Abstract
Excessive sodium (salt) intake in our diet is a main contributor to hypertension and a major risk factor for cardiovascular illnesses. As a result, research has made great efforts to develop salt alternatives, and Salicornia spp. offers a very high potential in the food industry for its promising functional characteristics. This review focuses on the nutritional profile, health effects and commercial potential of three specific species of the Salicornia genus: S. bigelovii, S. brachiata and S. herbacea. It also addresses the methods that are used to produce them as salt substitutes. Owing to the antinutritional and anti-inflammatory effects of its bioactive compounds, Salicornia spp. can serve as an organic biological preservative in foods with better consumer appeal when compared with chemical preservatives that are common in the food industry. Overall, the commercial use of these underutilized species will help to improve food security.
Keywords: Salicornia spp., S. bigelovii, S. brachiata, S. herbacea, salt substitute, nutrition, food industry, health, antioxidant, anti-inflammatory
1. Introduction
Salicornia, a genus of annual, rapidly growing euhalophytes, belongs to the Chenopodiaceae family. It has fleshy, articulated stems, scale-like leaves and flowers arranged in spike-like dense and thick thyrses [1,2]. Salicornia spp. often start their life cycles in spring as green plants, gradually become reddish-yellow in autumn and die in winter. In taxonomical terms, the Salicornia genus is complex with several species, aggregates and subspecies [3]. All around the world, Salicornia spp. naturally exist on saline inlands and in coastal locations, including saltpans and salt marshes. They feature among the most promising halophytes for commercial production because of their wide-ranging resistance to climate and salinity conditions [4,5]. Salicornia is eaten fresh, fermented, cooked, dehydrated or pickled (seasoning). Since ancient times, it has been extensively used in coastal regions of Asia, particularly as fermented food and seasoning. It is also employed in folk medicine to cure various ailments, including obesity, diabetes, constipation and cancer [6]. Consuming Salicornia is more recent and less common in North American and European markets and is quite appreciated in the gourmet market. Demand surpasses supply in certain nations, including the UK and Ireland, especially in winter when imports are required from other nations such as Portugal [5]. In addition to haute cuisine, traditional cuisine is starting to show an interest in using it as a salt alternative, but it presently comes in a powdered form. Salicornia is a promising novel functional component for its significant nutritional value, including its mineral richness and fiber content [6]. Additionally, research has demonstrated that Salicornia is an excellent source of bioactive substances (e.g., polysaccharides, phytosterols and phenolic compounds) for cosmetic and nutraceutical industries, which all make it a crucial component of goods marketed to rapidly expand natural and organic markets [7]. In addition to these uses, seeds are utilized for extracting high-quality edible oil, and leftover plants are employed as forage. Given its huge potential as a crop in saline soil, Salicornia is a very adaptable plant that possesses a range of applications and is now considered to be one of the “plants of the future” [5,7,8].
Between 0.18 and 0.23 g/day of sodium must be consumed daily to sustain essential biological functions [9]. However, in our modern culture, individuals often eat excessive sodium (salt), which has become an issue in Western nations and a problem in developing nations that have acquired a liking for intake a high-sodium diet [10]. According to Powles et al. [11], the average overall sodium in 2010 was 3.95 g/day, with regional intakes falling within the 2.18–5.51 g/day range (sub-Saharan Africa to Central Asia). This amount more than doubles the recommended World Health Organization’s (WHO) limit of 2 g sodium/day (this equals 5 g/d of salt intake) [12]. Additionally, 181 of 187 countries (99.2% of the adult population) report higher sodium consumption levels than WHO recommendations; in 119 of these countries (88.3% of the world’s adult population), sodium intake exceeds the recommended threshold value of 1 g/d. In 51 countries (44.8% of the world’ adult population), the estimated average sodium intake is more than two-fold the recommended level. Asians, followed by Europeans, are the populations with the highest sodium intakes worldwide [11]. According to recent data, studies on salt intake were conducted between January 2011 and September 2018, with findings ranging from 6.75 g/d (6.32–7.17) in Barbados [13] to 10.66 g/d (10.52–10.81) in Portugal [14]. Consuming too much sodium is associated with illnesses such as hypertension and cardiovascular diseases [15]. As a result, the creation of salt substitutes has been paid a lot of attention by researchers [16,17,18]. Indeed, numerous research works have been conducted recently to examine the potential of Salicornia spp. as a functional component for the food industry in light of its promising functional traits. These research works have led to novel products with enhanced qualities being developed, including a fiber-enriched fermented milk probiotic [19] and vinegar with antifatigue and antioxidant effects [20]. Salicornia spp. has also been discovered to be a fascinating potential salt alternative [6,16,21,22,23,24].
Based on these premises, this review aims to study in depth three particular species of the Salicornia genus (S. bigelovii, S. brachiata, S. herbacea) by focusing on: their commercial potentialities on various industries including the food market; the techniques to produce them as salt substitutes; and both their nutrition profile and health impacts.
2. Generalities of the Genus Salicornia
The family Amaranthaceae (formerly Chenopodiaceae) includes the genus Salicornia. This annual succulent plant has leafless stems and branches whose sessile flowers are frequently grouped in three-flower cymes per bract and aggregated in dense terminal spike-like thyrses [3]. Inbreeding appears to dominate reproductive biology in diploid species. However, out-crossing happens, especially in tetraploid species such as S. bigelovii [25]. The majority of species favor unshaded locations, have an erect or prostate growing style and range in height (10–60 cm) and degree of branching (depending on environmental and climate circumstances) [26]. Salicornia species may be found growing inside and near inland and coastal salt lakes, saltpans, salt marshes and mudflats across boreal, temperate and subtropical regions in the northern hemisphere. The length of time that Salicornia spends submerged, the amount of waterlogging and salinity levels fluctuate in the daytime and across seasons. Salicornia spp. have been discovered to have a large amount of physiological plasticity, which results in wide-ranging phenotypic diversity between populations in various environmental circumstances [27]. Salicornia spp. have evolved exceptional salt tolerance to deal with the demanding edaphic conditions present in salt marsh ecosystems, where salinities can almost double the concentration of seawater (1 M NaCl) [8,28,29]. This high salt tolerance depends on the compartmentalization of salts in vacuoles, together with the production of suitable solutes. This allows for osmotic adjustment while also preventing the harmful effects of Cl− and Na+ in the cytosol [30]. Compatible solutes, including sucrose, proline and the glycine-betaine function, act as osmoprotective substances that preserve protein integrity and shield the cytosol from ion toxicity and free radicals and maintain osmotic pressure [31].
Although no consensus about the precise numbers of recognized species has been reached, the Salicornia genus has 25–30 species [3]. A complex taxonomy has resulted from the high physiological adaptability level combined with a very restricted leaf and flower morphology that only provides a few identifying features [3,32]. The names Salicornia europaea L. and Salicornia herbacea L. have been broadly used to refer to a variety of genotypes due to taxonomic definition difficulties, and many names have been given to the same species depending on the area [26,32]. Salicornia is also called samphire, sea asparagus, pickled seaweed, crow’s foot green, hamcho, glasswort or sea beans depending on the location [33]. Although genetically different forms have been established by analyzing ribosomal DNA polymorphism and external transcribed spacer (ETS) sequence data, these methods have not been adequate for morphologically identifying distinct species [25,34]. Seed and fruit characteristics have been acknowledged as being potentially helpful diagnostic features for identifying species [35].
Despite the taxonomic challenges posed by both morphological parallelism and phenotypic plasticity, certain identified species have drawn more attention than others [36].
3. Salicornia bigelovii
The dwarf glasswort S. bigelovii (Figure 1), which is a member of the Salicornia tetraploid branch native to North America, may be identified from other species by the tips of its bracts and leaves, which are acute and sharply mucronate [3]. Its growth habit is erect, and it can grow as tall as 50 cm in subtropical areas. It has been one of the most sought-after species in the endeavor to produce halophytes in coastal desert areas using seawater [29,37,38,39,40], and it can accumulate salt from up to 37% to 52% in dry mass [41]. The stem of this plant is succulent, erect and photosynthetic. We can find S. bigelovii in the coastal estuaries of the Mexican Sonora and Baja California States and in salt flats [42]. Several experts regard it as the most salt-tolerant vascular plant worldwide [43]. S. bigelovii, also known as samphire, is a pickled sea vegetable employed in both appetizer platters and salads. Given its oceanic flavor, raw samphire pairs well with fish and seafood. The halophyte’s leaves can be utilized as a fodder crop alternative to Rhodes grass [29] and alfalfa with livestock such as sheep and goats [44].
By using seawater for irrigation, S. bigelovii has the enormous potential for being exploited as an oilseed crop in coastal regions of wastelands and deserts [29]. On Mexico’s arid coastline, it has been assessed as an oilseed crop [45]. This halophyte may be grown as an oilseed crop in the sandy areas bordering the Gulf of California, the Indian Ocean, the Arabian Gulf and the Red Sea [37]. It is the most promising future oilseed halophyte crop for its seed’s high oil contents (30%) and low salt concentration (less than 3%) [37]. Its oil is acknowledged as good quality because it has high linoleic acid (75%) and linolenic acid (2%) levels, which are, respectively, two important omega-3 fatty acids for human nutrition and help to fight coronary heart disease [46,47]. Its meal has a high protein content (42–45%), which renders it suitable for use as animal feed [29]. Bearing in mind the significance of S. bigelovii, a breeding program has been launched in the USA and Eritrea thanks to its enhancement [48]. S. bigelovii has been cultivated on several lines to be used as vegetables, fodder and oilseeds by the Saudi Arabian BEHAR (the Arabian Saline Water Technology Company Ltd., Jubail, Saudi Arabia), which has been researching several halophyte plant species. S. bigelovii is characterized by a high protein content with high concentration of amino acids (Glu, Asp, Cyst and Gly) in both its shoots and seeds, and high unsaturated fatty acids were also reported [49]. The authors also acknowledged its role as a valuable source of minerals, amino acids and antioxidants, which makes it valuable as a food ingredient.
4. Salicornia brachiata
With terminal fruit-bearing spikes and jointed, green succulent stems, S. brachiata (Figure 2) is one of some annual halophytes that can withstand high salt concentrations and grows without leaves [50]. According to Joshi et al. [51] and Glenn et al. [47], this plant is capable of thriving in salt marshes and even needs NaCl for in vitro regeneration. It also collects 30–40% NaCl in dry weight [52]. The plant is grown in high-salinity locations, commonly in the Gujarat coastal marshes of India, and is seen as a potential substitute seawater crop [52,53], making it an interesting option for animal feed. Given its protein-rich shoots and seeds, which are employed as salad greens, this plant provides nutritional benefits [54]. This extreme halophyte is a prospective contender with a wide range of applications given its potential for acting as a naturally adapted higher plant model for abiotic stress-responsive gene resources [55,56].
S. brachiata has been tested for its antiviral activities and is acknowledged as a traditional medicine to treat hepatitis [57]. There are reports about the presence of bioactive components, minerals, amino acids, polyphenols, proteins, reducing sugars and pigments with antioxidant qualities such as betacyanin and betaxanthin [58,59].
5. Salicornia herbacea
This flowering plant species belongs to the amaranth family and is called S. herbacea (Figure 3). This halophyte plant thrives in saltwater and can be referred to by the popular names dwarf glasswort and dwarf saltwort (e.g., salt marshes), having the capacity to collect more than 50% NaCl in dry weight [60]. It is indigenous to the coastal regions of China, southern and eastern USA, southern California, Belize and in coastal regions of Mexico (on both the west and east coastlines) [61,62,63]. S. herbacea is extremely promising as a domesticated oilseed, biomass and forage crop plant [3,64,65]. In light of all this, its evaluation as an oilseed and vegetable crop in the desert coasts of Mexico, Africa and the Middle East is favorable [41,44,48,66]. Seeds germinate immediately in seawater and possess a high percentage of protein (35%) and oil (30%) but very little salt (3%) [52]. Given the large amount of polyunsaturated linoleic (75%) and linolenic (omega 3) fatty acids, both quality and oil yield are equivalent to those presented by major oilseed crops. Oil can be utilized to make biodiesel and is valuable for human consumption [46,67,68]. Additionally, high-salt drainage water, e.g., the effluent that derives from farming in the Central Valley of California, can be used to irrigate plants [41]. Aquaculture farms in Eritrea’s wastewater have been utilized to produce the plant, which is then collected to be used as animal feed [64,67].
According to studies by Lu et al. [69], Salicornia plants are an excellent source of a number of vitamins, dietary fiber, the 18 essential amino acids, unsaturated fatty acids and microelements such as calcium, iodine iron and zinc. The plant may also provide raw materials for pharmaceutical chemical manufacturing purposes and biological salt [70].
6. Commercial Potentials towards Application in Various Industries
Interest is being shown in the potential applications of Salicornia, its uses and future trends (see Figure 4). Apart from it being utilized on the food market for human consumption, the plant can be used as a biofilter for mariculture effluents, be converted into bioethanol and employed as aviation biofuel [71,72,73].
Due to Salicornia plants’ contents of flavonoids, vitamin A, carotenoid, retinol and quercetin, they have many applications in the food and pharmacy markets [73]. Salicornia seeds are valuable because 30% of edible oil can be obtained from them, and the remainder can be utilized as fodder. There is a very high economic potential value in Salicornia seeds because they are an excellent source of polyunsaturated oil. Extracted oil from Salicornia seeds have been utilized as biofuel by the National Aeronautics and Space Administration (NASA) researchers in space expeditions [73]. According to previous research, approximately eight lipid patterns of Salicornia oil have been obtained from its seeds [74,75]. Kang et al. [76] and Min et al. [77] report that S. herbacea leaves and seeds are employed for their antioxidant properties. Additional details on the utilization of Salicornia as an ingredient in functional foods is provided under Section 8.2 “Utilization as functional foods”. Ahmed and co-workers reported on the synthesis of gold nanoparticles using S. brachiata, which had antibacterial and catalytic activity, with great potential applications in the food, pharmacy and cosmetic industries [78].
Apart from the commercial potential in the food industry, the pharmaceutical, cosmetic and aquaculture industries also benefit from the utilization of Salicornia. In addition, phytoremediation of saline soils polluted with heavy metals promotes its ecological role. In particular, bio-saline farming offers a feasible solution in marginal, coastal and salt-affected areas to utilize unconventional water resources such as seawater, brackish groundwater and the reject brine from desalination [79]. Much interest has been shown in living soil bacteria with proven beneficial effects on plants. For example, utilizing plant-growth-promoting rhizobacteria as bio-inoculants for enhancing the growth of several halophytic plants such as Salicornia has been described in the works of El-Terabily et al.; Mesa-Marín et al.; and Jímenez-Mejía et al. [80,81,82]. Actinobacteria Streptomyces euryhalinus and Actinoplanes deccanensis have been isolated from marine environments to promote the growth and seed yields of S. bigelovii by stimulating endogenous levels of polyamines and other plant growth regulators [83].
The opportunities to extend the Salicornia plant market can be further expanded when plant yields increase, which includes its roots, shoots and seeds. Mathew et al. have reported that individually treating S. bigelovii in vitro with some S. bigelovii rhizosphere actinobacteria, i.e., Streptomyces chartreusis, S. tritolerans and S. rochei, respectively, brings about 46.1%, 60.0%, and 69.1% increases in seed yields [84]. However, synergetically combining these three strains leads to increases in dry shoots and root biomass of 62.2% and 77.9%, respectively, while seed yields grow by 79.7%. Similarly, El-Tarabily et al. report that actinobacteria Actinoplanes deccanensis United Arab Emirates (UAE1) and Streptomyces euryhalinus UAE1, with very high polyamine production, have a synergistic effect by increasing the length and dry weight of S. bigelovii shoots (by 44.6% and 26.11%, respectively), roots (by 42.3% and 26.5%, respectively) and photosynthetic pigment and seed yields (by 57% and 41.4%, respectively) compared with the control plants left under greenhouse conditions [83].
The unique ability of Salicornia to adapt to salt is based on the reduction in the toxicity of sodium ion in the cytoplasm, restraining the vacuoles in order to maintain a normal cellular turgor pressure [34,73]. The signal transduction pathways of the plant have a vital role for the connection within the mechanism with regard to sensing and genetic response [85]. High levels of salinity interfere with plant growth since they lead to ion toxicity and physiological drought. Gene expression regulation and changes in transcript levels are part of plant salt-stress adaptation [73].
The first mechanism by Salicornia to overcome high Na+ concentrations is the water storage in the parenchyma. This will dilute the accumulated salts, thus helping to maintain cellular turgor, allowing the plant to cope efficiently with high salinity [86].
According to Yadav and co-workers, Salicornia species can use three different techniques for preventing and adapting to high salt concentrations: (1) active sodium efflux, (2) sodium compartmentalization in vacuoles and (3) inhibition of sodium, where antiporters (group of genes), such as the Salt Overly Sensitive 1 (SOS1) gene that encodes a plasma membrane Na+/H+ antiporter, have a regulating role in ion homeostasis of plants [87].
7. Techniques to Produce Salicornia as a Salt Substitute
In order to utilize Salicornia as a salt substitute, the first step involves collecting the plant. This is followed by a cleaning procedure, which slightly differs according to reports by several authors [16,88,89,90]. Plants may be washed with either seawater or salty water [90]. Then, they are normally cut and heated [16,79], or may be dried as reported by Ghosh et al. [88]. Drying is an important process that permits plants to be stored for a longer time, such as freeze-drying and oven-drying [89]. However, the drying procedure must be carefully carried out to avoid damaging plants [91]. After these steps, different methods may be included, some of which may incorporate filtration [16,88] or mix the extract with distilled water [21,88].
A standard procedure involves cleaning the fresh stalks of S. bigelovii under tap water, washed at 95–98 °C for 4–6 min, quickly cooled with water and broken down in a high-speed tamping machine homogenizer (DS-1, Yoycart, Shanghai, China). After filtering with 200 mesh gauze, the filtrate is concentrated by rotary evaporators at 85 °C (vacuum degree at 0.06 MPa) to give liquid plant salt, which is stored at −20 °C to prepare plant salt feed [92].
In another procedure, when S. bigelovii is harvested fresh, it can be fractionated by using a twin-screw press (Angelia 8500S Angel juicer, Angel Co., Ltd., Busan, South Korea) equipped with a coarse screen with hole sizes of 1 mm [93]. The fiber produced is rewetted in a 1:1 weight ratio of fiber and saline irrigation water after the first fractionation and is pressed in the screw press for a second time. The resulting samples of juice and fiber are frozen, and the remaining biomass is dried at 70 °C and ball milled to a powder [93].
Other drying procedures reported by various authors for S. bigelovii, S. brachiata and S. herbacea include hydrothermal liquefaction as an efficient technology to convert high moisture content feedstock such as S. bigelovii stems to biofuel intermediates [94]. According to the authors, the process reduces process energy consumption due to the omission of the drying step and using water in the biomass as a potent reaction medium at elevated temperatures (180–375 °C) and pressures (4–30 MPa) [94]. Oven-drying of S. brachiata by oven-drying at 80 °C for 7 days [95]. Oven-drying of S. herbacea at 70 °C for 48 h [96].
The entire saltwort (S. herbacea) plant can be micronized to develop a table salt substitute. In line with the Chinese National Standard GB/T 12457-90, the indirect precipitation titration method can be applied to establish the NaCl content of liquid plant salt [97]. Employing the entire plant can cut waste and provide beneficial effects compared with plant extracts. The micronization process can also cut waste and allow entire plants to be employed as food additives for preparing several health foods. Thus, applying micronization to entire plant sources has been paid plenty of attention and resulted in new food industry applications [92,98].
It is necessary to improve the characteristics of the micronized powders obtained from entire plant sources because their handling often tends to be difficult and their product flowability is low. One improvement can be made by employing fluid-bed dryers. The products acquired from fluid-bed coaters present excellent preservation characteristics, along with better flowability and controlled release, and they are more conveniently handled.
So, to develop saltwort as a table salt substitute, the entire saltwort plant is micronized with a pulverizer. The micronized powder is mixed with distilled water and converted into spherical granules by means of a fluid-bed coater. To enhance this powder’s dispersibility, the micronized powder is mixed with a solution that contains several soluble solid saltwort aqueous extract contents, which is made into spherical granules [21].
Instead of heating or drying plants, extraction from plants can be carried out with water after cutting. If extraction is performed at higher temperatures, sodium content increases, while amino acids decrease. The obtained result is inversely proportional when carried out at lower temperatures or for times shorter than 4–10 h [91]. This process can increase amino acids by up to 200–400% and lower sodium content to about 1–3%. Finally, the resulting product is then centrifuged and ultrafiltrated. The product can be utilized as salt substitutes made from Salicornia species plants [99,100]. Additionally, herbal salt with the oil of plants can be made by drying, incineration and filtration [99]. They are dried and pulverized to obtain a granulose extract [101].
8. Nutrition Profile and Health Impacts
One good option is to introduce Salicornia as a salt substitute for human consumption given its unique nutritional profile, as reviewed by several authors [21,99,102]. One research work into the mechanism and effect of S. bigelovii plant salt (SPS) on Sprague Dawley (SD) rats’ blood pressure revealed that edible salt induces hypertension, while SPS does not [24]. SPS as a salt substitute has a protective effect on the liver and kidneys and can improve the body’s antioxidant ability to protect the liver and kidneys from high salt intake damage and prevent hypertension [24].
The common names, geographical location, some highlights on the nutritional features and compositions including health benefits that are associated with the three species of interest included in this review article are shown in Table 1 below.
Table 1.
Salicornia Species | Common Name | Location | Nutritional Features and Compositions | Health Benefits | References |
---|---|---|---|---|---|
S. bigelovii | Dwarf saltwort | USA, Mexico | β-carotene (15.9 mg/100 g). polyphenols (1.2 GAE/g) Na (30.4 g/kg), Cl (45.8 g/kg), K (13.2 g/kg) |
protective effects on cardiovascular diseases, hypertension | [24,103] |
S. herbacea | Dwarf glasswort | South Korea | presence of tungtungmadic acid, quercetin | protective effects on diabetes, hepatitis, gastro-enteritis | [20,76,104,105] |
S. brachiata | Umari keerai | India | high cysteine and methionine | antioxidant effects, immune booster | [54,106] |
In the study by Ventura and co-workers (Table 1), it was shown that the S. bigelovii species has a high content of β-carotene (15.9 mg/100 g of fresh weight), as well as polyphenols at (1.2 gallic acid equivalent GAE/g) of fresh weight [107]. Kang et al. [103] stated that the seawater cultivation of S. herbacea could result in higher phenolic and flavonoid contents.
S. bigelovii is referred to as ‘green food’. It is apt for being developed into new plant salt as a salt substitute for preventing high blood pressure. Natural plant salt has been confirmed to be effective in controlling blood pressure and reducing morbidity from cardiovascular and cerebrovascular diseases, i.e., coronary disease, cerebral apoplexy, etc. [103]. Nevertheless, no key studies into the relation linking S. bigelovii Torr plant salt (SPS), SPS intake and high blood pressure have yet been reported [24]. In this study, Salicornia bigelovii Torr. stalks were made into plant salt for investigating the impact of a high-dose intake of SPS on the blood pressure of SD rats. The results will offer a sound basis for employing SPS as substitute salt to prevent and control high blood pressure [24].
Min et al. [77] reported the chemical composition and micronutrients from different parts of the S. herbacea plant such as leaves, stems and roots. They concluded that the stems and roots of the plant contained a significant content of important amino acids such as aspartic acid (140.1 and 165.5 mg/100 g), glutamic acid (160.5 and 182.3 mg/100 g) and isoleucine (107.5 and 94.7 mg/100 g), respectively. In addition, they found a significant amount of minerals such as sodium (1218.1 mg/100 g), calcium (158.8 mg/100 g), potassium (740.1 mg/100 g) and magnesium (52.2 mg/100 g), mainly in stems. Other studies by Man and co-workers stated that the leaves of S. herbacea have significant contents of fatty acids such as linoleic and oleic. They also showed that S. herbacea contained bioactive compounds such as tungtungmadic acid and quercetin 3−0 glucoside [35].
S. herbacea consumption is considered to be a slight risk due to its iodine content, which can lead to hypokalemic [7]. It is noteworthy that, to date, no problem has been reported from consuming it. However, there has been some incidence of this hypokalemic rare disease being referred to as “throtoxic periodic analysis” (TPP), which has been associated with hyperthyroidism. As a result of this, there have been recommendations about being careful with iatrogenic iodine compounds, especially when consuming S. herbacea [108].
S. herbacea are also unique for having a salty taste and a smaller quantity of sodium, as well as their nutritional quality of fatty acid content [4,46,109,110], especially polyunsaturated [111,112], in addition to minerals [4,16,20,53,103,105,108,113,114], vitamins [4,53] and antioxidants [4,7,20,29,105], which enrich their nutritional profile [4] and make Salicornia species S. herbacea, S. bigelovii and S. brachiata good options for making salt substitutes.
S. herbacea’s efficacy against inflammation, oxidative stress, asthma, diabetes, hepatitis, gastroenteritis and cancer has been reported [105]. S. herbacea leaves and seeds can also be employed for their antioxidant properties, as, respectively, reported by Min et al. [77] and Kang et al. [103]. The results obtained with the present study indicate that no experimental group (fresh mullet (FM) and salted semidried mullet (SSDM)) had Staphylococcus aureus. This indicates that the semidried salted method followed by using natural salt and S. herbacea treatment for preservation purpose is capable of preventing microbial contamination and prolonging shelf life [104].
Salicornia seeds are valuable for the amount of edible oil (30%) that can be extracted from them, whereas the remainder is employed as fodder. Some studies report the presence of proteins, lipids, bioactive polysaccharides, dietary fibers, sterols, minerals (Ca, Fe, K and Mg) and flavonoids in S. herbacea [105]. One study has shown S. herbacea seed oil as being stable to oxidation, which renders its use as eligible in food processing [115]. Oil is composed of oleic acid, linoleic acid, palmitic acid, arachidic acidtocopherol (α, γ, δ type), chlorophyll, phenol and β carotene, which all confer it a long shelf life as evidenced by the study of Choi et al. [115]. These authors observed that oil remained rancidity-free over a 60-day dark storage period. 24-ethyl-δ(22)-coprostenol, stigmastanol and some other bioactive fatty alcohols have been detected in oil [111].
S. bigelovii salt has been found to prevent the hypertensive effects usually related to sodium chloride. In a study by Zhang et al., a lower serum creatinine level was observed with S. bigelovii consumption due to its ameliorative effect on the liver and kidneys [24]. The same authors also showed that Na(+)-K(+)-ATPase activity and superoxide dismutase (SOD) increased, while malondialdehyde (MDA) content lowered. This finding advocates a beneficial effect on the body’s antioxidant profile [24]. S. bigelovii species are particularly noteworthy for having high contents of both β-carotene (15.9 mg 100 g−1 fresh weight-FW) and polyphenols (1.2 GAE g−1 FW) [107]. Kang et al. [103] report that Salicornia seawater cultivation may result in high flavonoid and phenolic contents.
In S. brachiata, a high content of sulfur-rich amino acids (cysteine and methionine) was detected because of the disruption of the sulfur bonds and release of these amino acids under stress [116]. Eganathan and co-workers identified the fatty acids present in S. brachiata fat as palmitic (16.48%), myristic (12.88%), oleic (32.79%) and, in particular, 10-undecenoic (37.85%), which has the potential for commercial exploitation for use in lubricants or pheromones in crop pests [109].
The metabolomic analysis of S. brachiata detected rich polyunsaturated fatty acids (PUFAs) and sulfur amino acids at up to 55–64% [116]. The authors also detected that selenium was present in S. brachiata [116]. Selenium is a micronutrient that is vital for growth with marked antioxidant effects whose deficiency can impair the immune system [63]. This justifies evaluating selenium extraction from Salicornia for human diet. Another study also revealed that S. brachiata is capable of absorbing nickel, arsenic and cadmium salts [117], which indicates that Salicornia plants can be an excellent source of the phytoremediation of heavy-metal-polluted saline coastal regions.
8.1. Antioxidant and Anti-Inflammatory Effects
The health impacts of Salicornia spp. are enhanced by its important role as an antioxidant and anti-inflammatory when added as a food ingredient. Plant-derived antioxidants are extracted from natural plants such as Salicornia spp. with antioxidant properties, they can effectively inhibit or delay the oxidative decomposition and deterioration of food ingredients, thereby enhancing the stability of food and extending their storage period [118].
Salicornia can be utilized as ‘functional foods’ since it contains metabolites with bioactivities [118]. For example, the S. brachiata plant possesses nutritional antioxidants, scavenging activities, amino acids, flavonoids, essential fatty acids and polyunsaturated fatty acids, making it a promising ideal plant that can used as a functional food or as a dietary supplement in nutraceutical industries [116]. An interesting application that uses S. brachiata to produce low-cost antibacterial nanoparticles for the food and pharmacy markets was created by Ahmed et al. [78].
In previous research, it was demonstrated that S. bigelovii contains a variety of chemical components with antioxidant properties [119], antitumor properties [119] and the molecular basis for anti-inflammatory effects [120]. The effect of S. bigelovii extract on the preservation of aquatic products as demonstrated by Wang and co-workers showed that S. bigelovii can significantly reduce the pH value and the content of total volatile basic nitrogen (TVB-N) in fish meat, leading to the reduction in amines by inhibiting the decomposition of protein and the oxidation of unsaturated fatty acids [118]. The antioxidant compound that was purified from S. herbacea, known as a 13-Oxo-9(Z), 11(E)-octadecadienoic acid, i.e., ‘13-KODE’, produced anti-inflammatory effects with great potential for use in treating inflammatory diseases [121].
Several natural compounds have been isolated from S. herbacea. Methanol-extracted compounds from S. herbacea includes stigmasterol, P-sitosterol, uracil and isorhamnetin-3-0-β-D-glucopyranoside [111]. The presence of several chlorogenic acid derivatives, such as 3-caffeoyl-4-dihydrocaffeoyl quinic acid, also known as tungtungmadic acid [122], methyl4-caffeoyl-3-dihydrocaffeoyl quinate (salicornate), methyl 3,5-dicaffeoyl quinate, 3,5-dicaffeoylquinic acid and 3,4-dicaffeoylquinic acid, as well as the flavonoid derivatives quercetin 3-0-p-o-glucopyranoside and isorhamnetin 3-0-p-o-glucopyranoside and isoquercetin 6″-0-methyloxalate, were also obtained [123].
Other authors have reported the isolation of isorhamnetin 3-0-p-o-glucopyranoside and quercetin 3-0-p-o-glucopyranoside from the n-butanol extract of S. herbacea [124,125,126].
In 2007, Oh et al., obtained S. herbacea viscozyme-treated extract and further extracted it with ethanol. This allowed the isolation of simple phenolic acids such as protocatechuic, caffeic and ferulic and also the flavanol derivatives quercetin and isorhamnetin [127]. Chung and co-workers also found that tungtungmadic acid prevents iron-induced liver microsomal lipid peroxidation (IC50 9.3 μM) and is effective in protection of plasmid DNA against strand breakage induced by hydroxyl radicals [122]. Hwang and co-workers reported that tungtungmadic acid is capable of inhibiting tumor cell invasion and migration in human fibrosarcoma HT-1080 cells by regulating protein kinase co-dependent matrix metalloproteinase-9 expression. They proposed that the anti-invasive effects occur through the inhibition of activator protein-1 (AP-1) and signaling pathways, which involves protein kinase C-delta (PKCծ) and three mitogen-activated protein kinases, i.e. extracellular signal-regulated kinases (ERK), a subfamily of mitogen-activated protein kinases that are responsive to stress stimuli (p38MAPK) and terminal kinases (JNK-c-Jun N) that belongs to the mitogen-activated protein kinase family leading to the down regulation of matrix metallopeptidase 9 (MMP-9)—key effectors of extracellular matrix remodeling that play a role in inflammation [128].
8.2. Utilization as Functional Foods
The utilization of these Salicornia species as functional foods lies in their compositional quality attributes and health impacts discussed above. For example, the chemical composition of S. bigelovii seeds had protein (31.2), ash (5.5), fiber (5.3) and oil (28.2), with a good balance of fatty acids (linoleic 74, linolenic 2.6, oleic, 2.5 palmitic 8.1 and stearic 2.2) [29]. The seeds from these Salicornia species are considered very valuable, since 30 edible oils can be extracted from them, and the rest of the biomass can be used as fodder. The seeds and leaves of S. herbacea are used due to their antioxidant properties, as reported by [76,77]. The presence of polyunsaturated oil in Salicornia seeds makes them of high economic value.
When monosaccharide composition in S. brachiata was analyzed, the obtained fractions revealed that mannose, rhamnose, galactose, arabinose and glucose dominated, with a meager presence of xylose and ribose [129]. The MALDI-TOF (matrix-assisted laser desorption/ionization time of flight mass spectrometry) proteomic analysis demonstrated that S. brachiata seeds contained a considerable amount of protein. In the globulin proteins of S. brachiata, high disulfide linkages were detected, and sulfur-rich proteins were noted to be suitable for nutritional purposes, which makes a strong case to consume it [54].
S. herbecea enhanced fermenting microbe propagation and improved the quality of vinegar quality [130]. The authors noted that S. herbecea activates the growth of microorganisms during the fermentation of nuruk, makgeolli, or vinegar but also serves as a nutritional supplement that improves the quality of vinegar [130]. The young stalks of S. herbacea, called hamcho and tungtungmadi in Korea, are consumed in a variety of ways such as a seasoned vegetable, salad and fermented food in coastal areas of Korea; they are also utilized as a main ingredient of salad in Europe [111,131]. In India, shoots of S. herbacea can also be transformed into beverages such as nuruk (fermentation starter), makgeolli (Korean rice wine), or vinegar [130]. Kang and co-workers reported that the seeds of S. herbecea are also used as tea [76].
The annual glasswort or saltwort S. bigelovii Torr. are used freshly in salad or boiled for jarring as pickles with vinegar, sugar, onion, bayberry leaves and mixed pickling spice in Nova Scotia, Canada [111,132]. The aerial parts of S. bigelovii have also been used as an ingredient in vinegar in Italy and France [111,123]. S. bigelovii is described as a very valuable source of minerals, amino acids and antioxidants that render it the most promising salt-loving plant for food use [49].
In the efforts to create a halophyte-based food industry with local produce in a desert environment, a project funded by Universal Exposition in Dubai (EXPO2020 Dubai) from 2019–2021 entitled ‘From Desert Farm to Fork: Value chain development for innovative halophyte-based food products’ will utilize the health-giving properties in S. bigelovii in newly formulated food products [79].
The following food products were developed with S. bigelovii: sorbet with mango, banana and S. bigelovii; camel laban with Salicornia; lasagna with Salicornia; charcoal bread with vegan Salicornia burger; falafel with Salicornia, quinoa, chickpea and kale; vegan Salicornia burger; steamed Salicornia bread; camel cheesecake with Salicornia; charcoal pizza with Salicornia; and vegan Salicornia, quinoa and peas balls. Such initiatives can be replicated industrially in similar climatic contexts and salt-affected areas.
The ratio of S. bigelovii as an ingredient in the recipes ranged between 20% and 40% for all the products and recipes that were developed. In this project, it was observed that Salicornia showed great versatility in cooking options and processing possibilities for both salty and sweet dishes, liquid and solid food products. As already discussed in the previous section, Salicornia is characterized by its antioxidant and anti-inflammatory effects, a high content of minerals and high vitamin C, especially at a later growth stage, which when combined with its rich content in zinc, magnesium and manganese will make it a good candidate to boost the immune system [79].
9. Conclusions and Future Perspectives
The role of Salicornia as a good salt substitute is very promising. It is quite sustainable as an underutilized flora and can form part of the human diet. It can also provide a source of income for growers. The three species considered in this review, namely S. bigelovii, S. brachiata and S. herbacea, are rich in dietary bioactive components, low in sodium and high in protein and fiber and can promote health. The salt-water-tolerant plant also helps to improve water quality through remediation and makes clean water available that is essential for food processing and sanitation. There is a need to investigate the nanoparticles with antibacteria activities that are found in S. brachiata; they will be useful in the food, pharmacy and cosmetic industries.
However, one major drawback of utilizing Salicornia is its non-perennial nature. So, it cannot be harvested all year round, unlike its counterpart genus Sarcocornia, which is non-seasonal and can be supplied all year long. For example, the native range of S. bigelovii plant is coastal salt marshes, where it germinates in winter or spring and flowers in summer in response to photoperiod [133]. The plants senesce and shed seeds in the fall. In order to overcome this challenge, efforts are being made to ensure the regular availability of Salicornia plants with efficient drying techniques in the future.
Acknowledgments
The authors extend their appreciation to the Deputyship for Research & Innovation, Ministry of Education, Saudi Arabia for funding this research work through the project number (QU-IF-01-02-28482). The authors would also thank Qassim University for technical support.
Author Contributions
Conceptualization, A.R., A.S. and D.R.; methodology, A.R., A.S. and D.R.; software, A.R., A.S. and D.R.; validation, A.R., A.S. and D.R.; formal analysis, A.R., A.S. and D.R.; investigation, A.R., A.S. and D.R.; resources, A.R., A.S. and D.R.; data curation, A.R., A.S. and D.R.; writing—original draft preparation, A.R., A.S. and D.R.; writing—review and editing, A.R., A.S. and D.R.; visualization, A.R., A.S., D.R., H.A.A., F.A., F.S.A., Z.D.A., J.H.A. and M.N.B.; funding acquisition, A.R., H.A.A., F.A., F.S.A., Z.D.A., J.H.A. and M.N.B.; project administration, A.R., A.S. and D.R.; supervision, A.R. All authors have read and agreed to the published version of the manuscript.
Institutional Review Board Statement
Not applicable.
Informed Consent Statement
Not applicable.
Data Availability Statement
Not applicable.
Conflicts of Interest
The authors declare no conflict of interest.
Funding Statement
The authors extend their appreciation to the Deputyship for Research & Innovation, Ministry of Education, Saudi Arabia for funding this research work through the project number (QU-IF-01-02-28482). The authors would also thank Qassim University for technical support.
Footnotes
Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations.
References
- 1.Lopes M., Castilho M.D.C., Sanches-Silva A., Freitas A., Barbosa J., Gonçalves M.J., Cavaleiro C., Ramos F. Evaluation of the mycotoxins content of Salicornia spp.: A gourmet plant alternative to salt. Food Addit. Contam. Part B. 2020;13:162–170. doi: 10.1080/19393210.2020.1741692. [DOI] [PubMed] [Google Scholar]
- 2.Valdés B., Castroviejo S. Platanaceae-Plumbaginaceae (partim) In: Castroviejo S., Laínz M., González G.L., Montserrat P., Garmendia F.M., Paiva J., Villar L., editors. Flora Iberica–Plantas Vasculares De La Península Ibérica E Islas Baleares. Volume II. Real Jardín Botánico, C.S.I.C.; Madrid, Spain: 1990. [(accessed on 15 September 2022)]. pp. 531–533. Available online: http://www.floraiberica.es/floraiberica/texto/pdfs/02_052_17_Salicornia.pdf. [Google Scholar]
- 3.Kadereit G., Ball P., Beer S., Mucina L., Sokoloff D., Teege P., Yaprak A.E., Freitag H. A taxonomic nightmare comes true: Phylogeny and biogeography of glassworts (Salicornia, L., Chenopodiaceae) Taxon. 2007;56:1143–1170. doi: 10.2307/25065909. [DOI] [Google Scholar]
- 4.Lu D., Zhang M., Wang S., Cai J., Zhou X., Zhu C. Nutritional characterization and changes in quality of Salicornia bigelovii Torr. during storage. LWT-Food Sci. Technol. 2010;43:519–524. doi: 10.1016/j.lwt.2009.09.021. [DOI] [Google Scholar]
- 5.Gunning D. Cultivating Salicornia europaea (marsh samphire) Dublin Irel. Ir. Sea Fish. Board. 2016;4:1–95. [Google Scholar]
- 6.Lopes M., Cavaleiro C., Ramos F. Sodium reduction in bread: A role for glasswort (Salicornia ramosissima J. Woods) Compr. Rev. Food Sci. Food Saf. 2017;16:1056–1071. doi: 10.1111/1541-4337.12277. [DOI] [PubMed] [Google Scholar]
- 7.Patel S. Salicornia: Evaluating the halophytic extremophile as a food and a pharmaceutical candidate. 3 Biotech. 2016;6:1–10. doi: 10.1007/s13205-016-0418-6. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 8.Ventura Y., Sagi M. Halophyte crop cultivation: The case for Salicornia and Sarcocornia. Environ. Exp. Bot. 2013;92:144–153. doi: 10.1016/j.envexpbot.2012.07.010. [DOI] [Google Scholar]
- 9.World Health Organization Reducing salt intake in populations: Report of a WHO forum and technical meeting; Proceedings of the WHO Forum and Technical Meeting; Paris, France. 5–7 October 2006. [Google Scholar]
- 10.Wei L., Mackenzie I.S., MacDonald T.M., George J. Cardiovascular risk associated with sodium-containing medicines. Expert Opin. Drug Saf. 2014;13:1515–1523. doi: 10.1517/14740338.2014.970163. [DOI] [PubMed] [Google Scholar]
- 11.Powles J., Fahimi S., Micha R., Khatibzadeh S., Shi P., Ezzati M., Engell R.E., Lim S.S., Danaei G., Mozaffarian D., et al. Global, regional and national sodium intakes in 1990 and 2010: A systematic analysis of 24 h urinary sodium excretion and dietary surveys worldwide. BMJ Open. 2013;3:e003733. doi: 10.1136/bmjopen-2013-003733. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 12.World Health Organization . Guideline: Sodium Intake for Adults and Children. World Health Organization; Geneva, Switzerland: 2012. [PubMed] [Google Scholar]
- 13.Harris R.M., Rose A., Hambleton I.R., Howitt C., Forouhi N.G., Hennis A.J., Samuels T.A., Unwin N. Sodium and potassium excretion in an adult Caribbean population of African descent with a high burden of cardiovascular disease. BMC Public Health. 2018;18:1–11. doi: 10.1186/s12889-018-5694-0. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 14.Polonia J., Martins L., Pinto F., Nazaré J. Prevalence, awareness, treatment and control of hypertension and salt intake in Portugal: Changes over a decade. The PHYSA study. J. Hypertens. 2014;32:1211–1221. doi: 10.1097/HJH.0000000000000162. [DOI] [PubMed] [Google Scholar]
- 15.Mcneely J.D., Windham B.G., Anderson D.E. Dietary sodium effects on heart rate variability in salt sensitivity of blood pressure. Psychophysiology. 2008;45:405–411. doi: 10.1111/j.1469-8986.2007.00629.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 16.Lee G.H. A salt substitute with low sodium content from plant aqueous extracts. Food Res. Int. 2011;44:537–543. doi: 10.1016/j.foodres.2010.11.018. [DOI] [Google Scholar]
- 17.Wick C.D., Dang L.X., Jungwirth P. Simulated surface potentials at the vapor-water interface for the KCl aqueous electrolyte solution. J. Chem. Phys. 2006;125:024706. doi: 10.1063/1.2218840. [DOI] [PubMed] [Google Scholar]
- 18.Braschi A., Gill L., Naismith D.J. Partial substitution of sodium with potassium in white bread: Feasibility and bioavailability. Int. J. Food Sci. Nutr. 2009;60:507–521. doi: 10.1080/09637480701782118. [DOI] [PubMed] [Google Scholar]
- 19.Choi S.C., Kim B.J., Rhee P.L., Chang D.K., Son H.J., Kim J.J., Rhee J.C., Kim S.I., Han Y.S., Sim K.H., et al. Probiotic fermented milk containing dietary fiber has additive effects in IBS with constipation compared to plain probiotic fermented milk. Gut Liver. 2011;5:22. doi: 10.5009/gnl.2011.5.1.22. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 20.Cho H.D., Lee J.H., Jeong J.H., Kim J.Y., Yee S.T., Park S.K., Lee M.K., Seo K.I. Production of novel vinegar having antioxidant and anti-fatigue activities from Salicornia herbacea L. J. Sci. Food Agric. 2016;96:1085–1092. doi: 10.1002/jsfa.7180. [DOI] [PubMed] [Google Scholar]
- 21.Shin M.G., Lee G.H. Spherical granule production from micronized saltwort (Salicornia herbacea) powder as salt substitute. Prev. Nutr. Food Sci. 2013;18:60. doi: 10.3746/pnf.2013.18.1.060. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 22.Kim H.W., Hwang K.E., Song D.H., Kim Y.J., Ham Y.K., Yeo I.J., Jeong T.-J., Choi Y.-S., Kim C.J. Effects of red and green glassworts (Salicornia herbacea L.) on physicochemical and textural properties of reduced-salt cooked sausages. Korean J. Food Sci. Anim. Resour. 2014;34:378. doi: 10.5851/kosfa.2014.34.3.378. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 23.Kim H.W., Hwang K.E., Song D.H., Kim Y.J., Lim Y.B., Ham Y.K., Yeo E.J., Chang S.J., Choi Y.S., Kim C.J. Effect of glasswort (Salicornia herbacea L.) on the texture of frankfurters. Meat Sci. 2014;97:513–517. doi: 10.1016/j.meatsci.2014.03.019. [DOI] [PubMed] [Google Scholar]
- 24.Zhang S., Wei M., Cao C., Ju Y., Deng Y., Ye T., Xia Z., Chen M. Effect and mechanism of Salicornia bigelovii Torr. plant salt on blood pressure in SD rats. Food Funct. 2015;6:920–926. doi: 10.1039/C4FO00800F. [DOI] [PubMed] [Google Scholar]
- 25.Noble S.M., Davy A.J., Oliver R.P. Ribosomal DNA variation and population differentiation in Salicornia L. New Phytol. 1992;122:553–565. doi: 10.1111/j.1469-8137.1992.tb00085.x. [DOI] [PubMed] [Google Scholar]
- 26.Davy A.J., Bishop G.F., Costa C.S.B. Salicornia L.(Salicornia pusilla J. woods, S. ramosissima J. woods, S. europaea L., S. obscura PW ball & tutin, S. nitens PW ball & tutin, S. fragilis PW ball & tutin and S. dolichostachya moss) J. Ecol. 2001;89:681–707. [Google Scholar]
- 27.Rozema J., Van Der List J.C., Schat H., Diggelen J.V., Broekman R.A. Vegetation between Land and Sea. Springer; Dordrecht, The Netherlands: 1987. Ecophysiological response of Salicornia dolichostachya and Salicornia brachystachya to seawater inundation; pp. 180–186. [Google Scholar]
- 28.Flowers T.J., Hajibagheri M.A., Clipson N.J.W. Halophytes. Q. Rev. Biol. 1986;61:313–337. doi: 10.1086/415032. [DOI] [Google Scholar]
- 29.Glenn E.P., O’Leary J.W., Watson M.C., Thompson T.L., Kuehl R.O. Salicornia bigelovii Torr.: An oilseed halophyte for seawater irrigation. Science. 1991;251:1065–1067. doi: 10.1126/science.251.4997.1065. [DOI] [PubMed] [Google Scholar]
- 30.Munns R., Tester M. Mechanisms of salinity tolerance. Annu. Rev. Plant Biol. 2008;59:651. doi: 10.1146/annurev.arplant.59.032607.092911. [DOI] [PubMed] [Google Scholar]
- 31.Slama I., Abdelly C., Bouchereau A., Flowers T., Savouré A. Diversity, distribution and roles of osmoprotective compounds accumulated in halophytes under abiotic stress. Ann. Bot. 2015;115:433–447. doi: 10.1093/aob/mcu239. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 32.Kadereit G., Piirainen M., Lambinon J., Vanderpoorten A. Cryptic taxa should have names: Reflections in the glasswort genus Salicornia (Amaranthaceae) Taxon. 2012;61:1227–1239. doi: 10.1002/tax.616005. [DOI] [Google Scholar]
- 33.Feng L., Ji B., Su B. Economic value and exploiting approaches of sea asparagus, a seawater-irrigated vegetable. Agric. Sci. 2013;4:40. doi: 10.4236/as.2013.49B007. [DOI] [Google Scholar]
- 34.Singh D., Buhmann A.K., Flowers T.J., Seal C.E., Papenbrock J. Salicornia as a crop plant in temperate regions: Selection of genetically characterized ecotypes and optimization of their cultivation conditions. AoB Plants. 2014;6 doi: 10.1093/aobpla/plu071. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 35.Man H.R., Hwa-Jin P., Jae Y.C. Salicornia herbacea: Botanical, chemical and pharmacological review of halophyte marsh plant. J. Med. Plants Res. 2009;3:548–555. [Google Scholar]
- 36.Chaturvedi T., Christiansen A.H., Gołębiewska I., Thomsen M.H. Future of Sustainable Agriculture in Saline Environments. CRC Press; Boca Raton, FL, USA: 2021. Salicornia Species: Current Status and Future Potential; pp. 461–482. [Google Scholar]
- 37.Glenn E.P., Brown J.J., O’Leary J.W. Irrigating crops with seawater. Sci. Am. 1998;279:76–81. doi: 10.1038/scientificamerican0898-76. [DOI] [Google Scholar]
- 38.Glenn E.P., Anday T., Chaturvedi R., Martinez-Garcia R., Pearlstein S., Soliz D., Nelson S.G., Felger R.S. Three halophytes for saline-water agriculture: An oilseed, a forage and a grain crop. Environ. Exp. Bot. 2013;92:110–121. doi: 10.1016/j.envexpbot.2012.05.002. [DOI] [Google Scholar]
- 39.Hodges C.N., Thompson T.L., Riley J.J., Glenn E.P. Reversing the flow: Water and nutrients from the sea to the land. Ambio. 1993;22:483–490. [Google Scholar]
- 40.Ventura Y., Eshel A., Pasternak D., Sagi M. The development of halophyte-based agriculture: Past and present. Ann. Bot. 2015;115:529–540. doi: 10.1093/aob/mcu173. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 41.Grattan S.R., Benes S.E., Peters D.W., Diaz F. Feasibility of irrigating pickleweed (Salicornia bigelovii Torr) with hyper-saline drainage water. J. Environ. Qual. 2008;37:S-149–S-156. doi: 10.2134/jeq2007.0450. [DOI] [PubMed] [Google Scholar]
- 42.Rueda-Puente E.O., García-Hernández J.L., Preciado-Rangel P., Murillo-Amador B., Tarazón-Herrera M.A., Flores-Hernández A., Holguin-Peña J., Aybar A.N., Hoyos J.M.B., Weimers D., et al. Germination of Salicornia bigelovii ecotypes under stressing conditions of temperature and salinity and ameliorative effects of plant growth-promoting bacteria. J. Agron. Crop Sci. 2007;193:167–176. doi: 10.1111/j.1439-037X.2007.00254.x. [DOI] [Google Scholar]
- 43.Ayala F., O’Leary J.W. Growth and physiology of Salicornia bigelovii Torr. at suboptimal salinity. Int. J. Plant Sci. 1995;156:197–205. doi: 10.1086/297241. [DOI] [Google Scholar]
- 44.Abdal M.S. Salicornia production in Kuwait. World Appl. Sci. J. 2009;6:1033–1038. [Google Scholar]
- 45.Troyo-Diéguez E., Ortega-Rubio A., Maya Y., León J.L. The effect of environmental conditions on the growth and development of the oilseed halophyte Salicornia bigelovii Torr. in arid Baja California Sur, Mexico. J. Arid Environ. 1994;28:207–213. doi: 10.1016/S0140-1963(05)80058-8. [DOI] [Google Scholar]
- 46.Anwar F., Bhanger M.I., Nasir M.K.A., Ismail S. Analytical characterization of Salicornia bigelovii seed oil cultivated in Pakistan. J. Agric. Food Chem. 2002;50:4210–4214. doi: 10.1021/jf0114132. [DOI] [PubMed] [Google Scholar]
- 47.Covington M.B. Omega-3 fatty acids. Am. Fam. Physician. 2004;70:133–140. [PubMed] [Google Scholar]
- 48.Zerai D.B., Glenn E.P., Chatervedi R., Lu Z., Mamood A.N., Nelson S.G., Ray D.T. Potential for the improvement of Salicornia bigelovii through selective breeding. Ecol. Eng. 2010;36:730–739. doi: 10.1016/j.ecoleng.2010.01.002. [DOI] [Google Scholar]
- 49.Lyra D.-A., Raman A., Hozayen A., Zaaboul R., Abou-Zaid F.O., El-Naggar A., Mansoor S., Mahmoudi H., Ammar K. Evaluation of Salicornia bigelovii Germplasm for Food Use in Egypt and the United Arab Emirates Based on Agronomic Traits and Nutritional Composition. Plants. 2022;11:2653. doi: 10.3390/plants11192653. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 50.Mishra A., Joshi M., Jha B. Oligosaccharide mass profiling of nutritionally important Salicornia brachiata, an extreme halophyte. Carbohydr. Polym. 2013;92:1942–1945. doi: 10.1016/j.carbpol.2012.11.055. [DOI] [PubMed] [Google Scholar]
- 51.Joshi M., Mishra A., Jha B. NaCl plays a key role for in vitro micropropagation of Salicornia brachiata, an extreme halophyte. Ind. Crops Prod. 2012;35:313–316. doi: 10.1016/j.indcrop.2011.06.024. [DOI] [Google Scholar]
- 52.Glenn E.P., Brown J.J., Blumwald E. Salt tolerance and crop potential of halophytes. Crit. Rev. Plant Sci. 1999;18:227–255. doi: 10.1080/07352689991309207. [DOI] [Google Scholar]
- 53.Stanley O.D. Bio prospecting marine halophyte Salicornia brachiata for medical importance and salt encrusted land development. J. Coast. Dev. 2008;11:62–69. [Google Scholar]
- 54.Jha B., Singh N.P., Mishra A. Proteome profiling of seed storage proteins reveals the nutritional potential of Salicornia brachiata Roxb., an extreme halophyte. J. Agric. Food Chem. 2012;60:4320–4326. doi: 10.1021/jf203632v. [DOI] [PubMed] [Google Scholar]
- 55.Chaturvedi A.K., Mishra A., Tiwari V., Jha B. Cloning and transcript analysis of type, 2 metallothionein gene (SbMT-2) from extreme halophyte Salicornia brachiata and its heterologous expression in E. coli. Gene. 2012;499:280–287. doi: 10.1016/j.gene.2012.03.001. [DOI] [PubMed] [Google Scholar]
- 56.Jha B., Sharma A., Mishra A. Expression of SbGSTU (tau class glutathione S-transferase) gene isolated from Salicornia brachiata in tobacco for salt tolerance. Mol. Biol. Rep. 2011;38:4823–4832. doi: 10.1007/s11033-010-0625-x. [DOI] [PubMed] [Google Scholar]
- 57.Bandaranayake W.M. Bioactivities, bioactive compounds and chemical constituents of mangrove plants. Wetl. Ecol. Manag. 2002;10:421–452. doi: 10.1023/A:1021397624349. [DOI] [Google Scholar]
- 58.Escribano J., Pedreño M.A., García-Carmona F., Muñoz R. Characterization of the antiradical activity of betalains from Beta vulgaris L. roots. Phytochem. Anal. Int. J. Plant Chem. Biochem. Tech. 1998;9:124–127. doi: 10.1002/(SICI)1099-1565(199805/06)9:3<124::AID-PCA401>3.0.CO;2-0. [DOI] [Google Scholar]
- 59.Parida A.K., Kumari A., Panda A., Rangani J., Agarwal P.K. Photosynthetic pigments, betalains, proteins, sugars, and minerals during Salicornia brachiata senescence. Biol. Plant. 2018;62:343–352. doi: 10.1007/s10535-017-0764-1. [DOI] [Google Scholar]
- 60.Shimizu K. Studies on the salinity tolerance of Salicornia herbacea L. Agric. For. Sci. 1996;8:1–65. [Google Scholar]
- 61.Balick M.J., Nee M., Atha D.E. Checklist of the Vascular Plants of Belize. New York Botanical Garden; New York, NY, USA: 2000. Checklist of the vascular plants of Belize. [Google Scholar]
- 62.Carnevali F.C.G., Tapia-Muñoz J.L., de Stefano R.D., Morillo I.R. Flora Ilustrada De La Península De Yucatán: Listado Florístico. Centro de Investigación Científica de Yucatán; AC Yucatán, México: 2010. [Google Scholar]
- 63.Godfrey R.K. Aquatic and Wetland Plants of Southeastern United States: Dicotyledons. Volume 2 University of Georgia Press; Athens, Greece: 1981. [Google Scholar]
- 64.Bashan Y., Moreno M., Troyo E. Growth promotion of the seawater-irrigated oilseed halophyte Salicornia bigelovii inoculated with mangrove rhizosphere bacteria and halotolerant Azospirillum spp. Biol. Fertil. Soils. 2000;32:265–272. doi: 10.1007/s003740000246. [DOI] [Google Scholar]
- 65.Masters D.G., Benes S.E., Norman H.C. Biosaline agriculture for forage and livestock production. Agric. Ecosyst. Environ. 2007;119:234–248. doi: 10.1016/j.agee.2006.08.003. [DOI] [Google Scholar]
- 66.Jaradat A.A. WFL publisher. Sci. Technol. 2005;3:302–306. [Google Scholar]
- 67.Dickerson M. Letting the sea cultivate the land. Los Angeles Times. Jul 10, 2008.
- 68.Hendricks R.C., Bushnell D.M., Shouse D.T. Aviation fueling: A cleaner, greener approach. Int. J. Rotating Mach. 2011;2011:782969. doi: 10.1155/2011/782969. [DOI] [Google Scholar]
- 69.Lu A.G., Zhang X.L., Ju X., Yang Y.Z. Quality analysis of the vacuum freezing drying Salicornia. Food Res. Dev. 2008;29:111–114. [Google Scholar]
- 70.Wang H., Xu Z., Li X., Sun J., Yao D., Jiang H., Zhou T., Liu Y., Li J., Wang C., et al. Extraction, preliminary characterization and antioxidant properties of polysaccharides from the testa of Salicornia herbacea. Carbohydr. Polym. 2017;176:99–106. doi: 10.1016/j.carbpol.2017.07.047. [DOI] [PubMed] [Google Scholar]
- 71.Al-Yamani W., Kennedy S., Sgouridis S., Yousef L. A land suitability study for the sustainable cultivation of the halophyte Salicornia bigelovii: The case of Abu Dhabi, UAE. Arid Land Res. Manag. 2013;27:349–360. doi: 10.1080/15324982.2013.771230. [DOI] [Google Scholar]
- 72.Shahid M., Jaradat A.A., Rao N.K. Use of Marginal Water for Salicornia bigelovii Torr. planting in the United Arab Emirates. In: Shahid S.A., Abdelfattah M.A., Taha F.K., editors. Developments in Soil Salinity Assessment and Reclamation. Springer; Dordrecht, The Netherlands: 2013. pp. 451–462. [Google Scholar]
- 73.Cárdenas-Pérez S., Piernik A., Chanona-Pérez J.J., Grigore M.N., Perea-Flores M.J. An overview of the emerging trends of the Salicornia, L. genus as a sustainable crop. Environ. Exp. Bot. 2021;191:104606. doi: 10.1016/j.envexpbot.2021.104606. [DOI] [Google Scholar]
- 74.Bañuelos J.A., Velázquez-Hernández I., Guerra-Balcázar M., Arjona N. Production, characterization and evaluation of the energetic capability of bioethanol from Salicornia bigelovii as a renewable energy source. Renew. Energy. 2018;123:125–134. doi: 10.1016/j.renene.2018.02.031. [DOI] [Google Scholar]
- 75.El-Mallah M.H., Turui T., El-Shami S. Detailed studies on seed oil of Salicornia SOS-7 cultivated at the Egyptian border of Red Sea. Grasas y Aceites. 1994;45:385–389. doi: 10.3989/gya.1994.v45.i6.1036. [DOI] [Google Scholar]
- 76.Kang S., Kim D., Lee B.H., Kim M.R., Chiang M., Hong J. Antioxidant properties and cytotoxic effects of fractions from glasswort (Salicornia herbacea) seed extracts on human intestinal cells. Food Sci. Biotechnol. 2011;20:115–122. doi: 10.1007/s10068-011-0016-7. [DOI] [Google Scholar]
- 77.Min J.G., Lee D.S., Kim T.J., Park J.H., Cho T.Y., Park D.I. Chemical Composition of Salicornia Herbacea, L. Prev. Nutr. Food Sci. 2002;7:105–107. doi: 10.3746/jfn.2002.7.1.105. [DOI] [Google Scholar]
- 78.Ahmed K.B.A., Subramanian S., Sivasubramanian A., Veerappan G., Veerappan A. Preparation of gold nanoparticles using Salicornia brachiata plant extract and evaluation of catalytic and antibacterial activity. Spectrochim. Acta Part A Mol. Biomol. Spectrosc. 2014;130:54–58. doi: 10.1016/j.saa.2014.03.070. [DOI] [PubMed] [Google Scholar]
- 79.Lyra D.A., Lampakis E., Al Muhairi M., Tarsh F.M.B., Dawoud M.A.H., Al Khawaldeh B., Moukayed M., Plewa J., Cobre L., Al Masjedi O.S., et al. Future of Sustainable Agriculture in Saline Environments. CRC Press; Boca Raton, FL, USA: 2021. From Desert Farm to Fork: Value Chain Development for Innovative Salicornia-Based Food Products in the United Arab Emirates; pp. 181–200. [Google Scholar]
- 80.El-Tarabily K.A., AlKhajeh A.S., Ayyash M.M., Alnuaimi L.H., Sham A., ElBaghdady K.Z., Saeed T., AbuQamar S.F. Growth promotion of Salicornia bigelovii by Micromonospora chalcea UAE1, an endophytic 1-aminocyclopropane-1-carboxylic acid deaminase-producing actinobacterial isolate. Front. Microbiol. 2019;10:1694. doi: 10.3389/fmicb.2019.01694. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 81.Mesa-Marín J., Mateos-Naranjo E., Rodríguez-Llorente I.D., Pajuelo E., Redondo-Gómez S. Halophytes and Climate Change: Adaptive Mechanisms and Potential Uses. CABI; Wallingford, UK: 2019. 15 Synergic Effects of Rhizobacteria: Increasing Use of Halophytes in a Changing World; p. 240. [Google Scholar]
- 82.Jiménez-Mejía R., Medina-Estrada R.I., Carballar-Hernández S., Orozco-Mosqueda M.D.C., Santoyo G., Loeza-Lara P.D. Teamwork to Survive in Hostile Soils: Use of Plant Growth-Promoting Bacteria to Ameliorate Soil Salinity Stress in Crops. Microorganisms. 2022;10:150. doi: 10.3390/microorganisms10010150. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 83.El-Tarabily K.A., ElBaghdady K.Z., AlKhajeh A.S., Ayyash M.M., Aljneibi R.S., El-Keblawy A., AbuQamar S.F. Polyamine-producing actinobacteria enhance biomass production and seed yield in Salicornia bigelovii. Biol. Fertil. Soils. 2020;56:499–519. doi: 10.1007/s00374-020-01450-3. [DOI] [Google Scholar]
- 84.Mathew B.T., Torky Y., Amin A., Mourad A.H.I., Ayyash M.M., El-Keblawy A., Hilal-Alnaqbi A., AbuQamar S.F., El-Tarabily K.A. Halotolerant marine rhizosphere-competent actinobacteria promote Salicornia bigelovii growth and seed production using seawater irrigation. Front. Microbiol. 2020;11:552. doi: 10.3389/fmicb.2020.00552. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 85.Hasegawa P.M., Bressan R.A., Zhu J.K., Bohnert H.J. Plant cellular and molecular responses to high salinity. Annu. Rev. Plant Biol. 2000;51:463–499. doi: 10.1146/annurev.arplant.51.1.463. [DOI] [PubMed] [Google Scholar]
- 86.Grigore M.N., Toma C. Handbook of Halophytes: From Molecules to Ecosystems towards Biosaline Agriculture. Springer; Berlin/Heidelberg, Germany: 2021. Morphological and anatomical adaptations of halophytes: A review; pp. 1079–1221. [Google Scholar]
- 87.Yadav N.S., Shukla P.S., Jha A., Agarwal P.K., Jha B. The SbSOS1 gene from the extreme halophyte Salicornia brachiata enhances Na+ loading in xylem and confers salt tolerance in transgenic tobacco. BMC Plant Biol. 2012;12:1–18. doi: 10.1186/1471-2229-12-188. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 88.Ghosh P.K., Reddy M.P., Pandya J.B., Patolia J.S., Vaghela S.M., Gandhi M.R., Sanghvi R.J., Kumar V.G.S., Shah M.T. Preparation of Nutrient Rich Salt of Plant Origin. 2005,6,929,809. US patent. 2005 August 16;
- 89.Oliveira-Alves S.C., Andrade F., Prazeres I., Silva A.B., Capelo J., Duarte B., Caçador I., Coelho J., Serra A.T., Bronze M.R. Impact of drying processes on the nutritional composition, volatile profile, phytochemical content and bioactivity of Salicornia ramosissima J. woods. Antioxidants. 2021;10:1312. doi: 10.3390/antiox10081312. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 90.Seong P., Seo H., Cho S., Kim Y., Kang S., Kim J., Kang G., Park B., Moon S., Hoa V. Potential use of glasswort powder as a salt replacer for production of healthier dry-cured ham products. Czech J. Food Sci. 2017;35:149–159. [Google Scholar]
- 91.Biswas S., Pal N., Biswas P., Zaman S., Mitra A. Nutritional status of food products developed from Salicornia brachiata. Int. J. Pharm. Biol. Sci. 2018;8:546–551. [Google Scholar]
- 92.Liang W.P., Liu M.H., Guo G.L. Microemulsions. In: Wang Z.L., Liu Y., Zhang Z., editors. Handbook of Nanophase and Nanostructured Materials-Synthesis. Kluwer Academic/PlenumPublishers; New York, NY, USA: 2002. pp. 1–25. [Google Scholar]
- 93.Christiansen A.H., Lyra D.A., Jørgensen H. Increasing the value of Salicornia bigelovii green biomass grown in a desert environment through biorefining. Ind. Crops Prod. 2021;160:113105. doi: 10.1016/j.indcrop.2020.113105. [DOI] [Google Scholar]
- 94.Dandamudi K.P.R., Luboowa K.M., Laideson M., Murdock T., Seger M., McGowen J., Lammers P.J., Deng S. Hydrothermal liquefaction of Cyanidioschyzon merolae and Salicornia bigelovii Torr.: The interaction effect on product distribution and chemistry. Fuel. 2020;277:118146. doi: 10.1016/j.fuel.2020.118146. [DOI] [Google Scholar]
- 95.Siddiqui S.A., Khatri K., Patel D., Rathore M.S. Photosynthetic Gas Exchange and Chlorophyll a Fluorescence in Salicornia brachiata (Roxb.) Under Osmotic Stress. J. Plant Growth Regul. 2022;41:429–444. doi: 10.1007/s00344-021-10311-8. [DOI] [Google Scholar]
- 96.Jung E.Y., Lee D.Y., Kim O.Y., Lee S.Y., Yim D.G., Hur S.J. Subacute feeding toxicity of low-sodium sausages manufactured with sodium substitutes and biopolymer-encapsulated saltwort (Salicornia herbacea) in a mouse model. J. Sci. Food Agric. 2020;100:794–802. doi: 10.1002/jsfa.10087. [DOI] [PubMed] [Google Scholar]
- 97.Yu Q.Q. Method for Determination of Chloride Sodium in Foods. Standard Press of China; Beijing, China: 1991. China National Standard GB/T 12457-90. [Google Scholar]
- 98.Ogawa S., Decker E.A., Mcclements D.J. Production and characterization of O/W emulsions containing cationic droplets stabilized by lecithin-chitosan membranes. J. Agric. Food Chem. 2003;51:2806–2812. doi: 10.1021/jf020590f. [DOI] [PubMed] [Google Scholar]
- 99.Ghosh P.K., Mody K.H., Reddy M.P., Patolia J.S., Eswaran K., Shah R.A., Barot B.K., Gandhi M.R., Mehta A.R., Bhatt M., et al. Low Sodium Salt of Botanic Origin. 7,208,189 B2. United States Patent and Trademark Office; Washington, DC, USA: States Patent. 2007 April 24;
- 100.Castañeda-Loaiza V., Oliveira M., Santos T., Schüler L., Lima A.R., Gama F., Salazar M., Neng N.R., Nogueira J.M.F., Varela J., et al. Wild vs cultivated halophytes: Nutritional and functional differences. Food Chem. 2020;333:127536. doi: 10.1016/j.foodchem.2020.127536. [DOI] [PubMed] [Google Scholar]
- 101.Kim J.H., Suk S., Jang W.J., Lee C.H., Kim J.E., Park J.K., Kweon M.H., Kim J.H., Lee K.W. Salicornia Extract Ameliorates Salt-Induced Aggravation of Nonalcoholic Fatty Liver Disease in Obese Mice Fed a High-Fat Diet. J. Food Sci. 2017;82:1765–1774. doi: 10.1111/1750-3841.13777. [DOI] [PubMed] [Google Scholar]
- 102.Antunes M.D., Gago C., Guerreiro A., Sousa A.R., Julião M., Miguel M.G., Faleiro M.L., Panagopoulos T. Nutritional characterization and storage ability of Salicornia ramosissima and Sarcocornia perennis for fresh vegetable salads. Horticulturae. 2021;7:6. doi: 10.3390/horticulturae7010006. [DOI] [Google Scholar]
- 103.Kang S., Kim M.R., Chiang M., Hong J. Evaluation and comparison of functional properties of freshwater-cultivated glasswort (Salicornia herbacea L.) with naturally-grown glasswort. Food Sci. Biotechnol. 2015;24:2245–2250. doi: 10.1007/s10068-015-0299-1. [DOI] [Google Scholar]
- 104.Jo H.-G., Chilakala R., Kim M.-J., Sin Y.-S., Lee K.-S., Cheong S.-H. Assessment of the Effects of Salt and Salicornia herbacea L. on Physiochemical, Nutritional, and Quality Parameters for Extending the Shelf-Life of Semi-Dried Mullets (Chelon haematocheilus) Foods. 2022;11:597. doi: 10.3390/foods11040597. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 105.Essaidi I., Brahmi Z., Snoussi A., Koubaier H.B.H., Casabianca H., Abe N., El Omri A., Chaabouni M.M., Bouzouita N. Phytochemical investigation of Tunisian Salicornia herbacea L., antioxidant, antimicrobial and cytochrome P450 (CYPs) inhibitory activities of its methanol extract. Food Control. 2013;32:125–133. doi: 10.1016/j.foodcont.2012.11.006. [DOI] [Google Scholar]
- 106.Finley J.W. Selenium accumulation in plant foods. Nutr. Rev. 2005;63:196–202. doi: 10.1111/j.1753-4887.2005.tb00137.x. [DOI] [PubMed] [Google Scholar]
- 107.Ventura Y., Wuddineh W.A., Myrzabayeva M., Alikulov Z., Khozin-Goldberg I., Shpigel M., Samocha T.M., Sagi M. Effect of seawater concentration on the productivity and nutritional value of annual Salicornia and perennial Sarcocornia halophytes as leafy vegetable crops. Sci. Hortic. 2011;128:189–196. doi: 10.1016/j.scienta.2011.02.001. [DOI] [Google Scholar]
- 108.Yun S.E., Kang Y., Bae E.J., Hwang K., Jang H.N., Cho H.S., Chang S.H., Park D.J. Iodine-induced thyrotoxic hypokalemic paralysis after ingestion of Salicornia herbace. Ren. Fail. 2014;36:461–463. doi: 10.3109/0886022X.2013.868296. [DOI] [PubMed] [Google Scholar]
- 109.Eganathan P., Subramanian H.S., Latha R., Rao C.S. Oil analysis in seeds of Salicornia brachiata. Ind. Crops Prod. 2006;23:177–179. doi: 10.1016/j.indcrop.2005.05.007. [DOI] [Google Scholar]
- 110.Tikhomirova N.A., Ushakova S.A., Tikhomirov A.A., Kalacheva G.S., Gros J.B. Possibility of Salicornia europaea use for the human liquid wastes inclusion into BLSS intrasystem mass exchange. Acta Astronaut. 2008;63:1106–1110. doi: 10.1016/j.actaastro.2008.01.003. [DOI] [Google Scholar]
- 111.Isca V., Seca A.M., Pinto D.C., Silva A. An overview of Salicornia genus: The phytochemical and pharmacological profile. Nat. Prod. Res. Rev. 2014;2:145–164. [Google Scholar]
- 112.Rathore A.P., Chaudhary D.R., Jha B. Biomass production, nutrient cycling, and carbon fixation by Salicornia brachiata Roxb.: A promising halophyte for coastal saline soil rehabilitation. Int. J. Phytoremediation. 2016;18:801–811. doi: 10.1080/15226514.2016.1146228. [DOI] [PubMed] [Google Scholar]
- 113.Im S.A., Kim K., Lee C.K. Immunomodulatory activity of polysaccharides isolated from Salicornia herbacea. Int. Immunopharmacol. 2006;6:1451–1458. doi: 10.1016/j.intimp.2006.04.011. [DOI] [PubMed] [Google Scholar]
- 114.Jha B., Agarwal P.K., Reddy P.S., Lal S., Sopory S.K., Reddy M.K. Identification of salt-induced genes from Salicornia brachiata, an extreme halophyte through expressed sequence tags analysis. Genes Genet. Syst. 2009;84:111–120. doi: 10.1266/ggs.84.111. [DOI] [PubMed] [Google Scholar]
- 115.Choi D., Lim G.S., Piao Y.L., Choi O.Y., Cho K.A., Park C.B., Chang Y.C., Song Y.I., Lee M.K., Cho H. Characterization, stability, and antioxidant activity of Salicornia herbaciea seed oil. Korean J. Chem. Eng. 2014;31:2221–2228. doi: 10.1007/s11814-014-0163-7. [DOI] [Google Scholar]
- 116.Mishra A., Patel M.K., Jha B. Non-targeted metabolomics and scavenging activity of reactive oxygen species reveal the potential of Salicornia brachiata as a functional food. J. Funct. Foods. 2015;13:21–31. doi: 10.1016/j.jff.2014.12.027. [DOI] [Google Scholar]
- 117.Sharma A., Gontia I., Agarwal P.K., Jha B. Accumulation of heavy metals and its biochemical responses in Salicornia brachiata, an extreme halophyte. Mar. Biol. Res. 2010;6:511–518. doi: 10.1080/17451000903434064. [DOI] [Google Scholar]
- 118.Wang D., Wang Y., Dong G., Shang Y., Lyu Y., Li F., Zhang C., Yu X. The chemical composition analysis of dwarf saltwort (Salicornia bigelovii Torr.) and its preservative effects on snakehead fish fillets. J. Food Process. Preserv. 2022;46:e16433. [Google Scholar]
- 119.Wang Q.Z., Liu X.F., Shan Y., Guan F.Q., Chen Y., Wang X.Y., Wang M., Feng X. Two new nortriterpenoid saponins from Salicornia bigelovii Torr. and their cytotoxic activity. Fitoterapia. 2012;83:742–749. doi: 10.1016/j.fitote.2012.02.013. [DOI] [PubMed] [Google Scholar]
- 120.Han E.H., Kim J.Y., Kim H.G., Chun H.K., Chung Y.C., Jeong H.G. Inhibitory effect of 3-caffeoyl-4-dicaffeoylquinic acid from Salicornia herbacea against phorbol ester-induced cyclooxygenase-2 expression in macrophages. Chem.-Biol. Interact. 2010;183:397–404. doi: 10.1016/j.cbi.2009.11.015. [DOI] [PubMed] [Google Scholar]
- 121.Ko Y.C., Choi H.S., Kim S.L., Yun B.S., Lee D.S. Anti-Inflammatory Effects of (9Z, 11E)-13-Oxooctadeca-9, 11-dienoic Acid (13-KODE) Derived from Salicornia herbacea L. on Lipopolysaccharide-Stimulated Murine Macrophage via NF-kB and MAPK Inhibition and Nrf2/HO-1 Signaling Activation. Antioxidants. 2022;11:180. doi: 10.3390/antiox11020180. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 122.Chung Y.C., Chun H.K., Yang J.Y., Kim J.Y., Han E.H., Kho Y.H., Jeong H.G. Tungtungmadic acid, a novel antioxidant, from Salicornia herbacea. Arch. Pharmacal. Res. 2005;28:1122–1126. doi: 10.1007/BF02972972. [DOI] [PubMed] [Google Scholar]
- 123.Kim J.Y., Cho J.Y., Ma Y.K., Park K.Y., Lee S.H., Ham K.S., Leea H.J., Park K.H., Moon J.H. Dicaffeoylquinic acid derivatives and flavonoid glucosides from glasswort (Salicornia herbacea L.) and their antioxidative activity. Food Chem. 2011;125:55–62. doi: 10.1016/j.foodchem.2010.08.035. [DOI] [Google Scholar]
- 124.Park S.H., Kim K.S. Isolation and identification of antioxidant flavonoids from Salicomia herbacen L. J. Korean Soc. Appl. Biol. Chem. 2004;47:120–123. [Google Scholar]
- 125.Kong C.S., Kim Y.A., Kim M.M., Park J.S., Kim S.K., Lee BJNam T.J., Seo Y. Antioxidant activity and inhibition of MMP-9 by isorhamnetin and quercetin 3-0-D glucopyranosides isolated from Salicornia herbacea in HT1080 cells. Food Sci. Biotechnol. 2008;17:983–989. [Google Scholar]
- 126.Kong C.-S., Lee J.I., Kim Y.A., Kim J.-A., Bak S.S., Hong J.W., Park H.Y., Yea S.S., Seo Y. Evaluation on anti-adipogenic activity of flavonoid glucopyranosides from Salicornia herbacea. Process Biochem. 2012;47:1073–1078. doi: 10.1016/j.procbio.2012.03.011. [DOI] [Google Scholar]
- 127.Oh J.-H., Kim E.-0., Lee S.-K., Woo M.-H., Choi S.-W. Antioxidant activities of the ethanol extract of Hamcho (Salicornia herbacea L.) cake prepared by enzymatic treatment. Food Sci. Biotechnol. 2007;1:90–98. [Google Scholar]
- 128.Hwang Y.P., Yun H.J., Choi J.H., Chun H.K., Chung Y.C., Kim S.K., Kim B.-H., Kwon K.-1., Jeong T.C., Lee K.Y., et al. 3-Caffeoyl, 4-dihydrocaffeoylquinic acid from Salicornia herbacea inhibits tumour cell invasion by regulating protein kinase C-ծ-dependent matrix metalloproteinase-9 expression. Toxicol. Lett. 2010;198:200–209. doi: 10.1016/j.toxlet.2010.06.018. [DOI] [PubMed] [Google Scholar]
- 129.Sanandiya N.D., Siddhanta A.K. Chemical studies on the polysaccharides of Salicornia brachiata. Carbohydr. Polym. 2014;112:300–307. doi: 10.1016/j.carbpol.2014.05.072. [DOI] [PubMed] [Google Scholar]
- 130.Seo H.N., Jeon B.Y., Yun A.R., Park D.H. Effect of glasswort (Salicornia herbacea L.) on microbial community variations in the vinegar-making process and vinegar characteristics. J. Microbiol. Biotechnol. 2010;20:1322–1330. doi: 10.4014/jmb.1003.03041. [DOI] [PubMed] [Google Scholar]
- 131.Jang H.S., Kim K.R., Choi S.W., Woo M.H., Choi J.H. Antioxidant and antithrombus activities of enzyme-treated Salicornia herbacea extracts. Ann. Nutr. Metab. 2007;51:119–125. doi: 10.1159/000100826. [DOI] [PubMed] [Google Scholar]
- 132.Mudie P.J., Greer S., Brakel J., Dickson J.H., Schinkel C., Peterson-Welsh R., Stevens M., Turner N.J., Shadow M., Washington R. Forensic palynology and ethnobotany of Salicornia species (Chenopodiaceae) in northwest Canada and Alaska. Can. J. Bot. 2005;83:111–123. doi: 10.1139/b04-159. [DOI] [Google Scholar]
- 133.York J., Lu Z., Glenn E.P., John M.E. Daylength affects floral initiation in Salicornia bigelovii Torr. Plant Biol. 2000:41–42. doi: 10.1139/b04-159. [DOI] [Google Scholar]
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