From Waste to Worth: The Role of Fermentation in a Sustainable Future
Abstract
1. Introduction—Sustainability and the Challenges of Contemporary Food Systems
2. Fermentation and Sustainable Development Goals (SDGs)
- Indicator 2.1.1 (Prevalence of undernourishment) is relevant to fermentation contributions to alternative protein sources;
- Indicator 2.3.1 (Volume of production per labour unit by classes of farming/pastoral/forestry enterprise size) can be influenced by fermentation-enhanced biostimulants and biofertilizers;
- Indicator 12.5.1 (National recycling rate, tons of material recycled) reflects fermentation’s role in valorizing bioeconomy side streams;
- Indicator 7.2.1 (Renewable energy share in total final energy consumption) captures biofuels and biogas production through fermentation;
- Indicator 13.2.1 (Number of countries that have communicated the establishment or operationalization of an integrated policy/strategy/plan which increases their ability to adapt to the adverse impacts of climate change, and foster climate resilience and low greenhouse gas emissions development in a manner that does not threaten food production (including a national adaptation plan, nationally determined contribution, national communication, biennial update report or other)) aligns with fermentation-based climate resilience technologies.
3. Definition and Types of Fermentation, the Importance of the Fermenta-Tion Process
3.1. Definition and Functional Role of Fermentation
3.2. Major Types of Fermentation
3.2.1. Classification by Metabolic Pathway
3.2.2. Classification by Production System Configuration
3.3. Strategic Importance in Food Systems and Human Nutrition
4. Fermentation in the Circular Bioeconomy
5. Valorization of Organic Waste Through Fermentation
5.1. Single-Cell Protein (SCP)
5.2. Biofuels
5.3. Organic Acids
5.4. Bioactive Compounds
5.5. Enzymes
6. Precision Fermentation—A Biotechnological Tool of the Future
7. Microbiome and Fermentation as an Element of a Health Strategy
8. Postbiotics and Sustainable Development
9. Challenges and Limitations of Fermentation-Based Waste Valorization
10. Concluding Perspectives
- −
- Resilient supply chains ensuring consistent feedstock quality,
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- Low-energy pretreatment and decentralized processing (e.g., solid-state fermentation),
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- Efficient downstream recovery strategies,
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- Clear regulatory frameworks for food-grade and feed applications,
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- Scaling technology and transferring knowledge to industry, while maintaining process safety and stability,
- −
- Life cycle assessment and environmental impact analysis to ensure real climate and environmental benefits,
- −
- Building social acceptance and consumer awareness of biotechnological value recovery methods,
- −
- Integrating fermentation with other bioprocess technologies within integrated biorefinery production systems.
Author Contributions
Funding
Institutional Review Board Statement
Informed Consent Statement
Data Availability Statement
Acknowledgments
Conflicts of Interest
Abbreviations
| SDGs | Sustainable Development Goals |
| GHG | Green-house gas |
| LAB | Lactic acid bacteria |
| SmF | Submerged fermentation |
| SSF | Solid-state fermentation |
| SCP | Single-cell protein |
| BDO | 2,3-butanediol |
| LCA | Life cycle assessment |
| LA | Lactic acid |
| CA | Citric acid |
| AA | Acetic acid |
| PFA | Precision Fermentation Alliance |
| FFE | Food Fermentation Europe |
| GRAS | Generally Recognized As Safe |
| FDA | Food and Drug Administration |
| EU | European Union |
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| Microorganism/Product | Substrate | SSF vs. SmF | Key Observation | Reference |
|---|---|---|---|---|
| Neurospora sitophila– cellulases | Wheat straw | SSF >> SmF | Higher cellulase activity in SSF | [60] |
| Aspergillus niger– cellulases | Coir waste | SSF >> SmF | SSF significantly increases cellulase activity | [61] |
| Aspergillus brasiliensis–inulinase/invertase | Agro residues | SSF > SmF | SSF improves enzyme production | [62] |
| Aspergillus oryzae– secreted proteins | Defined medium | Mode-dependent | Different growth/product profiles in SSF vs. SmF | [63] |
| Aspergillus niger–citric acid (industrial) | Sugars/molasses | SmF preferred | Commercial citric acid is mainly produced via SmF | [64] |
| Source of Waste | Microorganism | Product Obtained | References |
|---|---|---|---|
| Mango, prickly custard apple, pineapple, papaya, banana, mangosteen, cashew apple, cacao, jackfruit, and pomegranate | Saccharomyces cerevisiae | Single-cell proteins | [90] |
| Pineapple waste | Saccharomyces cerevisiae | Single-cell proteins | [91] |
| Orange, banana, sugarcane, garlic, and potato peels | Aspergillus niger | Single-cell proteins | [92] |
| Banana peel, citrus peel, carrot pomace, and potato peel | Saccharomyces cerevisiae | Single-cell proteins | [93] |
| Bread waste | Rhizopus delemar CBS 145940 | Protein biomass | [94] |
| Potato protein liquor | Rhizopus delemar | Protein biomass | [95] |
| Coffee wastewater | Candida sorboxylosa | Single-cell proteins | [96] |
| Source of Waste | Microorganism | Product Obtained | References |
|---|---|---|---|
| Leftover bread | Enterobacter ludwigii | 2,3-butanediol | [98] |
| Food waste | Fusarium oxysporum Saccharomyces cerevisiae | Ethanol | [99] |
| Kitchen waste | Saccharomyces cerevisiae and Pichia stipites | Ethanol | [100] |
| Corn by-products | Clostridium beijerinckii | Butanol | [101,102] |
| De-oiled rice bran | Clostridium acetobutylicum YM1 | Biohydrogen | [103] |
| Vegetable waste | Buttiauxella sp. 4, Rahnella sp. 10 and Raoultella sp. 47 | Biohydrogen | [104] |
| Source of Waste | Microorganism | Product Obtained | References |
|---|---|---|---|
| Cassava bagassa | Lactobacillus casei and Lactobacillus delbrueckii | Lactic acid | [107] |
| Restaurant waste | Streptococcus sp. Lactobacillus sp. | Lactic acid | [108] |
| Wood hydrolyzate | Enterococcus faecalis | Lactic acid | [109] |
| Orange peel | Lactobacillus delbrueckii | Lactic acid | [110] |
| Ricotta whey and pear residues | Lactobacillus casei DSM 20011 | Lactic acid | [110] |
| Pomegranate peel waste | Aspergillus niger | Citric acid | [111] |
| Banana peel | Aspergillus niger | Citric acid | [112] |
| Apple pomace | Aspergillus niger | Citric acid | [113] |
| Brewery wastes | Aspergillus niger | Citric acid | [114] |
| Cocoa pod husks | Aspergillus niger | Citric acid | [115] |
| Kitchen waste | Lactobacillus plantarum | Acetic acid | [116] |
| Pineapple peels | Acetobacter pasteurianus FPB2-3 | Acetic acid | [117] |
| Switchgrass, wheat straw, and sugarcane straw | Moorella thermoacetica and Aurantiochytrium limacinum | Acetic acid | [118] |
| Source of Waste | Microorganism | Product Obtained | References |
|---|---|---|---|
| Pineapple peels | Lactobacillus plantarum, Lactobacillus rhamnosus, and Aspergillus oryzae | Phenolic compounds, Antioxidant and anti-inflammatory activity | [123] |
| Rice bran | Rizhopus oryzae | Ferulic acid, gallic acid, and antioxidant activity | [124] |
| Soybean dregs | Neurospora crassa | Prebiotics | [125] |
| Crude olive pomace | Aspergillus niger | Phenolic compounds, antioxidant activity | [126] |
| Pineapple and guava wastes | Rhizopus oligosporus | Phenolic content, antioxidant activity, and antiamylolytic activity | [127] |
| Peanut press cake | Aspergillusawamori | Phenolic and antioxidant properties | [128] |
| Apricot press residues | Aspergillus niger and Rhizopus oligosporus | Quercetin 3-acetyl-glucoside, chlorogenic acid, neochlorogenic acid, rutin | [129] |
| Source of Waste | Microorganism | Product Obtained | References |
|---|---|---|---|
| Mango kernel | Fusarium solani | α-amylase | [134] |
| Groundnut, coconut, and sesame oil cakes | Aspergillus oryzae | α-amylase | [135] |
| Corn pericarp, rice bran, and wheat bran | Bacillus siamensis YC-9 | Protease, α-amylase, and cellulase | [136] |
| Banana peel | Yarrowia phangngaensis | Pectinases | [137] |
| Coffee pulp | Aspergillus sp. VTM5 | Pectinase | [138] |
| Peels of orange, banana, carrot, lemon, sweet lime, and apple | Aspergillus. cervinus ARS2 | Pectinase | [139] |
| Wheat bran, soybean meal | Aspergillus niger | Protease | [140] |
| Andiroba oil cake and soybean meal | Yarrowia lipolytica | Lipase | [141] |
| Castor bean biodiesel | Penicillium simplicissimum | Lipase | [142] |
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Share and Cite
Gabriele, M.; Peres Fabbri, L.; Ventimiglia, M.; Łepecka, A. From Waste to Worth: The Role of Fermentation in a Sustainable Future. Foods 2026, 15, 664. https://doi.org/10.3390/foods15040664
Gabriele M, Peres Fabbri L, Ventimiglia M, Łepecka A. From Waste to Worth: The Role of Fermentation in a Sustainable Future. Foods. 2026; 15(4):664. https://doi.org/10.3390/foods15040664
Chicago/Turabian StyleGabriele, Morena, Laryssa Peres Fabbri, Maria Ventimiglia, and Anna Łepecka. 2026. "From Waste to Worth: The Role of Fermentation in a Sustainable Future" Foods 15, no. 4: 664. https://doi.org/10.3390/foods15040664
APA StyleGabriele, M., Peres Fabbri, L., Ventimiglia, M., & Łepecka, A. (2026). From Waste to Worth: The Role of Fermentation in a Sustainable Future. Foods, 15(4), 664. https://doi.org/10.3390/foods15040664

