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Review

Microbial Resources, Fermentation and Reduction of Negative Externalities in Food Systems: Patterns toward Sustainability and Resilience

by
Vittorio Capozzi
1,
Mariagiovanna Fragasso
2 and
Francesco Bimbo
2,*
1
Institute of Sciences of Food Production, National Research Council (CNR), c/o CS-DAT, Via Michele Protano, 71121 Foggia, Italy
2
Department of Agriculture, Food, Natural Science, Engineering, University of Foggia, 71121 Foggia, Italy
*
Author to whom correspondence should be addressed.
Fermentation 2021, 7(2), 54; https://doi.org/10.3390/fermentation7020054
Submission received: 12 January 2021 / Revised: 29 March 2021 / Accepted: 3 April 2021 / Published: 6 April 2021

Abstract

:
One of the main targets of sustainable development is the reduction of environmental, social, and economic negative externalities associated with the production of foods and beverages. Those externalities occur at different stages of food chains, from the farm to the fork, with deleterious impacts to different extents. Increasing evidence testifies to the potential of microbial-based solutions and fermentative processes as mitigating strategies to reduce negative externalities in food systems. In several cases, innovative solutions might find in situ applications from the farm to the fork, including advances in food matrices by means of tailored fermentative processes. This viewpoint recalls the attention on microbial biotechnologies as a field of bioeconomy and of ‘green’ innovations to improve sustainability and resilience of agri-food systems alleviating environmental, economic, and social undesired externalities. We argue that food scientists could systematically consider the potential of microbes as ‘mitigating agents’ in all research and development activities dealing with fermentation and microbial-based biotechnologies in the agri-food sector. This aims to conciliate process and product innovations with a development respectful of future generations’ needs and with the aptitude of the systems to overcome global challenges.

1. Microbial Resources and Food Fermentations: The ‘Oldest Biotechnologies’

Microbes, the first forms of life that appeared on Earth at least 3.8 billion years ago, represent the organisms more diffused on the Earth [1,2]. Microorganisms have crucial roles in the environment (cycling of elements and, more generally, of nutrients), in the biology of macroorganisms (of outstanding importance for human, animal, and plant health), and in human advances (e.g., in agriculture, relevant food chains, and biotechnologies) [1,2]. The huge variable in terms of catabolic pathways and for the aptitude to survive to stress conditions make microbes versatile key players on the live planet and drivers of innovations for human activities, such as in biogeochemical processes, biotechnologies, and health [3,4]. Microbes associated with a given ‘macroorganism’ are defined as their microbiome. Microbiomes are involved in critical physiological activities of their hosts, contributing to the maintenance of a state of well-being. The microbiomes associated with plants and animals domesticated for food uses are fundamental to modulate their productivity and affect the quality of the obtained products.
Since the Neolithic period, humans have developed an unawareness of the management of microbes and experience the benefits of food fermentation, also known as the oldest biotechnologies [5], with a vast variability of raw matrices (cereals, vegetables, and bamboo shoots, legumes, roots/tubers, milk, meat, and fish products) and microorganisms involved (bacteria, yeasts, and molds belonging to several genera and species) [6]. It has been estimated that about one-third of the food and beverage consumption worldwide concern fermented matrices: more than 5000 different products that account for an essential part of global systems [6,7]. In general, a given food/beverage is reported as fermented when is “produced through controlled microbial growth, and the conversion of food components through enzymatic action” [8]. The controlled growth of desired bacteria, yeasts, and filamentous fungi modulate all the main aspects of fermented food/beverage safety and quality (organoleptic, nutritional, functional) (Figure 1) [9].
In addition, the target of microbial-based solutions has been broadened throughout the advances in microbial biotechnologies. In fact, protective cultures and microbial biocontrol agents can also be found on non-fermented products (e.g., fresh fruits and vegetables, fresh meat) [11,12].

2. Food Systems and Negative Externalities

Food systems embrace all resources and activities related to production, processing, distribution, preparation, and food consumption. Also, food systems include the product market, its institutional networks needed for its governance, and it is the ultimate responsibility for the socioeconomic and environmental outcomes of all the activities listed above [13]. According to Organization for Economic Co-operation and Development (OECD), the term externalities ‘refers to situations when the effect of production or consumption of goods and services imposes costs or benefits on others which are not reflected in the prices charged for the goods and services being provided’ [14].
The idea of sustainable development is tailored to mitigate the negative externalities [15]. In effect, these phenomena undermine the pillars of growth compatible with the needs of future generations. For instance, negative environmental externalities reflect into pollution, natural resource exhaustion/degradation threatening the long-term balance of the ecosystem. These trends also threaten the economic sustainability of markets when companies produce limited quantities leaving unsatisfactory market demand as well as whether companies produce low quality or without placing interest in saving energy, water and preventing pollution. Lastly, negative externalities also challenge sustainable development from a social point of view occur if companies produce with the limited observance of the code of good social responsibility practices: for instance, when companies pay unfair prices to supplies exploiting their work, as well as whether they produce unmatching consumers’ and societies’ priorities in terms of animal welfare or workers welfare standards.
The rising occurrence of negative externalities generated by food systems has called into action different sectoral stakeholders, such as policymakers, non-governmental organisations (NGOs), and academics, to prioritise the development of strategies contrasting the environmental, economic, and social externalities generated with the food production. Important examples of initiatives are reported in Table 1, testifying the global interest in tailored policies oriented toward sustainability and food systems resilience.
In association with food production, it is possible to highlight several significant negative externalities, ‘namely effects on the environment, the economy and the society that are not reflected in the cost of food’ [16]. These include the release of CO2 and other greenhouse gases, increase of wastes and pollution, contamination of freshwater, enhanced water deficiencies, soil depletion, a decrease of biological diversity, reduced benefits of microbiomes, the market of unsafe products, diffused antibiotic resistance, lessening of the supply for selected consumers groups, lastly whether the production is foster the rise of socioeconomic disparities [16,17,18,19,20]. Taken together, these undesirable trends threaten food security (Figure 2), human health, environmental resources, and economic networks, especially if we consider future generations.

3. Microbial Biotechnologies to Reduce Negative Externalities in Agri-Food Systems

Microbial-based solutions can find global applications in the food systems, counteracting, at the farm level, to relevant negative externalities on a global scale (Table 2). These include, among others, pollution in the animal/plant food chains, diffusion of contaminations, productions associated with and considerable environmental footprints, and reduction of water availability and soil fertility.
As reported in the scientific literature, it is possible to find so many examples as to suggest a potential systemic application of microbes as mitigating agents in the primary production. In several cases, the target is the ‘remediation’ of negative trends: microorganisms selected to reduce carbon dioxide [19,22], bioconversion of pollutants in water via microbial [19,26,27], microbial-driven bioremediation of soil [28,29], and microbial-based decomposition of endocrine disruptors from trophic chains [22]. In addition, we can find ‘green’ microbial alternatives to standard solutions, such as substitute to antibiotic [35,36,37], pesticides [32,34], fertilizers/stimulants [32,33], feeding regimen [42], nitrogen sources [19], protein production [19,25], and to make water potable [30,31]. Finally, there are positive activities exerted by microbial resources (e.g., biological fixation of nitrogen [22,23,24], microalgae beneficial application [40,41], modulation of nutrient crops quality [38,39], and breeding of ‘microbe-optimised plants’ [32]) that can counteract to the effects of negative externalities.

4. Tailored Food Fermentative Processes to Reduce Negative Externalities in Food Systems

Moving from the farm to the fork, we shift from general microbial biotechnologies to food/fermentative biotechnologies (Table 3). This technological exploitation of microorganisms can find direct application in food manufacture, with a considerable potential for in situ uses tailored to modulate specific aspects of food quality and, more generally, food production.
The examples reported in Table 3 encompass a broad spectrum of subjects of interest in the food and beverage industry. A family of solutions reduces the risk of biological and chemical contaminants, respectively, with biocontrol applications against microbial pathogens and spoilers [43,44,45,46,47] and exploiting microbial biochemical activities responsible for the degradation of chemical contaminants [49,50,51]. Another group of bio-based innovations oriented at ‘label cleaning’, conceive alternatives to chemical preservatives [52,53,54] and to fortification via the addition of exogenous nutrients [55,56,57]. Some studies proposed pathways towards enhanced nutrient bioavailability [10,58,59,60] and improved human health/well-being [61,62,63,64] (including microbiome therapies [63,64,65,66]), advances of interest to contrast the adverse effects of some negative externalities. Furthermore, the design of several works looking at reducing resource dissipation, saving energy [52,69], valorising foods by-products [52,70,71], foods wastes [72,73,74], and wastewater [75,76,77]. Finally, some strategies can preserve microbial diversity associated with food fermentation [78,79,80].
Some implementations are common to the primary sector and to the studies in food processing. It is the case of protein production that receives interest for both feed and food applications, involving biotechnologies to address a societal or a business need [19,25]. Fermentation and microbial cell factories for producing proteins [81], but also enhancing the nutritional quality of alternative protein sources [82].
It is crucial to underline that the safety of the microbial resources, to avoid any negative side-effects, represents a milestone to assure the sustainability of the solutions reported in Table 2 and Table 3 [83,84]. At the same time, the management of microbial resources as ‘commons’, following the standard of microbial biological resource centers (mBRCs), it is of outstanding interest to promote innovation in the field [85,86].

5. Microbes as Mitigating Agents: A Common Denominator of R&D Activities in the Field

This viewpoint article suggests that the challenge of lowering negative externalities would represent a constant part of research and development activities dealing with fermentation and microbial-based biotechnologies in the agri-food sector; a sort of ‘lateral thinking’ [87] with the aims to conciliate product and process innovations with a development respectful of the needs of future generations. In other terms, as the food industry, together with the ‘conventional’ quality of the product (e.g., hygienic, sensory, nutritional, functional) [9], has an increasing ‘side’ focus to sustainable product footprint [88,89], at the same way, food scientists (in the field of microbial-related solutions) could systematically consider the potential as mitigating agents, ‘laterally’ to the innovation proposed. This in consideration that microbial biotechnologies are a driver of innovation but may play a pivotal role in matching sustainability goals and fostering the agri-food system’s resilience. The exploitation of microbial resources is generally considered a knowledge-based reservoir of ‘green’ innovations susceptible to be used in an environmentally, social, and economically conscious manner [1]. However, microbial biotechnologies’ successful implementation needs careful attention since microbial-based solutions are resources of knowledge as created through creative processes and productions and are the primary output of universities and private research centers [90]. Then, microbial biotechnologies are adopted according to the economic conditions in which a company operates as well as to the extent the civil society and consumer accept the use of such biotechnologies [91,92]. Thus, to fully exploit the potential benefits of microbial biotechnologies, there is a need to raise the awareness of their ability to lower the many negative externalities across all the food systems stakeholders (industries, policymakers, academics, and civil society) (Figure 3) [93,94].
It is important to consider that microbial biotechnology can contribute to economic progress and employment creation [96]. Also, it is worth saying that microbes and fermented base foods are amply accepted by consumers given the widespread use of fermentation across the many food sectors since ancient time, as well as the general consumers’ acceptance of microbes and related fermentation is rising due to the consumer demand for a more ‘natural’ food that replaces chemical preservatives with natural alternatives (bio-preservatives) [91,97]. These findings contrast the widespread contention that consumers are opposed to the use of biotechnology as they mainly associate biotechnology terms with genetically modified (GM) foods that are, indeed, perceived as an unnatural modification of food and for which consumers ask restrictive policy measures [91,97]. Lastly, related to the microbial biotechnologies and the sustainable economic growth, it is crucial to underline the importance of specific educative programs in the field to favour the people inclination to fair behaviours concerning global challenges such as climate changes and the COVID-19 pandemic [98,99,100,101].

Author Contributions

Investigation, V.C., M.F. and F.B.; conceptualization, V.C., M.F. and F.B.; literature Search, V.C., M.F. and F.B.; writing—original draft preparation, V.C., M.F. and F.B.; writing—review and editing, V.C., M.F. and F.B. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Acknowledgments

We would like to thank Domenico Genchi of the Institute of Sciences of Food Production—CNR for its skilled technical support provided during the realisation of this work.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Timmis, K.; de Vos, W.M.; Ramos, J.L.; Vlaeminck, S.E.; Prieto, A.; Danchin, A.; Verstraete, W.; de Lorenzo, V.; Lee, S.Y.; Brüssow, H.; et al. The Contribution of Microbial Biotechnology to Sustainable Development Goals. Microb. Biotechnol. 2017, 10, 984–987. [Google Scholar] [CrossRef]
  2. 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]
  3. Martínez-Espinosa, R.M. Microorganisms and Their Metabolic Capabilities in the Context of the Biogeochemical Nitrogen Cycle at Extreme Environments. Int. J. Mol. Sci. 2020, 21, 4228. [Google Scholar] [CrossRef]
  4. Poli, A.; Finore, I.; Romano, I.; Gioiello, A.; Lama, L.; Nicolaus, B. Microbial Diversity in Extreme Marine Habitats and Their Biomolecules. Microorganisms 2017, 5, 25. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  5. Dimidi, E.; Cox, S.R.; Rossi, M.; Whelan, K. Fermented Foods: Definitions and Characteristics, Impact on the Gut Microbiota and Effects on Gastrointestinal Health and Disease. Nutrients 2019, 11, 1806. [Google Scholar] [CrossRef] [Green Version]
  6. Tamang, J.P.; Watanabe, K.; Holzapfel, W.H. Review: Diversity of Microorganisms in Global Fermented Foods and Beverages. Front. Microbiol. 2016, 7. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  7. Vogel, R.F.; Hammes, W.P.; Habermeyer, M.; Engel, K.-H.; Knorr, D.; Eisenbrand, G. Microbial Food Cultures—Opinion of the Senate Commission on Food Safety (SKLM) of the German Research Foundation (DFG). Mol. Nutr. Food Res. 2011, 55, 654–662. [Google Scholar] [CrossRef]
  8. Marco, M.L.; Heeney, D.; Binda, S.; Cifelli, C.J.; Cotter, P.D.; Foligné, B.; Gänzle, M.; Kort, R.; Pasin, G.; Pihlanto, A.; et al. Health Benefits of Fermented Foods: Microbiota and Beyond. Curr. Opin. Biotechnol. 2017, 44, 94–102. [Google Scholar] [CrossRef] [PubMed]
  9. Capozzi, V.; Fragasso, M.; Romaniello, R.; Berbegal, C.; Russo, P.; Spano, G. Spontaneous Food Fermentations and Potential Risks for Human Health. Fermentation 2017, 3, 49. [Google Scholar] [CrossRef]
  10. 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] [CrossRef]
  11. De Simone, N.; Pace, B.; Grieco, F.; Chimienti, M.; Tyibilika, V.; Santoro, V.; Capozzi, V.; Colelli, G.; Spano, G.; Russo, P. Botrytis cinerea and Table Grapes: A Review of the Main Physical, Chemical, and Bio-Based Control Treatments in Post-Harvest. Foods 2020, 9, 1138. [Google Scholar] [CrossRef]
  12. Castellano, P.; Pérez Ibarreche, M.; Blanco Massani, M.; Fontana, C.; Vignolo, G.M. Strategies for Pathogen Biocontrol Using Lactic Acid Bacteria and Their Metabolites: A Focus on Meat Ecosystems and Industrial Environments. Microorganisms 2017, 5, 38. [Google Scholar] [CrossRef] [Green Version]
  13. Ruben, R.; Verhagen, J.; Plaisier, C. The Challenge of Food Systems Research: What Difference Does It Make? Sustainability 2019, 11, 171. [Google Scholar] [CrossRef] [Green Version]
  14. OECD Glossary of Statistical Terms—Externalities—OECD Definition. Available online: https://stats.oecd.org/glossary/detail.asp?ID=3215 (accessed on 31 December 2020).
  15. Ziolo, M.; Filipiak, B.Z.; Bąk, I.; Cheba, K.; Tîrca, D.M.; Novo-Corti, I. Finance, Sustainability and Negative Externalities. An Overview of the European Context. Sustainability 2019, 11, 4249. [Google Scholar] [CrossRef] [Green Version]
  16. Godfray, H.C.J.; Beddington, J.R.; Crute, I.R.; Haddad, L.; Lawrence, D.; Muir, J.F.; Pretty, J.; Robinson, S.; Thomas, S.M.; Toulmin, C. Food Security: The Challenge of Feeding 9 Billion People. Science 2010, 327, 812–818. [Google Scholar] [CrossRef] [Green Version]
  17. Buzby, J.C.; Hyman, J. Total and per Capita Value of Food Loss in the United States. Food Policy 2012, 37, 561–570. [Google Scholar] [CrossRef]
  18. Shafiee-Jood, M.; Cai, X. Reducing Food Loss and Waste to Enhance Food Security and Environmental Sustainability. Environ. Sci. Technol. 2016, 50, 8432–8443. [Google Scholar] [CrossRef] [PubMed]
  19. Verstraete, W.; Vrieze, J.D. Microbial Technology with Major Potentials for the Urgent Environmental Needs of the next Decades. Microb. Biotechnol. 2017, 10, 988–994. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  20. Russo, P.; Berbegal, C.; De Ceglie, C.; Grieco, F.; Spano, G.; Capozzi, V. Pesticide Residues and Stuck Fermentation in Wine: New Evidences Indicate the Urgent Need of Tailored Regulations. Fermentation 2019, 5, 23. [Google Scholar] [CrossRef] [Green Version]
  21. Matkovski, B.; Đokić, D.; Zekić, S.; Jurjević, Ž. Determining Food Security in Crisis Conditions: A Comparative Analysis of the Western Balkans and the EU. Sustainability 2020, 12, 9924. [Google Scholar] [CrossRef]
  22. de Lorenzo, V. Seven Microbial Bio-Processes to Help the Planet. Microb. Biotechnol. 2017, 10, 995–998. [Google Scholar] [CrossRef]
  23. Soumare, A.; Diedhiou, A.G.; Thuita, M.; Hafidi, M.; Ouhdouch, Y.; Gopalakrishnan, S.; Kouisni, L. Exploiting Biological Nitrogen Fixation: A Route Towards a Sustainable Agriculture. Plants 2020, 9, 1011. [Google Scholar] [CrossRef]
  24. Alaswad, A.A.; Oehrle, N.W.; Krishnan, H.B. Classical Soybean (Glycine Max (L.) Merr) Symbionts, Sinorhizobium fredii USDA191 and Bradyrhizobium diazoefficiens USDA110, Reveal Contrasting Symbiotic Phenotype on Pigeon Pea (Cajanus Cajan (L.) Millsp). Int. J. Mol. Sci. 2019, 20, 1091. [Google Scholar] [CrossRef] [Green Version]
  25. Tagliavia, M.; Nicosia, A. Advanced Strategies for Food-Grade Protein Production: A New E. Coli/Lactic Acid Bacteria Shuttle Vector for Improved Cloning and Food-Grade Expression. Microorganisms 2019, 7, 116. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  26. Ajiboye, T.O.; Kuvarega, A.T.; Onwudiwe, D.C. Recent Strategies for Environmental Remediation of Organochlorine Pesticides. Appl. Sci. 2020, 10, 6286. [Google Scholar] [CrossRef]
  27. Hayat, K.; Menhas, S.; Bundschuh, J.; Chaudhary, H.J. Microbial Biotechnology as an Emerging Industrial Wastewater Treatment Process for Arsenic Mitigation: A Critical Review. J. Clean. Prod. 2017, 151, 427–438. [Google Scholar] [CrossRef]
  28. Wang, R.; Wu, B.; Zheng, J.; Chen, H.; Rao, P.; Yan, L.; Chai, F. Biodegradation of Total Petroleum Hydrocarbons in Soil: Isolation and Characterization of Bacterial Strains from Oil Contaminated Soil. Appl. Sci. 2020, 10, 4173. [Google Scholar] [CrossRef]
  29. Rigoletto, M.; Calza, P.; Gaggero, E.; Malandrino, M.; Fabbri, D. Bioremediation Methods for the Recovery of Lead-Contaminated Soils: A Review. Appl. Sci. 2020, 10, 3528. [Google Scholar] [CrossRef]
  30. Fowler, S.J.; Smets, B.F. Microbial Biotechnologies for Potable Water Production. Microb. Biotechnol. 2017, 10, 1094–1097. [Google Scholar] [CrossRef] [Green Version]
  31. Byrne, J.M.; Kappler, A. Current and Future Microbiological Strategies to Remove as and Cd from Drinking Water. Microb. Biotechnol. 2017, 10, 1098–1101. [Google Scholar] [CrossRef] [Green Version]
  32. Trivedi, P.; Schenk, P.M.; Wallenstein, M.D.; Singh, B.K. Tiny Microbes, Big Yields: Enhancing Food Crop Production with Biological Solutions. Microb. Biotechnol. 2017, 10, 999–1003. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  33. Backer, R.; Rokem, J.S.; Ilangumaran, G.; Lamont, J.; Praslickova, D.; Ricci, E.; Subramanian, S.; Smith, D.L. Plant Growth-Promoting Rhizobacteria: Context, Mechanisms of Action, and Roadmap to Commercialization of Biostimulants for Sustainable Agriculture. Front. Plant Sci. 2018, 9. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  34. Syed Ab Rahman, S.F.; Singh, E.; Pieterse, C.M.J.; Schenk, P.M. Emerging Microbial Biocontrol Strategies for Plant Pathogens. Plant Sci. 2018, 267, 102–111. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  35. Kawacka, I.; Olejnik-Schmidt, A.; Schmidt, M.; Sip, A. Effectiveness of Phage-Based Inhibition of Listeria monocytogenes in Food Products and Food Processing Environments. Microorganisms 2020, 8, 1764. [Google Scholar] [CrossRef] [PubMed]
  36. Romero-Calle, D.; Guimarães Benevides, R.; Góes-Neto, A.; Billington, C. Bacteriophages as Alternatives to Antibiotics in Clinical Care. Antibiotics 2019, 8, 138. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  37. Nowakiewicz, A.; Zięba, P.; Gnat, S.; Matuszewski, Ł. Last Call for Replacement of Antimicrobials in Animal Production: Modern Challenges, Opportunities, and Potential Solutions. Antibiotics 2020, 9, 883. [Google Scholar] [CrossRef]
  38. Goicoechea, N.; Antolín, M.C. Increased Nutritional Value in Food Crops. Microb. Biotechnol. 2017, 10, 1004–1007. [Google Scholar] [CrossRef] [Green Version]
  39. Pedone-Bonfim, M.V.L.; da Silva, F.S.B.; Maia, L.C. Production of Secondary Metabolites by Mycorrhizal Plants with Medicinal or Nutritional Potential. Acta Physiol. Plant. 2015, 37, 27. [Google Scholar] [CrossRef]
  40. García, J.L.; de Vicente, M.; Galán, B. Microalgae, Old Sustainable Food and Fashion Nutraceuticals. Microb. Biotechnol. 2017, 10, 1017–1024. [Google Scholar] [CrossRef] [Green Version]
  41. Molino, A.; Iovine, A.; Casella, P.; Mehariya, S.; Chianese, S.; Cerbone, A.; Rimauro, J.; Musmarra, D. Microalgae Characterization for Consolidated and New Application in Human Food, Animal Feed and Nutraceuticals. Int. J. Environ. Res. Public Health 2018, 15, 2436. [Google Scholar] [CrossRef] [Green Version]
  42. Immerseel, F.V.; Eeckhaut, V.; Moore, R.J.; Choct, M.; Ducatelle, R. Beneficial Microbial Signals from Alternative Feed Ingredients: A Way to Improve Sustainability of Broiler Production? Microb. Biotechnol. 2017, 10, 1008–1011. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  43. Berbegal, C.; Spano, G.; Fragasso, M.; Grieco, F.; Russo, P.; Capozzi, V. Starter Cultures as Biocontrol Strategy to Prevent Brettanomyces bruxellensis Proliferation in Wine. Appl. Microbiol. Biotechnol. 2018, 102, 569–576. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  44. Berbegal, C.; Garofalo, C.; Russo, P.; Pati, S.; Capozzi, V.; Spano, G. Use of Autochthonous Yeasts and Bacteria in Order to Control Brettanomyces bruxellensis in Wine. Fermentation 2017, 3, 65. [Google Scholar] [CrossRef] [Green Version]
  45. Odedina, G.F.; Vongkamjan, K.; Voravuthikunchai, S.P. Potential Bio-Control Agent from Rhodomyrtus tomentosa against Listeria monocytogenes. Nutrients 2015, 7, 7451–7468. [Google Scholar] [CrossRef] [Green Version]
  46. Russo, P.; Fares, C.; Longo, A.; Spano, G.; Capozzi, V. Lactobacillus plantarum with Broad Antifungal Activity as a Protective Starter Culture for Bread Production. Foods 2017, 6, 110. [Google Scholar] [CrossRef] [Green Version]
  47. Arena, M.P.; Russo, P.; Spano, G.; Capozzi, V. Exploration of the Microbial Biodiversity Associated with North Apulian Sourdoughs and the Effect of the Increasing Number of Inoculated Lactic Acid Bacteria Strains on the Biocontrol against Fungal Spoilage. Fermentation 2019, 5, 97. [Google Scholar] [CrossRef] [Green Version]
  48. De Simone, N.; Capozzi, V.; Amodio, M.L.; Colelli, G.; Spano, G.; Russo, P. Microbial-Based Biocontrol Solutions for Fruits and Vegetables: Recent Insight, Patents, and Innovative Trends. Recent Pat. Food Nutr. Agric. 2021. [Google Scholar] [CrossRef]
  49. Fang, Q.; Du, M.; Chen, J.; Liu, T.; Zheng, Y.; Liao, Z.; Zhong, Q.; Wang, L.; Fang, X.; Wang, J. Degradation and Detoxification of Aflatoxin B1 by Tea-Derived Aspergillus niger RAF106. Toxins 2020, 12, 777. [Google Scholar] [CrossRef]
  50. Ji, C.; Fan, Y.; Zhao, L. Review on Biological Degradation of Mycotoxins. Anim. Nutr. 2016, 2, 127–133. [Google Scholar] [CrossRef]
  51. Russo, P.; Capozzi, V.; Spano, G.; Corbo, M.R.; Sinigaglia, M.; Bevilacqua, A. Metabolites of Microbial Origin with an Impact on Health: Ochratoxin A and Biogenic Amines. Front. Microbiol. 2016, 7, 482. [Google Scholar] [CrossRef]
  52. Nardi, T. Microbial Resources as a Tool for Enhancing Sustainability in Winemaking. Microorganisms 2020, 8, 507. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  53. Mannazzu, I.; Domizio, P.; Carboni, G.; Zara, S.; Zara, G.; Comitini, F.; Budroni, M.; Ciani, M. Yeast Killer Toxins: From Ecological Significance to Application. Crit. Rev. Biotechnol. 2019, 39, 603–617. [Google Scholar] [CrossRef] [PubMed]
  54. Bai, J.; Kim, Y.-T.; Ryu, S.; Lee, J.-H. Biocontrol and Rapid Detection of Food-Borne Pathogens Using Bacteriophages and Endolysins. Front. Microbiol. 2016, 7, 474. [Google Scholar] [CrossRef] [PubMed]
  55. Arena, M.P.; Caggianiello, G.; Russo, P.; Albenzio, M.; Massa, S.; Fiocco, D.; Capozzi, V.; Spano, G. Functional Starters for Functional Yogurt. Foods 2015, 4, 15–33. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  56. Yépez, A.; Russo, P.; Spano, G.; Khomenko, I.; Biasioli, F.; Capozzi, V.; Aznar, R. In Situ Riboflavin Fortification of Different Kefir-like Cereal-Based Beverages Using Selected Andean LAB Strains. Food Microbiol. 2019, 77, 61–68. [Google Scholar] [CrossRef]
  57. Capozzi, V.; Russo, P.; Fragasso, M.; de Vita, P.; Fiocco, D.; Spano, G. Biotechnology and Pasta-Making: Lactic Acid Bacteria as a New Driver of Innovation. Front. Microbiol. 2012, 3. [Google Scholar] [CrossRef] [Green Version]
  58. Melini, F.; Melini, V.; Luziatelli, F.; Ficca, A.G.; Ruzzi, M. Health-Promoting Components in Fermented Foods: An Up-to-Date Systematic Review. Nutrients 2019, 11, 1189. [Google Scholar] [CrossRef] [Green Version]
  59. Petrova, P.; Petrov, K. Lactic Acid Fermentation of Cereals and Pseudocereals: Ancient Nutritional Biotechnologies with Modern Applications. Nutrients 2020, 12, 1118. [Google Scholar] [CrossRef] [Green Version]
  60. Krausova, G.; Kana, A.; Hyrslova, I.; Mrvikova, I.; Kavkova, M. Development of Selenized Lactic Acid Bacteria and Their Selenium Bioaccummulation Capacity. Fermentation 2020, 6, 91. [Google Scholar] [CrossRef]
  61. Sergeev, I.N.; Aljutaily, T.; Walton, G.; Huarte, E. Effects of Synbiotic Supplement on Human Gut Microbiota, Body Composition and Weight Loss in Obesity. Nutrients 2020, 12, 222. [Google Scholar] [CrossRef] [Green Version]
  62. Arena, M.P.; Russo, P.; Capozzi, V.; Rascón, A.; Felis, G.E.; Spano, G.; Fiocco, D. Combinations of Cereal β-Glucans and Probiotics Can Enhance the Anti-Inflammatory Activity on Host Cells by a Synergistic Effect. J. Funct. Foods 2016, 23, 12–23. [Google Scholar] [CrossRef]
  63. Markowiak, P.; Śliżewska, K. Effects of Probiotics, Prebiotics, and Synbiotics on Human Health. Nutrients 2017, 9, 1021. [Google Scholar] [CrossRef] [PubMed]
  64. Pérez-Ramos, A.; Mohedano, M.L.; López, P.; Spano, G.; Fiocco, D.; Russo, P.; Capozzi, V. In Situ β-Glucan Fortification of Cereal-Based Matrices by Pediococcus parvulus 2.6: Technological Aspects and Prebiotic Potential. Int. J. Mol. Sci. 2017, 18, 1588. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  65. O’Toole, P.W.; Paoli, M. The Contribution of Microbial Biotechnology to Sustainable Development Goals: Microbiome Therapies. Microb. Biotechnol. 2017, 10, 1066–1069. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  66. Satokari, R. Modulation of Gut Microbiota for Health by Current and Next-Generation Probiotics. Nutrients 2019, 11, 1921. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  67. Shinde, T.; Hansbro, P.M.; Sohal, S.S.; Dingle, P.; Eri, R.; Stanley, R. Microbiota Modulating Nutritional Approaches to Countering the Effects of Viral Respiratory Infections Including SARS-CoV-2 through Promoting Metabolic and Immune Fitness with Probiotics and Plant Bioactives. Microorganisms 2020, 8, 921. [Google Scholar] [CrossRef]
  68. Barathikannan, K.; Chelliah, R.; Rubab, M.; Daliri, E.B.-M.; Elahi, F.; Kim, D.-H.; Agastian, P.; Oh, S.-Y.; Oh, D.H. Gut Microbiome Modulation Based on Probiotic Application for Anti-Obesity: A Review on Efficacy and Validation. Microorganisms 2019, 7, 456. [Google Scholar] [CrossRef] [Green Version]
  69. Berbegal, C.; Fragasso, M.; Russo, P.; Bimbo, F.; Grieco, F.; Spano, G.; Capozzi, V. Climate Changes and Food Quality: The Potential of Microbial Activities as Mitigating Strategies in the Wine Sector. Fermentation 2019, 5, 85. [Google Scholar] [CrossRef] [Green Version]
  70. Karlović, A.; Jurić, A.; Ćorić, N.; Habschied, K.; Krstanović, V.; Mastanjević, K. By-Products in the Malting and Brewing Industries—Re-Usage Possibilities. Fermentation 2020, 6, 82. [Google Scholar] [CrossRef]
  71. Mora-Villalobos, J.A.; Montero-Zamora, J.; Barboza, N.; Rojas-Garbanzo, C.; Usaga, J.; Redondo-Solano, M.; Schroedter, L.; Olszewska-Widdrat, A.; López-Gómez, J.P. Multi-Product Lactic Acid Bacteria Fermentations: A Review. Fermentation 2020, 6, 23. [Google Scholar] [CrossRef] [Green Version]
  72. Costa, S.; Summa, D.; Semeraro, B.; Zappaterra, F.; Rugiero, I.; Tamburini, E. Fermentation as a Strategy for Bio-Transforming Waste into Resources: Lactic Acid Production from Agri-Food Residues. Fermentation 2021, 7, 3. [Google Scholar] [CrossRef]
  73. Krull, S.; Brock, S.; Prüße, U.; Kuenz, A. Hydrolyzed Agricultural Residues—Low-Cost Nutrient Sources for l-Lactic Acid Production. Fermentation 2020, 6, 97. [Google Scholar] [CrossRef]
  74. Alexandri, M.; López-Gómez, J.P.; Olszewska-Widdrat, A.; Venus, J. Valorising Agro-Industrial Wastes within the Circular Bioeconomy Concept: The Case of Defatted Rice Bran with Emphasis on Bioconversion Strategies. Fermentation 2020, 6, 42. [Google Scholar] [CrossRef]
  75. Kurniawan, A.; Kwon, S.Y.; Shin, J.-H.; Hur, J.; Cho, J. Acid Fermentation Process Combined with Post Denitrification for the Treatment of Primary Sludge and Wastewater with High Strength Nitrate. Water 2016, 8, 117. [Google Scholar] [CrossRef] [Green Version]
  76. Souza Filho, P.F.; Brancoli, P.; Bolton, K.; Zamani, A.; Taherzadeh, M.J. Techno-Economic and Life Cycle Assessment of Wastewater Management from Potato Starch Production: Present Status and Alternative Biotreatments. Fermentation 2017, 3, 56. [Google Scholar] [CrossRef] [Green Version]
  77. Harb, M.; Hong, P.-Y. Anaerobic Membrane Bioreactor Effluent Reuse: A Review of Microbial Safety Concerns. Fermentation 2017, 3, 39. [Google Scholar] [CrossRef] [Green Version]
  78. Capozzi, V.; Fragasso, M.; Russo, P. Microbiological Safety and the Management of Microbial Resources in Artisanal Foods and Beverages: The Need for a Transdisciplinary Assessment to Conciliate Actual Trends and Risks Avoidance. Microorganisms 2020, 8, 306. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  79. Capozzi, V.; Russo, P.; Spano, G. Microbial Information Regimen in EU Geographical Indications. World Pat. Inf. 2012, 34, 229–231. [Google Scholar] [CrossRef]
  80. Spano, G.; Capozzi, V. Food Microbial Biodiversity and “Microbes of Protected Origin”. Front. Microbiol. 2011, 2. [Google Scholar] [CrossRef] [Green Version]
  81. Matassa, S.; Boon, N.; Pikaar, I.; Verstraete, W. Microbial Protein: Future Sustainable Food Supply Route with Low Environmental Footprint. Microb. Biotechnol. 2016, 9, 568–575. [Google Scholar] [CrossRef]
  82. Kårlund, A.; Gómez-Gallego, C.; Korhonen, J.; Palo-oja, O.-M.; El-Nezami, H.; Kolehmainen, M. Harnessing Microbes for Sustainable Development: Food Fermentation as a Tool for Improving the Nutritional Quality of Alternative Protein Sources. Nutrients 2020, 12, 1020. [Google Scholar] [CrossRef] [Green Version]
  83. Berbegal, C.; Borruso, L.; Fragasso, M.; Tufariello, M.; Russo, P.; Brusetti, L.; Spano, G.; Capozzi, V. A Metagenomic-Based Approach for the Characterization of Bacterial Diversity Associated with Spontaneous Malolactic Fermentations in Wine. Int. J. Mol. Sci. 2019, 20, 3980. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  84. Russo, P.; Spano, G.; Capozzi, V. Safety evaluation of starter cultures. In Starter Cultures in Food Production; John Wiley & Sons, Ltd.: Hoboken, NJ, USA, 2017; pp. 101–128. ISBN 978-1-118-93379-4. [Google Scholar]
  85. Stackebrandt, E.; Schüngel, M.; Martin, D.; Smith, D. The Microbial Resource Research Infrastructure MIRRI: Strength through Coordination. Microorganisms 2015, 3, 890–902. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  86. De Vero, L.; Boniotti, M.B.; Budroni, M.; Buzzini, P.; Cassanelli, S.; Comunian, R.; Gullo, M.; Logrieco, A.F.; Mannazzu, I.; Musumeci, R.; et al. Preservation, Characterization and Exploitation of Microbial Biodiversity: The Perspective of the Italian Network of Culture Collections. Microorganisms 2019, 7, 685. [Google Scholar] [CrossRef] [Green Version]
  87. de Bono, E. Lateral Thinking; Creativity Step by Step; Penguin: London, UK, 1970. [Google Scholar]
  88. Topleva, S.A.; Prokopov, T.V. Integrated Business Model for Sustainability of Small and Medium-Sized Enterprises in the Food Industry: Creating Value Added through Ecodesign. Br. Food J. 2020, 122, 1463–1483. [Google Scholar] [CrossRef]
  89. Toussaint, M.; Cabanelas, P.; González-Alvarado, T.E. What about the Consumer Choice? The Influence of Social Sustainability on Consumer’s Purchasing Behavior in the Food Value Chain. Eur. Res. Manag. Bus. Econ. 2021, 27, 100134. [Google Scholar] [CrossRef]
  90. Demain, A.L. Microbial Biotechnology. Trends Biotechnol. 2000, 18, 26–31. [Google Scholar] [CrossRef] [Green Version]
  91. Pakseresht, A.; McFadden, B.R.; Lagerkvist, C.J. Consumer Acceptance of Food Biotechnology Based on Policy Context and Upstream Acceptance: Evidence from an Artefactual Field Experiment. Eur. Rev. Agric. Econ. 2017, 44, 757–780. [Google Scholar] [CrossRef] [Green Version]
  92. McFadden, J.R.; Huffman, W.E. Consumer Valuation of Information about Food Safety Achieved Using Biotechnology: Evidence from New Potato Products. Food Policy 2017, 69, 82–96. [Google Scholar] [CrossRef] [Green Version]
  93. Roman, M.; Varga, H.; Cvijanovic, V.; Reid, A. Quadruple Helix Models for Sustainable Regional Innovation: Engaging and Facilitating Civil Society Participation. Economies 2020, 8, 48. [Google Scholar] [CrossRef]
  94. Leydesdorff, L. The Triple Helix, Quadruple Helix, …, and an N-Tuple of Helices: Explanatory Models for Analyzing the Knowledge-Based Economy? J. Knowl. Econ. 2012, 3, 25–35. [Google Scholar] [CrossRef] [Green Version]
  95. Tobi, R.C.A.; Harris, F.; Rana, R.; Brown, K.A.; Quaife, M.; Green, R. Sustainable Diet Dimensions. Comparing Consumer Preference for Nutrition, Environmental and Social Responsibility Food Labelling: A Systematic Review. Sustainability 2019, 11, 6575. [Google Scholar] [CrossRef] [Green Version]
  96. Timmis, K.; de Lorenzo, V.; Verstraete, W.; Ramos, J.L.; Danchin, A.; Brüssow, H.; Singh, B.K.; Timmis, J.K. The Contribution of Microbial Biotechnology to Economic Growth and Employment Creation. Microb. Biotechnol. 2017, 10, 1137–1144. [Google Scholar] [CrossRef] [PubMed]
  97. Doyle, M.P.; Steenson, L.R.; Meng, J. Bacteria in Food and Beverage Production. In The Prokaryotes: Applied Bacteriology and Biotechnology; Rosenberg, E., DeLong, E.F., Lory, S., Stackebrandt, E., Thompson, F., Eds.; Springer: Berlin/Heidelberg, Germany, 2013; pp. 241–256. ISBN 978-3-642-31331-8. [Google Scholar]
  98. Timmis, K.; Cavicchioli, R.; Garcia, J.L.; Nogales, B.; Chavarría, M.; Stein, L.; McGenity, T.J.; Webster, N.; Singh, B.K.; Handelsman, J.; et al. The Urgent Need for Microbiology Literacy in Society. Environ. Microbiol. 2019, 21, 1513–1528. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  99. Galanakis, C.M. The Food Systems in the Era of the Coronavirus (COVID-19) Pandemic Crisis. Foods 2020, 9, 523. [Google Scholar] [CrossRef]
  100. Eilam, E.; Prasad, V.; Widdop Quinton, H. Climate Change Education: Mapping the Nature of Climate Change, the Content Knowledge and Examination of Enactment in Upper Secondary Victorian Curriculum. Sustainability 2020, 12, 591. [Google Scholar] [CrossRef] [Green Version]
  101. Capozzi, V.; Spano, G.; Fiocco, D. Transdisciplinarity and Microbiology Education. J. Microbiol. Biol. Educ. JMBE 2012, 13, 70–73. [Google Scholar] [CrossRef] [PubMed] [Green Version]
Figure 1. Nutritional enhancement in fermented foods; reproduced from Sharma et al. [10].
Figure 1. Nutritional enhancement in fermented foods; reproduced from Sharma et al. [10].
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Figure 2. ‘Dimensions of food security’; reproduced from Matkovski et al. [21].
Figure 2. ‘Dimensions of food security’; reproduced from Matkovski et al. [21].
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Figure 3. ‘Domains within a sustainable food system framework’; reproduced from Tobi et al. [95].
Figure 3. ‘Domains within a sustainable food system framework’; reproduced from Tobi et al. [95].
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Table 1. Example of tailored initiatives of policy organisations.
Table 1. Example of tailored initiatives of policy organisations.
OrganisationInitiativesWebsite
United Nations General Assembly2030 Agenda, Sustainable Development Goals (SDGs)https://www.un.org/sustainabledevelopment/, accessed on 13 December 2020
Food and Agriculture Organization (FAO)Food and agriculture in the 2030 Agenda for Sustainable Developmenthttp://www.fao.org/sustainable-development-goals/en/, accessed on 10 January 2021
European CommissionFood 2030https://ec.europa.eu/info/research-and-innovation/research-area/food-systems/food-2030_en, accessed on 14 December 2020
United States Environmental Protection AgencySustainable Management of Foodhttps://www.epa.gov/sustainable-management-food, accessed on 21 December 2020
United Kingdom GovernmentFood Industry Sustainability Strategy (FISS)https://www.gov.uk/government/publications/food-industry-sustainability-strategy-fiss, accessed on 20 November 2020
Table 2. A non-exhaustive list of possible microbial-based solutions as potential mitigating strategies against negative externalities.
Table 2. A non-exhaustive list of possible microbial-based solutions as potential mitigating strategies against negative externalities.
Microbial Biotechnologies to Counteract/Prevent Negative ExternalitiesRef.
Biological fixation of nitrogen[22,23,24]
Alternative nitrogen sources to be used as feed or food[19]
Microbial protein production[19,25]
Microbial biotechnology for CO2 capture[19,22]
Microbial biotechnology to limit diffuse methane emissions[19]
Microbial-based bioconversion of pollutants in water[19,26,27]
Microbial-based bioremediation of soil[28,29]
Microbial biotechnologies for potable water production[30,31]
Biodegradation of endocrine disruptors from trophic chains[22]
Optimisation of microbial biofertilizers/biostimulants [32,33]
Optimisation of microbial biopesticides[32,34]
Bioprotection and alternatives to antibiotics[35,36,37]
Rhizospheric microorganisms for improving the nutrient quality of crops[38,39]
Beneficial plant-microbe interactions to breed ‘microbe-optimized plants’[32]
Microalgae and new application in food, feed, and nutraceuticals chains[40,41]
Microbial-based tailored solutions for sustainable feeding regimen[42]
Table 3. A non-exhaustive list of possible microbial-based solutions as potential mitigating strategies against negative externalities.
Table 3. A non-exhaustive list of possible microbial-based solutions as potential mitigating strategies against negative externalities.
Fermentative Processes to Counteract/Prevent Negative ExternalitiesRef.
Microbial-based biocontrol of microbial pathogens and spoilers[43,44,45,46,47,48]
Microbial-based degradation of chemical contaminants[49,50,51]
Bioprotection and alternatives to chemical preservatives[52,53,54]
Microbial production of nutrients[55,56,57]
Microbes to improve nutrient bioavailability[10,58,59,60]
Synbiotic approaches to improve human health and well-being[61,62,63,64]
Microbial biotechnology and microbiome therapies[65,66,67,68]
Microbial resources and strategies to save energy during fermentation[52,69]
Fermentative valorization of foods by-products[52,70,71]
Fermentative valorization of foods wastes[72,73,74]
Microbial-based valorization of wastewater associated with food systems[75,76,77]
Strategies to preserve microbial diversity associated with food fermentation[78,79,80]
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Capozzi, V.; Fragasso, M.; Bimbo, F. Microbial Resources, Fermentation and Reduction of Negative Externalities in Food Systems: Patterns toward Sustainability and Resilience. Fermentation 2021, 7, 54. https://doi.org/10.3390/fermentation7020054

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Capozzi V, Fragasso M, Bimbo F. Microbial Resources, Fermentation and Reduction of Negative Externalities in Food Systems: Patterns toward Sustainability and Resilience. Fermentation. 2021; 7(2):54. https://doi.org/10.3390/fermentation7020054

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Capozzi, Vittorio, Mariagiovanna Fragasso, and Francesco Bimbo. 2021. "Microbial Resources, Fermentation and Reduction of Negative Externalities in Food Systems: Patterns toward Sustainability and Resilience" Fermentation 7, no. 2: 54. https://doi.org/10.3390/fermentation7020054

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