Bradney L, Dutta S, Xiong X, Tsang DCW, Ramadass K, Vinu A, Kirkham MB, Bolan NS. A review on the valorisation of food waste as a nutrient source and soil amendment. Environ Pollut. 2021;272:115985. doi: 10.1016/j.envpol.2020.115985. [DOI] [PubMed] [Google Scholar]
  245. Okoniewski A, Dobrzyńska M, Kusyk P, Dziedzic K, Przysławski J, Drzymała-Czyż S. The role of fermented dairy products on gut microbiota composition. Fermentation. 2023;9:231. doi: 10.3390/fermentation9030231. [DOI] [Google Scholar]
  246. Ortiz-Sanchez M, Inocencio-García P-J, Alzate-Ramírez AF, Alzate CAC. Potential and restrictions of food-waste valorization through fermentation processes. Fermentation. 2023;9(3):3. doi: 10.3390/fermentation9030274. [DOI] [Google Scholar]
  247. Østergaard DK. The role of microorganisms in soy sauce production. Adv Appl Microbiol. 2019;108:45–113. doi: 10.1016/bs.aambs.2019.07.002. [DOI] [PubMed] [Google Scholar]
  248. Østergaard A, Embarek PKB, Yamprayoon J, Wedell-Neergaard C, Huss HH, Gram L. Fermentation and spoilage of som fak, a Thai low-salt fish product. Trop Sci. 1998;38:105–112. [Google Scholar]
  249. Ouyang P, Wang H, Hajnal I, Wu Q, Guo Y, Chen GQ. Increasing oxygen availability for improving poly(3-hydroxybutyrate) production by Halomonas. Metab Eng. 2018;45:20–31. doi: 10.1016/j.ymben.2017.11.006. [DOI] [PubMed] [Google Scholar]
  250. Öz E, Kaban G, Barış Ö, Kaya M. Isolation and identification of lactic acid bacteria from pastırma. Food Control. 2017;77:158–162. doi: 10.1016/j.foodcont.2017.02.017. [DOI] [Google Scholar]
  251. Palacios S, Ruiz HA, Ramos-Gonzalez R, Martínez J, Segura E, Aguilar M, Aguilera A, Michelena G, Aguilar C, Ilyina A. Comparison of physicochemical pretreatments of banana peels for bioethanol production. Food Sci Biotechnol. 2017;26(4):993–1001. doi: 10.1007/s10068-017-0128-9. [DOI] [PMC free article] [PubMed] [Google Scholar]
  252. Panyawoot N, So S, Cherdthong A, Chanjula P. Effect of feeding discarded durian peel ensiled with Lactobacillus casei TH14 and additives in total mixed rations on digestibility, ruminal fermentation, methane mitigation, and nitrogen balance of Thai Native–Anglo-Nubian goats. Fermentation. 2022;8(2):2. doi: 10.3390/fermentation8020043. [DOI] [Google Scholar]
  253. Paramithiotis S, Das G, Shin H-S, Patra JK. Fate of bioactive compounds during lactic acid fermentation of fruits and vegetables. Foods. 2022;11(5):733. doi: 10.3390/foods11050733. [DOI] [PMC free article] [PubMed] [Google Scholar]
  254. Parente E, Cogan TM, Powell IB. Starter cultures: general aspects. In: McSweeney PLH, Fox PF, Cotter PD, Everett DW, editors. Dairy and dairy products. Academic Press; 2017. pp. 201–226. [Google Scholar]
  255. Park S, Bae JH. Fermented food intake is associated with a reduced likelihood of atopic dermatitis in an adult population (Korean National Health and Nutrition Examination Survey 2012–2013) Nutr Res. 2016;36(2):125–133. doi: 10.1016/j.nutres.2015.11.011. [DOI] [PubMed] [Google Scholar]
  256. Parlindungan E, Lugli GA, Ventura M, van Sinderen D, Mahony J. Lactic acid bacteria diversity and characterization of probiotic candidates in fermented meats. Foods. 2021;10(7):1519. doi: 10.3390/foods10071519. [DOI] [PMC free article] [PubMed] [Google Scholar]
  257. Patel A, Prajapat J. Food and health applications of exopolysaccharides produced by lactic acid bacteria. Adv Dairy Res. 2013 doi: 10.4172/2329-888x.1000107. [DOI] [Google Scholar]
  258. Pérez-Alva A, MacIntosh AJ, Baigts-Allende DK, García-Torres R, Ramírez-Rodrigues MM. Fermentation of algae to enhance their bioactive activity: a review. Algal Res. 2022;64:102684. doi: 10.1016/J.ALGAL.2022.102684. [DOI] [Google Scholar]
  259. Pérez-Díaz IM, Hayes J, Medina E, Anekella K, Daughtry K, Dieck S, Levi M, Price R, Butz N, Lu Z, Azcarate-Peril MA. Reassessment of the succession of lactic acid bacteria in commercial cucumber fermentations and physiological and genomic features associated with their dominance. Food Microbiol. 2017;63:217–227. doi: 10.1016/J.FM.2016.11.025. [DOI] [PubMed] [Google Scholar]
  260. Pham PV. Medical biotechnology: techniques and applications. In: Barh D, Azevedo V, editors. Omics technologies and bio-engineering. Academic Press; 2018. pp. 449–469. [Google Scholar]
  261. Pi X, Wan Y, Yang Y, Li R, Wu X, Xie M, Li X, Fu G. Research progress in peanut allergens and their allergenicity reduction. Trends Food Sci Technol. 2019;93:212–220. doi: 10.1016/j.tifs.2019.09.014. [DOI] [Google Scholar]
  262. Pi X, Peng Z, Liu J, Jiang Y, Wang J, Fu G, Yang Y, Sun Y (2022) Sesame allergy: mechanisms, prevalence, allergens, residue detection, effects of processing and cross-reactivity. Crit Rev Food Sci Nutr 1–16. 10.1080/10408398.2022.2128031 [DOI] [PubMed]
  263. Pihlanto A, Korhonen H. Bioactive peptides from fermented foods and health promotion. In: Korhonen H, editor. Advances in fermented foods and beverages. Elsevier; 2015. pp. 39–74. [Google Scholar]
  264. Piqué N, Berlanga M, Miñana-Galbis D. Health benefits of heat-killed (Tyndallized) probiotics: an overview. Int J Mol Sci. 2019;20(10):2534. doi: 10.3390/ijms20102534. [DOI] [PMC free article] [PubMed] [Google Scholar]
  265. Pires AF, Marnotes NG, Rubio OD, Garcia AC, Pereira CD. Dairy by-products: a review on the valorization of whey and second cheese whey. Foods. 2021;10(5):5. doi: 10.3390/foods10051067. [DOI] [PMC free article] [PubMed] [Google Scholar]
  266. Pleadin J, Kovačević D, Perković I. Impact of casing damaging on aflatoxin B 1 concentration during the ripening of dry-fermented meat sausages. J Immunoassay Immunochem. 2015;36(6):655–666. doi: 10.1080/15321819.2015.1032306. [DOI] [PubMed] [Google Scholar]
  267. Pleadin J, Zadravec M, Brnić D, Perković I, Škrivanko M, Kovačević D. Moulds and mycotoxins detected in the regional speciality fermented sausage ‘slavonski kulen’ during a 1-year production period. Food Addit Contam Part A. 2016 doi: 10.1080/19440049.2016.1266395. [DOI] [PubMed] [Google Scholar]
  268. Pleadin J, Lešić T, Milićević D, Markov K, Šarkanj B, Vahčić N, Kmetič I, Zadravec M. Pathways of mycotoxin occurrence in meat products: a review. Processes. 2021;9(12):2122. doi: 10.3390/pr9122122. [DOI] [Google Scholar]
  269. Połka J, Rebecchi A, Pisacane V, Morelli L, Puglisi E. Bacterial diversity in typical Italian salami at different ripening stages as revealed by high-throughput sequencing of 16S rRNA amplicons. Food Microbiol. 2015;46:342–356. doi: 10.1016/j.fm.2014.08.023. [DOI] [PubMed] [Google Scholar]
  270. Prado N, Sampayo M, González P, Lombó F, Díaz J. Physicochemical, sensory and microbiological characterization of Asturian Chorizo, a traditional fermented sausage manufactured in Northern Spain. Meat Sci. 2019;156:118–124. doi: 10.1016/j.meatsci.2019.05.023. [DOI] [PubMed] [Google Scholar]
  271. Profeta A, Baune MC, Smetana S, Bornkessel S, Broucke K, van Royen G, Enneking U, Weiss J, Heinz V, Hieke S, Terjung N. Preferences of German consumers for meat products blended with plant-based proteins. Sustainability. 2021;13(2):650. doi: 10.3390/SU13020650. [DOI] [Google Scholar]
  272. Rabie MA, Peres C, Malcata FX. Evolution of amino acids and biogenic amines throughout storage in sausages made of horse, beef and turkey meats. Meat Sci. 2014;96(1):82–87. doi: 10.1016/j.meatsci.2013.05.042. [DOI] [PubMed] [Google Scholar]
  273. Raffaelli F, Nanetti L, Montecchiani G, Borroni F, Salvolini E, Faloia E, Ferretti G, Mazzanti L, Vignini A. In vitro effects of fermented papaya (Carica papaya L.) on platelets obtained from patients with type 2 diabetes. Nutr Metab Cardiovasc Dis. 2015;25(2):224–229. doi: 10.1016/j.numecd.2014.10.013. [DOI] [PubMed] [Google Scholar]
  274. Ranadheera CS, Evans CA, Adams MC, Baines SK. In vitro analysis of gastrointestinal tolerance and intestinal cell adhesion of probiotics in goat’s milk ice cream and yogurt. Food Res Int. 2012;49(2):619–625. doi: 10.1016/j.foodres.2012.09.007. [DOI] [Google Scholar]
  275. Rastogi YR, Thakur R, Thakur P, Mittal A, Chakrabarti S, Siwal SS, Thakur VK, Saini RV, Saini AK. Food fermentation-significance to public health and sustainability challenges of modern diet and food systems. Int J Food Microbiol. 2022;371:109666. doi: 10.1016/j.ijfoodmicro.2022.109666. [DOI] [PubMed] [Google Scholar]
  276. Ravindran R, Jaiswal AK. Exploitation of food industry waste for high-value products. Trends Biotechnol. 2016;34(1):58–69. doi: 10.1016/j.tibtech.2015.10.008. [DOI] [PubMed] [Google Scholar]
  277. Ravyts F, Vuyst LD, Leroy F. Bacterial diversity and functionalities in food fermentations. Eng Life Sci. 2012;12(4):356–367. doi: 10.1002/elsc.201100119. [DOI] [Google Scholar]
  278. Read QD, Brown S, Cuéllar AD, Finn SM, Gephart JA, Marston LT, Meyer E, Weitz KA, Muth MK. Assessing the environmental impacts of halving food loss and waste along the food supply chain. Sci Total Environ. 2020;712:136255. doi: 10.1016/j.scitotenv.2019.136255. [DOI] [PMC free article] [PubMed] [Google Scholar]
  279. RedCorn R, Engelberth AS. Identifying conditions to optimize lactic acid production from food waste co-digested with primary sludge. Biochem Eng J. 2016;105:205–213. doi: 10.1016/j.bej.2015.09.014. [DOI] [Google Scholar]
  280. Ricci G, Andreozzi L, Cipriani F, Giannetti A, Gallucci M, Caffarelli C. Wheat allergy in children: a comprehensive update. Medicina. 2019;55(7):400. doi: 10.3390/medicina55070400. [DOI] [PMC free article] [PubMed] [Google Scholar]
  281. Ritala A, Häkkinen ST, Toivari M, Wiebe MG. Single cell protein-state-of-the-art, industrial landscape and patents 2001–2016. Front Microbiol. 2017;8:2009. doi: 10.3389/fmicb.2017.02009. [DOI] [PMC free article] [PubMed] [Google Scholar]
  282. Rodríguez A, Bernáldez V, Rodríguez M, Andrade MJ, Núñez F, Córdoba JJ. Effect of selected protective cultures on ochratoxin A accumulation in dry-cured Iberian ham during its ripening process. LWT Food Sci Technol. 2015;60(2):923–928. doi: 10.1016/j.lwt.2014.09.059. [DOI] [Google Scholar]
  283. Rodríguez-Figueroa JC, González-Córdova AF, Astiazaran-García H, Vallejo-Cordoba B. Hypotensive and heart rate-lowering effects in rats receiving milk fermented by specific Lactococcus lactis strains. Br J Nutr. 2013;109(5):827–833. doi: 10.1017/S0007114512002115. [DOI] [PubMed] [Google Scholar]
  284. Rosa DD, Dias MMS, Grześkowiak ŁM, Reis SA, Conceição LL, Peluzio do MCG. Milk kefir: nutritional, microbiological and health benefits. Nutr Res Rev. 2017;30(1):82–96. doi: 10.1017/S0954422416000275. [DOI] [PubMed] [Google Scholar]
  285. Saad N, Delattre C, Urdaci M, Schmitter JM, Bressollier P. An overview of the last advances in probiotic and prebiotic field. LWT Food Sci Technol. 2013;50(1):1–16. doi: 10.1016/j.lwt.2012.05.014. [DOI] [Google Scholar]
  286. Sabater C, Ruiz L, Delgado S, Ruas-Madiedo P, Margolles A. Valorization of vegetable food waste and by-products through fermentation processes. Front Microbiol. 2020;11:581997. doi: 10.3389/fmicb.2020.581997. [DOI] [PMC free article] [PubMed] [Google Scholar]
  287. Sadh P, Kumar S, Chawla P, Duhan J. Fermentation: a boon for production of bioactive compounds by processing of food industries wastes (by-products) Molecules. 2018;23(10):2560. doi: 10.3390/molecules23102560. [DOI] [PMC free article] [PubMed] [Google Scholar]
  288. Sahay S. Wine enzymes: potential and practices. In: Kuddus M, editor. Enzymes in food biotechnology: production, applications, and future prospects. Academic Press; 2019. pp. 73–92. [Google Scholar]
  289. Salque M, Bogucki PI, Pyzel J, Sobkowiak-Tabaka I, Grygiel R, Szmyt M, Evershed RP. Earliest evidence for cheese making in the sixth millennium bc in northern Europe. Nature. 2013;493(7433):522–525. doi: 10.1038/nature11698. [DOI] [PubMed] [Google Scholar]
  290. Şanlier N, Gökcen BB, Sezgin AC. Health benefits of fermented foods. Crit Rev Food Sci Nutr. 2019;59(3):506–527. doi: 10.1080/10408398.2017.1383355. [DOI] [PubMed] [Google Scholar]
  291. Santiago-Díaz P, Rico M, Rivero A, Santana-Casiano M. Bioactive metabolites of microalgae from canary ıslands for functional food and feed uses. Chem Biodivers. 2022 doi: 10.1002/cbdv.202200230. [DOI] [PubMed] [Google Scholar]
  292. Santos MHS. Biogenic amines: their importance in foods. Int J Food Microbiol. 1996;29(2–3):213–231. doi: 10.1016/0168-1605(95)00032-1. [DOI] [PubMed] [Google Scholar]
  293. Saqib S, Akram A, Halim SA, Tassaduq R. Sources of β-galactosidase and its applications in food industry. 3 Biotech. 2017;7(1):79. doi: 10.1007/s13205-017-0645-5. [DOI] [PMC free article] [PubMed] [Google Scholar]
  294. Savaiano DA. Lactose digestion from yogurt: mechanism and relevance. Am J Clin Nutr. 2014;99(5):1251S–1255S. doi: 10.3945/ajcn.113.073023. [DOI] [PubMed] [Google Scholar]
  295. Sawadogo-Lingani H, Owusu-Kwarteng J, Glover R, Diawara B, Jakobsen M, Jespersen L. Sustainable production of african traditional beers with focus on dolo, a west african sorghum-based alcoholic beverage. Front Sustain Food Syst. 2021;5:143. doi: 10.3389/FSUFS.2021.672410/BIBTEX. [DOI] [Google Scholar]
  296. Schiano AN, Harwood WS, Gerard PD, Drake MA. Consumer perception of the sustainability of dairy products and plant-based dairy alternatives. J Dairy Sci. 2020;103(12):11228–11243. doi: 10.3168/jds.2020-18406. [DOI] [PubMed] [Google Scholar]
  297. Sekwati-Monang B, Gänzle MG. Microbiological and chemical characterisation of ting, a sorghum-based sourdough product from Botswana. Int J Food Microbiol. 2011;150(2–3):115–121. doi: 10.1016/j.ijfoodmicro.2011.07.021. [DOI] [PubMed] [Google Scholar]
  298. Seong G, Lee S, Min YW, Jang YS, Kim HS, Kim E-J, Park S-Y, Kim C-H, Chang DK. Effect of heat-killed Lactobacillus casei DKGF7 on a rat model of irritable bowel syndrome. Nutrients. 2021;13(2):568. doi: 10.3390/nu13020568. [DOI] [PMC free article] [PubMed] [Google Scholar]
  299. Sepúlveda L, Laredo-Alcalá E, Buenrostro-Figueroa JJ, Ascacio-Valdés JA, Genisheva Z, Aguilar C, Teixeira J. Ellagic acid production using polyphenols from orange peel waste by submerged fermentation. Electron J Biotechnol. 2020;43:1–7. doi: 10.1016/j.ejbt.2019.11.002. [DOI] [Google Scholar]
  300. Shafi A, Naeem Raja H, Farooq U, Akram K, Hayat Z, Naz A, Nadeem HR. Antimicrobial and antidiabetic potential of synbiotic fermented milk: a functional dairy product. Int J Dairy Technol. 2019;72(1):15–22. doi: 10.1111/1471-0307.12555. [DOI] [Google Scholar]
  301. Sharma I, Yaiphathoi S. Role of microbial communities in traditionally fermented foods and beverages in North East India. In: Mandal SD, Bhatt P, editors. Recent advancements in microbial diversity. Academic Press; 2020. pp. 445–470. [Google Scholar]
  302. Sharma R, Garg P, Kumar P, Bhatia SK, Kulshrestha S. Microbial fermentation and its role in quality improvement of fermented foods. Fermentation. 2020;6(4):106. doi: 10.3390/fermentation6040106. [DOI] [Google Scholar]
  303. Sivamaruthi B, Kesika P, Prasanth M, Chaiyasut C. A mini review on antidiabetic properties of fermented foods. Nutrients. 2018;10(12):1973. doi: 10.3390/nu10121973. [DOI] [PMC free article] [PubMed] [Google Scholar]
  304. Smid EJ, Kleerebezem M. Production of aroma compounds in lactic fermentations. Annu Rev Food Sci Technol. 2014;5(1):313–326. doi: 10.1146/annurev-food-030713-092339. [DOI] [PubMed] [Google Scholar]
  305. Subrota H, Shilpa, Brij S, Vandna K, Surajit M. Antioxidative activity and polyphenol content in fermented soy milk supplemented with WPC-70 by probiotic Lactobacilli. Int Food Res J. 2013;20(5):2125–2131. [Google Scholar]
  306. Suez J, Zmora N, Segal E, Elinav E. The pros, cons, and many unknowns of probiotics. Nat Med. 2019;25(5):716–729. doi: 10.1038/s41591-019-0439-x. [DOI] [PubMed] [Google Scholar]
  307. Sun X, Zhou K, Gong Y, Zhang N, Yang M, Qing D, Li Y, Lu J, Li J, Feng C, Li C, Yang Y. Determination of biogenic amines in sichuan-style spontaneously fermented sausages. Food Anal Methods. 2016;9(8):2299–2307. doi: 10.1007/s12161-016-0417-6. [DOI] [Google Scholar]
  308. Sun W, Shahrajabian MH, Lin M. Research progress of fermented functional foods and protein factory-microbial fermentation technology. Fermentation. 2022;8(12):12. doi: 10.3390/fermentation8120688. [DOI] [Google Scholar]
  309. Tamang JP, Thapa N. Beneficial microbiota in ethnic fermented foods and beverages. In: de Bruijn FJ, Smidt H, Cocolin LS, Sauer M, Dowling D, Thomashow L, editors. Good microbes in medicine, food production, biotechnology, bioremediation, and agriculture. Wiley; 2022. pp. 130–148. [Google Scholar]
  310. Tamang JP, Tamang B, Schillinger U, Franz CMAP, Gores M, Holzapfel WH. Identification of predominant lactic acid bacteria isolated from traditionally fermented vegetable products of the Eastern Himalayas. Int J Food Microbiol. 2005;105(3):347–356. doi: 10.1016/J.IJFOODMICRO.2005.04.024. [DOI] [PubMed] [Google Scholar]
  311. Tamang JP, Shin DH, Jung SJ, Chae SW. Functional properties of microorganisms in fermented foods. Front Microbiol. 2016 doi: 10.3389/fmicb.2016.00578. [DOI] [PMC free article] [PubMed] [Google Scholar]
  312. Tamang JP, Cotter PD, Endo A, Han NS, Kort R, Liu SQ, Mayo B, Westerik N, Hutkins R. Fermented foods in a global age: east meets West. Compr Rev Food Sci Food Saf. 2020;19(1):184–217. doi: 10.1111/1541-4337.12520. [DOI] [PubMed] [Google Scholar]
  313. Tandon N, Gupta Y, Kapoor D, Lakshmi JK, Praveen D, Bhattacharya A, Billot L, Naheed A, De Silva A, Gupta I, Farzana N, John R, Ajanthan S, Divakar H, Bhatla N, Desai A, Pathmeswaran A, Prabhakaran D, Joshi R, et al. Effects of a lifestyle intervention to prevent deterioration in glycemic status among south asian women with recent gestational diabetes: a randomized clinical trial. JAMA Netw Open. 2022 doi: 10.1001/jamanetworkopen.2022.0773. [DOI] [PMC free article] [PubMed] [Google Scholar]
  314. Tang J, Wang XC, Hu Y, Ngo HH, Li Y. Dynamic membrane-assisted fermentation of food wastes for enhancing lactic acid production. Biores Technol. 2017;234:40–47. doi: 10.1016/j.biortech.2017.03.019. [DOI] [PubMed] [Google Scholar]
  315. Tasdemir SS, Sanlier N. An insight into the anticancer effects of fermented foods: a review. J Funct Foods. 2020;75:104281. doi: 10.1016/j.jff.2020.104281. [DOI] [Google Scholar]
  316. Teng TS, Chin YL, Chai KF, Chen WN. Fermentation for future food systems. EMBO Rep. 2021 doi: 10.15252/embr.202152680. [DOI] [PMC free article] [PubMed] [Google Scholar]
  317. Terpou A, Bekatorou A, Kanellaki M, Koutinas AA, Nigam P. Enhanced probiotic viability and aromatic profile of yogurts produced using wheat bran (Triticum aestivum) as cell immobilization carrier. Process Biochem. 2017;55:1–10. doi: 10.1016/j.procbio.2017.01.013. [DOI] [Google Scholar]
  318. Thakkar PN, Patel A, Modi HA, Prajapati JB. Hypocholesterolemic effect of potential probiotic Lactobacillus fermentum strains isolated from traditional fermented foods in wistar rats. Probiot Antimicrob Proteins. 2020;12(3):1002–1011. doi: 10.1007/s12602-019-09622-w. [DOI] [PubMed] [Google Scholar]
  319. Thi NBD, Lin CY, Kumar G. Waste-to-wealth for valorization of food waste to hydrogen and methane towards creating a sustainable ideal source of bioenergy. J Clean Prod. 2016;122:29–41. doi: 10.1016/j.jclepro.2016.02.034. [DOI] [Google Scholar]
  320. Thierry A, Valence F, Deutsch S-M, Even S, Falentin H, Le Loir Y, Jan G, Gagnaire V. Strain-to-strain differences within lactic and propionic acid bacteria species strongly impact the properties of cheese–a review. Dairy Sci Technol. 2015;95(6):895–918. doi: 10.1007/s13594-015-0267-9. [DOI] [Google Scholar]
  321. Topolska K, Florkiewicz A, Filipiak-Florkiewicz A. Functional food-consumer motivations and expectations. Int J Environ Res Public Health. 2021;18(10):5327. doi: 10.3390/ijerph18105327. [DOI] [PMC free article] [PubMed] [Google Scholar]
  322. Torres-León C, Chávez-González ML, Hernández-Almanza A, Martínez-Medina GA, Ramírez-Guzmán N, Londoño-Hernández L, Aguilar CN. Recent advances on the microbiological and enzymatic processing for conversion of food wastes to valuable bioproducts. Curr Opin Food Sci. 2021;38:40–45. doi: 10.1016/j.cofs.2020.11.002. [DOI] [Google Scholar]
  323. Tropea A. Food waste valorization. Fermentation. 2022;8:168. doi: 10.3390/fermentation8040168. [DOI] [Google Scholar]
  324. Tropea A, Potortì AG, Lo Turco V, Russo E, Vadalà R, Rando R, Di Bella G. Aquafeed production from fermented fish waste and lemon peel. Fermentation. 2021;7(4):272. doi: 10.3390/fermentation7040272. [DOI] [Google Scholar]
  325. Tsafack PB, Tsopmo A. Effects of bioactive molecules on the concentration of biogenic amines in foods and biological systems. Heliyon. 2022;8(9):e10456. doi: 10.1016/j.heliyon.2022.e10456. [DOI] [PMC free article] [PubMed] [Google Scholar]
  326. Tsafrakidou P, Michaelidou AM, Biliaderis CG. 2020. Fermented cereal-based products: nutritional aspects, possible impact on gut microbiota and health implications. Foods. [DOI] [PMC free article] [PubMed]
  327. Vakhrusheva DS, Sviridenko GM, Mordvinova VA, Delitskaya IN. New solutions in the technology of low-fat cheeses. IOP Conf Ser Earth Environ Sci. 2022;1052(1):012065. doi: 10.1088/1755-1315/1052/1/012065. [DOI] [Google Scholar]
  328. Valenti F, Porto SMC, Selvaggi R, Pecorino B. Co-digestion of by-products and agricultural residues: a bioeconomy perspective for a Mediterranean feedstock mixture. Sci Total Environ. 2020;700:134440. doi: 10.1016/j.scitotenv.2019.134440. [DOI] [PubMed] [Google Scholar]
  329. Valyasevi R, Rolle RS. An overview of small-scale food fermentation technologies in developing countries with special reference to Thailand: scope for their improvement. Int J Food Microbiol. 2002;75(3):231–239. doi: 10.1016/S0168-1605(01)00711-5. [DOI] [PubMed] [Google Scholar]
  330. Van Bloemendaal L, Ijzerman RG, ten Kulve JS, Barkhof F, Konrad RJ, Drent ML, Veltman DJ, Diamant M. GLP-1 receptor activation modulates appetite- and reward-related brain areas in humans. Diabetes. 2014;63(12):4186–4196. doi: 10.2337/db14-0849. [DOI] [PubMed] [Google Scholar]
  331. Vasilev D, Aleksic B, Tarbuk A, Dimitrijevic M, Karabasil N, Cobanovic N, Vasiljevic N. Identification of lactic acid bacteria isolated from serbian traditional fermented sausages Sremski and Lemeski Kulen. Procedia Food Sci. 2015;5:300–303. doi: 10.1016/j.profoo.2015.09.071. [DOI] [Google Scholar]
  332. Vasquez ZS, de Carvalho Neto DP, Pereira GVM, Vandenberghe LPS, de Oliveira PZ, Tiburcio PB, Rogez HLG, Góes Neto A, Soccol CR (2019) Biotechnological approaches for cocoa waste management: a review. Waste manag 90:72–83. 10.1016/j.wasman.2019.04.030 [DOI] [PubMed]
  333. Vera-Pingitore E, Jimenez ME, Dallagnol A, Belfiore C, Fontana C, Fontana P, von Wright A, Vignolo G, Plumed-Ferrer C. Screening and characterization of potential probiotic and starter bacteria for plant fermentations. LWT-Food Sci Technol. 2016;71:288–294. doi: 10.1016/j.lwt.2016.03.046. [DOI] [Google Scholar]
  334. Verotta L, Panzella L, Antenucci S, Calvenzani V, Tomay F, Petroni K, Caneva E, Napolitano A. Fermented pomegranate wastes as sustainable source of ellagic acid: antioxidant properties, anti-inflammatory action, and controlled release under simulated digestion conditions. Food Chem. 2018;246:129–136. doi: 10.1016/j.foodchem.2017.10.131. [DOI] [PubMed] [Google Scholar]
  335. Vidhyalakshmi R, Vallinachiyar C, Radhika R. Production of Xanthan from agro-industrial waste. J Adv Sci Res. 2012;3(2):56–59. [Google Scholar]
  336. Vieira Gomes A, Souza Carmo T, Silva Carvalho L, Mendonça Bahia F, Parachin N. Comparison of yeasts as hosts for recombinant protein production. Microorganisms. 2018;6(2):38. doi: 10.3390/microorganisms6020038. [DOI] [PMC free article] [PubMed] [Google Scholar]
  337. Vilela A, Bacelar E, Pinto T, Anjos R, Correia E, Gonçalves B, Cosme F. Beverage and food fragrance biotechnology, novel applications, sensory and sensor techniques: an overview. Foods. 2019;8(12):12. doi: 10.3390/foods8120643. [DOI] [PMC free article] [PubMed] [Google Scholar]
  338. Vitali B, Minervini G, Rizzello CG, Spisni E, Maccaferri S, Brigidi P, Gobbetti M, Di Cagno R. Novel probiotic candidates for humans isolated from raw fruits and vegetables. Food Microbiol. 2012;31(1):116–125. doi: 10.1016/J.FM.2011.12.027. [DOI] [PubMed] [Google Scholar]
  339. Voidarou C, Antoniadou Μ, Rozos G, Tzora A, Skoufos I, Varzakas T, Lagiou A, Bezirtzoglou E. Fermentative foods: microbiology, biochemistry, potential human health benefits and public health issues. Foods. 2021;10:69. doi: 10.3390/foods10010069. [DOI] [PMC free article] [PubMed] [Google Scholar]
  340. Walhe RA, Diwanay SS, Patole MS, Sayyed RZ, Al-Shwaiman HA, Alkhulaifi MM, Elgorban AM, Danish S, Datta R. Cholesterol reduction and vitamin B12 production study on Enterococcus faecium and Lactobacillus pentosus ısolated from yoghurt. Sustainability. 2021;13(11):5853. doi: 10.3390/su13115853. [DOI] [Google Scholar]
  341. Wanangkarn A, Liu DC, Swetwiwathana A, Jindaprasert A, Phraephaisarn C, Chumnqoen W, Tan FJ. Lactic acid bacterial population dynamics during fermentation and storage of Thai fermented sausage according to restriction fragment length polymorphism analysis. Int J Food Microbiol. 2014;186:61–67. doi: 10.1016/j.ijfoodmicro.2014.06.015. [DOI] [PubMed] [Google Scholar]
  342. Wang Y, Ling C, Chen Y, Jiang X, Chen GQ. Microbial engineering for easy downstream processing. Biotechnol Adv. 2019;37(6):107365. doi: 10.1016/j.biotechadv.2019.03.004. [DOI] [PubMed] [Google Scholar]
  343. Wang D, Cheng F, Wang Y, Han J, Gao F, Tian J, Zhang K, Jin Y. The changes occurring in proteins during processing and storage of fermented meat products and their regulation by lactic acid bacteria. Foods. 2022;11:2427. doi: 10.3390/foods11162427. [DOI] [PMC free article] [PubMed] [Google Scholar]
  344. Warda AK, Rea K, Fitzgerald P, Hueston C, Gonzalez-Tortuero E, Dinan TG, Hill C. Heat-killed lactobacilli alter both microbiota composition and behaviour. Behav Brain Res. 2019;362:213–223. doi: 10.1016/j.bbr.2018.12.047. [DOI] [PubMed] [Google Scholar]
  345. Wedajo Lemi B. Microbiology of Ethiopian traditionally fermented beverages and condiments. Int J Microbiol. 2020 doi: 10.1155/2020/1478536. [DOI] [PMC free article] [PubMed] [Google Scholar]
  346. Wendin K, Undeland I. Seaweed as food-Attitudes and preferences among Swedish consumers. A pilot study. Int J Gastronomy Food Sci. 2020;22:100265. doi: 10.1016/J.IJGFS.2020.100265. [DOI] [Google Scholar]
  347. Wesolowska A, Sinkiewicz-Darol E, Barbarska O, Strom K, Rutkowska M, Karzel K, Rosiak E, Oledzka G, Orczyk-Pawilowicz M, Rzoska S, Borszewska-Kornacka MK. New achievements in high-pressure processing to preserve human milk bioactivity. Front Pediatr. 2018;6:323. doi: 10.3389/FPED.2018.00323/BIBTEX. [DOI] [PMC free article] [PubMed] [Google Scholar]
  348. Xiong T, Guan Q, Song S, Hao M, Xie M. Dynamic changes of lactic acid bacteria flora during Chinese sauerkraut fermentation. Food Control. 2012;26(1):178–181. doi: 10.1016/J.FOODCONT.2012.01.027. [DOI] [Google Scholar]
  349. Xu Y, Hlaing MM, Glagovskaia O, Augustin MA, Terefe NS. Fermentation by probiotic Lactobacillus gasseri strains enhances the carotenoid and fibre contents of carrot juice. Foods. 2020;9(12):1803. doi: 10.3390/foods9121803. [DOI] [PMC free article] [PubMed] [Google Scholar]
  350. Yalemtesfa B, Tenkegna T. Solid substrate fermentation and conversion of orange waste in to fungal biomass using Aspergillus niger KA-06 and Chaetomium spp KC-06. Afr J Microbiol Res. 2010;4:1275–1281. [Google Scholar]
  351. Yan PM, Xue WT, Tan SS, Zhang H, Chang XH. Effect of inoculating lactic acid bacteria starter cultures on the nitrite concentration of fermenting Chinese paocai. Food Control. 2008;19(1):50–55. doi: 10.1016/J.FOODCONT.2007.02.008. [DOI] [Google Scholar]
  352. Yang Y, Deng Y, Jin Y, Liu Y, Xia B, Sun Q. Dynamics of microbial community during the extremely long-term fermentation process of a traditional soy sauce. J Sci Food Agric. 2017;97(10):3220–3227. doi: 10.1002/JSFA.8169. [DOI] [PubMed] [Google Scholar]
  353. Yang H, Qu Y, Li J, Liu X, Wu R, Wu J. Improvement of the protein quality and degradation of allergens in soybean meal by combination fermentation and enzymatic hydrolysis. LWT. 2020;128:109442. doi: 10.1016/j.lwt.2020.109442. [DOI] [Google Scholar]
  354. Yang R, Chen Z, Hu P, Zhang S, Luo G. Two-stage fermentation enhanced single-cell protein production by Yarrowia lipolytica from food waste. Biores Technol. 2022;361:127677. doi: 10.1016/j.biortech.2022.127677. [DOI] [PubMed] [Google Scholar]
  355. Yoon HS, Ju JH, Kim HN, Park HJ, Ji Y, Lee JE, Shin HK, Do MS, Holzapfel W. Reduction in cholesterol absorption in Caco-2 cells through the down-regulation of Niemann-Pick C1-like 1 by the putative probiotic strains Lactobacillus rhamnosus BFE5264 and Lactobacillus plantarum NR74 from fermented foods. Int J Food Sci Nutr. 2013;64(1):44–52. doi: 10.3109/09637486.2012.706598. [DOI] [PubMed] [Google Scholar]
  356. Yue H, Ling C, Yang T, Chen X, Chen Y, Deng H, Wu Q, Chen J, Chen GQ. A seawater-based open and continuous process for polyhydroxyalkanoates production by recombinant Halomonas campaniensis LS21 grown in mixed substrates. Biotechnol Biofuels. 2014;7(1):108. doi: 10.1186/1754-6834-7-108. [DOI] [Google Scholar]
  357. Zagorec M, Champomier-Vergès MC. Meat microbiology and spoilage. In: Toldrá F, editor. Woodhead publishing series in food science, technology and nutrition, Lawrie's Meat Science. 9. Elsevier, Woodhead Publishing; 2023. pp. 195–218. [Google Scholar]
  358. Zakharchenko A, Guz N, Laradji AM, Katz E, Minko S. Magnetic field remotely controlled selective biocatalysis. Nat Catal. 2018;1(1):1. doi: 10.1038/s41929-017-0003-3. [DOI] [Google Scholar]
  359. Zeng XQ, Pan DD, Guo YX. The probiotic properties of Lactobacillus buchneri P2. J Appl Microbiol. 2010;108(6):2059–2066. doi: 10.1111/J.1365-2672.2009.04608.X. [DOI] [PubMed] [Google Scholar]
  360. Zeuthen P (2007) A historical perspective of meat fermentation. In: Toldra F (ed) Handbook of fermented meat and poultry. Blackwell Publishing, Ames, Iowa, USA, p 308
  361. Zhang Y, Li X, Bartlett DH, Xiao X. Current developments in marine microbiology: high-pressure biotechnology and the genetic engineering of piezophiles. Curr Opin Biotechnol. 2015;33:157–164. doi: 10.1016/j.copbio.2015.02.013. [DOI] [PubMed] [Google Scholar]
  362. Zhang QA, Shen Y, Fan XH, García Martín JF. Preliminary study of the effect of ultrasound on physicochemical properties of red wine. CyTA J Food. 2016;14(1):55–64. doi: 10.1080/19476337.2015.1045036. [DOI] [Google Scholar]
  363. Zhang K, Chen X, Zhang L, Deng Z. Fermented dairy foods intake and risk of cardiovascular diseases: a meta-analysis of cohort studies. Crit Rev Food Sci Nutr. 2020;60(7):1189–1194. doi: 10.1080/10408398.2018.1564019. [DOI] [PubMed] [Google Scholar]
  364. Zhang M, Dang N, Ren D, Zhao F, Lv R, Ma T, Bao Q, Menghe B, Liu W. Comparison of bacterial microbiota in raw mare’s milk and koumiss using pacbio single molecule real-time sequencing technology. Front Microbiol. 2020 doi: 10.3389/fmicb.2020.581610. [DOI] [PMC free article] [PubMed] [Google Scholar]
  365. Zhang J, Zhao J, Li J, Xia Y, Cao J. Outer membrane vesicles derived from hypervirulent Klebsiella pneumoniae stimulate the inflammatory response. Microb Pathog. 2021;154:104841. doi: 10.1016/j.micpath.2021.104841. [DOI] [PubMed] [Google Scholar]
  366. Zhang L, Liao W, Huang Y, Wen Y, Chu Y, Zhao C. Global seaweed farming and processing in the past 20 years. Food Prod Process Nutr. 2022;4:23. doi: 10.1186/s43014-022-00103-2. [DOI] [Google Scholar]
  367. Zhao CJ, Schieber A, Gänzle MG. Formation of taste-active amino acids, amino acid derivatives and peptides in food fermentations–a review. Food Res Int. 2016;89:39–47. doi: 10.1016/j.foodres.2016.08.042. [DOI] [PubMed] [Google Scholar]
  368. Zhao Y, Kumar M, Caspers MPM, Nierop Groot MN, van der Vossen JMBM, Abee T. Short communication: growth of dairy isolates of Geobacillus thermoglucosidans in skim milk depends on lactose degradation products supplied by Anoxybacillus flavithermus as secondary species. J Dairy Sci. 2018;101(2):1013–1019. doi: 10.3168/jds.2017-13372. [DOI] [PubMed] [Google Scholar]
  369. Zhong H, Abdullah, Zhao M, Tang J, Deng L, Feng F. Probiotics-fermented blueberry juices as potential antidiabetic product: antioxidant, antimicrobial and antidiabetic potentials. J Sci Food Agric. 2021;101(10):4420–4427. doi: 10.1002/jsfa.11083. [DOI] [PubMed] [Google Scholar]

Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Data Citations

  1. Ha NI, Mun SK, Im SB, Jang HY, Jeong HG, Kang KY, Park KW, Seo KS, Ban SE, Kim KJ, Yee ST. 2022. Changes in functionality of tenebrio molitor larvae fermented by Cordyceps militaris mycelia. Foods. [DOI] [PMC free article] [PubMed]
  2. Maiorano G, Ramires FA, Durante M, Palamà IE, Blando F, De Rinaldis G, Perbellini E, Patruno V, Gadaleta Caldarola C, Vitucci S, Mita G, Bleve G. 2022. The controlled semi-solid fermentation of seaweeds as a strategy for their stabilization and new food applications. Foods. [DOI] [PMC free article] [PubMed]
  3. Tsafrakidou P, Michaelidou AM, Biliaderis CG. 2020. Fermented cereal-based products: nutritional aspects, possible impact on gut microbiota and health implications. Foods. [DOI] [PMC free article] [PubMed]

Data Availability Statement

The data that support the findings of this study are available from the corresponding author, [Shahida Anusha Siddiqui], upon reasonable request.


Articles from Bioresources and Bioprocessing are provided here courtesy of Springer

RESOURCES