Bio-Preservation of Meat by Lactic Acid Bacteria Strains: History
Please note this is an old version of this entry, which may differ significantly from the current revision.

Meat and some meat products are highly perishable due to their high-water content, pH, and high content of nutrients. Therefore, spoilage control in these products is one of the critical challenges in the food industry. On the other hand, the increasing widespread awareness about the undesirable effects of synthetic preservatives has promoted the breakthrough of the use of natural compounds or bio-preservation technology. Bio-preservation implies the application of microorganisms or their metabolites to extend the shelf life of food products. In this regard, according to the ancient and safe use of fermentation by lactic acid bacteria (LAB), their application in the bio-preservation of meat and meat products is gaining more attention.

  • bio-preservation
  • fermentation
  • lactic acid bacteria
  • meat products
  • natural anti-microbial

1. Introduction

Meat and meat products are rich sources of nutrients for humans due to their high content of vitamin B groups, protein, essential amino acids, and minerals. Also, they provide a favorable environment for the growth of several microorganisms due to their ideal pH, nutrient factors, and high water activity [1]. The main bacteria involved in meat spoilage include the genera Brochothrix, Enterobacter, Acinetobacter, Moraxella, Pseudomonas, Leuconostoc, and Proteus, meanwhile some of them (i.e., Enterobacter, Pseudomonas) secrete biogenic amines, which might cause food safety issues [2]. Furthermore, meat and meat products may be contaminated by pathogenic microorganisms such as Campylobacter jejuni, Clostridium botulinum, Escherichia coli, Bacillus cereus, Listeria monocytogenes, Clostridium perfringens, Salmonella spp., Yersinia enterocolitica, and Staphylococcus aureus [3][4].
One of the main concern for the meat industry is the spoilage of fresh meat and meat products caused by microbial contamination [5]. The meat industry applies different techniques to inhibit microbial growth and the production safe products with the suitable and desired shelf life [6]. Accordingly, the most common applied techniques include physical (e.g., drying, freezing, heat treatment, packaging, and curing) and especially chemical (e.g., use of synthetic preservative compounds) methods [7]. Nevertheless, chemical additives have many disadvantages such as the alteration of the nutritional and organoleptic properties of foods [8][9]. Also, the carcinogenicity and toxicity of many chemicals such as nitrates have been proven. Nitrates are the most common chemicals used in the meat industry for the inhibition of microbial growth, retardation of lipid oxidation, development of better flavor, taste, and aroma, and preserve the color of the meat. In fermented sausages, their conversion into nitrites by microbial nitrate reductases can inhibit the growth of spoilage bacteria such as Clostridium spp. [10]. It has been reported that their excess consumption can have dangerous effects on consumer health due to the formation of carcinogenic nitrosamines [11]. For example, nitrates can generate nitric oxide by nitrosation reactions, which can undergo a reaction with secondary amines and form N-nitrosamines [12][13]. So, the increasingly negative perceptions of synthetic preservative chemicals, the greater attention of consumers towards food quality, and increasing demand for high nutritional and synthetic chemical-free products has promoted the food industry to replace traditional preservation methods with green techniques, such as active packaging, modified atmosphere packaging, high hydrostatic pressure, pulsed electric fields, and bio-preservation [14][15][16][17]. In this field, bio-preservation is the most reliable and potent technique closely related to “from farm to fork” strategy. Bio-preservation is considered a method to extend the shelf life of food products using compounds derived from plants, animals, bacteria, or fungi [18]. However, most researchers focus on bio-preservation by using beneficial microorganisms and/or their antimicrobial compounds [19].
In this context, lactic acid bacteria (LAB) have attracted more attention than other bio-preservative microorganisms due to different reasons such as their encapsulation capability by extrusion during the production of the antimicrobial film [20] and their GRAS status approved by the U.S. Food and Drug Administration (FDA) as a preservative in some food [3][21]. On the other hand, increasing the demand for natural preservative methods in line with environmental protection led to an increase in researchers’ interest in finding efficient and sustainable preservative methods. In this regard, bio-preservation with LAB bacteria has no negative effects on consumers’ health and environment and have recently gained more attention as a useful and sustainable approach for the production of functional foods that lead to the sustainability of the consumers’ health [22][23]. So, the use of LAB and/or their metabolites, either alone or in combination with a low amount of natural or synthetic preservatives and moderate physicochemical treatments, may be an efficient solution to extend the shelf life and enhanced food safety (e.g., dairy products, fermented meat, and meat products) without negative effects on their nutritional quality [24]. Accordingly in the last two decades, intensive investigations have been focused on LAB and their antimicrobial metabolites to discover new LAB strains with food preservation potential to be used in sustainable preservative methods [25].

2. Fermented Meat Products and Their Health-Beneficial Properties

In the past, different techniques were used and developed for the preservation of meat and meat products, starting with adding some ingredients, such as salt and sugar to reduce microorganisms without an exact understanding of their preservative mechanisms. But today, the use of microorganisms in terms of fermentation of meat and meat products is known as an effective preservation method [5]. Microbial enzymatic activities during fermentation leads to various physicochemical and microbial changes based on the meat components (natural or added components) [26]. Fermentation can occur by two pathways: (1) the use of natural microflora of meat or (2) the use of starter cultures such as lactic acid bacteria and micrococci. Lactic acid bacteria breakdown the carbohydrates and micrococci reduce nitrates and nitrites to nitric oxide that leads to production of volatile and nonvolatile compounds and flavor and odor changes of the product [27]. Also, fermentation causes different health-beneficial properties in fermented meat products in comparison to non-fermented ones such as antioxidant, antimicrobial, anti-hypertensive, and antithrombotic [28][29]. Furthermore, some nutritional components are produced during fermentation that have the potential to prevent diabetes, cancers, and allergic sensitization [30]. More studies are needed to discover other health-beneficial potentials of these products and their exact mechanisms. Also, these products should be evaluated in terms of food safety.

3. A Brief Overview on LAB

LAB are part of the natural microbial flora of fermented meats and the intestinal microbiota of humans. These aerotolerant bacteria are mainly non-sporing, Gram-positive, Catalase-negative, and have either a spherical-shaped or rod-shaped cell (Figure 1) [31]. LAB are microaerophilic organisms and preferably require anaerobic conditions for growth. They play an important role in food fermentations; in fact, LAB can ferment carbohydrates to high amounts of lactic acid as the final product (homofermentative bacteria); in addition to lactic acid, heterofermentative bacteria produce acetic acid, carbon dioxide, and ethanol, as by-products [32]. These organisms are acidophilus with the optimum acidic pH values of 5.5–6.2, but few can tolerate pH as low as 3.0 [33]. LAB are Generally Regarded As Safe (GRAS) according to the FDA and the European Food Safety Authority (EFSA) that have granted many LAB species Qualified Presumption of Safety status (QPS) [25][34][35]. Lactic acid bacteria possess considerable bioactive properties such as cholesterol reduction and antimicrobial properties, which has led to an increased interest in their effective role as preservatives in innovative food preservation technology, much more than their application in traditional fermentation [36][37][38]. The antibacterial activity of LAB strains has been proven in different studies [39]. It has been reported that different LAB strains secrete various compounds that inhibit bacterial growth such as diacetyl, phenyl-lactate, organic acids, hydroxy fatty acid, hydroxy phenyl-lactate, hydrogen peroxide, propionate, and cyclic dipeptides. These bacteria also secrete biosurfactants, bacteriocins (i.e., acidophilin, lactacin, bifidocin, helveticin, plantarim, pediocin, bulgaricin, diplococcin, and nisin), and bacteriocin-like inhibitory substances [40][41].
Figure 1. Schematic of properties of lactic acid bacteria.

3.1. LAB Strains Involved in Fermented Meat Products

The technological characterization of LAB strains involved in the fermentation process of meat is essential to select the best strain to be utilized as starter cultures [42]. The genera Lactobacillus, Carnobacterium, Weissella, Pediococcus, Enterococcus, and Leuconostoc are the main LAB that play crucial role in the fermentation [42][43]. The list of some of GRAS LAB that are most commonly used in bio-preservation of meat and meat products are mentioned in Table 1. Members of the genus Lactobacillus are usually the dominant species in most fermented meat products, but in some slightly acidified sausages, both Enterococcus and Lactobacillus are present in similar amounts [43]; nevertheless, Lactobacillus plantarum and Lactobacillus curvatus are the most common LAB species in fermented sausages [26]. It has been reported that in many fermented sausages, Lactobacillus sakei has the most adaptability due to a higher maximum growth rate, higher final cell density, and a shorter lag phase [44][45]. It should be noted that in Southern European sausages, the most and least common species are Lactobacillus sakei and Pediococci spp., respectively [46]. Also, molds, such as Penicillium chrysogenum and Penicillium nalgiovense, are commonly used for sausage ripening in Southern Europe [47]. In artisan sausages from Southern Europe, a strain of Enterococcus faecium grows increasingly during the early stages of fermentation, producing a bacteriocin [48]. It has been reported that yeast genera, especially Debaryomyces hansenii, can be found in fermented meat products with appropriate organoleptic characteristics [49][50].
Table 1. Some of LAB species that are most commonly used in meat preservation.

Genus

Species

Genus

Species

Lactobacillus

Lactobacillus delbrueckii

Lacticaseibacillus

Lacticaseibacillus paracasei

Lactobacillus bulgaricus

Lacticaseibacillus rhamnosus

Lactobacillus gallinarum

Lacticaseibacillus casei

Lactobacillus gasseri

Pediococcus

Pediococcus acidilactici

Lactobacillus lactis

Pediococcus pentosaceus

Lactobacillus helveticus

Pediococcus parvulus

Lactobacillus reuteri

Leuconostoc

Leuconostoc mesenteroides

Lactobacillus acidophilus

Leuconostoc citreum

Lactobacillus curvatus

Leuconostoc pseudomesenteroides

Lactobacillus sakei

Leuconostoc carnosum

Lactobacillusalivarius

Lactiplantibacillus

Lactiplantibacillus pentosus

Latilactobacillus

Latilactobacillus sakei

Lactiplantibacillus plantarum

Latilactobacillus curvatus

Lactiplantibacillus brevis

Limosilactobacillus

Limosilactobacillus fermentum

Lactiplantibacillus casei

Limosilactobacillus reuteri

3.2. Bio-Preservation of Meat and Meat Products by LAB and Their Metabolites

As mentioned above, bio-preservation strategies are based on the application of natural compounds derived from microorganisms, plants, or animals for extending the shelf life of food products [18]. But most studies circumscribe the bio-preservation concept to the application of microorganisms such as LAB or their metabolites to enhance food safety and extend the shelf life of food products. Generally, the most important approach is to use of microorganisms or their metabolites with antimicrobial activity against food spoilage bacteria and especially foodborne pathogens [25]. A desirable bio-preservation compound should only show antimicrobial activity against the targeted spoilage or pathogenic microorganisms and should not adversely affect the intestinal microbial flora of consumers [18].
LAB can be used directly as a functional ingredient in meat and meat products or as starters in fermentation processes. When directly applied, LAB can be added in freeze-dried or fresh cultures in different ways such as addition to fresh meat, meat batter formulation, or spraying on the surface of ready-to-eat meat products or fresh meat [25].
Traditionally, LAB have been widely used in fermentation processes, converting carbohydrates to lactic acid and producing biologically active compounds such as antibacterial and antifungal peptides, diacetyl, organic acids, and flavor precursors [51].

3.3. LAB or Their Metabolites as a Part of Hurdle Technology

Hurdle technology refers to the combination of different preservative factors such as water activity (aw), temperature, redox potential (Eh), and novel preservative techniques, such as gas packaging, natural extracts, essential oils, and bacteriocins, to create more selective and efficient defensive systems to overcome pathogenic and spoilage microorganisms [52]. So, LAB and their metabolites can be used as a part of hurdles technology that act synergistically and inhibit food spoilage in combination with other preservative agents. In this way, less intensities of technological treatment and/or doses of preservative agents are required [53]. In the application of different antimicrobial agents, it is very important to select the best combination, so that desirable preservative effects are achieved. In this regard, it has been reported that the addition of chelating agents makes the outer membranes of Gram-negative bacteria more permeable and sensitive to the hydrophobic peptides such as bacteriocins [54]. Also, freezing temperatures and modified atmosphere packaging (MAP) in combination with LAB and their metabolites can be used in hurdles technology approaches [55]. Different studies have evaluated the effect of different LAB in combination with various bio-preservatives on the microbial quality of meat and fermented meat products (summarized in Table 2).
Table 2. The antibacterial effect of LAB or their metabolites in combination with other preservative agents in meat and meat products.

Product

Bio-Preservative Agent

Results

References

Ground beef

L. reuteri or L. plantarum in combination with garlic extract

1.4 and 1.5 log reduction of L. monocytogenes by using L. reuteri or L. plantarum in combination with 1% of garlic extract

[56]

Beef sausage

Bacteriocinogenic Enterococcus mundtii and 0.0075% ascorbic acid, 3% NaCl, 0.02% NaNO2, 0.75% glucose and 0.75% sucrose

>2 log cfu/g reduction of L. monocytogenes

[57]

Sliced beef

Bacteriocin from C. maltaromaticum combined with steam and chitosan

No synergistic effect 2 log reduction of S. typhimurium, E. coli and S. typhimurium

[58]

Minced beef meat

Mentha piperita essential oil with semipurified bacteriocin

Reduction in Enterobacteriaceae

[59]

Frozen ground beef patties

Bacteriocin-producing L. curvatus and L. lactis in combination with Na2EDTA

1 log reduction of E. coli

[60]

Fresh chicken meat burger

L. pseudomesenteroides combined with MAP (50% CO2 and 50% O2)

Reduction in L. monocytogenes and C. jejuni

[55]

Fresh pork sausage

Combination of essential oils, nisin, nitrite, and organic acid salts, encapsulated

Reduction in L. monocytogenes

[61]

Alheira paste

L. sakei and L. plantarum, vacuum packed or packed under MAP (20% CO2, 80% N2)

2 log reduction in L. monocytogenes by L. sakei. No significant differences between vacuum or MAP

[62]

Sliced lombo

Combination of Bacteriocin from P. acidilactici with HPP

Reduction in L. innocua

[63]

Goat meat emulsion

Combination of Pediocin from P. pentosaceus and Murraya koenigii berries extract

Reduction in L. innocua

[64]

Ready-to-eat porkham

Bacteriocin-like inhibitory substances (BLIS) from P. pentosaceus and nisin

Inhibition of growth of L. seeligeri

[65]

3.4. Kinetics Models for Microbial Inactivation

Different kinetic models have been widely used for predicting the inactivation patterns of microorganisms. In this regard, the first-order kinetic mode is employed for log-linear survival curves, while the Weibull, biphasic, and log-logistic models are used for non-log-linear inactivation patterns. The first-order kinetic mode, the Weibull, biphasic, and log-logistic are expressed by the following equations, respectively [66]:
l o g N t N O = t D T
l o g N t N O = b t n
l o g N t = l o g N o + l o g ( k × e α t + ( 1 k ) × e β t )
l o g N t N O = A 1 + e 4 σ ( τ l o g t ) A + A 1 + e 4 σ ( τ + 6 ) A
where 𝑁𝑂 and 𝑁𝑡 are the initial and surviving populations of bacteria at any time (CFU/g), t is time (min), 𝐷𝑇 is defined as the time at which 90% of the bacterial population is inactivated, b is the inverse of the shape factor (1/min), 𝑛 is the shape parameter (dimensionless), 𝛼 and 𝛽 are the inactivation kinetic rate constants (1/min), σ is the maximum inactivation rate (log (CFU/g)/log min), τ is the log time to attain the maximum inactivation rate (log min), 𝐴 is the log increase in population. The statistical criteria are used to determine the goodness of fit of the kinetic models for describing the survival data.

This entry is adapted from the peer-reviewed paper 10.3390/su151310154

References

  1. Bohrer, B.M. Nutrient Density and Nutritional Value of Meat Products and Non-Meat Foods High in Protein. Trends Food Sci. Technol. 2017, 65, 103–112.
  2. Gao, X.; Li, C.; He, R.; Zhang, Y.; Wang, B.; Zhang, Z.-H.; Ho, C.-T. Research Advances on Biogenic Amines in Traditional Fermented Foods: Emphasis on Formation Mechanism, Detection and Control Methods. Food Chem. 2022, 405, 134911.
  3. Favaro, L.; Todorov, S.D. Bacteriocinogenic LAB Strains for Fermented Meat Preservation: Perspectives, Challenges, and Limitations. Probiotics Antimicrob. Proteins 2017, 9, 444–458.
  4. Laukkanen-Ninios, R.; Fredriksson-Ahomaa, M.; Korkeala, H. Enteropathogenic Yersinia in the Pork Production Chain: Challenges for Control. Compr. Rev. Food Sci. Food Saf. 2014, 13, 1165–1191.
  5. Ashaolu, T.J.; Khalifa, I.; Mesak, M.A.; Lorenzo, J.M.; Farag, M.A. A Comprehensive Review of the Role of Microorganisms on Texture Change, Flavor and Biogenic Amines Formation in Fermented Meat with Their Action Mechanisms and Safety. Crit. Rev. Food Sci. Nutr. 2021, 20, 1–18.
  6. Deak, T. Thermal Treatment. In Food Safety Manag.; Elsevier: Amsterdam, The Netherlands, 2014; pp. 423–442.
  7. Buncic, S.; Nychas, G.-J.; Lee, M.R.F.; Koutsoumanis, K.; Hébraud, M.; Desvaux, M.; Chorianopoulos, N.; Bolton, D.; Blagojevic, B.; Antic, D. Microbial Pathogen Control in the Beef Chain: Recent Research Advances. Meat Sci. 2014, 97, 288–297.
  8. Kaveh, S.; Mahoonak, A.S.; Ghorbani, M.; Jafari, S.M. Fenugreek Seed (Trigonella Foenum Graecum) Protein Hydrolysate Loaded in Nanosized Liposomes: Characteristic, Storage Stability, Controlled Release and Retention of Antioxidant Activity. Ind. Crops Prod. 2022, 182, 114908.
  9. Radi, M.; Shadikhah, S.; Sayadi, M.; Kaveh, S.; Amiri, S.; Bagheri, F. Effect of Thymus Vulgaris Essential Oil-Loaded Nanostructured Lipid Carriers in Alginate-Based Edible Coating on the Postharvest Quality of Tangerine Fruit. Food Bioprocess Technol. 2023, 16, 185–198.
  10. Duarte, M.; de Fátima Carrijo, K. Quantificação Do Teor de Nitrito de Sódio Residual Em Linguiças Cozidas Tipo Calabresa Comercializadas No Sul Do Estado Do Rio de Janeiro, Brasil. Enciclopédia Biosf. 2014, 10, 1606–1615.
  11. Eskandari, M.H.; Hosseinpour, S.; Mesbahi, G.; Shekarforoush, S. New Composite Nitrite-free and Low-nitrite Meat-curing Systems Using Natural Colorants. Food Sci. Nutr. 2013, 1, 392–401.
  12. Bhattacharya, D.; Nanda, P.K.; Pateiro, M.; Lorenzo, J.M.; Dhar, P.; Das, A.K. Lactic Acid Bacteria and Bacteriocins: Novel Biotechnological Approach for Biopreservation of Meat and Meat Products. Microorganisms 2022, 10, 2058.
  13. Flores, M.; Toldrá, F. Chemistry, Safety, and Regulatory Considerations in the Use of Nitrite and Nitrate from Natural Origin in Meat Products-Invited Review. Meat Sci. 2021, 171, 108272.
  14. Hernández-Aquino, S.; Miranda-Romero, L.A.; Fujikawa, H.; Maldonado-Simán, E.D.E.J.; Alarcon-Zuniga, B. Antibacterial Activity of Lactic Acid Bacteria to Improve Shelf Life of Raw Meat. Biocontrol Sci. 2019, 24, 185–192.
  15. Jafarpour, D.; Hashemi, S.M.B. Pure and Co-Fermentation of Quinoa Seeds by Limosilactobacillus Fermentum and Lacticaseibacillus Rhamnosus: Bioactive Content, Antidiabetic and Antioxidant Activities. Fermentation 2023, 9, 80.
  16. Kaveh, S.; Gholamhosseinpour, A.; Mohammad, S.; Hashemi, B.; Jafarpour, D.; Castagnini, J.M. Original Article Recent Advances in Ultrasound Application in Fermented and Non-Fermented Dairy Products: Antibacterial and Bioactive Properties. Int. J. Food Sci. Technol. 2023, 58, 3591–3607.
  17. Rezazadeh-Bari, M.; Najafi-Darmian, Y.; Alizadeh, M.; Amiri, S. Numerical Optimization of Probiotic Ayran Production Based on Whey Containing Transglutaminase and Aloe Vera Gel. J. Food Sci. Technol. 2019, 56, 3502–3512.
  18. Pisoschi, A.M.; Pop, A.; Georgescu, C.; Turcuş, V.; Olah, N.K.; Mathe, E. An Overview of Natural Antimicrobials Role in Food. Eur. J. Med. Chem. 2018, 143, 922–935.
  19. Singh, V.P. Recent Approaches in Food Bio-Preservation-a Review. Open Vet. J. 2018, 8, 104–111.
  20. Radosavljević, M.; Lević, S.; Pejin, J.; Mojović, L.; Nedović, V. Encapsulation Technology of Lactic Acid Bacteria in Food Fermentation. In Lactic Acid Bacteria in Food Biotechnology; Elsevier: Amsterdam, The Netherlands, 2022; pp. 319–347.
  21. Register, F. Nisin Preparation: Affirmation of GRAS Status as a Direct Human Food Ingredient. Fed. Regist. 1988, 54, 11247–11251.
  22. Qiu, Y.; Lei, P.; Zhang, Y.; Sha, Y.; Zhan, Y.; Xu, Z.; Li, S.; Xu, H.; Ouyang, P. Recent Advances in Bio-Based Multi-Products of Agricultural Jerusalem Artichoke Resources. Biotechnol. Biofuels 2018, 11, 1–15.
  23. Venegas-Ortega, M.G.; Flores-Gallegos, A.C.; Martínez-Hernández, J.L.; Aguilar, C.N.; Nevárez-Moorillón, G. V Production of Bioactive Peptides from Lactic Acid Bacteria: A Sustainable Approach for Healthier Foods. Compr. Rev. Food Sci. Food Saf. 2019, 18, 1039–1051.
  24. Ananou, S.; Maqueda, M.; Martínez-Bueno, M.; Valdivia, E. Biopreservation, an Ecological Approach to Improve the Safety and Shelf-Life of Foods. Commun. Curr. Res. Educ. Top. Trends Appl. Microbiol. 2007, 1, 475–487.
  25. Barcenilla, C.; Ducic, M.; López, M.; Prieto, M.; Álvarez-Ordónez, A. Application of Lactic Acid Bacteria for the Biopreservation of Meat Products: A Systematic Review. Meat Sci. 2022, 183, 108661.
  26. Ojha, K.S.; Kerry, J.P.; Duffy, G.; Beresford, T.; Tiwari, B.K. Technological Advances for Enhancing Quality and Safety of Fermented Meat Products. Trends Food Sci. Technol. 2015, 44, 105–116.
  27. Lorenzo, J.M.; Bedia, M.; Bañón, S. Relationship between Flavour Deterioration and the Volatile Compound Profile of Semi-Ripened Sausage. Meat Sci. 2013, 93, 614–620.
  28. Ashaolu, T.J.; Reale, A. A Holistic Review on Euro-Asian Lactic Acid Bacteria Fermented Cereals and Vegetables. Microorganisms 2020, 8, 1176.
  29. Xing, L.; Liu, R.; Cao, S.; Zhang, W.; Guanghong, Z. Meat Protein Based Bioactive Peptides and Their Potential Functional Activity: A Review. Int. J. Food Sci. Technol. 2019, 54, 1956–1966.
  30. Ashaolu, T.J. Safety and Quality of Bacterially Fermented Functional Foods and Beverages: A Mini Review. Food Qual. Saf. 2020, 4, 123–127.
  31. Strafella, S.; Simpson, D.J.; Yaghoubi Khanghahi, M.; De Angelis, M.; Gänzle, M.; Minervini, F.; Crecchio, C. Comparative Genomics and in Vitro Plant Growth Promotion and Biocontrol Traits of Lactic Acid Bacteria from the Wheat Rhizosphere. Microorganisms 2020, 9, 78.
  32. Ribeiro, S.C.; Coelho, M.C.; Silva, C.C.G. A Rapid Screening Method to Evaluate Acidifying Activity by Lactic Acid Bacteria. J. Microbiol. Methods 2021, 185, 106227.
  33. Khalid, K. An Overview of Lactic Acid Bacteria. Int. J. Biosci. 2011, 1, 1–13.
  34. BIOHAZ; Koutsoumanis, K.; Allende, A.; Alvarez-Ordóñez, A.; Bolton, D.; Bover-Cid, S.; Chemaly, M.; Davies, R.; De Cesare, A.; Hilbert, F. Scientific Opinion on the Update of the List of QPS-recommended Biological Agents Intentionally Added to Food or Feed as Notified to EFSA (2017–2019). EFSA J. 2020, 18, e05966.
  35. Zheng, J.; Wittouck, S.; Salvetti, E.; Franz, C.M.A.P.; Harris, H.M.B.; Mattarelli, P.; O’toole, P.W.; Pot, B.; Vandamme, P.; Walter, J. A Taxonomic Note on the Genus Lactobacillus: Description of 23 Novel Genera, Emended Description of the Genus Lactobacillus Beijerinck 1901, and Union of Lactobacillaceae and Leuconostocaceae. Int. J. Syst. Evol. Microbiol. 2020, 70, 2782–2858.
  36. Saranraj, P.; Naidu, M.A.; Sivasakthivelan, P. Lactic Acid Bacteria and Its Antimicrobial Properties: A Review. Int. J. Pharm. Biol. Arch. 2013, 4, 1124–1133.
  37. Hashemi, S.M.B.; Abedi, E.; Kaveh, S.; Mousavifard, M. Hypocholesterolemic, Antidiabetic and Bioactive Properties of Ultrasound-Stimulated Exopolysaccharide Produced by Lactiplantibacillus Plantarum Strains. Bioact. Carbohydr. Diet. Fibre 2022, 28, 100334.
  38. Walhe, R.A.; Diwanay, S.S.; Patole, M.S.; Sayyed, R.Z.; Al-Shwaiman, H.A.; Alkhulaifi, M.M.; Elgorban, A.M.; Danish, S.; Datta, R. Cholesterol Reduction and Vitamin B12 Production Study on Enterococcus Faecium and Lactobacillus Pentosus Isolated from Yoghurt. Sustainability 2021, 13, 5853.
  39. Al-Dhabi, N.A.; Esmail, G.A.; Valan Arasu, M. Co-Fermentation of Food Waste and Municipal Sludge from the Saudi Arabian Environment to Improve Lactic Acid Production by Lactobacillus Rhamnosus AW3 Isolated from Date Processing Waste. Sustainability 2020, 12, 6899.
  40. Lee, N.-K.; Paik, H.-D. Prophylactic Effects of Probiotics on Respiratory Viruses Including COVID-19: A Review. Food Sci. Biotechnol. 2021, 30, 773–781.
  41. Mei, J.; Ma, X.; Xie, J. Review on Natural Preservatives for Extending Fish Shelf Life. Foods 2019, 8, 490.
  42. Hugo, C.J.; Hugo, A. Current Trends in Natural Preservatives for Fresh Sausage Products. Trends Food Sci. Technol. 2015, 45, 12–23.
  43. Ammor, S.; Dufour, E.; Zagorec, M.; Chaillou, S.; Chevallier, I. Characterization and Selection of Lactobacillus Sakei Strains Isolated from Traditional Dry Sausage for Their Potential Use as Starter Cultures. Food Microbiol. 2005, 22, 529–538.
  44. Hugas, M.; Garriga, M.; Aymerich, M.T. Functionalty of Enterococci in Meat Products. Int. J. Food Microbiol. 2003, 88, 223–233.
  45. Toldrá, F.; Hui, Y.H. Dry-Fermented Sausages and Ripened Meats: An Overview. In Handbook of fermented meat and poultry; Toldrá, F., Hui, Y.H., Astiasarán, I., Sebranek, J.G., Talon, R., Eds.; Wiley Online Library: New York, NY, USA, 2014; pp. 1–6.
  46. Franz, C.M.A.P.; Stiles, M.E.; Schleifer, K.H.; Holzapfel, W.H. Enterococci in Foods—A Conundrum for Food Safety. Int. J. Food Microbiol. 2003, 88, 105–122.
  47. Leroy, F.; Verluyten, J.; De Vuyst, L. Functional Meat Starter Cultures for Improved Sausage Fermentation. Int. J. Food Microbiol. 2006, 106, 270–285.
  48. Todorov, S.D.; Favaro, L.; Gibbs, P.; Vaz-Velho, M. Enterococcus Faecium Isolated from Lombo, a Portuguese Traditional Meat Product: Characterisation of Antibacterial Compounds and Factors Affecting Bacteriocin Production. Benef. Microbes 2012, 3, 319–330.
  49. Andrade, M.J.; Córdoba, J.J.; Casado, E.M.; Córdoba, M.G.; Rodríguez, M. Effect of Selected Strains of Debaryomyces Hansenii on the Volatile Compound Production of Dry Fermented Sausage “Salchichón”. Meat Sci. 2010, 85, 256–264.
  50. Cano-García, L.; Flores, M.; Belloch, C. Molecular Characterization and Aromatic Potential of Debaryomyces Hansenii Strains Isolated from Naturally Fermented Sausages. Food Res. Int. 2013, 52, 42–49.
  51. Egan, K.; Field, D.; Rea, M.C.; Ross, R.P.; Hill, C.; Cotter, P.D. Bacteriocins: Novel Solutions to Age Old Spore-Related Problems? Front. Microbiol. 2016, 7, 461.
  52. Castellano, P.; Belfiore, C.; Fadda, S.; Vignolo, G. A Review of Bacteriocinogenic Lactic Acid Bacteria Used as Bioprotective Cultures in Fresh Meat Produced in Argentina. Meat Sci. 2008, 79, 483–499.
  53. Gálvez, A.; Abriouel, H.; López, R.L.; Omar, N. Ben Bacteriocin-Based Strategies for Food Biopreservation. Int. J. Food Microbiol. 2007, 120, 51–70.
  54. Belfiore, C.; Castellano, P.; Vignolo, G. Reduction of Escherichia Coli Population Following Treatment with Bacteriocins from Lactic Acid Bacteria and Chelators. Food Microbiol. 2007, 24, 223–229.
  55. Melero, B.; Diez, A.M.; Rajkovic, A.; Jaime, I.; Rovira, J. Behaviour of Non-Stressed and Stressed Listeria Monocytogenes and Campylobacter Jejuni Cells on Fresh Chicken Burger Meat Packaged under Modified Atmosphere and Inoculated with Protective Culture. Int. J. Food Microbiol. 2012, 158, 107–112.
  56. Khalili Sadaghiani, S.; Aliakbarlu, J.; Tajik, H.; Mahmoudian, A. Anti-listeria Activity and Shelf Life Extension Effects of Lactobacillus along with Garlic Extract in Ground Beef. J. Food Saf. 2019, 39, e12709.
  57. Orihuel, A.; Bonacina, J.; Vildoza, M.J.; Bru, E.; Vignolo, G.; Saavedra, L.; Fadda, S. Biocontrol of Listeria Monocytogenes in a Meat Model Using a Combination of a Bacteriocinogenic Strain with Curing Additives. Food Res. Int. 2018, 107, 289–296.
  58. Hu, Z.Y.; Balay, D.; Hu, Y.; McMullen, L.M.; Gänzle, M.G. Effect of Chitosan, and Bacteriocin–Producing Carnobacterium Maltaromaticum on Survival of Escherichia Coli and Salmonella Typhimurium on Beef. Int. J. Food Microbiol. 2019, 290, 68–75.
  59. Smaoui, S.; Hsouna, A.B.; Lahmar, A.; Ennouri, K.; Mtibaa-Chakchouk, A.; Sellem, I.; Najah, S.; Bouaziz, M.; Mellouli, L. Bio-Preservative Effect of the Essential Oil of the Endemic Mentha Piperita Used Alone and in Combination with BacTN635 in Stored Minced Beef Meat. Meat Sci. 2016, 117, 196–204.
  60. Castellano, P.; Belfiore, C.; Vignolo, G. Combination of Bioprotective Cultures with EDTA to Reduce Escherichia Coli O157: H7 in Frozen Ground-Beef Patties. Food Control 2011, 22, 1461–1465.
  61. Ghabraie, M.; Vu, K.D.; Huq, T.; Khan, A.; Lacroix, M. Antilisterial Effects of Antibacterial Formulations Containing Essential Oils, Nisin, Nitrite and Organic Acid Salts in a Sausage Model. J. Food Sci. Technol. 2016, 53, 2625–2633.
  62. Vaz-Velho, M.; Jácomea, S.; Noronhab, L.; Todorovc, S.; Fonsecaa, S.; Pinheiro, R.; Moraisb, A.; Silvab, J.; Teixeirab, P. Comparison of Antilisterial Effects of Two Strains of Lactic Acid Bacteria during Processing and Storage of a Portuguese Salami-like Product “Alheira”. Chem. Eng. 2013, 32, 1807–1812.
  63. Castro, S.M.; Silva, J.; Casquete, R.; Queirós, R.; Saraiva, J.A.; Teixeira, P. Combined Effect of Pediocin BacHA-6111-2 and High Hydrostatic Pressure to Control Listeria Innocua in Fermented Meat Sausage. Int. Food Res. J. 2018, 25, 553–560.
  64. Kumar, Y.; Kaur, K.; Shahi, A.K.; Kairam, N.; Tyagi, S.K. Antilisterial, Antimicrobial and Antioxidant Effects of Pediocin and Murraya Koenigii Berry Extract in Refrigerated Goat Meat Emulsion. LWT-Food Sci. Technol. 2017, 79, 135–144.
  65. de Azevedo, P.O.S.; Mendonça, C.M.N.; Seibert, L.; Domínguez, J.M.; Converti, A.; Gierus, M.; Oliveira, R.P.S. Bacteriocin-like Inhibitory Substance of Pediococcus Pentosaceus as a Biopreservative for Listeria Sp. Control in Ready-to-Eat Pork Ham. Braz. J. Microbiol. 2020, 51, 949–956.
  66. Esua, O.J.; Sun, D.-W.; Ajani, C.K.; Cheng, J.-H.; Keener, K.M. Modelling of inactivation kinetics of Escherichia coli and Listeria monocytogenes on grass carp treated by combining ultrasound with plasma functionalized buffer. Ultrason. Sonochem. 2022, 88, 106086.
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