Microbial Secondary Metabolites via Fermentation Approaches for Dietary Supplementation Formulations
Abstract
:1. Introduction
- -
- Supplementation: Dietary supplements are meant to complement a person’s diet when it may be difficult to obtain all necessary nutrients through food alone. They aim to fill nutritional gaps and provide additional nutrients that may be lacking;
- -
- Nutrient types: Common nutrients found in dietary supplements include vitamins (such as vitamin C, vitamin D, or B-complex vitamins), minerals (like calcium, iron, or magnesium), and herbal or botanical extracts (such as ginkgo biloba or Echinacea);
- -
- Regulation: In many countries, dietary supplements are regulated as a category of food, rather than drugs. Regulations vary, but typically supplements must be labeled accurately and must not make false or misleading claims about their benefits;
- -
- Health claims: Dietary supplements are often marketed with various health claims, but it is important to approach these claims with skepticism. While some supplements have been studied extensively and may have proven benefits, others may have limited or no scientific evidence to support their claimed effects. The safety and quality of dietary supplements can vary. It is important to choose reputable brands that adhere to good manufacturing practices. Additionally, some supplements may interact with medications or have adverse effects, so it’s wise to consult a healthcare professional before starting any new supplement regimen;
- -
- Individual needs: Not all individuals require dietary supplements. In general, it is best to obtain nutrients through a balanced diet rich in fruits, vegetables, whole grains, lean proteins, and healthy fats. However, certain population groups, such as pregnant women, older adults, or individuals with specific dietary restrictions, may benefit from targeted supplementation under the guidance of a healthcare professional.
- (I)
- Multivitamins: These formulations contain a combination of essential vitamins and minerals to support general health; their aim is to provide a comprehensive range of nutrients that may be lacking in a person’s diet.
- (II)
- Omega-3 fatty acids: Omega-3 supplements often come in the form of fish oil or algae oil capsules. They provide essential fatty acids, such as eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA), which are beneficial for heart health, brain function, and inflammation reduction.
- (III)
- Protein supplements: These formulations are popular among athletes, bodybuilders, and individuals who may have increased protein needs. Protein supplements often come in powder form, are made from sources such as whey, casein, soy, or pea protein, and can be used to support muscle growth, recovery, and overall protein intake.
- (IV)
- Calcium and vitamin D: These supplements are commonly taken to support bone health. Calcium is essential for strong bones, while vitamin D aids in calcium absorption.
- (V)
- Iron supplements: Iron is crucial for the production of red blood cells and oxygen transport in the body. Iron supplementation is often recommended for individuals with iron deficiency or increased iron needs, such as pregnant women or those with certain medical conditions.
- (VI)
- Probiotics: Probiotic supplements contain beneficial bacteria that support a healthy gut microbiome. They can help improve digestion, boost immune function, and promote overall gut health.
- (VII)
- Herbal supplements: These formulations contain various plant extracts or botanical ingredients. Herbal supplements are often used to support specific health goals or address certain conditions, but their effectiveness and safety may vary.
2. Biotechnological Production’ Role in the Context of Sustainable Microbial Natural Products
3. Microbial Natural Products via Fermentation and Their Potential Applications for Dietary Supplements Formulations
3.1. Microbial Production of Essential Amino Acids
- -
- Histidine is an essential amino acid involved in various metabolic pathways and protein synthesis;
- -
- Lysine is an essential amino acid required for protein synthesis and growth in many microorganisms;
- -
- Isoleucine, Leucine, and Valine (Branched-chain amino acids, or BCAAs) are essential amino acids that are important for protein synthesis and energy metabolism. L-valine and L-isoleucine, are frequently utilized as fitness supplements and for individuals with hepatic encephalopathy;
- -
- Methionine is an essential amino acid that is important for protein synthesis, methylation reactions, and sulfur metabolism;
- -
- Phenylalanine is an essential amino acid that serves as a precursor for the synthesis of other important molecules, such as tyrosine and various neurotransmitters;
- -
- Threonine is an essential amino acid that plays a crucial role in protein synthesis and the maintenance of healthy cells;
- -
- Tryptophan is an essential amino acid needed for protein synthesis and various physiological processes.
- (a)
- Cell Disruption: The first step in extracting amino acids from bacteria is to disrupt the bacterial cells to release their contents. This can be achieved through mechanical disruption methods such as sonication (using ultrasonic waves), homogenization (using a blender or homogenizer), or bead beating (using glass or ceramic beads). These methods break the cell walls and release the intracellular components, including amino acids.
- (b)
- Filtration: After cell disruption, the resulting mixture needs to be separated to remove the cell debris and other large particles. Filtration techniques, such as centrifugation or microfiltration, can be employed to separate the liquid phase containing the extracted amino acids from the solid residue.
- (c)
- Precipitation: To concentrate and separate the amino acids from the liquid extract, precipitation methods can be used. The most common approach is to adjust the pH of the solution to the isoelectric point of the amino acids of interest, causing them to become insoluble and precipitate out. The precipitated amino acids can then be separated by centrifugation or filtration.
- (d)
- Chromatography: Chromatography techniques, such as ion exchange chromatography or high-performance liquid chromatography (HPLC), are often employed for further purification and separation of specific amino acids. These methods utilize the differences in charge, size, or hydrophobicity of the amino acids to separate them into individual components.
- (e)
- Desalting: If the extracted amino acids contain high levels of salts or other impurities, desalting steps may be necessary. It can be achieved by dialysis or using desalting columns, which remove the salts and other small molecules, leaving behind purified amino acids.
3.2. Microbial Production of Essential Vitamins
- (a)
- Cell disruption: Break open the bacterial cells to release the intracellular contents, including the vitamin. Cell disruption methods can include mechanical disruption (e.g., bead milling, high-pressure homogenization) or enzymatic treatments.
- (b)
- Filtration and clarification: After cell disruption, the resulting mixture is typically filtered to remove large debris and cell fragments. Further clarification steps, such as centrifugation or filtration through membranes, can be performed to obtain a clearer solution.
- (c)
- Purification: Purify the extracted vitamin from other cellular components and impurities. Various techniques can be employed, such as chromatography (e.g., column chromatography, high-performance liquid chromatography) or crystallization, depending on the specific vitamin and its properties.
- (d)
- Concentration and drying: Concentrate the purified vitamin solution to increase its potency. This can be performed through techniques like evaporation or freeze-drying (lyophilization) to remove the solvent and obtain a dry, stable vitamin powder.
- (e)
- Quality control: Perform rigorous quality control tests on the extracted and purified vitamin to ensure its potency, purity, and safety. These tests may include assays for vitamin content, impurity analysis, and microbial testing.
3.3. Microbial Production of Functional Compounds
- -
- Bacterial production: some bacteria have the ability to produce phenolic compounds through their metabolic pathways. For instance, E. coli has been engineered to produce various phenolics, including resveratrol [116], a well-known antioxidant compound found in grapes and red wine. It was initially believed that resveratrol was only produced by plants, but later studies revealed that certain species of bacteria and fungi can also synthesize this compound (e.g., Saccharomyces cerevisiae) [117,118,119]. By introducing specific genes encoding enzymes involved in phenolic biosynthesis, researchers have successfully developed bacterial strains capable of producing these compounds;
- -
- Yeast production: certain strains of yeast, such as Saccharomyces cerevisiae, have been engineered to produce phenolic compounds [117,118,119]. Through genetic modifications, key enzymes involved in the phenolic biosynthetic pathway can be introduced into the yeast, enabling them to convert simple precursors into desired phenolic compounds. This approach has been employed to produce compounds like vanillin, which is a commonly used flavoring agent [120,121];
- -
- Fungal production: fungi are also a promising source for phenolic compound production. Filamentous fungi, such as Aspergillus, Rhizopus and Penicillium species, have been studied for their ability to produce phenolics [122], like tannins and coumarins, lignin derivatives, and flavonoids like naringenin and apigenin [123].
- -
- Escherichia coli: Genetic engineering techniques have been used to introduce carotenoid biosynthetic pathways into E. coli, enabling the production of carotenoids such as β-carotene and lycopene. [130];
- -
- Agrobacterium sp.: The bacterium has been engineered to produce astaxanthin, a highly valued carotenoid pigment, through the introduction of genes from other carotenoid-producing organisms. [131];
- -
- Paracoccus sp.: Some species of Paracoccus (e.g., Paracoccus carotinifaciens) have been found to naturally produce carotenoids such as canthaxanthin and astaxanthin [132];
- -
- -
- Neurospora crassa: Genetic engineering approaches have been applied to N. crassa to enhance its carotenoid production capacity. [135];
- -
- Phycomyces blakesleeanus: This fungus naturally produces β-carotene and can be cultivated to enhance carotenoid yields. [136]
- (a)
- Cell Disruption: Break open the harvested cells to release the carotenoids. Cell disruption methods can include physical techniques like sonication (ultrasonication), high-pressure homogenization, or mechanical methods such as bead milling or grinding. The objective is to rupture the cell walls and release the intracellular contents.
- (b)
- Extraction: Extract the carotenoids from the disrupted cells using an appropriate solvent. Common solvents for carotenoid extraction include organic solvents like acetone, ethyl acetate, or hexane. The choice of solvent depends on the nature of the carotenoids and their solubility properties.
- (c)
- Separation and Purification: After extraction, the crude extract is obtained, which may contain impurities and other unwanted compounds. Purify the carotenoid extract using techniques such as liquid–liquid extraction, chromatography (e.g., column chromatography or high-performance liquid chromatography), or filtration methods to obtain a pure carotenoid fraction.
- (d)
- Concentration and Drying: Concentrate the purified carotenoid solution using techniques such as rotary evaporation or nitrogen gas blowdown. Finally, dry the concentrated carotenoid solution to remove any residual solvent and obtain a dry carotenoid powder.
4. Future Considerations
4.1. Aspects Related to Microbial Production
- -
- Selection of microorganism: Various microorganisms have been engineered or naturally occur with the ability to produce specific metabolites. Researchers select the appropriate microorganism based on its natural capabilities or modify its genetic makeup through genetic engineering techniques to enhance targeted metabolites production;
- -
- Substrate selection: Microorganisms require a carbon source for growth and metabolites production. Common substrates include glucose, molasses, starch, or other renewable biomass sources. The choice of substrate depends on the target metabolite and the cost-effectiveness of the production process;
- -
- Optimization of culture conditions: Microorganisms need specific environmental conditions to thrive and produce metabolites efficiently. Factors such as temperature, pH, oxygen levels, and nutrient availability are optimized to create an ideal growth environment for the microorganism;
- -
- Genetic Engineering: Genetic engineering techniques are employed to modify the metabolic pathways of microorganisms. This can involve introducing or overexpressing genes related to the metabolite biosynthesis pathway, removing competing pathways, or enhancing precursor supply. These modifications aim to increase the yield and productivity of the desired metabolite;
- -
- Fermentation process: The selected microorganism is cultured in a large-scale fermentation process. Fermenters provide controlled conditions for the microorganisms to grow and produce metabolites. The process typically involves batch, fed-batch, or continuous fermentation modes, depending on the specific requirements of the microorganism and the desired metabolite production;
- -
- Downstream processing: Once the fermentation process is complete, the metabolites need to be separated and purified from the fermentation broth. This process usually includes steps such as cell removal, filtration, precipitation, chromatography, and drying. The purification steps ensure the final product meets the required quality standards.
4.2. Aspects Related to Consumers Acceptance
4.3. Achievements versus Limitations
- -
- Standardization and quality control: Ensuring consistent and reliable production of microbial-produced dietary supplements can be challenging. Variability in microbial strains, fermentation processes, and product formulation can affect the quality and efficacy of the supplements. Strict quality control measures are necessary to ensure safety and effectiveness;
- -
- Shelf stability: Some microbial-produced dietary supplements may have limited shelf stability due to the presence of live microorganisms. These products require proper storage and handling conditions to maintain viability and efficacy. Additionally, some supplements may require refrigeration, which can limit their accessibility and convenience;
- -
- Efficacy and individual variation: The efficacy of microbial-produced dietary supplements can vary among individuals. Factors such as the existing gut microbiota composition, overall health status, and individual response can influence the effectiveness of these supplements. What works for one person may not work the same way for another;
- -
- Regulatory considerations: The regulatory landscape for microbial-produced dietary supplements can be complex and varies across countries. Ensuring compliance with regulations and standards can be challenging for manufacturers, and the lack of standardized guidelines can create uncertainties in the industry.
5. Conclusions
Author Contributions
Funding
Acknowledgments
Conflicts of Interest
References
- World Health Organization. About World Health Organization. Constitution. Available online: http://www.who.int/governance/eb/constitution/en/ (accessed on 27 April 2023).
- Svalastog, A.L.; Donev, D.; Jahren Kristoffersen, N.; Gajović, S. Concepts and definitions of health and health-related values in the knowledge landscapes of the digital society. Croat. Med. J. 2017, 58, 431–435. [Google Scholar] [CrossRef] [Green Version]
- Kruk, M.E.; Gage, A.D.; Arsenault, C.; Jordan, K.; Leslie, H.H.; Roder-DeWan, S.; Adeyi, O.; Barker, P.; Daelmans, B.; Doubova, S.V.; et al. High-quality health systems in the Sustainable Development Goals era: Time for a revolution. Lancet Glob. Health 2018, 6, e1196–e1252, Erratum in Lancet Glob. Health 2021, 9, e1067. [Google Scholar] [CrossRef] [Green Version]
- Baker, M.T.; Lu, P.; Parrella, J.A.; Leggette, H.R. Consumer Acceptance toward Functional Foods: A Scoping Review. Int. J. Environ. Res. Public Health 2022, 19, 1217. [Google Scholar] [CrossRef]
- Sharma, R.; Garg, P.; Kumar, P.; Bhatia, S.K.; Kulshrestha, S. Microbial Fermentation and Its Role in Quality Improvement of Fermented Foods. Fermentation 2020, 6, 106. [Google Scholar]
- Shaikh, S. Sources and Health Benefits of Functional Food Components. In Current Topics in Functional Food; Shiomi, N., Savitskaya, A., Eds.; IntechOpen: London, UK, 2022. [Google Scholar] [CrossRef]
- Directive 2002/46/EC of the European Parliament and of the Council of 10 June 2002 on the Approximation of the Laws of the Member States Relating to Food Supplements. 2023. Available online: https://eur-lex.europa.eu/legal-content/EN/TXT/PDF/?uri=CELEX:32002L0046 (accessed on 27 April 2023).
- EFSA. Food Supplements. 2020. Available online: http://www.efsa.europa.eu/en/topics/topic/food-supplements (accessed on 10 September 2020).
- Granato, D.; Barba, F.J.; Bursać Kovačević, D.; Lorenzo, J.M.; Cruz, A.G.; Putnik, P. Functional foods: Product development, technological trends, efficacy testing, and safety. Annu. Rev. Food Sci. Technol. 2020, 11, 93–118. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Bagchi, D. Nutraceutical and Functional Food Regulations in the United States and Around the World, 3rd ed.; Academic Press: London, UK, 2019. [Google Scholar]
- Bigliardi, B.; Galati, F. Innovation trends in the food industry: The case of functional foods. Trends Food Sci. Technol. 2013, 31, 118–129. [Google Scholar]
- Wortmann, L.; Enneking, U.; Daum, D. German consumers’ attitude towards selenium-biofortified apples and acceptance of related nutrition and health claims. Nutrients 2018, 10, 190. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Gonçalves, A.C.; Nunes, A.R.; Flores-Félix, J.D.; Alves, G.; Silva, L.R. Cherries and Blueberries-Based Beverages: Functional Foods with Antidiabetic and Immune Booster Properties. Molecules 2022, 27, 3294. [Google Scholar]
- Yang, S.-Y.; Yoon, K.-S. Effect of Probiotic Lactic Acid Bacteria (LAB) on the Quality and Safety of Greek Yogurt. Foods 2022, 11, 3799. [Google Scholar] [CrossRef] [PubMed]
- Moineau-Jean, A.; Champagne, C.P.; Roy, D.; Raymond, Y.; LaPointe, G. Effect of Greek-style yoghurt manufacturing processes on starter and probiotic bacteria populations during storage. Int. Dairy J. 2019, 93, 35–44. [Google Scholar] [CrossRef]
- Petrovna, L.G.; Vladimirovna, S.E.; Dashievna, Z.S.; Sergeevna, K.T. The Functional Properties of Bread Enriched with Essential Fatty Acids. KnE Life Sci. 2022, 7, 236–250. [Google Scholar] [CrossRef]
- Verni, M.; Rizzello, C.G.; Coda, R. Fermentation biotechnology applied to cereal industry by-products: Nutritional and functional insights. Front. Nutr. 2019, 6, 42. [Google Scholar]
- Fortune Business Insights. Europe Dietary Supplements Market Size, Trends|Analysis [2020–2027]. Market Report Research. 2019. Available online: https://www.fortunebusinessinsights.com/industry-reports/europe-dietary-supplements-market-101918 (accessed on 7 April 2023).
- Roobab, U.; Abida, A.; Chacha, J.S.; Athar, A.; Madni, G.M.; Ranjha, M.M.A.N.; Rusu, A.V.; Zeng, X.-A.; Aadil, R.M.; Trif, M. Applications of Innovative Non-Thermal Pulsed Electric Field Technology in Developing Safer and Healthier Fruit Juices. Molecules 2022, 27, 4031. [Google Scholar] [CrossRef] [PubMed]
- Provst, I. Functional foods in Europe: A focus on health claims. In Scientific, Health and Social Aspects of the Food Industry; IntechOpen: London, UK, 2012. [Google Scholar]
- Nasri, H.; Baradaran, A.; Shirzad, H.; Rafieian-Kopaei, M. New concepts in nutraceuticals as alternative for pharmaceuticals. Int. J. Prev. Med. 2014, 5, 1487–1499. [Google Scholar] [PubMed]
- Prakash, O.; Ved, A.; Kumar, S.; Kumar, R.; Mariappan, G.; Rawat, A.K.S. Exploring Role of Dietary Fibres, Nutraceuticals and Functional Foods in Cardiovascular Disorders. Curr. Top. Nutraceutical Res. 2017, 15, 67. [Google Scholar]
- Augustsson, A.; Qvarforth, A.; Engström, E.; Paulukat, C.; Rodushkin, I. Trace and major elements in food supplements of different origin: Implications for daily intake levels and health risks. Toxicol. Rep. 2021, 8, 1067–1080. [Google Scholar] [PubMed]
- Rani, V.; Yadav, U.C.S. Functional Food and Human Health; Springer: Berlin, Germany, 2018. [Google Scholar]
- Qin, Y. 6—Applications of Bioactive Seaweed Substances in Functional Food Products; Academic Press: Cambridge, MA, USA, 2018. [Google Scholar]
- Muscaritoli, M. The Impact of Nutrients on Mental Health and Well-Being: Insights from the Literature. Front. Nutr. 2021, 8, 656290. [Google Scholar] [CrossRef] [PubMed]
- Bechoff, A.; De Bruyn, J.; Alpha, A.; Wieringa, F.; Greffeuille, V. Exploring the complementarity of fortification and dietary diversification to combat micronutrient deficiencies: A scoping review. Curr. Dev. Nutr. 2023, 7, 100033. [Google Scholar] [CrossRef] [PubMed]
- Gombart, A.F.; Pierre, A.; Maggini, S. A review of micronutrients and the immune system-working in harmony to reduce the risk of infection. Nutrients 2020, 12, 236. [Google Scholar] [CrossRef] [Green Version]
- Hans, K.B.; Jana, T. Micronutrients in the life cycle: Requirements and sufficient supply. NFS J. 2018, 11, 1–11. [Google Scholar] [CrossRef]
- Vaz, B.D.S.; Moreira, J.B.; Morais, M.G.D.; Costa, J.A.V. Microalgae as a new source of bioactive compounds in food supplements. Curr. Opin. Food Sci. 2016, 7, 73–77. [Google Scholar] [CrossRef]
- Samtiya, M.; Aluko, R.E.; Dhewa, T.; Moreno-Rojas, J.M. Potential Health Benefits of Plant Food-Derived Bioactive Components: An Overview. Foods 2021, 10, 839. [Google Scholar] [CrossRef] [PubMed]
- Ghosh, S.; Sarkar, T.; Pati, S.; Kari, Z.A.; Edinur, H.A.; Chakraborty, R. Novel Bioactive Compounds from Marine Sources as a Tool for Functional Food Development. Front. Mar. Sci. 2022, 9, 832957. [Google Scholar] [CrossRef]
- Ali, S.; Shah, W.A.S.; Shah, M.A.; Zareef, M.; Arslan, M.; Hassan, M.; Ali, I.; Ali, M.; Ullah, S. Adulteration and Safety Issues in Nutraceuticals and Functional Foods. In Advances in Nutraceuticals and Functional Foods; Apple Academic Press: Palm Bay, FL, USA, 2022; pp. 79–103. [Google Scholar]
- Fogacci, F.; Fogacci, S. Cardiovascular Risk Factors Management in Pregnancy: A Role for Nutraceuticals? In Nutraceuticals and Cardiovascular Disease; Humana: Cham, Switzerland, 2021; pp. 245–253. [Google Scholar]
- Sirico, F.; Miressi, S.; Castaldo, C.; Spera, R.; Montagnani, S.; Di Meglio, F.; Nurzynska, D. Habits and beliefs related to food supplements: Results of a survey among Italian students of different education fields and levels. PLoS ONE 2018, 13, e0191424. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Hassan, S.; Egbuna, C.; Tijjani, H.; Ifemeje, J.C.; Olisah, M.C.; Patrick-Iwuanyanwu, K.C.; Onyeike, P.C.; Ephraim-Emmanuel, B.C. Dietary Supplements: Types, Health Benefits, Industry and Regulation. In Functional Foods and Nutraceuticals; Egbuna, C., Dable Tupas, G., Eds.; Springer: Cham, Switzerland, 2020. [Google Scholar] [CrossRef]
- Puri, V.; Nagpal, M.; Singh, I.; Singh, M.; Dhingra, G.A.; Huanbutta, K.; Dheer, D.; Sharma, A.; Sangnim, T. A Comprehensive Review on Nutraceuticals: Therapy Support and Formulation Challenges. Nutrients 2022, 14, 4637. [Google Scholar] [CrossRef]
- Vorderbruggen, M. Enhanced D Vitamin Nutraceutical Compositions and Methods for Making and Used Same. U.S. Patent 17/546,982, 16 June 2022. [Google Scholar]
- Ghorbanzade, T.; Jafari, S.M.; Akhavan, S.; Hadavi, R. Nano-encapsulation of fish oil in nano-liposomes and its application in fortification of yogurt. Food Chem. 2017, 216, 146–152. [Google Scholar] [PubMed]
- Verstringe, S.; Vandercruyssen, R.; Carmans, H.; Rusu, A.V.; Bruggeman, G.; Trif, M. Alternative Proteins for Food and Feed. In Biodiversity, Functional Ecosystems and Sustainable Food Production; Galanakis, C.M., Ed.; Springer: Cham, Switzerland, 2023. [Google Scholar] [CrossRef]
- Patel, P.; Jethani, H.; Radha, C.; Vijayendra, S.V.N.; Mudliar, S.N.; Sarada, R.; Chauhan, V.S. Development of a carotenoid enriched probiotic yogurt from fresh biomass of Spirulina and its characterization. J. Food Sci. Technol. 2019, 56, 3721–3731. [Google Scholar] [CrossRef]
- Voidarou, C.; Antoniadou, Μ.; Rozos, G.; Tzora, A.; Skoufos, I.; Varzakas, T.; Lagiou, A.; Bezirtzoglou, E. Fermentative Foods: Microbiology, Biochemistry, Potential Human Health Benefits and Public Health Issues. Foods 2021, 10, 69. [Google Scholar]
- Tullio, V. Yeast Genomics and Its Applications in Biotechnological Processes: What Is Our Present and Near Future? J. Fungi 2022, 8, 752. [Google Scholar] [CrossRef]
- Skowron, K.; Budzyńska, A.; Grudlewska-Buda, K.; Wiktorczyk-Kapischke, N.; Andrzejewska, M.; Wałecka-Zacharska, E.; Gospodarek-Komkowska, E. Two Faces of Fermented Foods—The Benefits and Threats of Its Consumption. Front. Microbiol. 2022, 13, 845166. [Google Scholar] [PubMed]
- Frazzetto, G. White biotechnology. EMBO Rep. 2003, 4, 835–837. [Google Scholar] [CrossRef] [PubMed]
- Kordi, M.; Salami, R.; Bolouri, P.; Delangiz, N.; Lajayer, B.A.; van Hullebusch, E.D. White biotechnology and the production of bio-products. Syst. Microbiol. Biomanuf. 2022, 2, 413–429. [Google Scholar] [CrossRef]
- Heux, S.; Meynial-Salles, I.; O’Donohue, M.J.; Dumon, C. White biotechnology: State of the art strategies for the development of biocatalysts for biorefining. Biotechnol. Adv. 2015, 33, 1653–1670. [Google Scholar] [CrossRef] [PubMed]
- Nout, M.J.R. Food Technologies: Fermentation. In Encyclopedia of Food Safety, Volume 3: Foods, Materials, Technologies and Risks; Elsevier: Amsterdam, The Netherlands, 2014. [Google Scholar] [CrossRef]
- Shaw, A.J.; Lam, F.H.; Hamilton, M.; Consiglio, A.; MacEwen, K.; Brevnova, E.E.; Greenhagen, E.; LaTouf, W.G.; South, C.R.; van Dijken, H.; et al. Metabolic engineering of microbial competitive advantage for industrial fermentation processes. Science 2016, 353, 583–586. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Pan, Y.; Wang, Y.; Hao, W.; Duan, C.; Wang, S.; Wei, J.; Liu, G. Metatranscriptomics Unravel Composition, Drivers, and Functions of the Active Microorganisms in Light-Flavor Liquor Fermentation. Microbiol. Spectr. 2022, 10, e0215121. [Google Scholar] [CrossRef] [PubMed]
- Parapouli, M.; Vasileiadis, A.; Afendra, A.S.; Hatziloukas, E. Saccharomyces cerevisiae and its industrial applications. AIMS Microbiol. 2020, 6, 1–31. [Google Scholar] [CrossRef] [PubMed]
- Li, H.; Yang, Y.; Hong, W.; Huang, M.; Wu, M.; Zhao, X. Applications of genome editing technology in the targeted therapy of human diseases: Mechanisms, advances and prospects. Sig. Transduct. Target. Ther. 2020, 5, 1. [Google Scholar] [CrossRef]
- Adli, M. The CRISPR tool kit for genome editing and beyond. Nat. Commun. 2018, 9, 1911. [Google Scholar] [CrossRef] [Green Version]
- Nielsen, J.C.; Nielsen, J. Development of fungal cell factories for the production of secondary metabolites: Linking genomics and metabolism. Synth. Syst. Biotechnol. 2017, 2, 5–12. [Google Scholar]
- Xu, Y.; Li, Z. CRISPR-Cas systems: Overview, innovations and applications in human disease research and gene therapy. Comput. Struct. Biotechnol. J. 2020, 18, 2401–2415. [Google Scholar] [CrossRef]
- Knott, G.J.; Doudna, J.A. CRISPR-Cas guides the future of genetic engineering. Science 2018, 361, 866–869. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Orsi, E.; Claassens, N.J.; Nikel, P.I.; Lindner, S.N. Growth-coupled selection of synthetic modules to accelerate cell factory development. Nat. Commun. 2021, 12, 5295. [Google Scholar] [CrossRef] [PubMed]
- Dietrich, T.; Villaran Velasco, M.C.; Echeverría, P.J.; Pop, B.; Rusu, A. Crop and Plant Biomass as Valuable Material for BBB. Alternatives for Valorization of Green Wastes. In Biotransformation of Agricultural Waste and By-Products: The Food, Feed, Fibre, Fuel (4F) Economy; Elsevier: San Diego, CA, USA, 2016. [Google Scholar]
- Punia Bangar, S.; Chaudhary, V.; Thakur, N.; Kajla, P.; Kumar, M.; Trif, M. Natural Antimicrobials as Additives for Edible Food Packaging Applications: A Review. Foods 2021, 10, 2282. [Google Scholar] [CrossRef] [PubMed]
- Berg, G.; Rybakova, D.; Fischer, D.; Cernava, T.; Vergès, M.C.; Charles, T.; Chen, X.; Cocolin, L.; Eversole, K.; Corral, G.H.; et al. Microbiome definition re-visited: Old concepts and new challenges. Microbiome 2020, 8, 103, Erratum in Microbiome 2020, 8, 119. [Google Scholar] [CrossRef] [PubMed]
- Bangar, S.P.; Sharma, N.; Kumar, M.; Ozogul, F.; Purewal, S.S.; Trif, M. Recent developments in applications of lactic acid bacteria against mycotoxin production and fungal contamination. Food Biosci. 2021, 44, 101444. [Google Scholar] [CrossRef]
- Roy, A.; Khan, A.; Ahmad, I.; Alghamdi, S.; Rajab, B.S.; Babalghith, A.O.; Alshahrani, M.Y.; Islam, S.; Islam, M.R. Flavonoids a Bioactive Compound from Medicinal Plants and Its Therapeutic Applications. Biomed. Res. Int. 2022, 2022, 5445291. [Google Scholar] [CrossRef]
- Abdelghani, Z.; Hourani, N.; Zaidan, Z.; Dbaibo, G.; Mrad, M.; Hage-Sleiman, R. Therapeutic applications and biological activities of bacterial bioactive extracts. Arch. Microbiol. 2021, 203, 4755–4776. [Google Scholar] [CrossRef] [PubMed]
- Tufail, T.; Ain, H.B.U.; Saeed, F.; Nasir, M.; Basharat, S.; Mahwish; Rusu, A.V.; Hussain, M.; Rocha, J.M.; Trif, M.; et al. A Retrospective on the Innovative Sustainable Valorization of Cereal Bran in the Context of Circular Bioeconomy Innovations. Sustainability 2022, 14, 14597. [Google Scholar] [CrossRef]
- Coughlan, L.M.; Cotter, P.D.; Hill, C.; Alvarez-Ordóñez, A. Biotechnological applications of functional metagenomics in the food and pharmaceutical industries. Front. Microbiol. 2015, 6, 672. [Google Scholar] [CrossRef] [Green Version]
- Zhang, Y.; Wang, Y.; Tang, M.; Zhou, J.; Zhang, T. The microbial dark matter and “wanted list” in worldwide wastewater treatment plants. Microbiome 2023, 11, 59. [Google Scholar] [CrossRef] [PubMed]
- Trif, M.; Rusu, A.V.; Francino, M.P.; Delgado, G.; Rufián-Henares, J.Á. Microbiome Applications for Sustainable Food Systems. In Biodiversity, Functional Ecosystems and Sustainable Food Production; Galanakis, C.M., Ed.; Springer: Cham, Switzerland, 2023. [Google Scholar] [CrossRef]
- Delompré, T.; Guichard, E.; Briand, L.; Salles, C. Taste Perception of Nutrients Found in Nutritional Supplements: A Review. Nutrients 2019, 11, 2050. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Wu, Q.; Gao, Z.J.; Yu, X.; Wang, P. Dietary regulation in health and disease. Sig. Transduct. Target. Ther. 2022, 7, 252. [Google Scholar] [CrossRef]
- Bott, M. Nutzung mikrobieller und pflanzlicher Diversität in der Biotechnologie. In Biodiversität im Meer und an Land. Vom Wert Biologischer Vielfalt; Kandarr, J., Jorzik, O., Klinghammer, P., Spreen, D., Eds.; Deutsches GeoForschungsZentrum GFZ: Potsdam, Germany, 2020; pp. 50–53. [Google Scholar] [CrossRef]
- Murray, J.E.; Laurieri, N.; Delgoda, R. Chapter 24—Proteins. In Pharmacognosy; Badal, S., Delgoda, R., Eds.; Academic Press: Boston, MA, USA, 2017; pp. 477–494. [Google Scholar]
- Hoffer, L.J. Parenteral Nutrition: Amino Acids. Nutrients 2017, 9, 257. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Parikh, P.; Semba, R.; Manary, M.; Swaminathan, S.; Udomkesmalee, E.; Bos, R.; Poh, B.K.; Rojroongwasinkul, N.; Geurts, J.; Sekartini, R.; et al. Animal source foods, rich in essential amino acids, are important for linear growth and development of young children in low- and middle-income countries. Matern. Child. Nutr. 2022, 18, e13264. [Google Scholar] [CrossRef] [PubMed]
- Lv, Z.; Shi, W.; Zhang, Q. Role of Essential Amino Acids in Age-Induced Bone Loss. Int. J. Mol. Sci. 2022, 23, 11281. [Google Scholar] [CrossRef] [PubMed]
- Endrinikapoulos, A.; Afifah, D.N.; Mexitalia, M.; Andoyo, R.; Hatimah, I.; Nuryanto, N. Study of the importance of protein needs for catch-up growth in Indonesian stunted children: A narrative review. SAGE Open Med. 2023, 11, 1–9. [Google Scholar] [CrossRef] [PubMed]
- Sanchez, S.; Rodríguez-Sanoja, R.; Ramos, A.; Demain, A.L. Our microbes not only produce antibiotics, they also overproduce amino acids. J. Antibiot. 2018, 71, 26–36. [Google Scholar] [CrossRef]
- Sanchez, S.; Demain, A.L. Bioprocess, Bioseparation, and Cell Technology EIB; Flickinger, M.C., Ed.; John Wiley and Sons: Chichester, UK, 2010; Volume 2, pp. 1186–1202. [Google Scholar]
- Eggeling, L.; Bott, M. A giant market and a powerful metabolism: L-lysine provided by Corynebacterium glutamicum. Appl. Microbiol. Biotechnol. 2015, 99, 3387–3394. [Google Scholar] [CrossRef] [PubMed]
- Becker, J.; Zelder, O.; Häfner, S.; Schröder, H.; Wittmann, C. From zero to hero-design-based systems metabolic engineering of Corynebacterium glutamicum for L-lysine production. Metabol. Eng. 2011, 13, 159–168. [Google Scholar] [CrossRef] [PubMed]
- Matano, C.; Uhde, A.; Youn, J.W.; Maeda, T.; Clermont, L.; Marin, K.; Kramer, R.; Wendisch, V.F.; Seibold, G.M. Engineering of Corynebacterium glutamicum for growth and L-lysine and lycopene production from N-acetyl-glucosamine. Appl. Microbiol. Biotechnol. 2014, 98, 5633–5643. [Google Scholar] [CrossRef]
- Sheng, Q.; Wu, X.Y.; Xu, X.; Tan, X.; Li, Z.; Zhang, B. Production of l-glutamate family amino acids in Corynebacterium glutamicum: Physiological mechanism, genetic modulation, and prospects. Synth. Syst. Biotechnol. 2021, 6, 302–325. [Google Scholar] [CrossRef] [PubMed]
- Xie, X.; Liang, Y.; Liu, H.; Liu, Y.; Xu, Q.; Zhang, C.; Chen, N. Modification of glycolysis and its effect on the production of L-threonine in Escherichia coli. J. Indust. Microbiol. Biotechnol. 2014, 41, 1007–1015. [Google Scholar] [CrossRef] [PubMed]
- Zhang, Y.; Meng, Q.; Ma, H.; Liu, Y.; Cao, G.; Zhang, X.; Zheng, P.; Sun, J.; Zhang, D.; Jiang, W.; et al. Determination of key enzymes for threonine synthesis through in vitro metabolic pathway analysis. Microb. Cell Factories 2015, 14, 86–95. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Huang, Q.; Liang, L.; Wu, W.; Wu, S.; Huang, J. Metabolic engineering of Corynebacterium glutamicum to enhance L-leucine production. Afr. J. Biotechnol. 2017, 16, 1048–1060. [Google Scholar] [CrossRef] [Green Version]
- Vogt, M.; Haas, S.; Klaffl, S.; Polen, T.; Eggeling, L.; van Ooyen, J.; Bott, M. Pushing product formation to its limit: Metabolic engineering of Corynebacterium glutamicum for L-leucine overproduction. Metab. Eng. 2013, 22, 40–52. [Google Scholar] [CrossRef]
- Ma, W.; Wang, J.; Li, Y.; Hu, X.; Shi, F.; Wang, X. Enhancing pentose phosphate pathway in Corynebacterium glutamicum to improve L-isoleucine production. Biotechnol. Appl. Biochem. 2016, 63, 877–885. [Google Scholar] [CrossRef]
- Oldiges, M.; Eikmanns, B.J.; Blombach, B. Applications of metabolic engineering for the biotechnological production of L-valine. Appl. Microbiol. Biotechnol. 2014, 98, 5859–5870. [Google Scholar] [CrossRef] [Green Version]
- Wu, H.; Tian, D.; Fan, X.; Fan, W.; Zhang, Y.; Jiang, S.; Wen, C.; Ma, Q.; Chen, N.; Xie, X. Highly Efficient Production of l-Histidine from Glucose by Metabolically Engineered Escherichia coli. ACS Synth. Biol. 2020, 9, 1813–1822. [Google Scholar] [CrossRef]
- Malykh, E.A.; Butov, I.A.; Ravcheeva, A.B.; Krylov, A.A.; Mashko, S.V.; Stoynova, N.V. Specific features of l-histidine production by Escherichia coli concerned with feedback control of AICAR formation and inorganic phosphate/metal transport. Microb. Cell Fact. 2018, 17, 42. [Google Scholar] [CrossRef] [PubMed]
- Mohany, N.A.M.; Totti, A.; Naylor, K.R.; Janovjak, H. Microbial methionine transporters and biotechnological applications. Appl. Microbiol. Biotechnol. 2021, 105, 3919–3929. [Google Scholar] [CrossRef] [PubMed]
- Ding, D.; Liu, Y.; Xu, Y.; Zheng, P.; Li, H.; Zhang, D. Improving the production of L-phenylalanine by identifying key enzymes through multi-enzyme reaction system in vitro. Sci. Rep. 2016, 6, 32208. [Google Scholar] [CrossRef] [Green Version]
- Wang, S.; Fang, Y.; Wang, Z.; Zhang, S.; Wang, L.; Guo, Y.; Wang, X. Improving l-threonine production in Escherichia coli by elimination of transporters ProP and ProVWX. Microb. Cell Fact. 2021, 20, 58. [Google Scholar] [CrossRef] [PubMed]
- Wang, J.; Cheng, L.; Wang, J.; Liu, J.; Shen, T.; Chen, N. Genetic engineering of Escherichia coli to enhance production of L-tryptophan. Appl. Microbiol. Biotechnol. 2013, 97, 7587–7596. [Google Scholar] [CrossRef]
- Ikeda, M.; Nakanishi, K.; Kino, K.; Katsumata, R. Fermentative production of tryptophan by a stable recombinant strain of Corynebacterium glutamicum with a modified serine-biosynthetic pathway. Biosci. Biotechnol. Biochem. 2014, 58, 674–678. [Google Scholar] [CrossRef] [PubMed]
- Wang, Y.; Liu, L.; Jin, Z.; Zhang, D. Microbial Cell Factories for Green Production of Vitamins. Front. Bioeng. Biotechnol. 2021, 9, 661562. [Google Scholar] [CrossRef] [PubMed]
- Brancaccio, M.; Mennitti, C.; Cesaro, A.; Fimiani, F.; Vano, M.; Gargiulo, B.; Caiazza, M.; Amodio, F.; Coto, I.; D’Alicandro, G.; et al. The Biological Role of Vitamins in Athletes’ Muscle, Heart and Microbiota. Int. J. Environ. Res. Public Health 2022, 19, 1249. [Google Scholar] [CrossRef] [PubMed]
- Amrein, K.; Scherkl, M.; Hoffmann, M.; Neuwersch-Sommeregger, S.; Köstenberger, M.; Berisha, A.T.; Martucci, G.; Pilz, S.; Malle, O. Vitamin D deficiency 2.0: An update on the current status worldwide. Eur. J. Clin. Nutr. 2020, 74, 1498–1513. [Google Scholar] [CrossRef] [PubMed]
- Acevedo-Rocha, C.G.; Gronenberg, L.S.; Mack, M.; Commichau, F.M.; Genee, H.J. Microbial Cell Factories for the Sustainable Manufacturing of B Vitamins. Curr. Opin. Biotechnol. 2019, 56, 18–29. [Google Scholar] [CrossRef] [PubMed]
- Calvillo, Á.; Pellicer, T.; Carnicer, M.; Planas, A. Bioprocess Strategies for Vitamin B12 Production by Microbial Fermentation and Its Market Applications. Bioengineering 2022, 9, 365. [Google Scholar] [CrossRef] [PubMed]
- Zhang, Y.; Li, X.; Wang, Z.; Wang, Y.; Ma, Y.; Su, Z. Metabolic Flux Analysis of Simultaneous Production of Vitamin B12 and Propionic Acid in a Coupled Fermentation Process by Propionibacterium freudenreichii. Appl. Biochem. Biotechnol. 2021, 193, 3045–3061. [Google Scholar] [CrossRef] [PubMed]
- Liu, J.; Liu, Y.; Wu, J.; Fang, H.; Jin, Z.; Zhang, D. Metabolic Profiling Analysis of the Vitamin B12 Producer Propionibacterium freudenreichii. Microbiologyopen 2021, 10, e1199. [Google Scholar] [CrossRef] [PubMed]
- Wang, P.; Shen, C.; Li, L.; Guo, J.; Cong, Q.; Lu, J. Simultaneous Production of Propionic Acid and Vitamin B12 from Corn Stalk Hydrolysates by Propionibacterium freudenreichii in an Expanded Bed Adsorption Bioreactor. Prep. Biochem. Biotechnol. 2020, 50, 763–767. [Google Scholar] [CrossRef]
- Ahmed, S.A.; Mesbah, M.K.; Youssef, D.T. Microbial production of 1α-hydroxyvitamin D3 from vitamin D3. Nat. Prod. Res. 2014, 28, 444–448. [Google Scholar] [CrossRef] [PubMed]
- Zhang, Q.; Lyu, S. Microbial Interactions in a Vitamin C Industrial Fermentation System: Novel Insights and Perspectives. Appl. Env. Microbiol. 2022, 88, e0121222. [Google Scholar] [CrossRef]
- Ren, L.; Peng, C.; Hu, X.; Han, Y.; Huang, H. Microbial production of vitamin K2: Current status and future prospects. Biotechnol. Adv. 2020, 39, 107453. [Google Scholar] [CrossRef] [PubMed]
- Kang, M.-J.; Baek, K.-R.; Lee, Y.-R.; Kim, G.-H.; Seo, S.-O. Production of Vitamin K by Wild-Type and Engineered Microorganisms. Microorganisms 2022, 10, 554. [Google Scholar] [CrossRef] [PubMed]
- Zhang, Z.; Liu, L.; Liu, C.; Sun, Y.; Zhang, D. New aspects of microbial vitamin K2 production by expanding the product spectrum. Microb. Cell Fact. 2021, 20, 84. [Google Scholar] [CrossRef] [PubMed]
- Bangar, S.P.; Trif, M.; Özogul, F.; Kumar, M.; Chaudhary, V.; Vukic, M.; Tomar, M.; Changan, S. Recent developments in cold plasma-based enzyme activity (browning, cell wall degradation, and antioxidant) in fruits and vegetables. Compr. Rev. Food Sci. Food Saf. 2022, 21, 1958–1978. [Google Scholar] [CrossRef]
- Cavicchioli, R.; Ripple, W.J.; Timmis, K.N.; Azam, F.; Bakken, L.R.; Baylis, M.; Behrenfeld, M.J.; Boetius, A.; Boyd, P.W.; Classen, A.T.; et al. Scientists’ warning to humanity: Microorganisms and climate change. Nat. Rev. Microbiol. 2019, 17, 569–586. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Pham, J.V.; Yilma, M.A.; Feliz, A.; Majid, M.T.; Maffetone, N.; Walker, J.R.; Kim, E.; Cho, H.J.; Reynolds, J.M.; Song, M.C.; et al. A Review of the Microbial Production of Bioactive Natural Products and Biologics. Front. Microbiol. 2019, 10, 1404. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Roy, A.; Das, S.; Chatterjee, I.; Roy, S.; Chakraborty, R. Anti-inflammatory Effects of Different Dietary Antioxidants. In Plant Antioxidants and Health; Reference Series in Phytochemistry; Ekiert, H.M., Ramawat, K.G., Arora, J., Eds.; Springer: Cham, Switzerland, 2022. [Google Scholar] [CrossRef]
- Barros, L.; Ferreira, I.C.F.R. Editorial: Phytochemicals and their Effects on Human Health. Curr. Pharm. Des. 2017, 23, 2695–2696. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Santhiravel, S.; Bekhit, A.E.-D.A.; Mendis, E.; Jacobs, J.L.; Dunshea, F.R.; Rajapakse, N.; Ponnampalam, E.N. The Impact of Plant Phytochemicals on the Gut Microbiota of Humans for a Balanced Life. Int. J. Mol. Sci. 2022, 23, 8124. [Google Scholar] [CrossRef] [PubMed]
- Mucha, P.; Skoczyńska, A.; Małecka, M.; Hikisz, P.; Budzisz, E. Overview of the Antioxidant and Anti-Inflammatory Activities of Selected Plant Compounds and Their Metal Ions Complexes. Molecules 2021, 26, 4886. [Google Scholar] [PubMed]
- Polat, S.; Trif, M.; Rusu, A.; Šimat, V.; Čagalj, M.; Alak, G.; Meral, R.; Özogul, Y.; Polat, A.; Özogul, F. Recent advances in industrial applications of seaweeds. Crit. Rev. Food Sci. Nutr. 2021, 8, 1–30. [Google Scholar] [CrossRef]
- Li, J.; Qiu, Z.; Zhao, G.R. Modular engineering of E. coli coculture for efficient production of resveratrol from glucose and arabinose mixture. Synth. Syst. Biotechnol. 2022, 7, 718–729. [Google Scholar] [CrossRef]
- Ibrahim, G.G.; Yan, J.; Xu, L.; Yang, M.; Yan, Y. Resveratrol Production in Yeast Hosts: Current Status and Perspectives. Biomolecules 2021, 11, 830. [Google Scholar] [CrossRef] [PubMed]
- Canedo-Santos, J.C.; Carrillo-Garmendia, A.; Mora-Martinez, I.; Gutierrez-Garcia, I.K.; Ramirez-Romero, M.G.; Regalado-Gonzalez, C.; Nava, G.M.; Madrigal-Perez, L.A. Resveratrol shortens the chronological lifespan of Saccharomyces cerevisiae by a pro-oxidant mechanism. Yeast 2022, 39, 193–207. [Google Scholar] [CrossRef]
- Meng, L.; Diao, M.; Wang, Q.; Peng, L.; Li, J.; Xie, N. Efficient biosynthesis of resveratrol via combining phenylalanine and tyrosine pathways in Saccharomyces cerevisiae. Microb. Cell Fact. 2023, 22, 46. [Google Scholar] [CrossRef] [PubMed]
- Luziatelli, F.; Brunetti, L.; Ficca, A.G.; Ruzzi, M. Maximizing the Efficiency of Vanillin Production by Biocatalyst Enhancement and Process Optimization. Front. Bioeng. Biotechnol. 2019, 7, 279. [Google Scholar] [CrossRef] [PubMed]
- Martău, G.A.; Călinoiu, L.F.; Vodnar, D.C. Bio-vanillin: Towards a sustainable industrial production. Trends Food Sci. Technol. 2021, 109, 579–592. [Google Scholar]
- Mark, R.; Lyu, X.; Lee, J.J.; Parra-Saldívar, R.; Chen, W.N. Sustainable production of natural phenolics for functional food applications. J. Funct. Foods 2019, 57, 233–254. [Google Scholar]
- Duda-Madej, A.; Stecko, J.; Sobieraj, J.; Szymańska, N.; Kozłowska, J. Naringenin and Its Derivatives—Health-Promoting Phytobiotic against Resistant Bacteria and Fungi in Humans. Antibiotics 2022, 11, 1628. [Google Scholar] [CrossRef] [PubMed]
- Abo-Kadoum, M.A.; Abouelela, M.E.; Al Mousa, A.A.; Abo-Dahab, N.F.; Mosa, M.A.; Helmy, Y.A.; Hassane, A.M.A. Resveratrol biosynthesis, optimization, induction, bio-transformation and bio-degradation in mycoendophytes. Front. Microbiol. 2022, 13, 1010332. [Google Scholar] [CrossRef] [PubMed]
- Martínez-Cámara, S.; Ibañez, A.; Rubio, S.; Barreiro, C.; Barredo, J.-L. Main Carotenoids Produced by Microorganisms. Encyclopedia 2021, 1, 1223–1245. [Google Scholar] [CrossRef]
- Sen, T.; Barrow, C.J.; Deshmukh, S.K. Microbial pigments in the food industry—Challenges and the way forward. Front. Nutr. 2019, 6, 7. [Google Scholar]
- Sankari, M.; Rao, P.R.; Hemachandran, H.; Pullela, P.K.; Tayubi, I.A.; Subramanian, B.; Gothandam, K.; Singh, P.; Ramamoorthy, S. Prospects and progress in the production of valuable carotenoids: Insights from metabolic engineering, synthetic biology, and computational approaches. J. Biotechnol. 2018, 266, 89–101. [Google Scholar] [PubMed]
- Rao, N.; Prabhu, M.; Xiao, M.; Li, W.J. Fungal and bacterial pigments: Secondary metabolites with wide applications. Front. Microbiol. 2017, 8, 1113. [Google Scholar]
- Pandey, N.; Jain, R.; Pandey, A.; Tamta, S. Optimisation and characterisation of the orange pigment produced by a cold adapted strain of Penicillium sp. (GBPI_P155) isolated from mountain ecosystem. Mycology 2018, 9, 81–92. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Wu, Y.; Yan, P.; Li, Y.; Liu, X.; Wang, Z.; Chen, T.; Zhao, X. Enhancing β-Carotene Production in Escherichia coli by Perturbing Central Carbon Metabolism and Improving the NADPH Supply. Front. Bioeng. Biotechnol. 2020, 8, 585. [Google Scholar] [CrossRef]
- Ma, T.; Zhou, Y.; Li, X.; Zhu, F.; Cheng, Y.; Liu, Y.; Deng, Z.; Liu, T. Genome mining of astaxanthin biosynthetic genes from Sphingomonas sp. ATCC 55669 for heterologous overproduction in Escherichia coli. Biotechnol. J. 2016, 11, 228–237. [Google Scholar] [CrossRef]
- Tam, L.T.; Hong, D.D.; Ranga Rao, A.; Ravishankar, G.A. Astaxanthin production and technology in Vietnam and other Asian countries. In Global Perspectives on Astaxanthin. From Industrial Production to Food, Health, and Pharmaceutical Applications; Elsevier: Amsterdam, The Netherlands, 2021; pp. 595–633. [Google Scholar]
- Bindea, M.; Rusu, B.; Rusu, A.; Trif, M.; Leopold, L.F.; Dulf, F.; Vodnar, D.C. Valorification of crude glycerol for pure fractions of docosahexaenoic acid and beta-carotene production by using Schizochytrium limacinum and Blakeslea trispora. Microb. Cell Factories 2018, 17, 97. [Google Scholar] [CrossRef] [PubMed]
- Papadaki, E.; Mantzouridou, F.T. Natural β-Carotene Production by Blakeslea trispora Cultivated in Spanish-Style Green Olive Processing Wastewaters. Foods 2021, 10, 327. [Google Scholar] [CrossRef] [PubMed]
- Li, C.; Swofford, C.A.; Sinskey, A.J. Modular engineering for microbial production of carotenoids. Metab. Eng. Commun. 2019, 10, e00118. [Google Scholar] [CrossRef]
- Sandmann, G. Carotenoids and Their Biosynthesis in Fungi. Molecules 2022, 27, 1431. [Google Scholar] [CrossRef] [PubMed]
- Pan, X.; Wang, B.; Duan, R.; Jia, J.; Li, J.; Xiong, W.; Ling, X.; Chen, C.; Huang, X.; Zhang, G.; et al. Enhancing astaxanthin accumulation in Xanthophyllomyces dendrorhous by a phytohormone: Metabolomic and gene expression profiles. Microb. Biotechnol. 2020, 13, 1446–1460. [Google Scholar] [CrossRef] [PubMed]
- Naz, T.; Ullah, S.; Nazir, Y.; Li, S.; Iqbal, B.; Liu, Q.; Mohamed, H.; Song, Y. Industrially Important Fungal Carotenoids: Advancements in Biotechnological Production and Extraction. J. Fungi 2023, 9, 578. [Google Scholar]
- Sanmartín, P.; Bosch-Roig, P.; Pangallo, D.; Kraková, L.; Serrano, M. Unraveling disparate roles of organisms, from plants to bacteria, and viruses on built cultural heritage. Appl. Microbiol. Biotechnol. 2023, 107, 2027–2037. [Google Scholar] [CrossRef] [PubMed]
- Solanki, P.; Putatunda, C.; Kumar, A.; Bhatia, R.; Walia, A. Microbial proteases: Ubiquitous enzymes with innumerable uses. 3 Biotech 2021, 11, 428. [Google Scholar] [CrossRef]
- Yang, X.; Zhang, Y.; Pang, H.; Yuan, S.; Wang, X.; Hu, Z.; Zhou, Q.; He, Y.; Yan, Y.; Xu, L. Codisplay of Rhizopus oryzae and Candida rugosa Lipases for Biodiesel Production. Catalysts 2021, 11, 421. [Google Scholar] [CrossRef]
- Septiani, D.I.A.; Suryadi, H.; Mun’im, A.; Mangunwardoyo, W. Production of cellulase from Aspergillus niger and Trichoderma reesei mixed culture in carboxymethylcellulose medium as sole carbon. Biodiversitas 2019, 20, 3539–3544. [Google Scholar] [CrossRef]
- Haile, S.; Ayele, A. Pectinase from Microorganisms and Its Industrial Applications. Sci. World J. 2022, 2022, 1881305. [Google Scholar] [CrossRef] [PubMed]
- Yan, S.; Wu, G. Bottleneck in secretion of α-amylase in Bacillus subtilis. Microb. Cell Factories 2017, 16, 124. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Raveendran, S.; Parameswaran, B.; Ummalyma, S.B.; Abraham, A.; Mathew, A.K.; Madhavan, A.; Rebello, S.; Pandey, A. Applications of Microbial Enzymes in Food Industry. Food Technol. Biotechnol. 2018, 56, 16–30. [Google Scholar] [CrossRef]
- Vachher, M.; Sen, A.; Kapila, R.; Nigam, A. Microbial therapeutic enzymes: A promising area of biopharmaceuticals. Curr. Res. Biotechnol. 2021, 3, 67–68. [Google Scholar] [CrossRef]
- Rodríguez-Sáiz, M.; de la Fuente, J.L.; Barredo, J.L. Xanthophyllomyces dendrorhous for the industrial production of astaxanthin. Appl. Microbiol. Biotechnol. 2010, 88, 645–658. [Google Scholar]
- Wang, E.; Dong, C.; Zhang, P.; Roberts, T.H.; Park, R.F. Carotenoid biosynthesis and the evolution of carotenogenesis genes in rust fungi. Fungal Biol. 2021, 125, 400–411. [Google Scholar] [CrossRef] [PubMed]
- Mohanty, S.S.; Koul, Y.; Varjani, S.; Pandey, A.; Ngo, H.H.; Chang, J.-S.; Wong, J.W.C.; Bui, X.-T. A critical review on various feedstocks as sustainable substrates for biosurfactants production: A way towards cleaner production. Microb. Cell Factories 2021, 20, 120. [Google Scholar] [CrossRef]
- Rinke, C.; Schwientek, P.; Sczyrba, A.; Ivanova, N.N.; Anderson, I.J.; Cheng, J.-F.; Darling, A.; Malfatti, S.; Swan, B.K.; Gies, E.A.; et al. Insights into the phylogeny and coding potential of microbial dark matter. Nature 2013, 499, 431–437. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Sreenikethanam, A.; Raj, S.; Banu, J.R.; Gugulothu, P.; Bajhaiya, A.K. Genetic Engineering of Microalgae for Secondary Metabolite Production: Recent Developments, Challenges, and Future Prospects. Front. Bioeng. Biotechnol. 2022, 10, 836056. [Google Scholar] [CrossRef] [PubMed]
- Graham, A.E.; Ledesma-Amaro, R. The microbial food revolution. Nat. Commun. 2023, 14, 2231. [Google Scholar] [CrossRef]
- Afzaal, M.; Saeed, F.; Shah, Y.A.; Hussain, M.; Rabail, R.; Socol, C.T.; Hassoun, A.; Pateiro, M.; Lorenzo, J.M.; Rusu, A.V.; et al. Human gut microbiota in health and disease: Unveiling the relationship. Front. Microbiol. 2022, 13, 999001. [Google Scholar] [PubMed]
- Kim, S.-H.; Kuo, W.-Y. The Role of Beliefs, Pride, and Perceived Barriers in Decision-Making Regarding Purchasing Value-Added Pulse Products among US Consumers. Foods 2022, 11, 824. [Google Scholar] [CrossRef]
- Singh, G.P.; Bangar, S.P.; Yang, T.; Trif, M.; Kumar, V.; Kumar, D. Effect on the Properties of Edible Starch-Based Films by the Incorporation of Additives: A Review. Polymers 2022, 14, 1987. [Google Scholar] [PubMed]
- Siegrist, M.; Hartmann, C. Consumer acceptance of novel food technologies. Nat. Food 2020, 1, 343–350. [Google Scholar] [CrossRef] [PubMed]
- Hassoun, A.; Jagtap, S.; Garcia-Garcia, G.; Trollman, H.; Pateiro, M.; Lorenzo, J.M.; Trif, M.; Rusu, A.V.; Aadil, R.M.; Šimat, V.; et al. Food quality 4.0: From traditional approaches to digitalized automated analysis. J. Food Eng. 2022, 337, 111216. [Google Scholar] [CrossRef]
Disclaimer/Publisher’s Note: The statements, opinions and data contained in all publications are solely those of the individual author(s) and contributor(s) and not of MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim responsibility for any injury to people or property resulting from any ideas, methods, instructions or products referred to in the content. |
© 2023 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
Share and Cite
Rusu, A.V.; Trif, M.; Rocha, J.M. Microbial Secondary Metabolites via Fermentation Approaches for Dietary Supplementation Formulations. Molecules 2023, 28, 6020. https://doi.org/10.3390/molecules28166020
Rusu AV, Trif M, Rocha JM. Microbial Secondary Metabolites via Fermentation Approaches for Dietary Supplementation Formulations. Molecules. 2023; 28(16):6020. https://doi.org/10.3390/molecules28166020
Chicago/Turabian StyleRusu, Alexandru Vasile, Monica Trif, and João Miguel Rocha. 2023. "Microbial Secondary Metabolites via Fermentation Approaches for Dietary Supplementation Formulations" Molecules 28, no. 16: 6020. https://doi.org/10.3390/molecules28166020