Clean-Label Antimicrobials in the  United States: History
Please note this is an old version of this entry, which may differ significantly from the current revision.
Contributor: , , , , ,

Food additives are employed in the food industry to enhance the color, smell, and taste of foods, increase nutritional value, boost processing efficiency, and extend shelf life. Consumers are beginning to prioritize food ingredients that they perceive as supporting a healthy lifestyle, emphasizing ingredients they deem acceptable as alternative or “clean-label” ingredients. Ready-to-eat (RTE) meat products can be contaminated with pathogens and spoilage microorganisms after the cooking step, contributing to food spoilage losses and increasing the risk to consumers for foodborne illnesses. More recently, consumers have advocated for no artificial additives or preservatives, which has led to a search for antimicrobials that meet these demands but do not lessen the safety or quality of RTE meats. Lactates and diacetates are used almost universally to extend the shelf life of RTE meats by reducing spoilage organisms and preventing the outgrowth of the foodborne pathogen Listeria monocytogenes. These antimicrobials applied to RTE meats tend to be broad-spectrum in their activities, thus affecting overall microbial ecology. It is to the food processing industry’s advantage to target spoilage organisms and pathogens specifically.

  • ready-to-eat food
  • alternative additives
  • clean-label
  • spoilage
  • antimicrobials

1. Introduction

Generally, food additives are used in the commercial food industry to improve foods’ color, smell, and taste, enhance nutritional value, increase processing efficiency, and extend shelf life [1][2]. Food additives are a broad group of compounds that potentially improve food quality [3]. Traditional food additives include salt, sugar, herbs or spices, vinegar, sulfur dioxide, and colorants [3]. However, the demand for types of food additives has changed with more emphasis on alternative additives deemed acceptable as “clean-label” [4]. The clean-label market trend for foods has become increasingly important to consumers in Western countries, and the onset of the pandemic in 2020 provided further motivation for consumers to prioritize food ingredients that they perceive as supporting a healthy lifestyle [5]. There is no legal or regulatory definition of a “clean-label” [4]. Consumers may equate clean-labels with minimally processed foods with no artificial flavors, artificial colors, or synthetic additives [4].
Consequently, food ingredients viewed as “healthier” or providing health-like benefits have gained commercial interest in the retail marketplace. These ingredients include those identified as part of a “clean-label” type of classification. A broad definition of “clean-label” foods is those with no artificial additives and are less processed, with simple and short ingredient lists that the average consumer recognizes [6][7]. Reduced fat, sugar, and sodium contents may also fall under the term “clean-label” when contributing to improved health [7].
In general, consumers rely on informational statements on packages such as “no preservatives” or “reduced fat” rather than reading the ingredient statements; for example, it has been reported that 65% of respondents to surveys responded that they never checked ingredient labels for additives [8], and some estimate that only 5 to 10% of consumers read the ingredients [9]. Delgado-Pando et al. [10] believe that consumers associate clean-label products with those with a short list of nonsynthetic or familiar ingredients. The Institute of Food Technologists (IFT) has proposed a definition: “clean-label means making a product using as few ingredients as possible and making sure those ingredients are items that consumers recognize and think of as wholesome” [11]. Cao and Miao [12] surveyed consumer-perceived clean-label attributes and found that the top three were minimally processed, eliminated undesired ingredients and exercised humane treatment. In order of perceived importance, they were minimally processed, had familiar ingredients, eliminated undesired ingredients, used local ingredients, and demonstrated an absence of allergens [12].
Clean-labeling in meat products, particularly further processed meats such as ready-to-eat (RTE) meats, has also become an issue. Most antimicrobials that are applied to RTE meats tend to be broad-spectrum in their activities, so it would be expected that overall microbial ecology would be impacted by their administration [13]. This, in turn, could alter the extent of shelf life and subsequent development of quality deterioration identified as spoilage. Historically, this has been difficult to characterize with conventional microbial culture-based approaches due to the limitations and selectivity of most media used for cultivation and enumeration. 

2. Clean-Label Antimicrobials in the U.S.

2.1. Organic Acids

Organic acids and salts of acids are theorized to exhibit antimicrobial activity in their un-dissociated and uncharged forms by being able to cross the bacterial cell membrane [14], where they increase osmotic stress and disrupt biomolecule synthesis, leading to bacterial death [15][16][17]. Organic acids have shown promise as natural antimicrobials but may affect color and flavor changes in products [18]. The most used acids are acetic, citric, lactic, propionic, malic, succinic, and tartaric [19][20]. Their many advantages include GRAS (generally regarded as safe) status by the U.S. Food and Drug Administration (FDA), no limits on acceptable daily intake, low cost, and ease of use, but caution must be observed as some Salmonella strains can develop resistance to acidic conditions [21].
Sodium lactate, the salt of lactic acid, has been used as an antimicrobial in Chinese-style sausages; lower total aerobic and anaerobic plates were seen with 3% sodium lactate during a storage time of 12 weeks at 4 °C [22]. Sodium lactate was also shown to inhibit the growth of several pathogens in inoculated cooked ham [23]. When samples were stored at 4 °C, 8 °C, or 10 °C, growth rates of L. monocytogenes, E. coli, or Salmonella decreased significantly for both 1% and 2% sodium lactate at all temperatures. However, the inhibition was more significant at lower storage temperatures [23]. The shelf life of ground beef treated with sodium lactate increased from 8 to 15 days when stored at 4 °C; aerobic plate counts, psychrotrophic counts, Enterobacteriaceae, and lactic acid bacteria counts decreased significantly compared to untreated controls [24]. Sodium lactate also effectively delayed the growth of aerobic plate counts (approximately 1.5 to 2 log reduction) in ground pork meat [25].
Barmpalia et al. [26] treated pork bologna sausage with 1.8% sodium lactate with 0.25% sodium diacetate and found that total spoilage organisms were reduced as much as 5 logs compared to the control when stored at 4 °C. Mohan and Pohlman [27] studied the effects of nine organic acids (30 g/L) and peroxyacetic acid (2 g/L) as antimicrobial treatments for beef trimmings. In general, most organic acids were effective at reducing bacterial populations, but caprylic acid produced a considerable reduction in coliforms (4.78 log reduction), E. coli O157:H7 (4.73 log reduction), and aerobic plate count bacteria (2.48 log reduction) [27].
The use of organic acids and their salts extends the shelf life of meat products and increases their safety due to their strong inhibitory effect against pathogenic and spoilage bacteria [28]. However, it has become apparent that some microorganisms have the means to counteract the effects of such acid-based agents, allowing them to become resistant to antimicrobial activity and to be able to survive under severe acidic conditions [29][30], leading to the emergence of acid-tolerant foodborne pathogens [31].

2.2. Botanicals

Botanically derived compounds, especially polyphenols, have antimicrobial effects and could be incorporated into RTE meats to reduce spoilage and increase food safety [32][33]. Polyphenols have one or more aromatic rings and one or more -OH groups, giving them their antibacterial properties [18]. These plant-based compounds can be further divided into extracts (normally hydrophilic, obtained by aqueous extractions) and essential oils (lipophilic, obtained by distillation or extraction by organic solvents) [34]. Extraction and separation of these plant substances are performed to confirm antimicrobial effects [34], but using extracts rather than plant powders also has advantages. Bioactive molecules are concentrated in the extracts so they can be used at lower concentrations than powders; the extracts are more stable, accessible, and economical to ship [18].
McDonnell et al. [35] evaluated the addition of vinegar, lemon, and cherry powder blend (1.5%) against the growth of L. monocytogenes inoculated on the surface of cured ham and deli-style turkey breast. They detected no growth of L. monocytogenes during 12 weeks of storage at 4 °C. Red fruit extracts (plum, red grapes, and elderberries) also inhibited pathogens, including B. cereus, S. aureus, and E. coli, while also increasing the growth of probiotic bacteria [36].
Extracts obtained from green tea, stinging nettle, and olive leaves produced a greater than 1 log CFU/g reduction in the total viable count, resulting in shelf-life extension when used in a frankfurter-type sausage [37]. Fresh chicken sausages were treated with 1% lemongrass extract, which significantly reduced the counts of total psychrotrophic and aerobic mesophilic microorganisms compared to controls [38]. Similarly, lemongrass extract extended the shelf life of cooked and shredded chicken breast and inhibited Staphylococcus spp., Salmonella spp., and coliforms [39].
A broad range of essential oils (EOs) and their active compounds possess antimicrobial effects. They are widely used in meat production to prevent spoilage and inhibit the growth of foodborne pathogens [40][41]. Many of these are considered GRAS [41][42], and lemon balm, basil, clove, vanilla, thyme, coriander, and others are approved for food in the U.S. [43]. Oregano oil has been proven to inhibit spoilage bacteria, extend shelf life in meat [44][45][46], and possess activity against pathogens including Sal. Enteritidis [47], Sal. Typhimurium [45][48], St. aureus, and L. monocytogenes [49].
Essential oils often have a strong odor and flavor, which may impact consumer acceptance and limit their use in foods [12]. In addition to their sensory effects, botanical-based antimicrobials may not mix well in food matrices or may be inactivated by standard processing techniques [50]. Other considerations include variations in the effectiveness of extracts prepared at different times from different batches of plant material and the possibility of bacteria developing resistance to the compounds [51]. There have also been concerns about the safety of these compounds since there is a potential for plants to be contaminated with heavy metals [52], mycotoxins [53], or pesticides [54]. Hurdle technology should be explored with EOs combined with other compounds or processing methods to lessen the organoleptic effects of EOs. Some suggested techniques include the encapsulation of EOs in nanostructures, which should be explored to extend the shelf life and safety of RTE meats [50].

2.3. Digestible Films and Coatings

Digestible films, also more commonly referred to as edible films, are usually cast over an inert surface, dried, and then used on food products in the form of pouches, wraps, capsules, bags, or casings [55]. Edible coatings, on the other hand, are food-grade suspensions that are sprayed or spread over the surface of a product, or the product is dipped in the suspension; when the suspension dries, it forms a transparent thin layer over the food surface and becomes a part of the final product [56]. These products can extend the shelf life of RTE meats by acting as barriers to water vapor, oxygen, and carbon dioxide, or they may also be used to carry antimicrobials [55]. These edible films and coatings can be based on lipids, proteins, or carbohydrates [55].

2.3.1. Protein-Based Films and Coatings

The proteins for these products can be from both animal (casein, whey protein concentrate and isolate, collagen, gelatin, and egg albumin) and plant sources (corn, soybean, wheat, cottonseed, peanut, and rice) [55]. These protein-based films work well on hydrophilic surfaces and act as a barrier to oxygen and carbon dioxide but not water [57]. Adding hydrophobic materials such as beeswax or oils can improve the moisture barrier properties [58][59][60]. Collagen, keratin, and proteins from quinoa, milk, egg, whey, zein, and soy are widely used to make protein-based films [61]. Protein-based edible films have been investigated for salami [62], chicken breast [63][64], beef [65][66], and pork [67]. However, these films can potentially be degraded by innate enzymes in the meat or prove allergenic for some portion of the population [68].

2.3.2. Lipid-Based Films and Coatings

Lipids used in edible films and coating come from both animal and plant sources. For instance, vegetable oils such as peanut, coconut, or palm oil and animal-based products including lard, butter, and fatty acids have all been utilized [69]. Fat has been used as a food coating since the 16th century [70]. Waxes and oils have been used for years as protective coatings for fresh fruits and vegetables [71]. However, wax-based fat- and oil-based coatings can be too thick, inconsistent, and greasy, or the coatings may crack [72]. There can also be a waxy or rancid taste that limits their use [72]. Therefore, lipids are usually used in a multi-component system with proteins, starch, cellulose, and their derivatives [57].

2.3.3. Carbohydrate-Based Coatings and Films

Polysaccharides are carbohydrates used in coatings; they are relatively poor moisture barriers but have low permeability to O2 and CO2 and are resistant to fats and oils [73]. Cellulose, starch, pectin, seaweed extracts, gums, and chitosan can be used to make polysaccharide films [55]. These films and coatings extend the shelf life of meats by preventing dehydration, oxidative rancidity, and surface browning [55]. If these coatings are used on meat products that are smoked or steamed, the film dissolves and becomes part of the product, thus increasing yield, improving texture, and reducing loss of moisture [57].
Cellulose is the most abundant renewable resource on the planet, and cellulose derivatives are often used for edible films because they are biodegradable, tasteless, and odorless [74][75][76]. The most frequently utilized cellulose derivatives for edible films are methylcellulose (MC), carboxymethyl cellulose (CMC), and hydroxypropyl methylcellulose (HPMC) [77]. Films made from these cellulose derivatives are transparent and strong [78][79], and bioactive compounds can be added to impart antimicrobial properties [76]. Xie et al. [80] studied cellulose-based films with ZnO nanopillars as an antimicrobial packaging material. They concluded that these films possessed good mechanical properties, were excellent barriers to water and oxygen, and had optimal antimicrobial activity against both Gram-positive (St. aureus) and Gram-negative (E. coli) bacteria [80].
Starch is another abundant plant-derived polysaccharide considered cost-effective and forms desirable films [75][81][82]. Corn, potatoes, rice, cassava, tapioca, and sweet potatoes are the most common starch sources for edible films [83]. Radha Krishnan et al. [84] added clove and cinnamon essential oils to corn starch film, extending beef fillets’ shelf life. Grape juice incorporated into maize starch films increased the shelf life of chicken breast fillets [85]. Curcumin extract incorporated into a rice film increased the shelf life of chicken and fish stored at refrigeration temperatures [86].
Chitosan, a high-molecular-weight cationic polysaccharide obtained from the shells of crustaceans (mainly lobster and shrimp), exhibits a pronounced film-forming capacity and antimicrobial activities [76][87][88]. Chitosan-based films are transparent, flexible, tough, and very resistant to fat, oil, and oxygen but are highly sensitive to moisture [76][89]. Chitosan also possesses antimicrobial properties. Alaskan pollock sausages stored in chitosan–gelatin films had both Gram-positive and Gram-negative bacteria growth inhibited in the sausages over 42 days of storage [90].
Cyclodextrins (CDs) are water-soluble cyclic oligosaccharides made up of D-glucopyranoside units linked by α-1,4-glycosidic bonds [91]. The positions of hydroxyl groups in CDs allow the exterior to be hydrophilic while the interior is hydrophobic [92], enabling them to form inclusion complexes with hydrophobic molecules [93][94]. These CD inclusion complexes are used to maintain firmness and freshness and aid in water retention in fresh-cut fruits and vegetables [95]. Empty CDs are used to encapsulate detrimental volatile compounds inside their hollow cavity. Ethylene is the compound responsible for the ripening of fruits, but the control of ripening during shipping is desirable, and it has been successfully controlled by using CDs [96]. For example, α-CD complexes were used in one study to encapsulate ethylene to prevent the ripening of mangoes [97]. Antimicrobial compounds can also be encapsulated in CDs for slow release with various triggers. Eucalyptus essential oil was treated with CD to form an inclusion complex, and zein was added to enhance antimicrobial results; L. monocytogenes was reduced by 28.5% and S. aureus by 24.3% when using these films [98]. CD-based films have also been used to eliminate fish odors and preserve meat, juices, milk, beverages of all types, processed foods, ready-to-eat foods, and cheese [99].
As already noted, edible films produced from polysaccharides are suitable barriers to gas but inadequate for water vapors and have poor mechanical strength [73]. Protein-based films also have poor water vapor resistance but good mechanical strength [57]. However, lipids cannot be used to make edible films as they cannot form a cohesive structure and are used as edible coatings, primarily for fruits and vegetables, or combined with proteins or polysaccharides to make composite films [100]. Edible films have yet to be commercialized for various reasons, not the least of which is that edible films are not as strong as plastic films and do not elongate well [101]. Jeevahan et al. [101] have written an excellent article addressing the problems with the commercialization of edible films, addressing six problem areas: (a) functional properties, (b) film making and drying methods, (c) nanotechnology on edible films, (d) lack of knowledge, and (e) consumer acceptance.

2.4. Bacteriocins: Sources and Applications for RTE Meats in the U.S.

Bacteriocins are peptides produced by certain bacteria that can exhibit activity against Gram-positive and Gram-negative bacteria [102][103]. They are known to be safe for human consumption because they are inactivated by proteases in the gastrointestinal tract (GIT) without affecting the normal microbiota of the GIT [104]. An attractive feature is that target bacteria do not form resistance against them [105]. There are three different approaches to the use of bacteriocins in food: (1) direct addition of the bacteriocin into the product; (2) incorporation of the bacteriocin into an edible film; (3) inclusion of bacteriocin-producing cultures into the formula or in a coating [104].
Lactococcus lactis subsp. lactis produces a bacteriocin, nisin, which has been found to inhibit the growth of Clostridium and Bacillus [106]. Many countries, including the U.S., allow the use of nisin in food products such as milk, processed cheese, grated cheese, dairy products, canned vegetables, soups, and meat, as well as brewery products and mayonnaise [107][108][109]. However, the use of nisin in meat is limited because it has low solubility in meat products, innate enzymes in the meat may destroy nisin, and it has shown limited effectiveness against several meat spoilage organisms [110].
Pediocin PA-1/AcH, produced by Pediococcus acidilactici, is another bacteriocin that can be used in dried sausages and fermented meat products [103][105][110]. P. acidilactici MCH14, which produces pediocin PA-1, was incorporated into dry fermented sausages and was shown to inhibit the growth of both L. monocytogenes and Cl. perfringens [111]. Strain P. pentosaceus BCC3772, which produces pediocin PA-1/AcH, inhibited L. monocytogenes during the fermentation of a Thai pork sausage without significantly altering its odor or taste [112]. Pediocin and nisin were used in vacuum-packed sliced ham and reduced the counts of Lactobacillus sakei, an important spoilage organism [113]. Pediocin PA-1 minimizes the growth of spoilage microorganisms during the storage of meat products; it is active at low pH and acts synergistically with lactate or organic acids [114].
A bacteriocin produced by Leuconostoc mesenteroides ssp. mesenteroides IMAU: 10231 was incorporated into a fermented sausage product, reducing the growth of L. monocytogenes during 21 days of refrigerated storage [115]. This strain of Leuconostoc produces CO2 during fermentation, which means the bacteriocin itself must be used rather than the bacteria being incorporated as a part of the culture [116]. However, a homofermentative lactic acid bacteria (LAB) that produces lactic acid instead of CO2 could be used as a starter culture [104]. For example, Weissella paramesenteroides DX produces the bacteriocin weissellin A. When this organism is grown in oxygen, sodium nitrite inhibits the bacteriocin production [116]. However, in anaerobic conditions such as those found when fermenting meat sausages, sodium nitrite does not inhibit the production of bacteriocin, making this organism an optimal candidate as a starter culture [116]. The bacteriocin BacFL31 produced by Enterococcus faecium sp. FL 31 inhibited the growth of spoilage microorganisms, L. monocytogenes, and Sal. Typhimurium in ground turkey meat during refrigerated storage [117].
Direct application of bacteriocins in the meat matrix reduces the antimicrobial activity of some other bacteriocins [118]. To avoid reductions in the efficacy of other bacteriocins, an alternative application method is to incorporate the bacteriocin into the food packaging material to serve as an active packaging component, therefore reducing the direct contact of the bacteriocin with the food product [104]. This approach allows the use of a smaller quantity of bacteriocins and controlled release, as the activity is on the product’s surface [119]. Over the past ten years, nisin has been widely utilized as an active packaging component [120]. Nisin used in various films and coatings has been shown to reduce the growth of L. monocytogenes, B. thermosphacta, Enterobacteriaceae, and spoilage LAB in raw meat, sliced ham, and ground beef [65][121][122][123]. Pediocin incorporated into cellulose-based packages also reduced the growth of L. monocytogenes in sliced ham, turkey, and beef [124][125]. Marcos et al. [126] demonstrated the increased safety of sliced ham by delaying or reducing the growth of L. monocytogenes using enterocins incorporated into alginate, zein, or polyvinyl alcohol-based biodegradable film.
Despite the success of nisin and pediocin, the use of bacteriocins in foods may be limited by their poor solubility and the uneven distribution and partitioning in the food matrix [104][127]. Their narrow spectrum of activity means that specific spoilage organisms must be identified and bacteriocins discovered that inactivate these bacteria [128]. Purification of bacteriocins can be difficult and expensive [128].

2.5. Bacteriophage for RTE Meats in the U.S.

Bacteriophages (phages), viruses that infect bacteria, are ubiquitous in the world, existing everywhere that there are bacteria [129][130][131]. Bacteriophages have been studied for use as antimicrobials to increase food safety [132]. Since bacteriophages are specific for a particular bacterium, most studies in RTE meats and bacteriophages have been conducted on pathogens, especially L. monocytogenes [133]. The U.S. Food and Drug Administration (FDA) has approved two bacteriophage preparations, using phages P100 and LMP-102, as food ingredients to control L. monocytogenes [134].
Alves et al. [135] incorporated bacteriophage IBB-PF7A in a sodium alginate film to limit meat spoilage caused by Pseudomonas fluorescens. The number of Ps. fluorescens organisms decreased by 2 Logs CFU/cm2 during the first two days of refrigerated storage and then only dropped by 1 Log CFU/cm2 over the next five days [135]. This highlights one of the problems with using bacteriophage in food products: their stability [135].
A more significant problem is the specificity of phages [133]. To target specific spoilage organisms, there is a need to definitively identify most, if not all, members of the microbial community of meat and meat products, especially regarding spoilage. Another limitation is that phages cannot be combined with other methods because the other techniques would inactivate the phages [136]. There are two types of bacteriophages, lytic and lysogenic, which also challenge their use [130]. Lytic phages take over the protein synthesis of the target cell and produce more phages, which then burst the target cell to infect other bacteria [130]. Lysogenic phages, on the other hand, integrate themselves into the host cell’s chromosome, making lytic phages the most suitable for food applications [130][136]. Bacteriophages cannot diffuse throughout food and are limited to surface application [136].

This entry is adapted from the peer-reviewed paper 10.3390/foods13030464

References

  1. Wu, L.; Zhang, Q.; Shan, L.; Chen, Z. Identifying critical factors influencing the use of additives by food enterprises in China. Food Control 2013, 31, 425–432.
  2. Wang, C.; Wu, J.; Gao, X. Basic attributives, functions and characteristics of food additives. China Food Addit. 2015, 10, 154–158.
  3. FDA. Overview of Food Ingredients, Additives & Colors. 2010. Available online: https://www.fda.gov/food/food-ingredients-packaging/overview-food-ingredients-additives-colors (accessed on 22 May 2023).
  4. Chen, W.; Hart, H. Consumers Turn an Eye to Clean Labels. 2016. Available online: https://www.food-safety.com/articles/5009-consumers-turn-an-eye-to-clean-labels (accessed on 23 May 2023).
  5. Jacobsen, J. Consumer Awareness of Clean Label Drives Demand for Ingredient Solutions. 2022. Available online: https://www.bevindustry.com/articles/95110-consumer-awareness-of-clean-label-drives-demand-for-ingredient-solutions (accessed on 4 April 2023).
  6. Asioli, D.; Aschemann-Witzel, J.; Caputo, V.; Vecchio, R.; Annunziata, A.; Næs, T.; Varela, P. Making sense of the “clean label” trends: A review of consumer food choice behavior and discussion of industry implications. Food Res. Int. 2017, 99, 58–71.
  7. Hutt, C.A.; Sloan, A.E. Coming clean: What clean label means for consumers and industry. In Proceedings of the Global Food Forum Clean Label Conference, Itasca, IL, USA, 31 March 2015; pp. 5–8.
  8. Koyratty, B.N.S.; Aumjaud, B.; Neeliah, S.A. Food additive control: A survey among selected consumers and manufacturers. Br. Food J. 2014, 116, 353–372.
  9. Sosland, J. Research Suggests Few Consumers Actually Read Package Labels. 2022. Available online: https://www.supermarketperimeter.com/articles/8428-research-suggests-few-consumers-actually-read-package-labels (accessed on 6 April 2023).
  10. Delgado-Pando, G.; Ekonomou, S.I.; Stratakos, A.C.; Pintado, T. Clean Label Alternatives in Meat Products. Foods 2021, 10, 1615.
  11. IFT. What Is Clean Label? 2021. Available online: https://www.ift.org/news-and-publications/blog/2018/november/what-is-clean-label (accessed on 23 May 2023).
  12. Cao, Y.; Miao, L. Consumer perception of clean food labels. Br. Food J. 2022, 125, 433–448.
  13. Abdelhamid, A.G.; El-Dougdoug, N.K. Controlling foodborne pathogens with natural antimicrobials by biological control and antivirulence strategies. Heliyon 2020, 6, e05020.
  14. Russell, J. Another explanation for the toxicity of fermentation acids at low pH: Anion accumulation versus uncoupling. J. Appl. Bacteriol. 1992, 73, 363–370.
  15. Kashket, E.R. Bioenergetics of lactic acid bacteria: Cytoplasmic pH and osmotolerance. FEMS Microbiol. Lett. 1987, 46, 233–244.
  16. Hirshfield, I.N.; Terzulli, S.; O’Byrne, C. Weak Organic Acids: A Panoply of Effects on Bacteria. Sci. Prog. 2003, 86, 245–270.
  17. Salsali, H.; Parker, W.J.; Sattar, S.A. The effect of volatile fatty acids on the inactivation of Clostridium perfringens in anaerobic digestion. World J. Microbiol. Biotechnol. 2007, 24, 659–665.
  18. Santiesteban-López, N.A.; Gómez-Salazar, J.A.; Santos, E.M.; Campagnol, P.C.B.; Teixeira, A.; Lorenzo, J.M.; Sosa-Morales, M.E.; Domínguez, R. Natural Antimicrobials: A Clean-label Strategy to Improve the Shelf Life and Safety of Reformulated Meat Products. Foods 2022, 11, 2613.
  19. Sohaib, M.; Anjum, F.M.; Arshad, M.S.; Rahman, U.U. Postharvest intervention technologies for safety enhancement of meat and meat based products; a critical review. J. Food Sci. Technol. 2016, 53, 19–30.
  20. Ben Braïek, O.; Smaoui, S. Chemistry, Safety, and Challenges of the Use of Organic Acids and Their Derivative Salts in Meat Preservation. J. Food Qual. 2021, 2021, 6653190.
  21. Mani-López, E.; García, H.; López-Malo, A. Organic acids as antimicrobials to control Salmonella in meat and poultry products. Food Res. Int. 2012, 45, 713–721.
  22. Lin, K.-W.; Lin, S.-N. Effects of sodium lactate and trisodium phosphate on the physicochemical properties and shelf life of low-fat Chinese-style sausage. Meat Sci. 2002, 60, 147–154.
  23. Hwang, C.-A.; Sheen, S.; Juneja, V. Effects of Sodium Lactate on the Survival of Listeria Monocytogenes, Escherichia coli O157:H7, and Salmonella spp. in Cooked Ham at Refrigerated and Abuse Temperatures. Food Nutr. Sci. 2011, 02, 464–470.
  24. Sallam, K.I.; Samejima, K. Effects of trisodium phosphate and sodium chloride dipping on the microbial quality and shelf life of refrigerated tray-packaged chicken breasts. Food Sci. Biotechnol. 2004, 13, 425–429.
  25. Brewer, M.S.; Rostogi, B.K.; Argoudelis, L.; Sprouls, G.K. Sodium Lactate/Sodium Chloride Effects on Aerobic Plate Counts and Color of Aerobically Packaged Ground Pork. J. Food Sci. 1995, 60, 58–62.
  26. Barmpalia, I.M.; Geornaras, I.; Belk, K.E.; Scanga, J.A.; Kendall, P.A.; Smith, G.C.; Sofos, J.N. Control of Listeria monocytogenes on Frankfurters with Antimicrobials in the Formulation and by Dipping in Organic Acid Solutions. J. Food Prot. 2004, 67, 2456–2464.
  27. Mohan, A.; Pohlman, F. Role of organic acids and peroxyacetic acid as antimicrobial intervention for controlling Escherichia coli O157:H7 on beef trimmings. LWT Food Sci. Technol. 2016, 65, 868–873.
  28. Yu, H.H.; Chin, Y.-W.; Paik, H.-D. Application of Natural Preservatives for Meat and Meat Products against Food-Borne Pathogens and Spoilage Bacteria: A Review. Foods 2021, 10, 2418.
  29. Theron, M.M.; Lues, J.F. Organic Acids and Meat Preservation: A Review. Food Rev. Int. 2007, 23, 141–158.
  30. Hauser, C.; Thielmann, J.; Muranyi, P. Organic acids: Usage and potential in antimicrobial packaging. In Antimicrobial Food Packaging; Academic Press: Cambridge, MA, USA, 2016; pp. 563–580.
  31. Quintavalla, S.; Vicini, L. Antimicrobial food packaging in meat industry. Meat Sci. 2002, 62, 373–380.
  32. Cordery, A.; Rao, A.P.; Ravishankar, S. Antimicrobial activities of essential oils, plant extracts and their applications in foods—A review. J. Agric. Environ. Sci. 2018, 7, 76–89.
  33. dos Santos, L.R.; Alía, A.; Martin, I.; Gottardo, F.M.; Rodrigues, L.B.; A Borges, K.; Furian, T.Q.; Córdoba, J.J. Antimicrobial activity of essential oils and natural plant extracts against Listeria monocytogenes in a dry-cured ham-based model. J. Sci. Food Agric. 2022, 102, 1729–1735.
  34. Alirezalu, K.; Pateiro, M.; Yaghoubi, M.; Alirezalu, A.; Peighambardoust, S.H.; Lorenzo, J.M. Phytochemical constituents, advanced extraction technologies and techno-functional properties of selected Mediterranean plants for use in meat products. A comprehensive review. Trends Food Sci. Technol. 2020, 100, 292–306.
  35. Mcdonnell, L.M.; Glass, K.A.; Sindelar, J.J. Identifying Ingredients That Delay Outgrowth of Listeria monocytogenes in Natural, Organic, and Clean-Label Ready-to-Eat Meat and Poultry Products. J. Food Prot. 2013, 76, 1366–1376.
  36. Coman, M.M.; Oancea, A.M.; Verdenelli, M.C.; Cecchini, C.; Bahrim, G.E.; Orpianesi, C.; Cresci, A.; Silvi, S. Polyphenol content and in vitro evaluation of antioxidant, antimicrobial and prebiotic properties of red fruit extracts. Eur. Food Res. Technol. 2017, 244, 735–745.
  37. Alirezalu, K.; Hesari, J.; Eskandari, M.H.; Valizadeh, H.; Sirousazar, M. Effect of Green Tea, Stinging Nettle and Olive Leaves Extracts on the Quality and Shelf Life Stability of Frankfurter Type Sausage. J. Food Process. Preserv. 2017, 41, e13100.
  38. Boeira, C.P.; Piovesan, N.; Soquetta, M.B.; Flores, D.C.B.; Lucas, B.N.; da Rosa, C.S.; Terra, N.N. Extraction of bioactive compounds of lemongrass, antioxidant activity and evaluation of antimicrobial activity in fresh chicken sausage. Ciência Rural 2018, 48, e20180477.
  39. Kieling, D.D.; Delarco, M.F.; Prudencio, S.H. Lemongrass Extract as a Natural Preservative of Cooked and Shredded Chicken Breast during Storage. J. Culin. Sci. Technol. 2019, 19, 55–66.
  40. Wińska, K.; Mączka, W.; Łyczko, J.; Grabarczyk, M.; Czubaszek, A.; Szumny, A. Essential Oils as Antimicrobial Agents—Myth or Real Alternative? Molecules 2019, 24, 2130.
  41. Pateiro, M.; Munekata, P.E.S.; Sant’Ana, A.S.; Domínguez, R.; Rodríguez-Lázaro, D.; Lorenzo, J.M. Application of essential oils as antimicrobial agents against spoilage and pathogenic microorganisms in meat products. Int. J. Food Microbiol. 2021, 337, 108966.
  42. Singh, S.; Chaurasia, P.K.; Bharati, S.L. Functional roles of Essential oils as an effective alternative of synthetic food preservatives: A review. J. Food Process. Preserv. 2022, 46, e16804.
  43. Coimbra, A.; Ferreira, S.; Duarte, A.P. Biological properties of Thymus zygis essential oil with emphasis on antimicrobial activity and food application. Food Chem. 2022, 393, 133370.
  44. Tsigarida, E.; Skandamis, P.; Nychas, G.J. Behaviour of Listeria monocytogenes and autochthonous flora on meat stored under aerobic, vacuum and modified atmosphere packaging conditions with or without the presence of Oregano essential oil at 5 degrees C. J. Appl. Microbiol. 2000, 89, 901–909.
  45. Skandamis, P.; Tsigarida, E.; Nychas, G.-J. The effect of oregano essential oil on survival/death of Salmonella typhimurium in meat stored at 5 °C under aerobic, VP/MAP conditions. Food Microbiol. 2002, 19, 97–103.
  46. Chouliara, E.; Karatapanis, A.; Savvaidis, I.; Kontominas, M. Combined effect of oregano essential oil and modified atmosphere packaging on shelf-life extension of fresh chicken breast meat, stored at 4 °C. Food Microbiol. 2007, 24, 607–617.
  47. Govaris, A.; Solomakos, N.; Pexara, A.; Chatzopoulou, P. The antimicrobial effect of oregano essential oil, nisin and their combination against Salmonella Enteritidis in minced sheep meat during refrigerated storage. Int. J. Food Microbiol. 2010, 137, 175–180.
  48. Ahn, J.; Grün, I.U.; Mustapha, A. Antimicrobial and Antioxidant Activities of Natural Extracts In Vitro and in Ground Beef. J. Food Prot. 2004, 67, 148–155.
  49. Barbosa, L.N.; Rall, V.L.M.; Fernandes, A.A.H.; Ushimaru, P.I.; Probst, I.d.S.; Fernandes, A. Essential Oils Against Foodborne Pathogens and Spoilage Bacteria in Minced Meat. Foodborne Pathog. Dis. 2009, 6, 725–728.
  50. Jackson-Davis, A.; White, S.; Kassama, L.S.; Coleman, S.; Shaw, A.; Mendonca, A.; Cooper, B.; Thomas-Popo, E.; Gordon, K.; London, L. A Review of Regulatory Standards and Advances in Essential Oils as Antimicrobials in Foods. J. Food Prot. 2023, 86, 100025.
  51. Pinto, L.; Tapia-Rodríguez, M.R.; Baruzzi, F.; Ayala-Zavala, J.F. Plant Antimicrobials for Food Quality and Safety: Recent Views and Future Challenges. Foods 2023, 12, 2315.
  52. Iordache, A.M.; Nechita, C.; Voica, C.; Roba, C.; Botoran, O.R.; Ionete, R.E. Assessing the Health Risk and the Metal Content of Thirty-Four Plant Essential Oils Using the ICP-MS Technique. Nutrients 2022, 14, 2363.
  53. Ałtyn, I.; Twarużek, M. Mycotoxin Contamination Concerns of Herbs and Medicinal Plants. Toxins 2020, 12, 182.
  54. Fillâtre, Y.; Gray, F.-X.; Roy, C. Pesticides in essential oils: Occurrence and concentration in organic and conventional orange essential oils from eleven geographical origins. Anal. Chim. Acta 2017, 992, 55–66.
  55. Sánchez-Ortega, I.; García-Almendárez, B.E.; Santos-López, E.M.; Amaro-Reyes, A.; Barboza-Corona, J.E.; Regalado, C. Antimicrobial Edible Films and Coatings for Meat and Meat Products Preservation. Sci. World J. 2014, 2014, 248935.
  56. Han, J.H. Edible Films and Coatings: A Review. In Innovations in Food Packaging, 2nd ed.; Han, J., Ed.; Pepsico Inc.: Plano, TX, USA, 2014; pp. 213–255.
  57. Cutter, C.N. Opportunities for bio-based packaging technologies to improve the quality and safety of fresh and further processed muscle foods. Meat Sci. 2006, 74, 131–142.
  58. Cagri, A.; Ustunol, Z.; Ryser, E.T. Antimicrobial Edible Films and Coatings. J. Food Prot. 2004, 67, 833–848.
  59. Oussalah, M.; Caillet, S.; Salmiéri, S.; Saucier, L.; Lacroix, M. Antimicrobial and Antioxidant Effects of Milk Protein-Based Film Containing Essential Oils for the Preservation of Whole Beef Muscle. J. Agric. Food Chem. 2004, 52, 5598–5605.
  60. Hong, Y.H.; Lim, G.O.; Song, K.B. Physical properties of Gelidium corneum-gelatin blend films containing grapefruit seed extract or green tea extract and its application in the packaging of pork loins. J. Food Sci. 2009, 74, 6–10.
  61. Cazón, P.; Velazquez, G.; Ramírez, J.A.; Vázquez, M. Polysaccharide-based films and coatings for food packaging: A review. Food Hydrocoll. 2017, 68, 136–148.
  62. Moreira, M.d.R.; Pereda, M.; Marcovich, N.E.; Roura, S.I. Antimicrobial Effectiveness of Bioactive Packaging Materials from Edible Chitosan and Casein Polymers: Assessment on Carrot, Cheese, and Salami. J. Food Sci. 2011, 76, M54–M63.
  63. Fernández-Pan, I.; Carrión-Granda, X.; Maté, J.I. Antimicrobial efficiency of edible coatings on the preservation of chicken breast fillets. Food Control 2014, 36, 69–75.
  64. Di Giorgio, L.; Salgado, P.R.; Mauri, A.N. Flavored oven bags for cooking meat based on proteins. LWT 2019, 101, 374–381.
  65. Emiroğlu, Z.K.; Yemiş, G.P.; Coşkun, B.K.; Candoğan, K. Antimicrobial activity of soy edible films incorporated with thyme and oregano essential oils on fresh ground beef patties. Meat Sci. 2010, 86, 283–288.
  66. Cardoso, G.P.; Dutra, M.P.; Fontes, P.R.; de Lemos Souza Ramos, A.; de Miranda Gomide, L.A.; Ramos, E.M. Selection of a chitosan gelatin-based edible coating for color preservation of beef in retail display. Meat Sci. 2016, 114, 85–94.
  67. Kaewprachu, P.; Osako, K.; Benjakul, S.; Rawdkuen, S. Quality attributes of minced pork wrapped with catechin–lysozyme incorporated gelatin film. Food Packag. Shelf Life 2015, 3, 88–96.
  68. Gennadios, A.; Hanna, M.; Kurth, L. Application of Edible Coatings on Meats, Poultry and Seafoods: A Review. LWT 1997, 30, 337–350.
  69. Debeaufort, F.; Voilley, A. Lipid based edible films and coatings. In Edible Films and Coatings for Food Applications; Embuscado, M.E., Huber, K.C., Eds.; Springer: New York, NY, USA, 2009; pp. 135–168.
  70. Labuza, T.P.; Contreras-Medellin, R. Prediction of moisture protection requirements for foods. Cereal Foods World 1981, 26, 335–343.
  71. Baldwin, E.A. Edible coatings for fresh fruits and vegetables: Past, present, and future. In Edible Coatings and Films to Improve Food Quality; Krochta, J.M., Baldwin, E.A., Nisperos-Carriedo, M., Eds.; Technomic Publishing Company, Inc.: Lancaster, PA, USA, 1994; pp. 25–64.
  72. Bolívar-Monsalve, J.; Ramírez-Toro, C.; Bolívar, G.; Ceballos-González, C. Mechanisms of action of novel ingredients used in edible films to preserve microbial quality and oxidative stability in sausages—A review. Trends Food Sci. Technol. 2019, 89, 100–109.
  73. Soliva-Fortuny, R.; Rojas-Graii, M.A.; Martin-Belloso, O. Polysaccharide coatings. In Edible Coatings and Films to Improve Food Quality; Baldwin, E., Hagenmaier, R., Bai, J., Eds.; CRC Press: Boca Raton, FL, USA, 2012; pp. 103–136.
  74. Erginkaya, Z.; Kalkan, S.; Ünal, E. Use of Antimicrobial Edible Films and Coatings as Packaging Materials for Food Safety. In Food Processing: Strategies for Quality Assessment; Springer: New York, NY, USA, 2014; pp. 261–295.
  75. Asgher, M.; Qamar, S.A.; Bilal, M.; Iqbal, H.M. Bio-based active food packaging materials: Sustainable alternative to conventional petrochemical-based packaging materials. Food Res. Int. 2020, 137, 109625.
  76. Mohamed, S.A.A.; El-Sakhawy, M.; El-Sakhawy, M.A.M. Polysaccharides, protein and lipid-based natural edible films in food packaging: A review. Carbohydr. Polym. 2020, 238, 116178.
  77. Von Schantz, L.; Schagerlöf, H.; Karlsson, E.N.; Ohlin, M. Characterization of the substitution pattern of cellulose derivatives using carbohydrate-binding modules. BMC Biotechnol. 2014, 14, 113.
  78. Agustin, M.B.; Ahmmad, B.; Alonzo, S.M.M.; Patriana, F.M. Bioplastic based on starch and cellulose nanocrystals from rice straw. J. Reinf. Plast. Compos. 2015, 33, 2205–2213.
  79. Guzman-Puyol, S.; Ceseracciu, L.; Tedeschi, G.; Marras, S.; Scarpellini, A.; Benítez, J.J.; Athanassiou, A.; Heredia-Guerrero, J.A. Transparent and Robust All-Cellulose Nanocomposite Packaging Materials Prepared in a Mixture of Trifluoroacetic Acid and Trifluoroacetic Anhydride. Nanomaterials 2019, 9, 368.
  80. Xie, Y.; Pan, Y.; Cai, P. Cellulose-based antimicrobial films incroporated with ZnO nanopillars on surface as biodegradable and antimicrobial packaging. Food Chem. 2022, 368, 130784.
  81. Mose, B.R.; Maranga, S.M. A review on starch based nanocomposites for bioplastic materials. J. Mater. Sci. Eng. B 2011, 1, 239–245.
  82. Pająk, P.; Socha, R.; Łakoma, P.; Fortuna, T. Antioxidant properties of apple slices stored in starch-based films. Int. J. Food Prop. 2017, 20, 1117–1128.
  83. Putri, T.R.; Adhitasari, A.; Paramita, V.; Yulianto, M.E.; Ariyanto, H.D. Effect of different starch on the characteristics of edible film as functional packaging in fresh meat or meat products: A review. Mater. Today Proc. 2023, 87, 192–199.
  84. Krishnan, K.R.; Babuskin, S.; Rakhavan, K.; Tharavin, R.; Babu, P.A.S.; Sivarajan, M.; Sukumar, M. Potential application of corn starch edible films with spice essential oils for the shelf life extension of red meat. J. Appl. Microbiol. 2015, 119, 1613–1623.
  85. Yıldırım-Yalçın, M.; Sadıkoğlu, H.; Şeker, M. Characterization of edible film based on grape juice and cross-linked maize starch and its effects on the storage quality of chicken breast fillets. LWT 2021, 142, 111012.
  86. Erna, K.H.; Felicia, W.X.L.; Rovina, K.; Vonnie, J.M.; Huda, N. Development of curcumin/rice starch films for sensitive detection of hypoxanthine in chicken and fish meat. Carbohydr. Polym. Technol. Appl. 2022, 3, 100189.
  87. Ferreira, C.O.; Nunes, C.A.; Delgadillo, I.; Lopes-Da-Silva, J. Characterization of chitosan–whey protein films at acid pH. Food Res. Int. 2009, 42, 807–813.
  88. Campos, C.A.; Gerschenson, L.N.; Flores, S.K. Development of Edible Films and Coatings with Antimicrobial Activity. Food Bioprocess Technol. 2011, 4, 849–875.
  89. Nayik, G.A.; Majid, I.; Kumar, V. Developments in edible films and coatings for the extension of shelf life of fresh fruits. Am. J. Nutr. Food Sci. 2015, 2, 16–20.
  90. Alemán, A.; González, F.; Arancibia, M.; López-Caballero, M.; Montero, P.; Gómez-Guillén, M. Comparative study between film and coating packaging based on shrimp concentrate obtained from marine industrial waste for fish sausage preservation. Food Control 2016, 70, 325–332.
  91. Jansook, P.; Ogawa, N.; Loftsson, T. Cyclodextrins: Structure, physicochemical properties and pharmaceutical applications. Int. J. Pharm. 2018, 535, 272–284.
  92. Muñoz-Shugulí, C.; Vidal, C.P.; Cantero-López, P.; Lopez-Polo, J. Encapsulation of plant extract compounds using cyclodextrin inclusion complexes, liposomes, electrospinning and their combinations for food purposes. Trends Food Sci. Technol. 2021, 108, 177–186.
  93. van der Veen, B.A.; Uitdehaag, J.C.; Penninga, D.; van Alebeek, G.-J.W.; Smith, L.M.; Dijkstra, B.W.; Dijkhuizen, L. Rational design of cyclodextrin glycosyltransferase from Bacillus circulans strain 251 to increase α-cyclodextrin production. J. Mol. Biol. 2000, 296, 1027–1038.
  94. Messner, M.; Kurkov, S.V.; Flavià-Piera, R.; Brewster, M.E.; Loftsson, T. Self-assembly of cyclodextrins: The effect of the guest molecule. Int. J. Pharm. 2011, 408, 235–247.
  95. Ayala-Zavala, J.F.; Del-Toro-Sánchez, L.; Alvarez-Parrilla, E.; González-Aguilar, G.A. High relative humidity in-package of fresh-cut fruits and vegetables: Advantage or disadvantage considering microbiological problems and antimicrobial delivering systems? J. Food Sci. 2008, 73, R41–R47.
  96. Capozzi, L.C.; Bazzano, M.; Sangermano, M.; Pisano, R. Inclusion complexes dispersed in polystyrene-based labels for fruit ripening on demand. Int. J. Food Sci. Technol. 2018, 53, 389–394.
  97. Buendía, L.; Sánchez, M.J.; Antolinos, V.; Ros, M.; Navarro, L.; Soto, S.; Martínez, G.B.; López, A. Active cardboard box with a coating including essential oils entrapped within cyclodextrins and/or halloysite nanotubes. A case study for fresh tomato storage. Food Control 2020, 107, 106763.
  98. Antunes, M.D.; da Silva Dannenberg, G.; Fiorentini, Â.M.; Pinto, V.Z.; Lim, L.-T.; da Rosa Zavareze, E.; Dias, A.R.G. Antimicrobial electrospun ultrafine fibers from zein containing eucalyptus essential oil/cyclodextrin inclusion complex. Int. J. Biolog. Macromol. 2017, 104, 874–882.
  99. Liu, Y.; Sameen, D.E.; Ahmed, S.; Wang, Y.; Lu, R.; Dai, J.; Li, S.; Qin, W. Recent advances in cyclodextrin-based films for food packaging. Food Chem. 2022, 370, 131026.
  100. Jeevahan, J.; Chandrasekaran, M.; Durairaj, R.; Mageshwaran, G.; Joseph, G.B. A brief review on edible food packing materials. J. Glob. Eng. Probl. Solut. 2017, 1, 9–19.
  101. Jeevahan, J.J.; Chandrasekaran, M.; Venkatesan, S.P.; Sriram, V.; Joseph, G.B.; Mageshwaran, G.; Durairaj, R.B. Scaling up difficulties and commercial aspects of edible films for food packaging: A review. Trends Food Sci. Technol. 2020, 100, 210–222.
  102. And, H.C.; Hoover, D.G. Bacteriocins and their food applications. Comp. Rev. Food Sci. Food Saf. 2003, 2, 82–100.
  103. Cotter, P.D.; Hill, C.; Ross, R.P. Bacteriocins: Developing innate immunity for food. Nat. Rev. Microbiol. 2005, 3, 777–788.
  104. da Costa, R.J.; Voloski, F.L.S.; Mondadori, R.G.; Duval, E.H.; Fiorentini, M. Preservation of Meat Products with Bacteriocins Produced by Lactic Acid Bacteria Isolated from Meat. J. Food Qual. 2019, 2019, 4726510.
  105. Gálvez, A.; Abriouel, H.; López, R.L.; Ben Omar, N. Bacteriocin-based strategies for food biopreservation. Int. J. Food Microbiol. 2007, 120, 51–70.
  106. Delves-Broughton, J. Nisin and its application as a food preservative. Int. J. Dairy Technol. 1990, 43, 73–76.
  107. Ross, R.P.; Galvin, M.; McAuliffe, O.; Morgan, S.M.; Ryan, M.P.; Twomey, D.P.; Meaney, W.J.; Hill, C. Developing applications for lactococcal bacteriocins. Antonie van Leeuwenhoek 1999, 76, 337–346.
  108. De Martinis, E.C.P.; Alves, V.F.; Franco, B.D.G.M. Fundamentals and perspectives for the use of bacteriocins produced by lactic acid bacteria in meat products. Food Rev. Int. 2002, 18, 191–208.
  109. Sobrino-López, A.; Martín-Belloso, O. Use of nisin and other bacteriocins for preservation of dairy products. Int. Dairy J. 2008, 18, 329–343.
  110. Gálvez, A.; López, R.L.; Abriouel, H.; Valdivia, E.; Ben Omar, N. Application of Bacteriocins in the Control of Foodborne Pathogenic and Spoilage Bacteria. Crit. Rev. Biotechnol. 2008, 28, 125–152.
  111. Nieto-Lozano, J.C.; Reguera-Useros, J.I.; Peláez-Martínez, M.D.C.; Sacristán-Pérez-Minayo, G.; Gutiérrez-Fernández, Á.J.; de la Torre, A.H. The effect of the pediocin PA-1 produced by Pediococcus acidilactici against Listeria monocytogenes and Clostridium perfringens in Spanish dry-fermented sausages and frankfurters. Food Control 2010, 21, 679–685.
  112. Kingcha, Y.; Tosukhowong, A.; Zendo, T.; Roytrakul, S.; Luxananil, P.; Chareonpornsook, K.; Valyasevi, R.; Sonomoto, K.; Visessanguan, W. Anti-listeria activity of Pediococcus pentosaceus BCC 3772 and application as starter culture for Nham, a traditional fermented pork sausage. Food Control 2012, 25, 190–196.
  113. Kalschne, D.L.; Geitenes, S.; Veit, M.R.; Sarmento, C.M.; Colla, E. Growth inhibition of lactic acid bacteria in ham by nisin: A model approach. Meat Sci. 2014, 98, 744–752.
  114. Alvarez-Sieiro, P.; Montalbán-López, M.; Mu, D.; Kuipers, O.P. Bacteriocins of lactic acid bacteria: Extending the family. Appl. Microbiol. Biotechnol. 2016, 100, 2939–2951.
  115. Moracanin, S.V.; Turubatovic, L.; Skrinjar, M.; Obradovic, D. Antilisterial activity of bacteriocin isolated from Leuconostoc mesenteroides ssp. mesenteroides IMAU: 10231 in the production of sremska sausages: Lactic acid bacteria isolation, bacteriocin identification and meat application experiments. Food Technol. Biotechnol. 2013, 51, 247–256.
  116. Papagianni, M.; Sergelidis, D. Effects of the presence of the curing agent sodium nitrite, used in the production of fermented sausages, on bacteriocin production by Weissella paramesenteroides DX grown in meat simulation medium. Enzym. Microb. Technol. 2013, 53, 1–5.
  117. Chakchouk-Mtibaa, A.; Smaoui, S.; Ktari, N.; Sellem, I.; Najah, S.; Karray-Rebai, I.; Mellouli, L. Biopreservative Efficacy of Bacteriocin BacFL31 in Raw Ground Turkey Meat in terms of Microbiological, Physicochemical, and Sensory Qualities. Biocontrol Sci. 2017, 22, 67–77.
  118. Rivas, F.P.; Castro, M.P.; Vallejo, M.; Marguet, E.; Campos, C.A. Sakacin Q produced by Lactobacillus curvatus ACU-1: Functionality characterization and antilisterial activity on cooked meat surface. Meat Sci. 2014, 97, 475–479.
  119. Kristo, E.; Koutsoumanis, K.P.; Biliaderis, C.G. Thermal, mechanical and water vapor barrier properties of sodium caseinate films containing antimicrobials and their inhibitory action on Listeria monocytogenes. Food Hydrocoll. 2008, 22, 373–386.
  120. Realini, C.E.; Marcos, B. Active and intelligent packaging systems for a modern society. Meat Sci. 2014, 98, 404–419.
  121. Ye, M.; Neetoo, H.; Chen, H. Effectiveness of chitosan-coated plastic films incorporating antimicrobials in inhibition of Listeria monocytogenes on cold-smoked salmon. Int. J. Food Microbiol. 2008, 127, 235–240.
  122. Kuorwel, K.K.; Cran, M.J.; Sonneveld, K.; Miltz, J.; Bigger, S.W. Essential Oils and Their Principal Constituents as Antimicrobial Agents for Synthetic Packaging Films. J. Food Sci. 2011, 76, R164–R177.
  123. La Storia, A.; Mauriello, G.; Villani, F.; Ercolini, D. Coating-Activation and Antimicrobial Efficacy of Different Polyethylene Films with a Nisin-Based Solution. Food Bioprocess Technol. 2013, 6, 2770–2779.
  124. Ming, X.; Weber, G.H.; Ayres, J.W.; Sandine, W.E. Bacteriocins Applied to Food Packaging Materials to Inhibit Listeria monocytogenes on Meats. J. Food Sci. 1997, 62, 413–415.
  125. Santiago-Silva, P.; Soares, N.F.; Nóbrega, J.E.; Júnior, M.A.; Barbosa, K.B.; Volp, A.C.P.; Zerdas, E.R.; Würlitzer, N.J. Antimicrobial efficiency of film incorporated with pediocin (ALTA® 2351) on preservation of sliced ham. Food Control 2009, 20, 85–89.
  126. Marcos, B.; Aymerich, T.; Monfort, J.M.; Garriga, M. Use of antimicrobial biodegradable packaging to control Listeria monocytogenes during storage of cooked ham. Int. J. Food Microbiol. 2007, 120, 152–158.
  127. Ünlü, G.; Nielsen, B.; Ionita, C. Inhibition of Listeria monocytogenes in Hot Dogs by Surface Application of Freeze-Dried Bacteriocin-Containing Powders from Lactic Acid Bacteria. Probiotics Antimicrob. Proteins 2016, 8, 102–110.
  128. Almeida-Santos, A.C.; Novais, C.; Peixe, L.; Freitas, A.R. Enterococcus spp. as a Producer and Target of Bacteriocins: A Double-Edged Sword in the Antimicrobial Resistance Crisis Context. Antibiotics 2021, 10, 1215.
  129. Brenner, S.; Streisinger, G.; Horne, R.; Champe, S.; Barnett, L.; Benzer, S.; Rees, M. Structural components of bacteriophage. J. Mol. Biol. 1959, 1, 281–292.
  130. Campbell, A. The future of bacteriophage biology. Nat. Rev. Genet. 2003, 4, 471–477.
  131. Hendrix, R.W. Bacteriophage genomics. Curr. Opin. Microbiol. 2003, 6, 506–511.
  132. Tauxe, R. Emerging Foodborne Pathogens. Int. J. Food Microbiol. 2002, 78, 31–41.
  133. 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.
  134. U.S. Food and Drug Administration. Food Additives Permitted for Direct Addition to Food for Human Consumption; Bacteriophage Preparation. 21 CFR Part. 2006; pp. 47729–47732. Available online: http://edocket.access.gpo.gov/2006/E6-13621.htm (accessed on 24 March 2023).
  135. Alves, D.; Marques, A.; Milho, C.; Costa, M.J.; Pastrana, L.M.; Cerqueira, M.A.; Sillankorva, S.M. Bacteriophage ϕIBB-PF7A loaded on sodium alginate-based films to prevent microbial meat spoilage. Int. J. Food Microbiol. 2019, 291, 121–127.
  136. Dülger, M.M.; Özpinar, H. Bakteriyofajların Gıda Güvenliğini Artırmak Amacıyla Kullanılması. İstanbul Gelişim Üniversitesi Sağlık Bilimleri Dergisi 2021, 15, 705–712.
More
This entry is offline, you can click here to edit this entry!
Video Production Service