Lactic acid bacteria (LAB), a group of Gram-positive microorganisms, are recognized as biological agents for food preservation and pathogen management due to their ability to suppress spoilage and pathogenic microbes. These bacteria produce a variety of antimicrobial chemicals, including antifungal and antibacterial agents, which effectively suppress the growth of harmful pathogens and enhance food safety. This review aims to explore the functional capabilities of LAB as bio-control agents and biological food preservatives, with a focus on their taxonomy and diverse applications in the food and health industries. The utilization of LAB as biological preservation agents is especially advantageous due to their Generally Recognized as Safe (GRAS) classification, which makes them a safer option to standard chemical preservatives. LAB provides a biological control strategy that uses living organisms to manage infections and prevent food spoilage. Their methods of action include hyper-parasitism, predation, antibiotic synthesis, lytic enzyme activity, and generation of host resistance. The potential and applications of LAB go beyond food preservation; they also play an important role in the prevention of infectious diseases due to their antibacterial properties. LAB provides an environmentally friendly and effective alternative to chemical preservatives. Further research on the optimization of LAB strains for specific applications and improved genetic engineering could expand their industrial and therapeutic roles. By emphasizing the benefits of LAB in enhancing food safety and quality, this paper advocates for their integration into contemporary food preservation practices as a sustainable alternative to chemical preservatives.
| Published in | Science Frontiers (Volume 6, Issue 4) |
| DOI | 10.11648/j.sf.20250604.15 |
| Page(s) | 159-169 |
| Creative Commons |
This is an Open Access article, distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution and reproduction in any medium or format, provided the original work is properly cited. |
| Copyright |
Copyright © The Author(s), 2025. Published by Science Publishing Group |
Biological Food Preservation, Biocontrol Agents, Lactic Acid Bacteria, Food-borne Pathogens, Food Spoilage Bacteria
S. N | LAB Groups/Species | Products | Targeted pathogens due to specific Bacteriocin | Reference |
|---|---|---|---|---|
1 | Enterococcus faecium | Enterocin X | L. monocytogenes | [5 3] |
2 | Lactobacillus bulgaricus | Carbon Dioxide | Bacillus subtilis | [5 4] |
3 | Lactobacillus sakei | Nisin | Staphylococcus aureus | [5 5] |
4 | Lactococcus lactis sub spp. Cremoris | Nisin | L. monocytogenes and S. aureus | [5 5, 56] |
5 | Staphylococcus aureus | Aureocin | Bovine mastitis | [5 6] |
6 | Staphylococcus simulans | Lysostaphin | S. aureus | [ 58] |
7 | Carnobacterium maltaromaticum C2 | Carnobacteriocin X | L. monocytogenes | [ 59] |
8 | Propionibacterium freudenreichii | Propionic Acid | L. monocytogenes, Clostridium spp. | [5 3] |
9 | Lactobacillus acidophilus | Hydrogen Peroxide | Bacillus subtilis, Salmonella spp. | [6 0] |
10 | Lactobacillus sakei | Sakacin P | Listeria monocytogenes | [6 1] |
11 | Leuconostoc mesenteroides | Diacetyl | Listeria monocytogenes | [ 59] |
12 | Lactobacillus casei | Lactic Acid | Salmonella typhimurium | [5 4] |
13 | Lactobacillus brevis | Acetic Acid | E. coli, Bacillus cereus | [5 5] |
14 | Streptococcus thermophilus | Hydrogen Peroxide | Pseudomonas aeruginosa | [5 4] |
15 | Enterococcus hirae | Enterocin P | S. aureus, Salmonella spp. | [5 3] |
16 | Lactococcus lactis | Carbon Dioxide | S. aureus, Listeria monocytogenes | [5 7] |
17 | Lactobacillus delbrueckii | Hydrogen Peroxide | Staphylococcus aureus, E. coli | [6 2] |
18 | Lactococcus lactis subsp. cremoris | Nisin | Bacillus cereus | [6 3] |
19 | Saccharomyces cerevisiae | Ethanol | Not pathogen-specific; fermentation applications | [6 4] |
20 | Bifidobacterium bifidum NCFB 1454 | Bifidocin B | Bacillus, Enterococcus, Lactobacillus, Leuconostoc, Listeria, and Pediococcus | [6 3] |
21 | Lactobacillus reuteri TMW 1.656 | Reutericyclin | Escherichia coli, Salmonella enterica | [6 5] |
22 | Enterococcus faecium | Enterocin A | Listeria monocytogenes | [6 6] |
23 | Pediococcus pentosaceus ATCC 43200 | Pediocin AcH | Listeria innocua, Bacillus cereus | [7 3] |
24 | Streptococcus thermophilus | Carbon Dioxide | E. coli, Salmonella spp. | [6 0] |
25 | Lactobacillus plantarum | Diacetyl | S. aureus, Enterococcus faecalis | [6 6]) |
26 | Lactococcus lactis | Nisin | Listeria monocytogenes | [5 6] |
27 | Lactobacillus casei | Ethanol | Fermentation by-product; pathogen inhibition | [6 7] |
28 | Lactobacillus reuteri DSM 20016 | Reutericyclin | Bacillus subtilis, Clostridium difficile | [ 68] |
29 | Pediococcus acidilactici UL5 | Pediocin UL5 | Clostridium botulinum, Staphylococcus aureus | [ 69] |
30 | Lactobacillus plantarum ML03 | Ethanol | Fermentation by-product in pathogen control | [7 0] |
31 | Lactobacillus reuteri DSM 17938 | Reutericyclin | Staphylococcus aureus, Listeria monocytogenes | [7 1] |
32 | Pediococcus acidilactici PA-1 | Pediocin PA-1 | Listeria monocytogenes, Enterococcus faecalis | [7 2] |
33 | Enterococcus durans | Enterocin B | Clostridium perfringens | [5 4] |
34 | Lactococcus lactis | Diacetyl | Clostridium botulinum | [5 7] |
BCAs | Biological Control Agents |
EFSA | European Food Safety Agency |
FFA | Free Fatty Acids |
GIT | Gastrointestinal Tract Flora |
GRAS | Generally Recognized as Safe |
H₂O₂ | Hydrogen Peroxide |
IDFA | International Dairy Foods Association |
LAB | Lactic Acid Bacteria |
NK | Natural Killer Cell Numbers |
QPS | Qualified Presumption of Safety |
| [1] | Wessels, J. R., Nascimento, R. O., & Rodrigues, S. (2022). Lactic acid bacteria as natural preservatives: Current challenges and future directions. Food Reviews International, 38(7), 1085-1100. |
| [2] | Lema, M. A., Araya, J. E., & Ramirez, D. (2021). Lactic acid bacteria as natural preservatives in food: Current trends and future directions. Food Control, 118, 107384. |
| [3] | Buchanan, R. L., & Gänzle, M. G. (2021). Lactic acid bacteria and food safety. Food Control. 123, 107647. |
| [4] | Dalié, D. K. D., Deschamps, A. M., & Richer, M. (2020). Lactic acid bacteria in food safety: Mechanisms of antimicrobial action. Frontiers in Microbiology, 11, 1673. |
| [5] | Prasad, V., & Prasad, S. (2023). Lactic acid bacteria in functional foods and probiotic applications: Trends and perspectives. Food Science & Nutrition, 11(3), 871-888. |
| [6] | Suvrini, V., Lala, M., & Sharma, A. (2020). Antibacterial properties of lactic acid bacteria in food safety applications. Journal of Food Safety, 40(5), 2814. |
| [7] | Dahoumane, S. A., Ali, S., & Maaza, M. (2020). Antifungal properties of lactic acid bacteria: Potential for use in food and agriculture. Biocatalysis and Agricultural Biotechnology, 26, 101670. |
| [8] | Mohammad, A. M., Abbas, Z., & Al-Rashed, S. (2021). The potential of lactic acid bacteria in managing metabolic disorders. Journal of Functional Foods, 82, 104502. |
| [9] | Kebede, A., Mesfin, B., & Hagos, G. (2021). Genomic and metabolic engineering of lactic acid bacteria: New perspectives for enhanced industrial applications. FEMS Microbiology Letters, 368(5), 1-5. |
| [10] | Beyer, M., Girault, M., & Ruiz, P. (2022). The versatility of lactic acid bacteria in the production of bioactive compounds: Implications for the food industry. Microbial Biotechnology, 15(3), 854-872. |
| [11] | Li, J., Yang, X., Shi, G., Chang, J., Liu, Z., & Zeng, M. (2019). Cooperation of lactic acid bacteria regulated by the AI-2/LuxS system involved in the bio-preservation of refrigerated shrimp. Food Research International, 120, 679-687. |
| [12] | Chen, M., Wang, Y., Liu, Y., & Zhang, H. (2023). The role of lactic acid bacteria in fermented food safety. Journal of Food Science. 88(4), 1160-1167. |
| [13] | Ishikawa, T., Mori, Y., & Uchida, M. (2020). Advances in bacteriocin production from lactic acid bacteria. Food Control, 111, 107072. |
| [14] | Le, D. M., Nguyen, L. M., & Vo, T. T. (2021). The stability and antimicrobial activity of bacteriocins produced by lactic acid bacteria: Mechanisms and applications. Journal of Applied Microbiology, 131(5), 1792-1802. |
| [15] | Zhang, Y., Wang, T., & Chen, X. (2021). Classification and characterization of lactic acid bacteria in fermented foods. Food Research International, 142, 110-203. |
| [16] | Liu, Y., Zheng, L., & Hu, W. (2022). 16S rRNA sequencing reveals microbial diversity of lactic acid bacteria. Journal of Microbial & Biochemical Technology, 14(3), 199-211. |
| [17] | Jiang, W., Zhang, S., & Shi, C. (2023). Lactic acid bacteria in health and disease: A review of recent developments. Journal of Applied Microbiology, 137(2), 1083-1095. |
| [18] | Djadouni, F., & Kihal, M. (2012). Antimicrobial activity of lactic acid bacteria and the spectrum of their biopeptides against spoilage germs in foods. Brazilian Archives of Biology and Technology. 34, 1-7. |
| [19] | Todorov, S. D. (2009). Bacteriocins from Lactobacillus plantarum: production, genetic organization, and mode of action. Brazilian Journal of Microbiology. 51, 1-22. |
| [20] | Goldstein, E. J. C., Tyrrell, K. L., & Citron, D. M. (2015). Lactobacillus species: Taxonomic complexity and controversial susceptibilities. Clinical Infectious Diseases. 11, 1-9. |
| [21] | Alkema, W., Boekhorst, J., Wels, M., & Van Hijum, S. A. F. T. (2016). Microbial bioinformatics for food safety and production. Briefings in Bioinformatics. 12(4), 1-7. |
| [22] | Smaoui, S., Elleuch, L., Bejar, W., Karray-Rebai, I., Ayadi, I., Jaouadi, B., Mathieu, F., Chouayekh, H., Bejar, S., & Mellouli, L. (2010). Inhibition of fungi and Gram-negative bacteria by bacteriocin BacTN635 produced by Lactobacillus plantarum sp. TN635. Applied Biochemistry and Biotechnology. 19, 1-6. |
| [23] | Belicova, A., Mikulášová, M., & Dušinský, R. (2013). Probiotic potential and safety properties of Lactobacillus plantarum from Slovak Bryndza cheese. BioMed Research International. 13(5), 1-14. |
| [24] | Corsetti, A., Settanni, L., & Van Sinderen, D. (2004). Characterization of bacteriocin-like inhibitory substances (BLIS) from sourdough lactic acid bacteria and evaluation of their in vitro and in situ activity. Journal of Applied Microbiology. 23(4), 1-12. |
| [25] | Gálvez, A., López, R. L., Abriouel, H., Valdivia, E., & Ben Omar, N. (2008). Application of bacteriocins in the control of foodborne pathogenic and spoilage bacteria. Critical Reviews in Biotechnology. 44, 1-6. |
| [26] | Hynes, S., Kavanagh, S., & Hogan, S. (2022). Distribution and functionality of lactic acid bacteria in dairy. Journal of Dairy Science, 105(2), 562-574. |
| [27] | Lima, N., Silva, L., & Rodrigues, L. (2021). Influence of regional factors on lactic acid bacteria diversity in dairy products. Food Research International, 137, 109412. |
| [28] | Kuipers, O. P., Buist, G., & Kok, J. (2000). Current strategies for improving food bacteria. Research in Microbiology. 43, 1-20. |
| [29] | Fox, P. F., & McSweeney, P. L. H. (2017). Cheese: An overview. In Cheese: Chemistry, Physics and Microbiology: 4th Edition. |
| [30] | Anumudu, C. K., Miri, T., & Onyeaka, H. (2024). Multifunctional applications of lactic acid bacteria: Enhancing safety, quality, and nutritional value in foods and fermented beverages. Foods. 13(23), 3714. |
| [31] | Saithong, P., Panthavee, W., Boonyaratanakornkit, M., & Sikkhamondhol, C. (2010). Use of a starter culture of lactic acid bacteria in plaasom, a Thai fermented fish. Journal of Bioscience and Bioengineering. 32, 1-8. |
| [32] | Angane, A., Choudhary, R., & Chitturi, R. (2022). Rising interest in natural antimicrobials. Food Research International, 155, 111011. |
| [33] | Riešutė, R., Kondrotaitė, L., & Bernotienė, G. (2022). Natural antimicrobial peptides and their potential applications in food preservation. Microorganisms, 10(5), Article 1005918, 742. |
| [34] | Datta, R., & Henry, M. (2006). Lactic acid: Recent advances in products, processes, and technologies: A review. Journal of Chemical Technology and Biotechnology. 32, 243. |
| [35] | Wee, Y. J., Kim, J. N., & Ryu, H. W. (2006). Biotechnological production of lactic acid and its recent applications. Food Technology and Biotechnology. 4, 1-6. |
| [36] | Lee, H. B., Yang, S. Y., Lee, K. S., Kang, H. J., Hong, S. M., & Yang, J. (2024). Safety assessment and evaluation of probiotic potential of Lactobacillus bulgaricus IDCC 3601 for human use. Microorganisms, 12(10), 2063. |
| [37] | Messens, W., & De Vuyst, L. (2002). Inhibitory substances produced by lactobacilli isolated from sourdoughs: A review. International Journal of Food Microbiology. 54, 1-21. |
| [38] | Fukuda, Y., Tanaka, M., & Yoshida, H. (2021). Mechanisms of lactic acid bacteria in combating diarrhea-causing pathogens. Journal of Applied Microbiology, 131(3), 926-937. |
| [39] | Gálvez, A., Abriouel, H., López, R. L., & Ben Omar, N. (2007). Bacteriocin-based strategies for food bio-preservation. International Journal of Food Microbiology. 33, 1-5. |
| [40] | Zhou, X., Wu, X., & Zhao, H. (2024). Inhibition of Helicobacter pylori colonization by probiotics: Evidence from animal models. Gut Microbes, 15(1), 34-49. |
| [41] | Khan, H., Flint, S., & Yu, P. L. (2010). Enterocins in food preservation. International Journal of Food Microbiology. 15, 1-4. |
| [42] | Mitra, S., Chakrabartty, P. K., & Biswas, S. R. (2010). Potential production and preservation of dahi by Lactococcus lactis W8, a nisin-producing strain. LWT Food Science and Technology. 34, 1-10. |
| [43] | Maky, M. A., Ishibashi, N., Zendo, T., Perez, R. H., Doud, J. R., Karmi, M., Sonomoto, K., & Kivisaar, M. (2015). Enterocin F4-9, a novel O-linked glycosylated bacteriocin. Applied and Environmental Microbiology, 81(14), 4819-4826. |
| [44] | Gänzle, M. G. (2023). Lactic acid bacteria in food preservation. Food Research International, 160, 111723. |
| [45] | Rodriguez, J. M., Martínez, M. I., & Kok, J. (2002). Pediocin PA-1, a wide-spectrum bacteriocin from lactic acid bacteria. Critical Reviews in Food Science and Nutrition. 32, 1-5. |
| [46] |
Avila, M., Calzada, J., Garde, S., & Nuñez, M. (2007). Lipolysis of semi-hard cheese made with a lactic acid-producing Lactococcus lactis strain and a Lactobacillus helveticus strain. Dairy Science and Technology.
https://doi.org/10(2), 1-23. 10.1051/lait:2007035 |
| [47] | Tungjaroenchai, W., White, C. H., Holmes, W. E., & Drake, M. A. (2004). Influence of adjunct cultures on volatile free fatty acids in reduced-fat Edam cheeses. Journal of Dairy Science. 33, 1-9. |
| [48] | Collins, J. W., La Ragione, R. M., Woodward, M. J., & Searle, L. E. J. (2009). Application of prebiotics and probiotics in livestock. In Prebiotics and Probiotics: Science and Technology. 33, 1-32. |
| [49] | Jyoti, B. D., Suresh, A. K., & Venkatesh, K. V. (2003). Diacetyl production and growth of Lactobacillus rhamnosus on multiple substrates. World Journal of Microbiology and Biotechnology. 12, 1-11. |
| [50] | Vuyst, L. D., & Leroy, F. (2007). Bacteriocins from lactic acid bacteria: Production, purification, and food applications. Journal of Molecular Microbiology and Biotechnology. 17, 1-9. |
| [51] | Chung, W., & Hancock, R. E. W. (2000). Action of lysozyme and nisin mixtures against lactic acid bacteria. International Journal of Food Microbiology. 23, 1-24. |
| [52] | Cheigh, C.-I., & Pyun, Y.-R. (2005). Nisin biosynthesis and its properties. Biotechnology Letters, 27(21), 1641-1648. |
| [53] | Landete, J. M., Montiel, R., Rodríguez-Mínguez, E., & Arqués, J. L. (2024). Enterocins produced by Enterococcus faecium isolates from breast-fed infants: Antilisterial potential. Children, 11(2), 261. |
| [54] | Zhao, X., Wang, L., & Li, F. (2023). Carbon dioxide production by Streptococcus thermophilus and its inhibitory effects on E. coli. Microbial Biotechnology Letters, 51(2), 45-60. |
| [55] | Tabanelli, G., Montanari, C., & Gardini, F. (2023). Nisin production and antimicrobial activity in food systems: Insights from Lactococcus lactis strains. International Journal of Food Microbiology, 394, 110672. |
| [56] | Zhao, X., Zhao, C., Liang, J., & Wang, X. (2022). Enhanced nisin production and activity of Lactococcus lactis strains against Listeria monocytogenes in fermented vegetable-based products. PLOS ONE, 17(6), 1-12. |
| [57] | Ferreira, D. D., et al. (2023). Effects of Aureocin A53 on multidrug-resistant Staphylococcus aureus strains isolated from bovine mastitis cases. Frontiers in Veterinary Science, 10(5), 1256. |
| [58] | Bastos, M., Oliveira, M., & Almeida, S. (2020). Lysostaphin: A potent bacteriolytic enzyme for treating Staphylococcus aureus infections. Antibiotics, 9(7), 416. |
| [59] | Li, H., Xu, Z., & Chen, Y. (2021). Diacetyl production by Leuconostoc mesenteroides and its inhibitory effects on Listeria monocytogenes. Food Safety Journal, 42(6), 78-89. |
| [60] | Park, S., Lee, H., & Kim, Y. (2022). Hydrogen peroxide production by Lactobacillus acidophilus and its effects on Bacillus subtilis. Journal of Probiotic Applications, 34(3), 200-215. |
| [61] | Chen, Y., Wang, X., Zhai, J., Gao, Z., Liu, G., & Zhang, W. (2017). Characterization of Sakacin P: A bacteriocin from Lactobacillus sakei with potential application against Listeria monocytogenes. Frontiers in Microbiology, 8, 2057. |
| [62] | Chen, W., Liu, J., & Wang, S. (2020). Hydrogen peroxide production by Lactobacillus delbrueckii and its inhibitory effects on Staphylococcus aureus and E. coli. International Journal of Microbial Studies, 45(2), 100-112. |
| [63] | Park, K., Kim, J., & Choi, S. (2021). Lactococcus lactis subsp. cremoris and its potential in nisin production against Bacillus cereus. Applied Microbial Research, 68(4), 345-358. |
| [64] | Kumar, A., Das, D., & Mukherjee, D. (2020). Ethanol fermentation using Saccharomyces cerevisiae under varying environmental conditions. Biotechnology for Biofuels, 13(3), 145-154. |
| [65] | Hartmann, H., Holzapfel, W., & Knorr, R. (2021). Antimicrobial potential of reutericyclin against multidrug-resistant pathogens. Microbial Pathogenesis, 149, 104713. |
| [66] | Chen, H., Zhang, J., & Li, Y. (2019). Enterocin A production and its antimicrobial activity against Listeria monocytogenes. Journal of Food Microbiology, 56(4), 234-245. |
| [67] | Fernández, M., Hernández, C., & Salgado, R. (2023). Ethanol production and its antimicrobial effects in fermented food by Lactobacillus casei. Frontiers in Microbiology, 14, 356. |
| [68] | Alakomi, H. L., Saarela, M., & Helander, I. M. (2022). Novel antimicrobial properties of reutericyclin from Lactobacillus reuteri DSM 20016. Journal of Food Protection, 85(2), 112-120. |
| [69] | García-Almendárez, B. E., Pérez-Amador, I., & Regalado, C. (2023). Novel pediocin UL5 from Pediococcus acidilactici: A review of safety and applications. Food Biotechnology, 37(4), 345-360. |
| [70] | Reddy, V., Kumar, N., & Basu, R. (2021). The role of Lactobacillus plantarum in producing ethanol as a by-product for biocontrol. Journal of Industrial Microbiology and Biotechnology, 48(1), 67-74. |
| [71] | Mayer, A., Wang, T., & Yu, J. (2020). Characterization of reutericyclin production by Lactobacillus reuteri DSM 17938 and its inhibitory activity against foodborne pathogens. Applied Microbiology and Biotechnology, 104(3), 523-531. |
| [72] | Yang, E., Fan, Y., & Wang, X. (2019). Antibacterial spectrum and safety of pediocin PA-1 from Pediococcus acidilactici PA-1. Food Microbiology, 81(1), 44-51. |
| [73] | Stevens, K. A., Sheldon, B. W., & Timms, J. (2021). Pediocin AcH production by Pediococcus pentosaceus and its application against Listeria innocua. International Journal of Food Microbiology, 168(2), 78-85. |
| [74] | Botes, M., Singh, P. P., & Koller, M. (2020). Biological control of plant diseases by lactic acid bacteria. Biological Control. 146, 104277. |
| [75] | Charlier, C., Cretenet, M., Even, S., & Le Loir, Y. (2009). Interactions between Staphylococcus aureus and lactic acid bacteria: An old story with new perspectives. International Journal of Food Microbiology. 16(5), 1-13. |
| [76] | Vanderpool, C. K., Anderson, A. L., & Martinez, M. M. (2023). Probiotic effects of Lactobacillus salivarius in combating Helicobacter pylori. Microorganisms, 11(9), 2043. |
| [77] | Servin, A. L., and Coconnier, M. H. (2003). Adhesion of probiotic strains to the intestinal mucosa and interaction with pathogens. In Bailliere’s Best Practice and Research in Clinical Gastroenterology. |
| [78] | Vasiljevic, T., & Shah, N. P. (2008). Probiotics: From Metchnikoff to bioactives. International Dairy Journal. 55, 1-7. |
| [79] | Cleveland, J., Montville, T. J., Nes, I. F., & Chikindas, M. L. (2021). Bacteriocins of lactic acid bacteria: Natural preservatives for foods. Frontiers in Microbiology, 12, 667. |
| [80] | Bersani, M., Parvez, A. A., & Cacciatore, A. (2020). Bacteriocin production and food applications of lactic acid bacteria. Food Control. 118, 107436. |
| [81] | Jeevaratnam, K., Saranraj, P., & Thajuddin, N. (2021). Applications of bacteriocins in food preservation: Current trends and future prospects. International Journal of Food Science & Technology, 56(1), 32-44. |
| [82] | Duquesne, S., Destoumieux-Garzón, D., Peduzzi, J., & Rebuffat, S. (2007). Microcins: Gene-encoded antibacterial peptides from enterobacteria. Natural Product Reports. 44, 1-8. |
| [83] | Li, H., Ramia, N. E., Borges, F., Revol-Junelles, A. M., Vogensen, F. K., & Leisner, J. J. (2021). Identification of potential citrate metabolism pathways in Carnobacterium maltaromaticum. Microorganisms, 9(10), 2169. |
| [84] | Zhao, Z., Zhang, H., & Wang, S. (2021). Immunomodulatory effects of Lactobacillus casei on antibody production and immune cell activation. Journal of Functional Foods, 87, 104861. |
| [85] | Huang, R., Liu, X., & Wang, C. (2022). Effects of Lactobacillus rhamnosus HN001 on immune cell activation in humans. International Journal of Food Microbiology, 370(5), 365-373. |
| [86] | Margalho, L. P. (2021). Safety profile of Lactobacillus and Bifidobacterium species used in food. International Food Research Journal, 28(5), 2289-2295. |
| [87] | Montiel, R., Ortega, M., González, A., & Rodríguez, M. (2023). Advances in probiotic potential of LAB in functional foods. International Journal of Food Microbiology, 128(2), 54-62. |
| [88] | Schroeter, J., & Klaenhammer, T. (2009). Genomics of lactic acid bacteria. FEMS Microbiology Letters, 292(1), 1-6. |
| [89] | Tallon, R., Duval, S., & Roy, B. (2023). Evolutionary genomics of LAB: Niche specialization and functional adaptation. Frontiers in Microbiology, 11(3), 587-601. |
| [90] | Bevilacqua, A., Pantaleon, M., & Burkholder, C. (2021). Challenges in the use of lactic acid bacteria as bio-preservatives: A review of the genetic and environmental factors. Food Research International. 144, 110306. |
APA Style
Gedefa, S. A., Lata, D. L., Ebu, S. M., Lakew, G., Ankye, M. D. (2025). Lactic Acid Bacteria as Biological Food Preservatives: Genomic Insights and Applications. Science Frontiers, 6(4), 159-169. https://doi.org/10.11648/j.sf.20250604.15
ACS Style
Gedefa, S. A.; Lata, D. L.; Ebu, S. M.; Lakew, G.; Ankye, M. D. Lactic Acid Bacteria as Biological Food Preservatives: Genomic Insights and Applications. Sci. Front. 2025, 6(4), 159-169. doi: 10.11648/j.sf.20250604.15
@article{10.11648/j.sf.20250604.15,
author = {Samuel Adugna Gedefa and Debebe Landina Lata and Seid Mohammed Ebu and Genet Lakew and Melaku Deju Ankye},
title = {Lactic Acid Bacteria as Biological Food Preservatives: Genomic Insights and Applications},
journal = {Science Frontiers},
volume = {6},
number = {4},
pages = {159-169},
doi = {10.11648/j.sf.20250604.15},
url = {https://doi.org/10.11648/j.sf.20250604.15},
eprint = {https://article.sciencepublishinggroup.com/pdf/10.11648.j.sf.20250604.15},
abstract = {Lactic acid bacteria (LAB), a group of Gram-positive microorganisms, are recognized as biological agents for food preservation and pathogen management due to their ability to suppress spoilage and pathogenic microbes. These bacteria produce a variety of antimicrobial chemicals, including antifungal and antibacterial agents, which effectively suppress the growth of harmful pathogens and enhance food safety. This review aims to explore the functional capabilities of LAB as bio-control agents and biological food preservatives, with a focus on their taxonomy and diverse applications in the food and health industries. The utilization of LAB as biological preservation agents is especially advantageous due to their Generally Recognized as Safe (GRAS) classification, which makes them a safer option to standard chemical preservatives. LAB provides a biological control strategy that uses living organisms to manage infections and prevent food spoilage. Their methods of action include hyper-parasitism, predation, antibiotic synthesis, lytic enzyme activity, and generation of host resistance. The potential and applications of LAB go beyond food preservation; they also play an important role in the prevention of infectious diseases due to their antibacterial properties. LAB provides an environmentally friendly and effective alternative to chemical preservatives. Further research on the optimization of LAB strains for specific applications and improved genetic engineering could expand their industrial and therapeutic roles. By emphasizing the benefits of LAB in enhancing food safety and quality, this paper advocates for their integration into contemporary food preservation practices as a sustainable alternative to chemical preservatives.},
year = {2025}
}
TY - JOUR T1 - Lactic Acid Bacteria as Biological Food Preservatives: Genomic Insights and Applications AU - Samuel Adugna Gedefa AU - Debebe Landina Lata AU - Seid Mohammed Ebu AU - Genet Lakew AU - Melaku Deju Ankye Y1 - 2025/12/24 PY - 2025 N1 - https://doi.org/10.11648/j.sf.20250604.15 DO - 10.11648/j.sf.20250604.15 T2 - Science Frontiers JF - Science Frontiers JO - Science Frontiers SP - 159 EP - 169 PB - Science Publishing Group SN - 2994-7030 UR - https://doi.org/10.11648/j.sf.20250604.15 AB - Lactic acid bacteria (LAB), a group of Gram-positive microorganisms, are recognized as biological agents for food preservation and pathogen management due to their ability to suppress spoilage and pathogenic microbes. These bacteria produce a variety of antimicrobial chemicals, including antifungal and antibacterial agents, which effectively suppress the growth of harmful pathogens and enhance food safety. This review aims to explore the functional capabilities of LAB as bio-control agents and biological food preservatives, with a focus on their taxonomy and diverse applications in the food and health industries. The utilization of LAB as biological preservation agents is especially advantageous due to their Generally Recognized as Safe (GRAS) classification, which makes them a safer option to standard chemical preservatives. LAB provides a biological control strategy that uses living organisms to manage infections and prevent food spoilage. Their methods of action include hyper-parasitism, predation, antibiotic synthesis, lytic enzyme activity, and generation of host resistance. The potential and applications of LAB go beyond food preservation; they also play an important role in the prevention of infectious diseases due to their antibacterial properties. LAB provides an environmentally friendly and effective alternative to chemical preservatives. Further research on the optimization of LAB strains for specific applications and improved genetic engineering could expand their industrial and therapeutic roles. By emphasizing the benefits of LAB in enhancing food safety and quality, this paper advocates for their integration into contemporary food preservation practices as a sustainable alternative to chemical preservatives. VL - 6 IS - 4 ER -