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Fermentation: A Broader Perspective

Written By

Margaret M.A. Danladi, Mary F. Istifanus, Musa S. Makeri, John O. Egbere, Luka S. Danahap, Brains O. Okechalu and Abigail I. Ogbonna

Submitted: 22 April 2024 Reviewed: 29 April 2024 Published: 03 July 2024

DOI: 10.5772/intechopen.115055

The Science of Fermentation IntechOpen
The Science of Fermentation Edited by María Chávarri Hueda

From the Edited Volume

The Science of Fermentation [Working Title]

Dr. María Chávarri Hueda

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Abstract

Fermentation is as old as man. It is a technology where growth and metabolic activities of microbes are used to preserve foods. The global increase in population and scarcity of food necessitated actions that will lead to increased and efficient food production, improved storage and transportation. Bacteria, fungi and yeast are capable of converting substrates of different kinds such as cereals, legumes, milk, meat, vegetables, palm sap, tubers and roots to produce variety of fermented foods consumed and enjoyed globally such as koji, kununzaki, yogurt, cheese, sauerkraut, peperoni, palmwine, fufu, Kefir, ogi, chhurpi and many others. Submerged and solid-state fermentation techniques are employed to produce fermented products which have applications in the food and non-food industries. Fermentation improves the, nutrition, enhances the shelf life and preserves of foods, baked foods production, produces biofuels and biopolymers as well as improves health.

Keywords

  • fermentation
  • fermented products
  • solid state fermentation
  • submerged fermentation
  • fermentation benefits

1. Introduction

Fermentation is an ancient technique for preserving food and drinks that has been practiced since long before the days of refrigeration. During fermentation, microorganisms like bacteria, yeast or fungi convert organic compounds like sugars and starch into alcohol [1]. Yeasts like Saccharomyces cerevisiae and their close relatives are dominant in many niches because of their high sugar consumption, ethanol production and their ability to survive anaerobic conditions, though aerobic which are the winning characteristics attributed to their competitive outcome as good brewers [2]. Lactic acid act to reduce bacterial load and improve sensory characteristics [3]. Many fungi are desirable in food applications and fermentation processes such as Aspergillus, Penicillium and many others [4].

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2. Categories of fermentation

Solid state fermentation occurs in aerobic conditions on solid state substrate with minimal moisture content, commonly used in traditional food production like Indonesian tempeh and bread [5]. Solid State fermentation is disadvantageous for some microorganisms, especially bacteria is greatly explored using fungal species because fungi grow on solid substrates such as wood, roots, stem, dry parts of animal skin and low moisture fecal matter [6]. Going down the history of fermentation technology, solid state fermentation process was almost completely sidelined in western countries after 1940s due to adaptation of submerged fermentation [7]. Patents and publications later came up on the use of solid-state fermentation, development of bioreactors, production of food and feeds, microbial metabolites, bio processes such as bioleaching, biopulping, bioremediation and so on [8, 9, 10, 11, 12, 13, 14]. Food, pharmaceuticals, energy and chemical sectors use solid state fermentation [15]. Though solid-State fermentation is important and acceptable, fermentation time is key to achieving this type of fermentation and has been employed in the production of biopesticide and biostimulant using green waste [16].

Submerged fermentation take place in liquid media, promoting anaerobic growth of microorganisms and is widely used in industries like sucrose laven, enzymes, and pigment production [17, 18]. Submerged fermentation is advantageous because it takes shorter fermentation time, large volume processing, low labour intensity and widely applied in industrial biotechnological processes [19, 20]. During submerged fermentation dispersed fungal mycelia, clumped aggregates and mycelial pellets are observed [21, 22]. Fungal metabolites such as antibiotics, hormones, enzymes which are not needed for their growth are used in the food and drug industry [23, 24].

2.1 Fermentation in food processing

The growing global population poses a threat to food security [25] which has necessitated actions that will lead to increased and efficient food production, improved storage and transportation [26]. Food fermentation utilizes the growth and metabolic activity of microorganisms which improve organoleptic and general value addition associated with fermented foods [27]. Fermentation is also employed in modern food processing for food preservation and improvement of its quality from the time of manufacture to the time of consumption [28].

The discovery of the role of microorganisms as fermenting agents began from the time pasteurization was discovered in 1861 AD [28] which led to an industrial revolution in the production of fermented foods and beverages using yeast and lactic acid bacteria for the production of beer, spirits, wines as well as fermented diary, vegetable and meat products respectively [28]. Depending on the type of microorganisms, the substrate, the environmental conditions and the processing methods, fermentation can result in various food products that may be peculiar to a region of the world such as yogurt, cheese, bread, kunun- zaki, masa, ogi, wine, beer, burukutu, and many more. An overview of some fermented foods produced worldwide is represented in Table 1.

SubstrateFermented food productCountry of origin
MilkAiragMongolia
MilkAmasiSouth Africa, Zimbabwe
MilkCheeseGlobal
MilkChhuIndia, Nepal, Bhutan, China (Tibet)
MilkChhurpiIndia, Nepal, Bhutan, China (Tibet)
MilkDhadiIndonesia
MilkKefir, KoumissRussia
MilkLaban rayebEgypt
MilkLebenNorth, East, Central Africa
MilkDahiIndia, Nepal, Sri Lanka, Bangladesh, Pakistan
MilkNunuGhana
MilkPhiluIndia, Nepal, Bhutan, China (Tibet)
MilkYogurtEurope, America, Australia
MilkViiliFinland
Milk, sugar, starterSua chuaVietnam
Maize, Sorghum, MilletKunu-zakiNigeria
Sorghum, Maize, Rice, MilletMasaNigeria
SorghumKisraSudan
Maize, SorghumPitoWest Africa
Maize, Sorghum, MilletOgiNigeria
Rye, WheatSourdoughEurope, America, Australia
Maize, Sorghum, Millet, Cassava flourUjiKenya, Tanzania, Uganda
MaizePozolMexico
MaizePoto PotoCongo
SoybeanMisoJapan
SoybeanMejuKorea
Melon seeds, Castor oil seeds, Sesame, Pumpkin beanOgiri/OgiliWest, East, Central Africa
SoybeanTempeIndonesia, The Netherlands, Japan. USA
SoybeanThua naoThailand
Locust beanSoumbalaBurkina Faso
SoybeanShoyuJapan, Korea, China
Pork, BeefPeperoniUSA, Europe, Australia
Pork or Beef meat, Fat, NaCl, SpicesSalchichanSpain
Chopped pork meat, Spices, NaClSalsicciaItaly
Pork, Salt, Cooked riceNem-chuaVietnam
Pork, Salt, Sugar, Potassium nitrateTocinoPhilippines
FishSidraIndia
Small sardine, saltMyulchijeotKorea
Horse mackerel, saltKusayaJapan
Marne FishNuoc mamVietnam
ShrimpSaeoo JeotKorea
CucumbersCucumbersEurope, Canada, USA
CupersCupersSpain
MustardBurong mustalaPhilippines
Bamboo shootsNaw-mai-dongThailand
Bamboo shootMesuIndia, Nepal, Bhutan
CassavaTapai UbiMalaysia
CassavaGarri, Fufu, LafunWest Africa
CassavaTapéIndonesia
CassavaChikwangueCentral Africa, Zaire
CassavaChingwadaEast and Central Africa
MaizeMangisiZimbabwe
Palm sapPalm winePalm growing regions
MolassesRumWorld wide
Sugar caneKojiJapan
GrapesSparkling wineWorldwide
MolassesRumWorldwide
BarleyWhiskyWorldwide
GrapesWineWorldwide
PotatoVodkaRussia, Finland, Poland

Table 1.

Geographical distribution of fermented foods.

Source: [29, 30, 31, 32, 33, 34, 35, 36, 37, 38].

Fermented foods are produced and enjoyed all over the world [29, 34, 35, 36, 37, 39, 40] using different raw materials such as cereals, legumes, tubers, roots, milk, fish and meat [41].

2.2 Benefits of fermentation

2.2.1 Baking industries (e.g. Bread)

Sourdough is produced by the use of lactic acid bacteria and yeast mixed in water and flour [42, 43, 44]. A good sourdough is dependent on parameters such as temperature, enzymatic composition of the flour, redox potential, water content, fermentation time [44]. The use of sourdough results in a better characteristic of bread and specific LAB strains delay staling in bread [45].

2.2.2 Energy production (e.g. Biofuel)

Although it may sound ridiculous, bacteria are often used to produce biofuels. The global demand for non-renewable fossil fuel is increasingly becoming unsustainable, therefore the need to seek alternative fuel sources such as biofuels [46]. The genus Clostridium have been studied and shown to have the ability to degrade sugars, starches, and other complex substrates to produce biofuel [47]. The production of biofuel is through alcoholic fermentation which has been reported in Clostridium sp. on Casava waste residue [48].

2.2.3 Synthesis of biopolymers

Fermentation plays an essential role in the production of biopolymers. Biopolymers are made of gelatin, xanthan gum cellulose, collagen and other related substances gotten from agri-food waste [49] which have been studied to have food and pharmaceutical uses [49]. Many genera of microorganisms produce polymers like cellulose, xanthan, alginate, cellulose and so on which are completely broken down into carbondioxide, methane, water and biomass [50]. Azobacter, Pseudomonas, Bacillus, Rhizopus, are among the numerous genera of microorganisms capable of producing biopolymers with various duration of degradation [51, 52, 53, 54].

2.2.4 Food preservation and shelf-life extension

Fermentation is a traditional method that extends the usability of foods by months, preventing spoilage. This process transforms perishable items like cabbage into long-lasting sauerkraut, enhancing food safety and reducing waste [51].

2.2.5 Toxin mitigation and nutritional enhancement

Fermentation not only mitigates harmful substances but also enriches foods with essential nutrients. Through fermentation, natural compounds like phytic acid in legumes are broken down, improving the availability of vitamins and minerals for better absorption. This process also removes anti-nutrients, making nutrients more accessible and boosting the health potential of the food [51]. Bacteria, yeast, algae and fungi are microorganisms that can be relied on for the protein need of man. Microbial based protein known as bioprotein can be multicellular [55]. Microbial protein can be obtained from environmental waste by microbial activity, thereby reducing environmental pollutants and addition of value-added feed and food as high nutritional biomass [56]. Oleaginous yeast such as Yarrowia lipolytica and Candida spp. clean up the environment and are capable of growing on biofuel waste, alkanes, petroleum bye-products, natural gas, glycerol as well as waste products from pants and animals [55, 57, 58, 59, 60, 61, 62]. Filamentous fungi such as Aspergillus, Penicillium, Rhizopus, and Fusarium are regarded as highly nutritious because of their ability to provide variety of essential nutrients and bioactive compounds which contribute to healthy diet, including protein, carbohydrates, fatty acids, minerals, vitamins and antioxidants and hence used in a wide range of fermented food technologies [4, 63, 64, 65, 66, 67]. Lactic acid bacteria (LAB) play an important role in degrading harmful substances in food. Lactic Acid Bacteria has been used in reduction of aflatoxin [68], breakdown of ethyl carbamate [69], decomposition of phytic acid [70] and hydrolysis of bitter peptides in cheese production [71].

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3. Conclusions

Fermentation is an ancient preserving technique adopted by man. Bacteria, yeast or fungi convert fermentable organic compounds like sugars and starch into alcohol. Fermentation can be categorized into solid state fermentation and submerged fermentation. Solid state fermentation occurs in aerobic conditions on solid state substrate with minimal moisture content which is commonly employed in traditional food production like Indonesian tempeh and bread. Submerged fermentation take place in liquid media, promoting anaerobic growth of microorganism and is widely employed in industries like sucrose laven, enzymes, and pigment production. Food fermentation utilizes the growth and metabolic activity of microorganisms which improve organoleptic and general value addition associated with fermented foods. Many fermented foods such as yogurt, cheese, bread, kunun- zaki, masa, ogi, and wines are produced as a result of fermentation of different substrates. Fermented foods are produced and enjoyed all over the world. Fermentation is beneficial to both food and nonfood industries especially in the production of bread with better characteristic using specific LAB strains, production of biofuel through alcoholic fermentation which has been reported in Clostridium sp. on Casava waste residue, production of biopolymers, extension of shelf life as well as food preservation especially in perishable items like cabbage which is transformed to long-lasting sauerkraut, enhancing food safety and reducing waste. Fermentation not only mitigates harmful substances but also enriches foods with essential nutrients. Microbial protein can be obtained from waste obtained from the environment by microbial action, thereby reducing environmental pollutants and addition of value to feed and food as high nutritional biomass. Harmful aflatoxins are degraded and reduced in foods by lactic acid bacteria.

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Acknowledgments

We appreciate intechopen for giving us the opportunity for contributing to this chapter. We also appreciate in anticipation, the sponsorship by Australian Society for Microbiology, World Bank Group, Akwa Ibom State University, Australian Commission on Safety and Quality in Health Care, Society for General Microbiology, Third World Organization for Women in Science, Academy of Science Research and Technology, AAIR Charity, Thrivent Financial Foundation and Abu Dhabi National Oil Company.

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Conflict of interest

The authors declare no conflict of interest.

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Notes/thanks/other declarations

Thanks to the authors whose rich contribution to science was used to write this piece of chapter and to intechopen, we are grateful for the opportunity to contribute to your book.

References

  1. 1. Binod P, Sindhu R, Pandey A. The alcohol fermentation step: The most common ethanologenic microorganisms among yeasts, bacteria and filamentous fungi. In: Faraco V, editor. Lignocellulose Conversion. Berlin, Heidelberg: Springer; 2013:131-149. DOI: 10.1007/978-3-642-37861-4_7
  2. 2. Piskur J, Rozpedowska E, Polakova S, Merico A, Compagno C. How did Saccharomyces evolve to become a good brewer? TRENDS in Genetics. 2006;22(4):183-186. DOI: 10.1016/j.tig.2006.02.002
  3. 3. Rodriguez-Melcon C, Alonso-Calleja C, Capita R. Lactic acid concentrations that reduce microbial load yet minimally impact colour and sensory characteristics of beef. Meat Science. 2017;129:169-175. DOI: 10.1016/j.meatsci.2017.01.007
  4. 4. Cao L, Barzee TJ, El Mashad HM, Pan Z, Zhang R. Potential of utilizing almond hull extract for filamentous fungi production by submerged cultivation. Food Bioengineering. 2024;3:3-13. DOI: 10.1002/fbe2.12079
  5. 5. Baker PW, Charlton A, Hale MDC. Fibre degradation of wheat straw by Pleurotus erygnii under low moisture conditions during solid-state fermentation. Letters in Applied Microbiology. 2019;68(2):182-187. DOI: 10.1111/lam.13104
  6. 6. Bhargav S, Panda BP, Ali M, Javed S. Solid-state fermentation: An overview. Chemical and Biochemical Engineering Quarterly. 2008;22(1):49-70
  7. 7. Pandey A. Solid-state fermentation. Biochemical Engineering Journal. 2003;13(2-3):81-84
  8. 8. Ogbonna DN, Sokari TG, Achinewhu SC. Development of an owoh-type product from African yam beans (Sphenostylis stenocarpa) (Hoechst (ex. A. Rich.) Harms.) seeds by solid substrate fermentation. Plant Foods for Human Nutrition. 2001;56:183-194. DOI: 10.1023/A:1011185513717
  9. 9. Haddadin MS, Abu-Reesh IM, Haddadin FA, Robinson RK. Utilisation of tomato pomace as a substrate for the production of vitamin B12–a preliminary appraisal. Bioresource Technology. 2001;78(3):225-230. DOI: 10.1016/S0960-8524(01)00018-9
  10. 10. Han BZ, Rombouts FM, Nout MJR. A Chinese fermented soybean food. International Journal of Food Microbiology. 2001;65(1-2):1-10. DOI: 10.1016/S0168-1605(00)00523-7
  11. 11. Yang XX, Chen HZ, Gao HL, Li ZH. Bioconversion of corn straw by coupling ensiling and solid-state fermentation. Bioresource Technology. 2001;78(3):277-280. DOI: 10.1016/S0960-8524(01)00024-4
  12. 12. Pandey A, Selvakumar P, Soccol CR, Nigam P. Solid-state fermentation for the production of industrial enzymes. Current Science. 1999;77(1):149-162
  13. 13. Classen JJ, Engler CR, Kenerley CM, Whittaker AD. A logistic model of subsurface fungal growth with application to bioremediation. Journal of Environmental Science and Health Part A. 2000;35(4):465-488. DOI: 10.1080/10934520009376982
  14. 14. Medeiros ABP, Pandey A, Freitas RJS, Christen P, Soccol CR. Optimization of production of aroma compounds by Kluyveromyces marxianus in solid-state fermentation using factorial design and response surface methodology. Biochemical Engineering Journal. 2000;6(1):33-39. DOI: 10.1016/s1369-703x(00)00065-6
  15. 15. Mattedi A, Sabbi E, Farda B, Djebaili R, Mitra D, Ercole C, et al. Solid-state fermentation: Applications and future perspectives for biostimulant and biopesticides production. Microorganisms. 2023;11(6):1408. DOI: 10.3390/microorganisms11061408
  16. 16. Ghoreishi G, Barrena R, Font X. Using green waste as substrate to produce biostimulant and biopesticide products through solid-state fermentation. Waste Management. 2023;159:84-92. DOI: 10.1016/j.wasman.2023.01.026
  17. 17. Gonzalez-Torres M, Hernandez-Rosas F, Pacheco N, Salinas-Ruiz J, Herrera-Corredor JA, Hernandez-Martinez R. Levan production by Suhomyces kilbournensis using sugarcane molasses as a carbon source in submerged fermentation. Molecules. 2024;29(5):1105. DOI: 10.3390/molecules29051105
  18. 18. Venkatachalam M. Pigment production using submerged fermentation. Fermentation. 2024;10(2):91. DOI: 10.3390/fermentation10020091
  19. 19. Liu J, Chai X, Guo T, Wu J, Yang P, Luo Y, et al. Disruption of the Ergosterol biosynthetic pathway results in increased membrane permeability, causing overproduction and secretion of extracellular Monascus pigments in submerged fermentation. Journal of Agricultural and Food Chemistry. 2019;67:13673-13683. DOI: 10.1021/acs.jafc.9b05872
  20. 20. Liu J, Guo T, Luo Y, Chai X, Wu J, Zhao W, et al. Enhancement of Monascus pigment productivity via a simultaneous fermentation process and separation system using immobilized-cell fermentation. Bioresource Technology. 2019;272:552-560. DOI: 10.1016/j.biortech.2018.10.072
  21. 21. Niu K, Mao J, Zheng Y. Effect of microparticle on fermentation process of filamentous microorganisms—A review. Wei Sheng Wu Xue Bao. 2015;55:258-263
  22. 22. Cairns TC, Feurstein C, Zheng X, Zheng P, Sun J, Meyer V. A quantitative image analysis pipeline for the characterization of filamentous fungal morphologies as a tool to uncover targets for morphology engineering: A case study using aplD in Aspergillus niger. Biotechnology for Biofuels. 2019;12:149. DOI: 10.1186/s13068-019-1473-0
  23. 23. Ruiz B, Chavez A, Forero A, Garcia-Huante Y, Romero A, Sanchez M, et al. Production of microbial secondary metabolites: Regulation by the carbon source. Critical Reviews in Microbiology. 2010;36:146-167. DOI: 10.3109/10408410903489576
  24. 24. Gong Z, Zhang S, Liu J. Recent advances in chitin biosynthesis associated with the morphology and secondary metabolite synthesis of filamentous fungi in submerged fermentation. Journal of Fungi. 2023;9(2):205. DOI: 10.3390/jof9020205
  25. 25. Linder T. Making the case for edible microorganisms as an integral part of a more sustainable and resilient food production system. Food Security. 2019;11:265-278. DOI: 10.1007/s12571-019-00912-3
  26. 26. Teng TS, Chin YL, Chai KF, Chen WN. Fermentation for future food systems: Precision fermentation can complement the scope and applications of traditional fermentation. EMBO Reports. 2021;22(5):e52680. DOI: 10.15252/embr.202152680
  27. 27. Geraldo R, Santos CS, Pinto E, Vasconcelos MW. Widening the perspectives for legume consumption: The case of bioactive non-nutrients. Frontiers in Plant Science. 2022;13:772054. DOI: 10.3389/fpls.2022.772054
  28. 28. Ross RP, Morgan S, Hill C. Preservation and fermentation: Past, present and future. International Journal of Food Microbiology. 2002;79:3-16. DOI: 10.1016/S0168-1605(02)00174-5
  29. 29. Rezac S, Kok CR, Heermann M, Hutkins R. Fermented foods as a dietary source of live organisms. Frontiers in Microbiology. 2018;9:396129. DOI: 10.3389/fmicb.2018.01785
  30. 30. Campbell-Platt G. Fermented Foods of the World: A Dictionary and Guide. London: Butterworths; 1987
  31. 31. Olukoya DK, Ebigwei SI, Olasupo NA, Ogunjimi AA. Production of DogiK: An improved Ogi (Nigerian fermented weaning food) with potentials for use in diarrhoea control. Journal of Tropical Pediatrics. 1994;40:108-113. DOI: 10.1093/tropej/40.2.108
  32. 32. Akande OA, Jolayemi OS, Familusi A, Idowu B. Nutritional, antioxidant and sensory properties of rice-based masa enriched with grain amaranth and carrot powder. Annals of Food Science and Technology. 2018;19(40):645-656
  33. 33. Samuel FO, Oluwaseun I, Bolanle O. Nutritional and sensory evaluation of rice -based masa enriched with soybean and crayfish. Food and nutrition. Science. 2015;6:234-241. DOI: 10.4236/fns.2015.62024
  34. 34. Egbere OJ, Onwuliri FC, Oyero SK, Henry UI. Accelerated fermentation process of kunun-zaki (A Nigerian non-alcoholic beverage). Advances in Science and Technology. 2008;2(1):36-41
  35. 35. Tamang JP, Holzapfel WH, Watanabe K. Diversity of microorganisms in global fermented foods and beverages. Frontiers in Microbiology. 2016;7:377. DOI: 10.3389/fmicb.2016.00377
  36. 36. Tamang JP, Samuel D. Dietary culture and antiquity of fermented foods and beverages. In: Tamang JP, Kailasapathy K, editors. Fermented Foods and Beverages of the World. New York: CRC Press; 2010. pp. 1-40
  37. 37. Tamang JP, Shin DH, Jung SJ, Chae SW. Functional properties of microorganisms in fermented foods. Frontiers in Microbiology. 2016b;7:578. DOI: 10.3389/fmicb.2016.00578
  38. 38. Tamang JP, Kailasapathy K, editors. Fermented Foods and Beverages of the World. United States of America: CRC Press; 2010
  39. 39. Steinkraus KH. Handbook of Indigenous Fermented Food. 2nd ed. New York: Marcel Dekker, Inc; 1996. p. 792. DOI: 10.1201\9780203752821
  40. 40. Franz CMAP, Huch M, Mathara JM, Abriouel H, Benomar N, Reid G, et al. African fermented foods and probiotics. International Journal of Food Microbiology. 2014;190:84-96. DOI: 10.1016/j.ijfoodmicro.2014.08.033
  41. 41. Liu A, Liu Q , Bu Y, Hao H, Liu T, Gong P, et al. Aroma classification and characterization of Lactobacillus delbrueckii subsp. bulgaricus fermented milk. Food Chemistry. 2022;15:100385. DOI: 10.1016/j.fochx.2022.100385
  42. 42. Poutanen K, Flander L, Katina K. Sourdough and cereal fermentation in a nutritional perspective. Food Microbiology. 2009;26(7):693-699. DOI: 10.1016/j.fm.2009.07.011
  43. 43. De Vuyst L, Van Kerrebroeck S, Leroy F. Microbial ecology and process technology of sourdough fermentation. Advances in Applied Microbiology. 2017;100:49-160. DOI: 10.1016/bs.aambs.2017.02.003
  44. 44. Rizzello CG, Portincasa P, Montemurro M, Di Palo DM, Lorusso MP, De Angelis M, et al. Sourdough fermented breads are more digestible than those started with baker’s yeast alone: An in vivo challenge dissecting distinct gastrointestinal responses. Nutrients. 2019;11(12):2954. DOI: 10.3390/nu11122954
  45. 45. Corsetti A, Gobbetti M, Balestrieri F, Paoletti F, Russi L, Rossi J. Sourdough lactic acid bacteria effects on bread firmness and staling. Journal of Food Science. 2000;63(2):347-351. DOI: 10.1021/jf990853e
  46. 46. Kordala N, Walter M, Brzozowski B, Lewandowska M. 2G-biofuel ethanol: An overview of crucial operations, advances and limitations. Biomass Conversion and Biorefinery. 2024;14(3):2983-3006. DOI: 10.1007/s13399-022-02861-y
  47. 47. Li C, Wang Y, Xie G, Peng B, Zhang B, Chen W, et al. Complete genome sequence of Clostridium butyricum JKY6D1 isolated from the pit mud of a Chinese flavor liquor-making factory. Journal of Biotechnology. 2016;220:23-24. DOI: 10.1016/j.jbiotec.2016.01.003
  48. 48. Johnravindar D, Elangovan N, Gopal NO, Muthaiyan A, Fei Q. Biobutanol production from cassava waste residue using Clostridium sp. AS3 in batch culture fermentation. Biofuels. 2019, 2019;12(10):1259-1266. DOI: 10.1080/17597269.2019.1608671
  49. 49. Panda J, Mishra AK, Mohanta YK, Patowary K, Rauta PR, Mishra B. Exploring biopolymer for food and pharmaceuticals application in the circular bioeconomy: An agro-food waste-to-wealth approach. Waste Biomass Valor. 2024:1-31. DOI: 10.1007/s12649-024-02452-0
  50. 50. Saharan BS, Kamal N, Badoni P, Kumar R, Saini M, Kumar D, et al. Biopolymer and polymer precursor production by microorganisms: Applications and future prospects. Journal of Chemical Technology & Biotechnology. 2024;99(1):17-30. DOI: 10.1002/jctb.7524
  51. 51. Zahan KA, Azizul NM, Mustapha M, Tong WY, Rahman MSA. Application of bacterial cellulose film as a biodegradable and antimicrobial packaging material. Mater Today: Proceedings. 2020;31:83-88. DOI: 10.1016/j.matpr.2020.01.201
  52. 52. Cho JY, Park SL, Lee HJ, Kim SH, Suh MJ, Ham S, et al. Polyhydroxyalkanoates (PHAs) degradation by the newly isolated marine Bacillus sp. JY14. Chemosphere. 2021;283:131172
  53. 53. Fischer M, Gebhard F, Hammer T, Zurek C, Meurer G, Marquardt C, et al. Microbial alginate dressings show improved binding capacity for pathophysiological factors in chronic wounds compared to commercial alginate dressings of marine origin. Journal of Biomaterial Application. 2017;31:1267-1276. DOI: 10.1177/0885328217702173
  54. 54. Mbarki K, Fersi M, Louati I, Elleuch B, Sayari A. Biodegradation study of PDLA/cellulose microfibres biocomposites by Pseudomonas aeruginosa. Environmental Technology. 2021;42:731-742. DOI: 10.1080/09593330.2019.1643926
  55. 55. Jach ME, Serefko A. Nutritional yeast biomass: Characterization and application. In: Grumezescu A, Holban AM, editors. Diet, Microbiome and Health. Handbook of Food Bioengineering. Vol. 11. London, UK: Academic Press; 2018. pp. 237-270
  56. 56. Suman G, Nupur M, Anuradha S, Pradeep B. Single cell protein production: A review. International Journal of Current Microbiology and Applied Science. 2015;4:251-262
  57. 57. Dourou M, Aggeli D, Papanikolaou S, Aggelis G. Critical steps in carbon metabolism affecting lipid accumulation and their regulation in oleaginous microorganisms. Applied Microbiology and Biotechnology. 2018;102:2509-2523. DOI: 10.1007/s00253-018-8813-z
  58. 58. Katre G, Joshi C, Khot M, Zinjarde S, RaviKumar A. Evaluation of single cell oil (SCO) from a tropical marine yeast Yarrowia lipolytica NCIM 3589 as a potential feedstock for biodiesel. AMB Express. 2012;2:36. DOI: 10.1186/2191-0855-2-36
  59. 59. Lopes M, Gomes AS, Silva CM, Bel I. Microbial lipids and added value metabolites production by Yarrowia lipolytica from pork lard. Journal of Biotechnology. 2018;265:76-85. DOI: 10.1016/j.jbiotec.2017.11.007
  60. 60. Rywinska A, Juszczyk P, Wojtatowicz M, Robak M, Lazar Z, Tomaszewska L, et al. Glycerol as a promising substrate for Yarrowia lipolytica biotechnological applications. Biomass and Bioenergy. 2013;48:148-166. DOI: 10.1016/j.biombioe.2012.11.021
  61. 61. Lopes M, Miranda SM, Alves JM, Pereira AS, Belo I. Waste cooking oils as feedstock for lipase and lipid-rich biomass production. European Journal of Lipid Science and Technology. 2019;121:1800188. DOI: 10.1002/ejlt.201800188
  62. 62. Jach ME, Sajnaga E, Swider R, Baier A, Mickowska B, Juda M, et al. Yarrowia lipolytica grown on biofuel waste as a source of single cell protein and essential amino acids for human diet. Saudi Journal of Medical and Pharmaceutical Science. 2017;3:1344-1351. DOI: 10.21276/sjmps.2017.3.12.14
  63. 63. Barzee TJ, Cao L, Pan Z, Zhang R. Fungi for future foods. Journal of Future Foods. 2021;1(1):25-37. DOI: 10.1016/j.jfutfo.2021.09.002
  64. 64. Chandra P, Sharma RK, Arora DS. Antioxidant compounds from microbial sources: A review. Food Research International. 2020;129:108849. DOI: 10.1016/j.foodres.2019.108849
  65. 65. Chakraborty A, Majumdar S, Bhowal J. Phytochemical screening and antioxidant and antimicrobial activities of crude extracts of different filamentous fungi. Archives of Microbiology. 2021;203:6091-6108. DOI: 10.1007/s00203-021-02572-4
  66. 66. Chan LG, Cohen J, de Moura B. Conversion of agricultural streams and food-processing by- products to value-added compounds using filamentous fungi. Annual Review of Food Science and Technology. 2018;9:503-523. DOI: 10.1146/annurev-food-030117-012626
  67. 67. Strong PJ, Self R, Allikian K, Szewczyk E, Speight R, O'Hara I, et al. Filamentous fungi for future functional food and feed. Current Opinion in Biotechnology. 2022;76:102729. DOI: 10.1016/j.copbio.2022.102729
  68. 68. Taheur FB, Mansour C, Kouidhi B, Chaieb K. Use of lactic acid bacteria for the inhibition of aspergillus flavusand aspergillus carbonarius growth and mycotoxin production. Toxicon. 2019;166:15-23. DOI: 10.1016/j.toxicon.2019.05.004
  69. 69. Fang R, Zhou W, Chen Q. Ethyl carbamate regulation and genomic expression of Saccharomyces cerevisiae during mixed-culture yellow rice wine fermentation with Lactobacillus sp. Food Chemistry. 2019;292:90-97. DOI: 10.1016.2019.04.014
  70. 70. Batista NN, Ramos CL, de Figueiredo VL, Dias DR, Schwan RF. Fermentation of yam (Dioscorea spp. L.) by indigenous phytase-producing lactic acid bacteria strains. Brazilian Journal of Microbiology. 2019;50:507-514. DOI: 10.1007/s42770-019-00059-5
  71. 71. Komprda T, Burdychova R, Dohnal V, Cwikova O, Sladkova P, Dvorackova H. Tyramine production in dutch-type semi-hard cheese from two different producers. Food Microbiology. 2008;25:219-227. DOI: 10.1016/j.fm.2007.11.006

Written By

Margaret M.A. Danladi, Mary F. Istifanus, Musa S. Makeri, John O. Egbere, Luka S. Danahap, Brains O. Okechalu and Abigail I. Ogbonna

Submitted: 22 April 2024 Reviewed: 29 April 2024 Published: 03 July 2024