LAB is known for its capability to produce a variety of antimicrobial agents that can inhibit the growth of pathogenic bacteria. In 1988, the FDA approved the use of nisin and pediocin, a bacteriocin produced from Lactococcus lactis and Pediococcus sp. as preservatives for application in the food industry. Nisin and pediocin have been successfully commercialized widely ^[1][7]. In addition to nisin and pediocin, a bacteriocin from Enterococcus sp. namely enterocin has also gained significant academic interest following the research conducted on the effectiveness of antimicrobial agents produced by this species for use in food as a preservative. Ben Braïek et al. ^[2][17] stated that enterocin produced by Enterococcus sp. has high anti-listerial properties due to the bacteriocins produced by Enterococcus species being mostly classified as class III. It has a C-terminal disulfide bridge that stabilizes the posterior fold in the structure, which is crucial in enhancing the antimicrobial activity of the species ^[3][18]. In a study conducted by Fathizadeh et al. ^[4][19], recombinant bacteriocin, enterocin A and colicin E1 (ent A-col E1) exhibited antibacterial characteristics against both Gram positive and negative bacteria. Enterocin 12a produced by E. faecium was able to inhibit the growth of pathogens, such as Salmonella enterica, Shigella flexneri, Vibrio cholerae, E. E. colicoli and L. monocytogenes ^[5][20]. Several studies have reported the effectiveness of bacteriocin produced by LAB in inhibiting the growth of L.monocytogenes as shown in (Table 12). LAB are mainly from the genus of Enterococcus (E. lactis Q1, E. lactis 4CP3, E. faecalis), Lactobacillus (L. paracasei, L. plantarum, L. sakei, L. reuteri), and Pediococcus. Most of the bacteriocins produced by these LAB were able to inhibit the growth of L. monocytogenes. Based on Table 12, the treatment of E. lactis 4CP3 (enterocin A, B, P), and E. faecalis (enterocin AS-48) against L. monocytogenes resulted in growth inhibition activity as reported by Ben Braïek et al. ^[2][6][17,21] and Sparo et al. ^[7][22]. Meanwhile, enterocin P produced by E. lactis Q1 reportedly exhibited antimicrobial activity, as observed in the stunted growth of L. monocytogenes after 7 days of treatment as compared to the untreated sample ^[8][23]. Paracin C by Lactobacillus paracasei, Plantaricin (EF, W, JK, S) produced by Lactobacillus plantarum and bacteriocins produced by Lactobacillus sakei, L. reuteri, L. plantarum, L. fermentum inhibited the growth of L. monocytogenes while the treatment of Sakacin G produced by Lactobacillus sakei resulted in a decrease in the number of L. monocytogenes cells on roasted meat ^[9][24]. In addition, pediocin produced by Pediococcus sp. was found to exert broad spectrum antimicrobial activity against L. monocytogenes ^[10][25].

^[18][2,16].

Abts et al. ^[29][42] stated that enterocin is used as a food preservative through two methods: (1) direct inoculation of bacteria producing enterocin directly as a starter or protective culture, and (2) the use of purified or semi-purified cell-free supernatant. However, enterocin is often widely applied as a starter culture. For example, E. faecium, E. mundtii, and E. classeliflavus have been used as a starter culture in the production of fermented sausage ^[1][30][26][7,8,39]. As a result, Enterococcus sp. competes partially during the meat fermentation process, inhibiting the growth of Listeria sp. in the product ^[30][8].

Enterocin is also associated with several biochemical activities that stimulate aroma development through glycolysis, proteolysis, and lipolysis activities. In addition, it also plays a role in reducing the activity of metmyoglobin (MetMbO), which is an important mechanism for maintaining meat color ^[31][43]. Furthermore, enterocin also helps the degradation of stachyose and raffinose, the non-digestive oligosaccharides known as anti-nutrient factors ^[32][11]. The use of purified or semi-purified cell-free supernatant is also one of the methods often used for raw products, conferring the same benefits as that of the inoculation method in terms of inhibiting the growth of L. monocytogenes. This method is particularly useful in stimulating the formation of compounds that give aroma and taste to the product. However, this preservation method also has several disadvantages. While bacteriocin can inhibit oxidative rancidity due to damage that occurs in fats or oils, the production of unwanted flavors may also occur as a result of fat hydrolysis by lipase enzymes or from contaminating microorganisms ^[17][2].

Several researchers have suggested that the use of purified or semi-purified cell-free supernatants is suitable for application in food products, as it is more effective than the direct inoculation of the bacteriocin-producing bacteria. The latter may cause damage to the food in hostile environments ^[33][44]. During the purification process, all contaminants with low molecular weight are removed, leaving only the bacteriocin with a specific activity. The purification step allows for a more accurate determination of the biological activity of bacteriocin ^[29][42]. On the other hand, it has been reported in some cases that the use of cell-free supernatant on raw meat can potentially reduce the antimicrobial activity of bacteriocin due to the protein degradation that takes place when the supernatant is absorbed into the meat matrix ^[17][2]. Thus, Silva et al. ^[34][45] and, Borges and Teixeir ^[35][46] have suggested an alternative method by incorporating the purified or semi-purified bacteriocin in packaging material to increase the activity and stability of the bacteriocin in complex food systems. Referring to Table 23, enterocin A and B from E. faecium were incorporated into an alginate film, which is one of the packaging techniques used for fermented dried sausages, minced pork, and ham ^[23][36].

Characterization of bacteriocin is important to evaluate its effectiveness to be applied in the food industry. According to previous researchers, E. faecalis and E. faecium are the most commonly used bacteria from the genus Enterococcus, particularly in the food industry. The bacteria are used for the preservation of raw materials due to their high stability against extreme temperature and pH as compared to other species of Enterococcus as shown in (Table 34). The sensitivity of bacteriocin towards pH is diverse. The bacteriocin, known as enterocin As-48 produced by E. faecalis maintains its activity at pHs as high as 12 and temperatures of 121 °C for 15 min. Meanwhile, the activity of bacteriocin produced by E. lactis and E. durans was inhibited at 121 °C after 15 min. On the other hand, E. mundtii, which produces mundticin, can maintain its stability at 121 °C for 15 min; however, its activity is typically inhibited at pH 12. By referring to Table 34, E. faecalis and E. faecium are suitable for application on food products, such as raw meats and vegetables since they are stable at high temperatures and pH.

Strain	Bacteriocin	Stability															References
		Enzyme					Temperature (°C/min)				pH
		Proteases K	Trypsin	Chymotrypsin	Lipase	Catalase	65 °C/30 min	80 °C/30 min	100 °C/30 min	121 °C/15 min	2	4	6	8	10	12
E. faecalis	Enterocin As-48	−	−	+	+	+	+	+	+	+	+	+	+	+	+	+	[19][36]]	[32,51,]
E. faecium	17	,	21]
Enterocin L50A-like bacteriocin & L50B (Dur 152A)				Ham	Semi-purified bacteriocin/anti-listerial protection	L. monocytogenes	[	20][21][22]	[33,34,35]	Enterocin A and B	−	−	+	+	+	+	+	+	−	+	+	+	+	+	+	[25	The inhibition of L. monocytogenes growth on the rabbit meat during cold storage was detected on day 28.
]	[	38	]	E. faecium	Enterocin A and B	Fermented dried sausage, minced pork, and ham	Applied on the surface of meat/alginate film/high hydrostatic pressure	Listeria spp, L. sakei	[18][23][24][25]	[16,36,37,38
E. durans	]	Enterocin L50A- like bacteriocin and L50B, Durancin GL	−	−	+	+	+	+	+	+	−	+	+	+	+	−	−	[19][21][22]	[32,34,35]
Enterococcus faecalis	Enterocin AS-48	There was no detection of L. monocytogenes growth on the beef after 24 h treated with E. faecalis.	[7]
Enterococcus faecalis	Enterocin AS-48	There was no detection of L. monocytogenes growth on the beef after 24 h treated with E. faecalis.	[22]
E. classeliflavus	Enterocin 416kk1	Cacciatore (Italian sausage)	Starter culture/low-density polyethylene film	L. monocytogenes	[26][27]	[39,40]
E. mundtii	Mudticin	−	−	+	+	+	+	+	+	+	+	+	+	+	+	−	[28]	[41]
Lactobacillus paracasei	Paracin C
Lactobacillus paracasei	Paracin C
The growth of pathogenic bacteria was inhibited, and the color of the meat was retained until day 15.	[	11]
The growth of pathogenic bacteria was inhibited, and the color of the meat was retained until day 15.	[26]
E. mundtii	Mundticin	Fermented fish and seafood, sausage	Starter culture/chitosan
Lactobacillus plantarum	Plantaricin EF, W, JK and S	The growth of both spoilage bacteria was inhibited by L. plantarum until day 15 at 22 °C.	[12]
Lactobacillus plantarum	Plantaricin EF, W, JK and S	The growth of both spoilage bacteria was inhibited by L. plantarum until day 15 at 22 °C.	[27]
Lactobacillus sakei	Sakacin G
Sakacin G
The application of		L.sakei takes on roasted meat resulted in a decrease in the number of L. monocytogenes cells. Meanwhile, for chicken breast, the inhibition effect depleted.
The application of	L.sakei takes on roasted meat resulted in a decrease in the number of L. monocytogenes cells. Meanwhile, for chicken breast, the inhibition effect depleted.
[	9	]
Lactobacillus sakei	[24]
Lactobacillus sakei, L. reuteri, L. plantarum, L. fermentum	Bacteriocins	The formation of the inhibition zone after the treatment of bacteriocin demonstrated the growth inhibition of L. monocytogenes.	[13]
Lactobacillus sakei, L. reuteri, L. plantarum, L. fermentum	Bacteriocins	The formation of the inhibition zone after the treatment of bacteriocin demonstrated the growth inhibition of L. monocytogenes.	[28]
Pediococcus sp.	Pediocin	Pediocin and pediocin-like bacteriocins exerted a broad spectrum of activity against L. monocytogenes through the formation of pores in the cytoplasmic membrane and cell membrane dysfunction.	[10]
Pediococcus sp.	Pediocin	Pediocin and pediocin-like bacteriocins exerted a broad spectrum of activity against L. monocytogenes through the formation of pores in the cytoplasmic membrane and cell membrane dysfunction.	[25]

Nowadays, the preservation methods in the food industry are evolving, with the use of bacteriocin aiding the process of preserving raw products. Bacteriocin is known for its capability to inhibit the growth of spoilage bacteria, such as L. monocytogenes, Salmonella sp., and E. coli in commercial food products so the quality can be maintained over a certain period. A newly reported byproduct rich in enterocin AS-48, and known to have a wide spectrum of antibacterial activity, might have good potential to be used as an additive since it achieved a good safety profile indicated by the negative result of the mutagenicity and genotoxicity assay test ^[14][29]. About 500 µL/animal/d of enterocin have been used as additives and were administrated in the drinking water of rabbits. As a result, the enterocin significantly affected the quality and mineral content of the rabbit meat, mainly iron and phosphorus ^[15][30]. There are several species of Enterococcus used as preservatives in raw products. For instance, the cell-free supernatant of Enterococcus faecium TJUQ1 combined with the bacterial cellulose of Gluconabacter xylinus forms a composite film, BC-E, which shows antibacterial activity against L. monocytogenes after being soaked and applied on ground meat ^[16][31]. Other examples were recorded as shown in (Table 23). There are several techniques for incorporating bacteriocin into food products: (1) inoculation of bacteria producing bacteriocin directly onto the meat or meat products as a starter or protective culture, (2) the use of purified or semi-purified cell-free supernatant directly as a food preservative, and (3) incorporation of purified and semi-purified bacteriocin and in packaging material ^[17]

E. lactis

Enterocin A, B, and P

−

−

+

+

+

+

+

+

−

+

+

+

+

+

−

[

2

][6]

[17,21]

Bacteriocin produced by Enterococcus sp. as listed in Table 34 is typically sensitive to proteolytic enzymes, such as protease K and trypsin, which demonstrated the proteinaceous properties of the bacteria. Meanwhile, chymotrypsin, lipase, and catalase do not exert any effect on enterocin activity, indicating that the inhibition of bacterial growth is not due to the production of hydrogen peroxide ^[37][47]. Application of this proteolytic enzyme leads to protein degradation, and therefore, is safe for human consumption ^[32][11]. In the meantime, the loss of activity of bacteriocin depends on the formation of peptides and amino acid sequences.

According to Gao et al. ^[38][48] lowering the pH will gradually deactivate the growth of microorganisms. Most cationic bacteria will undergo cell lysis as a result of stimuli formed by negatively charged molecules found on the bacterial cell surface, such as lipopolysaccharide (LPS), lipoteichoic and teichoic acids. The findings demonstrate that the bacteriocin produced by Enterococcus sp. has a high resistance to extreme pH ranges and has the potential to be used in acidic and alkaline processed foods ^[39][49].

Temperature is crucial in ensuring the stability of bacteriocin activity. Based on Table 34, the activity of enterocin from E. faecalis, and E. mundtii is stable at a maximum temperature of 121 °C for 15 min while E. faecium, E. durans, and E. lactis could only withstand temperatures up to 100 °C for 30 min. Enterocin produced by Enterococcus is a heat-tolerant bacteriocin. The activity performed differs according to the species and molecular structure of the respective bacteriocin ^[19][39][32,49]. Some highly heat-sensitive bacteriocin lose their activity at 50 °C due to the loss of their original secondary and tertiary structure as a result of denaturation ^[40][50]. The resistance of Enterococcus at pasteurization temperature and its adaptability to substrate and growth conditions demonstrates its potential application in food products.