Abstract
Objectives:
The aim of the study was to assess the feasibility of fodder Sorghum as poultry feed in terms of growth performance (plant height and fresh weight), nutritional quality (moisture, ash, crude protein, extract ether, crude fiber, extract material without nitrogen, and metabolic energy), and scanning electron microscopy energy dispersive X-ray (SEM-EDX).
Materials and Methods:
The study used a completely randomized design with six treatments and three replications. The treatments consisted of planting times of 24, 48, 72, 120, and 240 h and a control (0 h).
Results:
The results showed that there was a significant effect (p ≤ 0.05) when planting Sorghum fodder (SGF) on growth performance and moisture, but it had no significant effect on fresh weight, ash, crude protein, extract ether, crude fiber, nitrogen-free extract, energy metabolic aspects, and SEM-EDX.
Conclusion:
SGF is suitable as a feed ingredient for poultry in terms of nutrition and contains ZrO2, which functions as an antifungal.
Keywords: Feed, fodder, Sorghum, proximate, SEM-EDX
Introduction
Fodder is a plant or forage that can be used as feed, which is grown in a short time. The fodder method is done by sowing grains such as corn, Sorghum, and wheat in a medium [1]. Sorghum has the potential to be developed as green fodder because it can thrive in a tropical environment and is efficient in its maintenance process [2]. Sorghum fodder (SGF) contains 15.41% crude protein, 8.44% extract ether, and 11,03% crude fiber [3]. Fodder is suitable for use as poultry feed because of its low crude fiber content and reduced tannin content [4]. Sorghum cultivation can be done using a fodder system to reduce its anti-nutritional content [5]. The low crude fiber content of 2%–5% fodder has an impact on the increased digestibility of the material. The age of the plants, humidity levels, light, temperature, and media conditions all have an impact on the cultivation of fodder. The relatively short harvesting age makes fodder one of the solutions for the shortage of feed ingredients [6].
SGF can be used as an alternative source of energy for poultry. The use of fodder as broiler chicken feed can increase carcass weight. Colă and Colă [7] reported that using 23% fodder in broiler feed increased the carcass weight of broiler chickens by about 5%–10%. Based on the research of Aqilla et al. [8], the use of fodder as a hybrid chicken feed can increase egg production by 19.75%. Saputra et al. [9] added that using fodder with a composition of 6%–9% in hybrid chickens can increase the index of egg shape, fertility, hatchability, and hatching weight of chickens. The advantages of fodder are its relatively short planting time, good nutritional and digestibility content, and reduced anti-nutritional content [10]. The fodder planting system is mostly applied to corn plants. This study used Sorghum with a fodder planting system because of its large availability and good nutritional content. The purpose of the study was to assess the feasibility of fodder Sorghum as poultry feed in terms of growth performance (plant height and fresh weight), nutritional quality [moisture, ash, crude protein, extract ether, crude fiber, nitrogen-free extract (NFE), and energy metabolism (EM)], and scanning electron microscopy energy-dispersive X-ray (SEM-EDX). The benefit of the research is to provide information about the use of SGF as poultry feed. The research hypothesis is that fodder Sorghum can be used as feed for poultry.
Materials and Methods
The materials used were white Sorghum (Sorghum vulgare) from the local market, an analytical balance kern ABJ-220 with an accuracy of 0.001 gm, a 30 × 20 cm tray, a Universal Drying Oven UN 55, a Thermo F48010-26 furnace, a Normax Portugal desiccator, a Boro3.3 Germany glass beaker, a 50-ml Erlenmeyer, a filter paper, a Whatman filter paper, a Kjeldahl flask, a filter flask, an aluminum foil, and a Soxhlet Type II Flask /1-4360-04.
The research used a complete randomized design with six treatments and three repeats. The treatments were as follows:
T0: Planting age 0 h (control)
T1: Planting age 24 h
T2: Planting age 48 h
T3: Planting age 72 h
T4: Planting age 120 h
T5: Planting age 240 h
Planting of SGF begins with the cleaning of 1 kg of Sorghum seeds for each treatment. The clean seeds were then lowered using water at 100°C for 24 h, and then the seeds were spread on the planting medium according to the treatment. Watering is done twice a day, in the morning and evening. Parameters observed were growth performance (plant height and fresh weight), nutrient content (moisture, ash, crude protein, extract ether, crude fiber, NFE, and EM), and SEM-EDX.
Growth performance
Growth performance was tested by measuring plant height and fresh weight. The measurement of plant height was carried out before harvesting by measuring from the base of the planting medium to the top of the plant using a ruler. Fresh weight was measured during the harvesting process by weighing the yields.
Nutritional content
Parameters of nutrient content were tested by proximate analysis according to AOAC [11], including moisture by oven at 110°C, ash content by ashing, protein content by Kjeldahl method, extract ether content by Soxhlet method, and fiber content by gravimetric method. The content of the NFE was calculated using the formula, according to the method of Traughber et al. [12], namely, NFE = 100—crude protein—extract ether—ash—crude fiber. Metabolic energy is calculated using Balton’s formula, namely, EM (kcal/kg) = 40.81 [0.87 (crude protein + 2.25 × extract ether + NFE) + 2.5] [13].
SEM-EDX testing
SEM-EDX testing was carried out using a scanning electron microscope (SEM) (US) and energy dispersive X-ray using Fourier transform infrared spectroscopy (Perkin Elmer, US). The sample is then tested in the laboratory to determine the elemental composition with energy dispersive X-ray, according to the procedure.
Data analysis
The data obtained were analyzed using the analysis of variance test to test data diversity and determine if there is a real influence, followed by Duncan’s multiple range test with a 95% confidence level.
Results and Discussions
Growth performance of SGF with different planting times
The results of the data analysis showed that the height of fodder Sorghum plants with different planting times showed significant differences (Table 1). The lowest plant height was at T0, with 0 cm, and the highest was at T5, with a height of 6.1 cm. The value of plant height and fresh weight of SGF increased with the increasing age of harvest. Chrisdiana [2] stated that the biomass of green fodder would increase along with the increasing age of harvest. The ratio of stems and leaves will increase so that it will increase plant height, which is a representation of plant biomass [14].
Table 1. Growth performance of SGF with different planting time.
Parameters | Treatment | |||||
---|---|---|---|---|---|---|
T0 | T1 | T2 | T3 | T4 | T5 | |
Plant height (cm) | 0a | 1.6b | 1.9b | 2.4bc | 4.8d | 6.1d |
Fresh weight (gm) | 1,097 | 1,166 | 1,187 | 1,156 | 956 | 946 |
Different superscripts on the same line show a noticeable difference (p < 0.05).
The fresh weight of SGF with different planting times did not experience any significant difference. The value of plant weight can be increased by the increased conversion of nutrients obtained from water and stored in seeds during the rearing process into plant parts. Kusdiana et al. [15] stated that fresh weight per clump is one of the parameters in the growth of a plant and also plays a role in determining the quality of yield or production, which data is taken after harvest. Green fodder plant growth is strongly influenced by the availability of nutrients in the seeds. Rousseau et al. [16] stated that plants that lack nutritional elements experience obstacles in the formation of green leaves, which play a very important role in photosynthesis so that the formation of carbohydrates that function for energy and cell formation for plant growth is reduced as a result of plants turning yellow and slow growth. Fodder Sorghum can produce a dry weight of about 60%–70% of its fresh weight.
Nutritional content of SGF with different planting time
The nutritional content of SGF with different sowing times is shown in Table 2.
Table 2. Nutritional content of SGF with different planting time.
Parameters | Treatments | |||||
---|---|---|---|---|---|---|
T0 | T1 | T2 | T3 | T4 | T5 | |
Moisture (%) | 36.44 ± 5.89a | 22.30 ± 2.55b | 21.85 ± 2.31b | 21.68 ± 2.18b | 21.60 ± 2.36b | 22.84 ± 2.01b |
Ash (%) | 1.24 ± 0.22 | 0.85 ± 0.21 | 1.04 ± 0.20 | 1.48 ± 0.27 | 1.34 ± 0.22 | 1.32 ± 0.21 |
Crude protein (%) | 9.43 ± 0.24 | 9.65 ± 0.22 | 9.71 ± 0.27 | 9.74 ± 0.28 | 10.17 ± 0.31 | 9.75 ± 0.26 |
Extract ether (%) | 3.46 ± 0.69 | 2.24 ± 0.52 | 2.49 ± 0.61 | 1.76 ± 0.60 | 3.51 ± 0.72 | 2.73 ± 0.59 |
Crude fiber (%) | 2.49 ± 0.41 | 2.32 ± 0.37 | 1.87 ± 0.32 | 1.26 ± 0.31 | 5.33 ± 0.49 | 2.90 ± 0.47 |
Nitrogen-free extract (%) | 83.37 ± 2.41 | 84.94 ± 2.78 | 84.89 ± 2.83 | 85.75 ± 2.52 | 79.66 ± 2.33 | 83.30 ± 2.39 |
EM (kcal/kg) | 3,673.59 ± 35.41 | 3,639.41 ± 35.35 | 3,659.63 ± 35.27 | 3,633.33 ± 34.87 | 3,571.43 ± 34.22 | 3,623.86 ± 35.19 |
Different superscripts on the same line show a noticeable difference (p < 0.05).
Moisture
Based on data analysis, the difference in planting time affects the water content of SGF. The water content of SGF in treatment T0 was 36.44%, significantly different from treatments T1, T2, T3, T4, and T5, while treatments T1, T2, T3, T4, and T5 were not significantly different between the five treatments, with a water content of around 21.60%–22.84%. Chrisdiana [2] stated that the water content of SGF ranges from 60% to 74.5%. The high water content in the T0 treatment was caused by the lack of nutrients, so the water component was still high. Wahyono et al. [4] stated that the conversion of plant nutrients would increase along with the increasing age of harvest. The moisture of SGF is influenced by differences in plant commodities, the use of nutrient solutions, and the determination of harvest age [17].
Ash
SGF ash content at different planting times was not significantly different. The SGF in this study contained an ash content of around 0.85%–1.48%. The ash content value of hydroponic sorghum fodder with a planting time of 8 days was 2.25% [2]. The value of the ash content of a feed ingredient shows the large number of minerals contained in the feed material [18]. The low value of SGF ash content is possible because of the shorter research planting age. Soni et al. [19] stated that the age of Sorghum planting would affect the mineral and organic matter content.
Crude protein
Differences in planting time did not affect the protein content of SGF. The protein content of SGF ranged from 9.43% to 10.17%. The absence of significance in the protein content is possible because the carbohydrate fraction content of the SGF is relatively the same. Pan et al. [20] stated that during germination and growth, plants use carbohydrate reserves, which are assimilated by their metabolic activities, thereby increasing the crude protein fraction. Factors that affect protein content are harvesting age, type of seed, and plant food reserves. Chrisdiana [2] reported that the longer the harvest, the higher the crude protein content of Sorghum.
Extract ether
The results of the data analysis showed that the extract ether content of Sorghum feed was not affected by planting time. The extract ether content of Sorghum feed is 1.76%–3.51%. Sriagtula et al. [3] stated that the extract ether content of feed Sorghum extract was around 8.44%. There was no effect of differences in planting time on extract ether content due to soaking in hot water, which changed the fat fraction to free fatty acids. Chrisdiana [2] stated that soaking the seeds will increase the activity of enzymes that can convert fat into free fatty acids. The low extract ether content can minimize feed damage.
Crude fiber
Different planting times had no impact on the crude fiber content of Sorghum feed. The value of fiber content was not significantly different because of the relatively short planting time. Suhartanto et al. [21] stated that in connection with the development and increasing age of plants, there would also be an increase in fiber concentration. Short planting aims to reduce the crude fiber content so that digestibility increases. In the early phase of plant growth, the development of the fiber fraction is very important to support metabolism and strengthen plant stands. Wahyono et al. [4] stated that the accumulation of an increased cell wall fraction was associated with an increase in crude fiber content with increasing harvest time.
Nitrogen-free extract
The NFE value of fodder Sorghum did not significantly differ between the different planting time treatments. This is because planting time has no effect on other components such as crude fiber, crude fat, and crude protein. The factors that affect the NFE value are ash, crude fiber, crude protein, and extract ether levels. Aqilla et al. [8] stated that NFE comprises carbohydrates, amino acids, and vitamins. NFE contains monosaccharides, disaccharides, trisaccharides, and polysaccharides, especially starch, which is easily soluble in acid and alkaline solutions in crude fiber analysis and has high digestibility.
Energy metabolism
The results of the data analysis showed that the metabolic energy value of SGF was not affected by planting time. The EM value of fodder Sorghum ranged from 3,571.43 to 3,673.59 kcal/kg. The high and low metabolic energy content of a feed ingredient is influenced by the content of other nutrients, such as crude fiber content. According to Hidayat [22], the content of crude fiber in a material will affect the value of metabolic energy. The content of the metabolic energy value of a feed will affect the level of feed consumption. The higher the metabolic energy value, the lower the feed consumption; in addition, the metabolic energy value is also related to the digestibility value [23].
SEM-EDX observation
The results of observing the composition of fodder Sorghum using SEM-EDX are shown in Table 3 and Figure 1.
Table 3. Composition of fodder Sorghum using SEM-EDX.
Elemental composition | Treatment | |||||
---|---|---|---|---|---|---|
T0 | T1 | T2 | T3 | T4 | T5 | |
__________ % __________ | ||||||
C | 91.48 | 85.55 | 93.91 | 96.89 | 89.39 | 94.00 |
K2O | – | 1.15 | 0.60 | 0.04 | 0.48 | 0.28 |
MgO | – | 1.03 | – | – | 0.49 | 0.06 |
SO3 | – | 1.78 | – | – | – | – |
P2O5 | – | 1.91 | – | – | – | – |
ZrO2 | 8.52 | 8.58 | 5.49 | 3.07 | 9.63 | 5.67 |
Figure 1. Observation of the composition of fodder Sorghum through SEM-EDX (5,000×).
Table 3 shows that the duration of planting SGF has an elemental composition of carbon (C) ranging from 85.55% to 96.89% or dominates compared to other elements. The element C contained in SGF comes from the natural constituent components of Sorghum seeds. The source of these elements can come from protein, where the protein content of SGF in the study was 9.43%–10.17%. The accumulation of Sorghum seed protein is influenced by carbon and nitrogen metabolisms because both depend on each other. Mrid et al. [24] stated that providing carbon skeletons for amino acids determines the protein content of grains such as cereals, where carbon and nitrogen metabolism depend on each other. Furthermore, the element C in Sorghum seeds comes from the plant’s ability to absorb nutrients from the soil through the roots. Rad et al. [25] stated that Sorghum is a type of legume that can live in warm/dry climates and can absorb nutrients from various soil levels as well as fix nitrogen (increase nitrogen content) in the soil, thereby increasing protein in seeds and forage. The duration of planting did not show changes in the composition of C elements in a certain direction, so it can be said that different planting times did not affect the SGF.
The elemental compositions of potassium oxide (K2O), magnesium oxide (MgO), sulfur trioxide (SO3), and phosphorus pentaoxide (P2O5) had different compositions in each treatment, except for T0, which was not found at all. Elements of K2O and MgO in SGF ranged between 0.28%–1.15% and 0.06%–1.03%. Longer planting gives the Sorghum seeds time to form sprouts that can be a source of potassium and magnesium in fodder. The elements SO3 and P2O5 were only found in the T1 treatment at 1.78% and 1.91%, but the amounts were not too significant with other treatments. Elements of zirconium dioxide (ZrO2) in SGF amounted to 3.07%–9.63%. The element ZrO2 is obtained from rocks or the earth’s crust, which can be absorbed by Sorghum because of its ability to live in various soil conditions, so the element is also found in Sorghum seeds and, subsequently, in SGF. Joshi et al. [26] stated that the element ZrO2 could be useful as an antifungal agent for Aspergillus fumigatus with a maximum inhibition zone of 34 mm, Aspergillus niger (32 mm), and antibacterial Bacillus subtilis (36 mm), Escherichia coli (34 mm), Pseudomonas aeruginosa (32 mm), and Streptococcus mutans (28 mm).
The study results in Figure 1 show that different planting times affect the SEM image of fodder Sorghum. The SEM image of the SGF at T0 looks like it is still in the form of small and fine particles. The particles then enlarge with increasing duration of implantation until T4. The particle size again decreased at the time of T5 planting but by a higher amount than T0. The increasing particle size is an indication of the germination of Sorghum seeds into sprouts that have better nutritional content because they are at their maximum condition, so T4 treatment is the most recommended. Figure T4 shows a larger number of particles with a larger size. This is also supported by the data from Table 2 for nutritional content, where the T4 treatment had better protein than other treatments. Fodder constituent cells multiply and divide, as shown in the T5 treatment.
Conclusion
SGF is considered suitable as a feed ingredient for poultry in terms of nutrition and contains ZrO2, which functions as an antifungal.
Acknowledgment
A big thanks to the Universitas Diponegoro Institute Research and Community Service for facilitating the assignment of RPI activities No. 569-92/UN7.D2/PP/VII/2022.
List of Abbreviations
C, Carbon; EM, Energy metabolism; FTIR, Fourier transform Infrared Spectroscopy; K2O, Potassium oxide; MgO, Magnesium oxide; NFE, Nitrogen-free extract; SEM-EDX, Scanning electron microscope energy dispersive X-ray; SGF, Sorghum fodder; SO3, Sulfur trioxide; P2O5, Phosphorus pentoxide; ZrO2, Zirconium dioxide.
Conflict of interests
The authors declare that they have no conflict of interest.
Authors’ contributions
CSU is responsible for coordinating research activities, data processing, and finalization of scientific articles; BS provides suggestions, recommendations, and finalization of scientific articles; MFH is responsible for research, preparation of tools and materials, and research data processing.
References
- [1].Aghaeipoor R, Sharifi Hosseini MM, Tahmasbi R, Dayani O. Comparison the effect of corn, Sorghum and millet silages on feed intake, digestibility and ruminal parameters in goat. Anim Sci J. 2022;35(134):43–58. https://doi.org/10.22092/ASJ.2021.354391.2151. [Google Scholar]
- [2].Chrisdiana R. Quality and quantity of Sorghum hydroponic fodder from different varieties and harvest time. Environ Earth Sci. 2018;119:1–5. https://doi.org/10.1088/1755-1315/119/1/012014. [Google Scholar]
- [3].Sriagtula R, Martaguri I, Sowmen S. Evaluation of nutrient solution dose and harvest time on forage Sorghum (Sorghum bicolor L. Moench) in hydroponic fodder system. In IOP Conference Series: Earth and Environmental Science, IOP Publishing. 2021;888(1):012068. https://doi.org/10.1088/1755-1315/888/1/012068. [Google Scholar]
- [4].Wahyono T, Hardani SNW, Sugoro I. Low irradiation dose for Sorghum seed sterilization: hydroponic fodder system and in vitro study. Bul Peter. 2018;42(3):215–21. https://doi.org/10.21059/buletinpeternak.v42i3.30888. [Google Scholar]
- [5].Etuk EB, Okeudo NJ, Esonu BO, Udedibie ABI. Antinutritional factors in Sorghum: chemistry, mode of action and effects on livestock and poultry. Online J Anim Feed Res. 2012;2(2):113–9. [Google Scholar]
- [6].Ghorbel R, Koşum N. Hydroponic fodder production: an alternative solution for feed scarcity. In 6th International Students Science Congress Proceedings; 2022. https://doi.org/10.52460/issc.2022.005. [Google Scholar]
- [7].Colă M, Colă F. Influence of feeding on the weight of broiler chickens. An Univ Craiova Ser Agric. 2014;44:63–6. [Google Scholar]
- [8].Aqilla HR, Latif H, Daud M. Effect of the use of black soldier fly (Hermetia Illucens) and sprouted fodder for chicken (Sf2C) in fermentation feed on the production and quality of hybrid chicken eggs. J Ilmiah Mahas Pert. 2021;6(3):79–87. https://doi.org/10.17969/jimfp.v6i3.18260. [Google Scholar]
- [9].Saputra EN, Latif H, Daud M. The effect of substitution maggot flour (Hermetia illucens) and sprouted fodder for chicken (SF2C) in fermented feed on fertility, hatchability, and hatching weight of ALOBRA chickens. J Ilmiah Mahas Pert. 2021;6(3):61–9. https://doi.org/10.17969/jimfp.v7i1.18182. [Google Scholar]
- [10].Wahyono T, Sugoro I, Jayanegara A, Wiryawan KG, Astuti DA. Nutrient profile and in vitro degradability of new promising mutant lines Sorghum as forage in Indonesia. Adv Anim Vet Sci. 2019;7(9):810–8. https://doi.org/10.17969/journal.aavs/2019/7.9.810.818. [Google Scholar]
- [11].AOAC. Gaithersburg, MD: AOAC International; 2005. Official method of analysis of the association of official analytical chemist. [Google Scholar]
- [12].Traughber ZT, Detweiler KB, Price AK, Knap KE, Harper TA, Swanson KS, et al. Effect of crude fiber and total dietary fiber on the calculated nitrogen-free extract and metabolizable energy content of various dog foods fed to client-owned dogs with osteoarthritis. Am J Vet Res. 2021;82(10):787–94. doi: 10.2460/ajvr.82.10.787. https://doi.org/10.2460/ajvr.82.10.787. [DOI] [PubMed] [Google Scholar]
- [13].Sugiharto S, Yudiarti T, Isroli I, Widiastuti E, Putra FD. Effects of feeding cassava pulp fermented with Acremonium charticola on growth performance, nutrient digestibility and meat quality of broiler chicks. South Afr J Anim Sci. 2017;47(2):130–8. https://doi.org/10.4314/sajas.v47i2.4. [Google Scholar]
- [14].Koten BB, Lita Y, Wea R, Dato TOD. Response of arbila (Phaseolus Lunatus L.) plants to different water volumes during the dry season. Pastura. 2019;10(1):9–12. https://doi.org/10.24843/Pastura.2020.v10.i01.p03. [Google Scholar]
- [15].Kusdiana D, Hadist I, Dan E, Herawati The effect row spacing to plant high and fresh weight per clump of dwarf nafier (Pennisetum purpureum cv. Mott) J Anim Sci. 2017;1(2):32–7. http://doi.org/10.52434/janhus.v1i2.245. [Google Scholar]
- [16].Rousseau S, Kyomugasho C, Celus M, Hendrickx ME, Grauwet T. Barriers impairing mineral bioaccessibility and bioavailability in plant-based foods and the perspectives for food processing. Crit Rev Food Sci Nut. 2020;60(5):826–43. doi: 10.1080/10408398.2018.1552243. https://doi.org/10.1080/10408398.2018.1552243. [DOI] [PubMed] [Google Scholar]
- [17].Mbeong YSN, Umami N, Hanim C, Astuti A, Rahayu ERV. In International Conference on Improving Tropical Animal Production for Food Security (ITAPS 2021) Atlantis Press; 2022. The effect of mycorrhizal provision and watering frequency on the nutrient and prussic acid content of Sorghum (Sorghum bicolor (L.) Moench) pp. 230–6. https://doi.org/10.2991/absr.k.220309.047. [Google Scholar]
- [18].Sulaiman SA, Igwegbe AO, Nassarawa SS. Proximate and mineral composition of some selected Sorghum varieties in Kano Metropolis. J Food Nutr Res. 2020;8(1):1–5. https://doi.org/10.12691/ajfn-8-1-1. [Google Scholar]
- [19].Soni PG, Yadav RK, Kumar A, Yadav G, Kumar G, Yadav T. Effect of domestic wastewater and irrigation schedules on quality of fodder Sorghum. J Soil Salin Water Qual. 2016;8(2):173–9. [Google Scholar]
- [20].Pan L, Li P, Ma XK, Xu YT, Tian QY, Liu L, et al. Tannin is a key factor in the determination and prediction of energy content in Sorghum grains fed to growing pigs. Am Soc Anim Sci. 2016;94:2879–89. doi: 10.2527/jas.2016-0457. https://doi.org/10.2527/jas2016-0457. [DOI] [PubMed] [Google Scholar]
- [21].Suhartanto B, Widodo S, Umami N, Prasadita R, Utomo R. The effect of cutting age and ratooning on growth, production, and nutrient content of brown midrib resistance Sorghum. In IOP Conference Series: Earth and Environmental Science, IOP Publishing. 2020;465(1):012027. https://doi.org/10.1088/1755-1315/465/1/012027. [Google Scholar]
- [22].Hidayat C. The use of Sorghum as corn replacer for energy resources feedstuff in broiler chicken diet; a review. Indones J Anim Sci. 2021;2(3):262–75. https://doi.org/10.25077/jpi.23.3.262-275.2021. [Google Scholar]
- [23].Kalalo MN, Wolayan FR, Imbar MR, Liwe H. Determination of nitrogen retention and metabolic energy of banana peels (Musa paradisiaca) fermentation with Rhizopus oligosporus on broiler ransom. Zootec. 2021;41(1):166–73. https://doi.org/10.35792/zot.41.1.2021.32534. [Google Scholar]
- [24].Mrid BR, Bouargalne Y, Omari R, Mourabit NE, Nhiri M. Activities of carbon and nitrogen metabolism enzymes of Sorghum (Sorghum bicolor L. Moench) during seed development. J Crop Sci Biotechnol. 2018;21(3):283–9. https://doi.org/10.1007/s12892-017-0140-0. [Google Scholar]
- [25].Rad SV, Valadabadi SAR, Pouryousef M, Saifzadeh S, Zakrin HR, Mastinu A. Quantitative and qualitative evaluation of Sorghum bicolor L. under intercropping with legumes and different weed control methods. J Hortic. 2020;6(4):1–15. https://doi.org/10.3390/horticulturae6040078. [Google Scholar]
- [26].Joshi NC, Chaudhary N, Rai N. Medicinal plant leaves extract based synthesis, characterisations and antimicrobial activities of ZrO2 nanoparticles (ZrO2 NPs) J Bionanosci. 2021;11(2):497–505. https://doi.org/10.1007/s12668-021-00829-2. [Google Scholar]