Scholarly article on topic 'Class IIa Bacteriocins: Diversity and New Developments'

Class IIa Bacteriocins: Diversity and New Developments Academic research paper on "Biological sciences"

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Academic research paper on topic "Class IIa Bacteriocins: Diversity and New Developments"

Int. J. Mol. Sci. 2012, 13, 16668-16707; doi:10.3390/ijms131216668


International Journal of

Molecular Sciences

ISSN 1422-0067


Class IIa Bacteriocins: Diversity and New Developments

Yanhua Cui \ Chao Zhang Yunfeng Wang John Shi 3, Lanwei Zhang Zhongqing Ding 1, Xiaojun Qu 4 and Hongyu Cui 2

1 School of Food Science and Engineering, Harbin Institute of Technology, Harbin 150090, China; E-Mails: (Y.C.); (C.Z.); (Z.D.)

2 State Key Laboratory of Veterinary Biotechnology, Harbin Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Harbin 150001, China;


3 Guelph Food Research Center, Agriculture and Agri-Food Canada, Guelph, ON N1G5C9, Canada; E-Mail:

4 Institute of Microbiology, Heilongjiang Academy of Sciences, Harbin 150010, China; E-Mail:

* Authors to whom correspondence should be addressed; E-Mails: (Y.W.); (L.Z.); Tel.: +86-451-8593-5058 (Y.W.); Fax: +86-451-5199-7166 (Y.W.); Tel.: +86-451-8628-2901 (L.Z.); Fax: +86-451-8628-2906 (L.Z.).

Received: 10 September 2012; in revised form: 10 October 2012 /Accepted: 12 November 2012 / Published: 6 December 2012

Abstract: Class IIa bacteriocins are heat-stable, unmodified peptides with a conserved amino acids sequence YGNGV on their N-terminal domains, and have received much attention due to their generally recognized as safe (GRAS) status, their high biological activity, and their excellent heat stability. They are promising and attractive agents that could function as biopreservatives in the food industry. This review summarizes the new developments in the area of class IIa bacteriocins and aims to provide uptodate information that can be used in designing future research.

Keywords: class IIa bacteriocin; lactic acid bacteria; diversity; genetic organization; discovery

1. Introduction

Many Gram-positive bacteria, particularly many lactic acid bacteria (LAB) are known to secrete ribosomally-synthesized peptides or proteins that have antimicrobial activity. These compounds (bacteriocins) have been shown to display inhibitory activity against closely related bacteria [1,2]. Four classes of bacteriocins have been defined based on common characteristics, mainly primary structure, molecular weight, mode of action, heat stability and their genetic properties [1,2]. Among these classes, class II, consisting of small peptides that do not contain modified residues, has been divided further into subgroups. Class Ila bacteriocins are characterized by the occurrence of a highly conserved hydrophilic and charged ^-terminal region that has a disulphide bond linkage [1,2]. In some bacteriocins, an additional disulphide bond is present. The unambiguous consensus amino acid sequence of class IIa bacteriocins is the "pediocin box" YGNGV (where V can be replaced by L in some cases) [1-3]. This consensus sequence is included in the conserved ^-terminal region YGNGVxCxK/NxxC (where X is any amino acid) [1,2]. Class IIa bacteriocins show their strong inhibitory effect on Listeria sp. as well as other food spoilage and pathogenic bacteria. They have received much attention due to their generally recognized as safe (GRAS) status, their high biological activity, and their heat stability. These compounds show great promise and are attractive candidates for use as biopreservatives in the food industry [4-7].

2. Diversity of Class IIa Bacteriocins

To date, there are about 50 different kinds of class IIa bacteriocins that have been characterized to the extent that one can with a high degree of certainty determine whether the bacteriocin differs significantly from other bacteriocins (Supplementary Table 1). These bacteriocins have been isolated from a wide variety of LAB, including Lactobacillus sp., Enterococcus sp., Pediococcus sp., Carnobacterium sp., Leuconostoc sp., Streptococcus sp., as well as Weissella sp. [8,9]. They have also been found in the non-LAB Bifidobacterium bifidum [10,11], Bifidobacterium infantis [12], Bacillus coagulans [13] and Listeria innocua [14]. These bacteriocin-producing LAB have been isolated from various environments, including dairy products, fermented sausages, vegetables, and the mammalian gastrointestinal tract.

The class IIa bacteriocins are initially produced as a protein precursor containing an N-terminal leader peptide. This leader peptide is removed by site-specific proteolytic cleavage during export, to yield the mature bacteriocins [2,15]. These mature bacteriocins rang in length from 25 amino acids for mutacin F-59.1 to 58 amino acids for acidocin A. The classification of Gram-positive bacteriocins is complex and several authors have proposed different classifications based on different criteria [1-3,16-18]. The present direction for defining novel classification schemes of Gram-positive bacteriocins tends to take into account the composition, three-dimensional (3D) structure and mode of action of the bacteriocins. Classification of class IIa bacteriocins have been broadly defined first on the basis of their conserved ^-terminal region, the "pediocin box," and then subdivided into 4 subclasses through sequence alignments of the less conserved C-terminal region [3,17,19,20].

The most recent repertoire of class IIa bacteriocins consists of 28 peptides [3]. In this paper, some class IIa bacteriocins were supplemented, including avicin A [21], bavaricin A [22], curvaticin

L442 [23], enterocin CRL35 [24], enterocin HF (P86183), bifidocin B [10,11], ubericin A [8], weissellin A [25], bacteriocin 602 [26], bacteriocin 1580 [26], bacteriocin 37 [26], bavaricin MN [27], bacteriocin (P86291.1), bacteriocin E50-52 [28], acidocin A [29], bacteriocin OR-7 [30], bacteriocin L-1077 [31], mundticin L [32], leucocin B [33], prebacterioncin SkgA2, bacteriocin MC4-1 [34], and duracin GL. The 3D structures of bacteriocins were evaluated by SWISS-MODEL Workspace [35-37]. The 50 class IIa bacteriocins were classified into eight groups on the basis of their conserved primary structures, 3D structures and mode of action (See Figure 1). The results showed high consistency with the classification of class IIa bacteriocins that were described earlier and discussed by Nissen-Meyer et al. [3] (see Supplementary Table 1).

Group I contains 24 bacteriocins with a sequence length of between 25 and 49 amino acid residues. These peptides are secreted by 17 species of seven genera, including Bacillus sp., Bifidobacterium sp., Carnobacterium sp., Enterococcus sp., Lactobacillus sp., Leuconostoc sp., and Weissella sp. The bacteriocins in this group belong to subgroup 1 which was described in the classification of Nissen-Meyer et al. [3]. The bacteriocins of group I have a flexible hinge at the conserved Asp 17residue. This group can be further subdivided into three subgroups according to their sequence similarities and differences.

Subgroup I-1: includes avicin A, bavaricin A, curvaticin L442, enterocin CRL35, enterocin HF, listeriocin 743A, mundticin, mundticin CRL35, mundticin L, piscicocin CS526, piscicolin 126, sakacin P, and sakacin X. Members of this subgroup exhibit a common consensus motif IGNNxxANxxTGG located at the C-terminal region. Avicin A is produced by Enterococcus avium XA83 which was isolated from feces of healthy infants, and is a probiotic bacterium with diverse antimicrobial potential [21]. Mundticin L is virtually identical to enterocin CRL35. The only difference in sequence occurs in the fifth amino acid residue of the conserved sequence (YGNGX) of these mature bacteriocins, but this change has no influence on antimicrobial activity [32]. Sakacin P is produced by several L. curvatus strains LTH1174, L442 and CRL 705, which were isolated from Greek fermented sausages and fermented meat [38,39]; and by several Lactobacillus sakei strains I151 and LTH673 isolated from sausage and fermented meat [40,41].

Subgroup I-2 encompasses bifidocin B, coagulin, pediocin PA-1, which are produced by B. bifidum, B. coagulans, Enterococcus faecium, Lactobacillus plantarum, Pediococcus acidilactici, Pediococcus pentosaceus and Streptococcus mutans. The common consensus of this subgroup is KYYGNGVTCGK(L)HS(D)CS(R)VDW(R)GKATT(C)C(G)IINNG.

Pediocin PA-1/AcH is a 44-amino-acid class IIa bacteriocin produced primarily by strains of the genus Pediococcus, including Pediococcus acidilactici strains PAC1.0 [42], H [43,44], E, F, M [45,46], K10 [47], HA-6111-2, HA-5692-3 [48], MM33 [49]; Pediococcus parvulus ATO34, ATO77 [50] and P. pentosaceus FBB61 [51]. Pediocin PA-1/AcH is also synthesized by L. plantarum WHE92 [52], L. plantarum DDEN 11007 [53] and E. faecium Acr4.

The genetic determinants for the biosynthesis of pediocin PA-1/AcH are located within a plasmid-borne operon cassette in all producing lactic acid bacterial strains examined to date. In several strains, the sizes and organization of the various pediocin-encoding plasmids are similar [54-59]. It has been shown that the plasmids responsible for production in P. acidilactici H can be transferred intragenerically by conjugation [60]. The pediocin PA-1/AcH is the only class IIa bacteriocin for which both cross-species and cross-genera synthesis are known to occur [61].

Figure 1. Multiple sequence alignment of class IIa bacteriocins.

The entire amino acid sequences of curvaticin L442 and bifidocin B have not been determined and the reported sequence for the bifidocin B contains some uncertainties. The mature sequence of enterocin CRL35 is identical to that of mundticin CRL35, but their leader sequences have some differences. The mature sequence of leucocin A was identical to that of leucocin B and they also had differences in their leader sequences. Sakacin P was identical to bavaricin A, and the peptide we list as sakacin P was a variant of sakacin P.

Coagulin is produced by no-LAB B. coagulans [13]. Interestingly, coagulin is almost identical to pediocin PA-1/AcH, showing 97.7% identity with pediocin PA-1/AcH. More specifically, the coagulin encoding DNA (coaABCD operon) showed 99% identity to that of the papABCD operon encoding the pediocin PA-1/AcH genes [62] (see Figure 2). A putative mob-pre (plasmid recombination enzyme) gene was identified in the coagulin-encoding plasmid pI4 [13]. The mob-pre genes present on several plasmids extracted from various Gram-positive genera, including Bacillus, Lactococcus, Streptococcus, Lactobacillus, Enterococcus, and Staphylococcus [13]. In several cases, the corresponding mob genes have been shown to be required for conjugative mobilization and site-specific recombination [63]. Therefore, it was speculated that horizontal gene/operon transfer between P. acidilactici and B. coagulans was possible despite they being relatively unrelated, one is LAB, and the other is no-LAB [13,62].

Interestingly, mutacin F-59.1 from Streptococcus mutans 59.1 shared the conserved sequence KYYGNGVTCGKHSxSVDWxKXT [9]. S. mutans is a human indigenous oral bacterial species. It possesses an advantage against competitive species living in the same niche because of its bacteriocins [64]. The mutacin F-59.1 has a wide activity spectrum inhibiting human and food-borne pathogens [9]. Some amino acids of mutacin F-59.1 have not been determined.

In this subgroup, the bacteriocin-producing strains B. bifidum NCFB 1454 (bifidocin B) and P. acidilactici MM33 (pediocin PA-1), are from human intestinal origin [49,65]. They could be developed for their probiotic properties and as inhibitors of pathogenic bacteria in the gut. Pediocin PA-1 from L. plantarum DDEN 11007 and pediocin A from P. pentosaceus FBB61, are produced by bacteria with established probiotic properties [51,53,66].

Bifidocin B is the first class IIa bacteriocin from a member of the genus Bifidobacterium, sharing 56.8% homology with coagulin and inhibiting the growth of some species of the genera Listeria, Bacillus, Enterococcus, Lactobacillus, Leuconostoc and Pediococcus [11]. Recently, a new bacteriocin bifidin I from Bifidobacterium sp. was reported. Bifidin I from B. infantis BCRC 14602 and showed similarity with bifidocin B, but its whole sequences has not been determined [12]. Bifidin I showed a broad spectrum antimicrobial activity against Gram-positive bacteria and Gram-negative bacteria, including some food-borne pathogens, such as Staphylococcus aureus, Bacillus subtilis, Bacillus cereus, Listeria monocytogenes, Clostridium butyricum, Salmonella enteritidis, Salmonella enterica ssp., and Shigella dysenteriae [12].

Subgroup I-3 is represented by leucocin C, and weissellin A, which are produced by Leuconostoc mesenteroides, Streptococcus uberis and Weissella paramesenteroides. The common consensus of this subgroup is NYGNG(X)2C(X)4CXVXW(X)6IXNNS(X)3GLTG.

Figure 2. Organization of the gene clusters of class IIa bacteriocins. The figure was involved in production of avicin A in Enterococcus avium XA83 (avc, GenBank ID: FJ851402.1); bacteriocin MC4-1 in Enterococcus faecalis MC4 (bac, GenBank ID: EU047916.1); carnobacteriocin B2 in Carnobacterium maltaromaticum LV17B (cbn, GenBank ID: L47121.1); coagulin in Bacillus coagulans I4 (coa, GenBank ID AF300457.1); divercin V41 in Carnobacterium divergens V41 (dvn, GenBank ID AJ224003.1); enterocin A in Leuconostoc gelidum UAL 187 (ent, GenBank ID AF099088); enterocin P in Enterococcus faecium P13 (ent, GenBank ID: AF005726.1); leucocin A in Leuconostoc gelidum UAL 187 (lca, GenBank ID: L40491.1); mesentericin 52A in Leuconostoc mesenteroides subsp. mesenteroides FR52 (mes, GenBank ID: AY286003.1); mundticin KS in Enterococcus mundtii NFRI 7393/AT06 (mun, GenBank ID: AB066267); mundticin L in E. mundtii CUGF08 (mun, GenBank ID: FJ899708.1); pediocin PA-1 in E. faecium Acr4 (pap, GenBank ID: HQ876214.1); penocin A in Pediococcuspentosaceus ATCC 25745 (pen, GenBank ID: NC_008525.1); piscicolin 126 in Carnobacterium piscicola JG126 (pis, GenBank ID: AF275938.1); plantaricin 423 in Lactobacillus plantarum 423 (pla, GenBank ID: AF304384); sakacin A in Lactobacillus sakei Lb706 (sap, GenBank ID: Z46867.1); sakacin G in Lactobacillus sakei CWBI-B1365 (skg, GenBank ID: EU570253.1) ; sakacin P in Lactobacillus sakei LTH673 (spp, GenBank ID: AF002276.1); sakacin X in L. sakei 5 (sak, GenBank ID: AAP44569.1); ubericin A in Streptococcus uberis E (uba, GenBank IDs: EF203953.1 and EF203954.1). Open reading frames (ORFs) encoding the related proteins are marked with the different color. The number of amino acid residues within each encoded protein is shown below the corresponding ORF.

Figure 2. Cont.

Leucocin C and leucocin C-TA33a are produced by different strains of L. mesenteroides, but they showed similar sequences [67]. Leucocin C-TA33a is from L. mesenteroides TA33a, which produced three bacteriocins (leucocin C-TA33a, leucocin B-TA33a and leucocin A-TA33a) with different inhibitory activity spectra [68,69]. The related research revealed that production of leucocin A-, B- and C-type bacteriocins was widespread in Leuconostoc/Weissella strains, including Leuconostoc carnosum LA54a, W. paramesenteroides LA7a, and Leuconostoc gelidum UAL 187-22 [68]. Weissellin A is a unique 4450 Da peptide which is produced by W. paramesenteroides DX which was isolated from a traditional Greek sausage. This bacteriocin exhibits strong activity against L. monocytogenes, Listeria inocua and Clostridium sporogenes [25].

Subgroup I-4 is represented by bacteriocin 602 [26], bavaricin MN [27], divercin V41, divergicin M35, duracin GL, enterocin A, which come from Carnobacterium divergens, Enterococcus durans, E. faecium, L. sakei and Paenibacillus polymyxa. The common consensus of this subgroup is YYGNGV(L)YC.

Group II contains bacteriocin 31, bacteriocin RC714, enterocin SE-K4, bacteriocin T8 (hiracin JM79), penocin A, bacteriocin 1580 and carnobacteriocin B2. The common consensus of this group is YGNGL(V)xCxKxxCxVxW. The bacteriocins in this group belong to subgroup 4 which was described in the classification of Nissen-Meyer et al. [3]. Most class II bacteriocin precursors contain a double-glycine-type signal peptide, and are translocated by dedicated ABC transporters and accessory proteins. However it is likely that some of these bacteriocins contain a different signal peptide. The sequence of hiracin JM79 is identical to that of bacteriocin T8. Hiracin JM79 is produced by Enterococcus hirae DCH5 isolated from wild mallard ducks, and contains a typical sec signal peptide that is believed to direct bacteriocins to the sec translocase embedded in the cytoplasmic

membranes [70]. The bacteriocin 31, bacteriocin RC714 and enterocin SE-K4 are also sec-dependent class II bacteriocin [71,72].

Group III contains 10 bacteriocins, which can be further subdivided into two subgroups according to their sequence similarities and differences. The bacteriocins in this group belong to subgroup 2 which was described in the classification of Nissen-Meyer et al. [3].

Subgroup III-1, represented by 8 bacteriocins (bacteriocin MC4-1, leucocin A, leucocin B-Ta11a, mesentericin Y105, plantaricin 423, plantaricin C19, prebacteriocin SkgA2, and sakacin G) has a conserved N-terminal region YYGNGxxCxxxxCxVNWGxA. Plantaricin 423 is bactericidal for many Gram-positive food-borne pathogens and spoilage bacteria, including Listeria spp., Staphylococcus spp., Pediococcus spp., Lactobacillus spp. and so on [73]. Structurally, the N terminus of leucocin A (LeuA) consists of a three-strand antiparallel ß-sheet (residues 2-16) that is rigidified by this (9-14)-disulfide moiety [74]. Bacteriocin MC4-1 and prebacteriocin SkgA2 are similar to leucocin A and leucocin A variant (C9L, C14L) in the 3D structures. There structures were determined by the SWISS-MODEL Workspace [35-37,75].

Subgroup III-2 consists of lactococcin MMFII and bacteriocin (P86291.1). Lactococcin MMFII is produced by Lactococcus lactis MMFII, which was isolated from a traditional Tunisian cheese [76]. Lactococcin MMFII is the first class IIa bacteriocin produced by a lactococcal strain. It has activity against closely related Gram-positive bacteria, including Lactococcus lactis subsp. cremoris, Lactococcus lactis subsp. lactis, Lactobacillus delbrueckii, Lactobacillus casei, E. faecium, Enterococcus faecalis, and Listeria ivanovi. The bacteriocin (P86291.1) is also produced by Lactococcus sp., showing 90.2% identity with lactococcin MMFII.

Group IV contains carnobacteriocin BM1, curvacin A, enterocin P and ubericin A. This group has the conserved sequences YGNGV(L)YCNxxKCWVNxxE. The group IV bacteriocins lack the hairpin-stabilizing tryptophan and/or cysteine residues that are present at or near the C-terminal end in most class IIa bacteriocins [3]. Carnobacteriocin BM1 is produced by Carnobacterium piscicola LV17B, which is isolated from fresh pork [77]. Curvacin A is produced by Lactobacillus curvatus LTH 1174, which originates from fermented sausage [78]. Enterocin P is produced by several E. faecium strains: IJ-31, P13, GM-1, ATB 197a, JCM5804T, LHICA 51, LHICA 28-4, and LHICA 40-4, which were isolated from various environments, such as fermented sausage, dairy products, feces of newborn infants, and non-fermented animal foods [79-84]. Enterocin P showed strong inhibitory action toward Listeria sp. It was processed and secreted by the sec-dependent pathway [79]. Ubericin A is the first streptococcal class IIa bacteriocin to be characterized [8]. It is composed of 49 amino acids with an YGNGL motif at the N-terminal half [8]. Although ubericin A showed high similarity with bacteriocins of subgroup I-3 in amino acid sequences, it showed high similarity with curvacin A in its 3D structure that was determined by SWISS-MODEL Workspace [35-37].

The bacteriocin E50-52, bacteriocin 37 and bacteriocin L-1077 are very different and form their own separate group. Bacteriocin E50-52 is produced by E. faecium NRRL B-30746, and shows diverse antimicrobial activity against both Gram-negative and Gram-positive bacteria, including Campylobacter jejuni, Yersinia spp., Salmonella spp., Escherichia coli O157:H7, S. dysenteriae, Morganella morganii, Staphylococcus spp., and Listeria spp. [28]. Bacteriocin 37 is produced by P. polymyxa NRRL B-30507, isolated from broiler chicken, and hasstrong antimicrobial activity against C. jejuni [26]. Bacteriocin L-1077 is produced by Lactobacillus salivarius 1077 (NRRL

B-50053), isolated from poultry intestinal materials, and has broad-spectrum antimicrobial activity against 33 bacterial isolates (both Gram-negative and Gram-positive bacteria), including L. monocytogenes A 9-72, E. coli O157:H7, Pseudomonas aeruginosa 508 [31].

The group VII bacteriocins consists of acidocin A and bacteriocin OR-7. This group has a conserved N-terminal region KTYYGTNGVHCTKxSLWGKVRLKN and conserved C-terminal region ILLGWATGAFGKTFH. Acidocin A is produced by L. acidophilus with activity against L. monocytogenes and other closely related Gram-positive bacteria [29]. Bacteriocin OR-7 has 65.5% amino acids sequence similarity with acidocin A with a C-terminal region that is 100% identical to that of acidocin A. Interestingly, bacteriocin OR-7 has different antimicrobial activity from acidocin A. It is active against both Gram-negative and Gram-positive bacteria [30] and has strong antimicrobial activity to Gram-negative bacterium C. jejuni in the chicken gastrointestinal system [30].

The bacteriocin OR-7 and acidocin A have some differences with other class IIa bacteriocins. As a result there is a divergence of opinion as to whether bacteriocin OR-7 and acidocin A should be placed in the class IIa family of bacteriocin [3,19,29,30]. The position of the second cysteine is very different from the very conserved position of this cysteine in the class IIa bacteriocins, suggesting that bacteriocin OR-7 and acidocin A have a different 3D structure in their N-terminal region than the well conserved 3-stranded antiparallel P -sheet like structure which seems to be conserved in most class IIa bacteriocins [3]. Moreover, the sequence and length of the C-terminal region of bacteriocin OR-7 and acidocin A are also very different from other class IIa bacteriocins.

Both bacteriocin OR-7 and acidocin A contained a "pediocin box"-like motif, YGNGVXCXnV, in the N-terminal region of the peptide typical of class IIa bacteriocins, except that a T was present as YGTNGV in the sequence [29,30]. Based on our assessment of previous studies, we are in agreement that bacteriocin OR-7 and acidocin A belong to class IIa family [19,29,30].

3. Biosynthesis of Class IIa Bacteriocins

At least four genes are required for the production of class IIa bacteriocins, including a bacteriocin structural gene encoding a precursor, an immunity gene encoding an immunity protein, genes encoding an ATP-binding cassette transporter and an accessory protein for extracellular translocation of bacteriocin [2].

The class IIa bacteriocin production was regulated by quorum sensing (QS) system. QS systems are present in the majority of Gram-positive and Gram-negative bacteria, as one primary mechanism for bacteria to monitor the environment for other bacteria and to alter behavior on a population-wide scale in response to changes in the number and/or species present in a community [85-87].

QS systems used for the regulation of class IIa bacteriocin production are composed of three gene products, including an inducer peptide, a membrane-associated histidine protein kinase (HPK), and a cytoplasmic response regulator (RR) [88]. The inducer peptide is ribosomally synthesized at low levels as a precursor which appears not to be biologically active and contain an N-terminal extension or leader sequence [89]. Subsequent cleavage of the precursor at a specific processing site removes the leader sequence from the antimicrobial molecule concomitantly. Then inducer peptide is secreted and exported through the dedicated transport system involving an ABC-type translocator and an accessory protein [15,88,89]. The presequence of the bacteriocin plays a dual role in bacteriocin biosynthesis [2].

One is a protective role at the cytosolic side of the cell membrane by keeping the bacteriocin inactive. The other is as a recognition signal during export [2].

At a certain concentration threshold of the externalized inducer peptide, the transmembrane HPK detects a change in environmental signal and is activated, leading to its autophosphorylation [88,90]. Then the phosphorylated HPK transfers a phosphate group to its cognate RR. The phosphorylated RR acts as a transcriptional activator and activates expression of bacteriocin-related genes, including genes encoding bacteriocin, immunity protein, secretory apparatus, and regulatory proteins [2,88]. Bacteriocin and immunity genes most often reside on the same operon and are expressed concomitantly. The bacteriocin producer cells protect themselves from their own bacteriocin by the immunity protein. At a certain time, essentially all bacteriocin producer cells in the population are believed to secrete bacteriocins, and this result in a rapid activation of the bacteriocin production [89].

4. Genetic Organization of DNA Coding for Class IIa Bacteriocins

Generally, most class IIa bacteriocin genes are arranged in one or a few operons, which include a bacteriocin structural gene encoding a precursor, an immunity gene encoding an immunity protein, genes encoding an ATP-binding cassette transporter and an accessory protein for extracellular translocation of bacteriocin, and in several cases two regulatory genes encoding a two component system for regulations of the biosynthesis of bacteriocin [19] (Figure 2).

Production of bacteriocins is often correlated with the presence of a plasmid. Several class IIa bacteriocins, for example, enterocin A, divercin V41, sakacin P, carnobacteriocin B2 and carnobacteriocin BM1, have genes that have been shown to be located on chromosome fragments [19,77,91-93]. In many bacteriocin-producing bacteria, the bacteriocin structural gene and other related genes were located in one operon. However, genes encoding immunity and secretion functions may not always be linked to structure genes [89,94].

At the present time, all known class IIa bacteriocins are ribosomally synthesized as precursor peptides with an N-terminal leader sequence. The leader sequences of most bacteriocins contain two conserved glycine residues, which may serve as a recognition signal for protein processing and secretion. This double-glycine-type leader sequences were cleaved and removed by ATP-binding cassette (ABC) transporters and their accessory proteins [2]. However, a few class IIa bacteriocins, including bacteriocin 31, enterocin P, enterocin SE-K4, listeriocin 743A, and hiracin JM79 are secreted by the general sec-dependent export system [14,70-72,79,95]. These bacteriocins have a hydrophobic ^-terminal sec-dependent leader sequence, which directs the secretory protein to the cytoplasmic membrane and is processed by a signal peptidase during translocation across the cytoplasmic membrane. The related genes for production of these bacteriocins are unknown [14,71,72,79,95-98].

Class IIa bacteriocins show a remarkable conservation of gene arrangement (Figure 2). The genetic organization of leucocin A gene cluster (lea locus) from L. gelidum UAL187 is a typical bacteriocin locus [99]. The lea locus includes two different directions operons with four bacteriocin-related genes leaA, lcaB, lcaC and lcaD. The immunity protein gene lcaB is located immediately downstream of the structural leucocin A gene lcaA. The accessory transporter gene lcaD occurs also downstream of gene lcaC encoding an ABC transporter [99].

The genetic organization of sakacin P gene cluster (spp locus) from L. sakei LTH673 and LTH674 is complicate, when compared to leuconcin A [40,93]. It is composed of three operons, which encode a 61-amino-acid sakacin P precursor SppA, a sakacin P immunity protein SpiA; a transport and secretory system (a 718-amino-acid ABC transporter protein SppT and an accessory factor for ABC transporter protein SppE); and a three-component regulatory system (inducing peptide preprotein SppIP, HPK SppK and RR SppR), respectively [40,93]. The production of sakacin P in L. sakei Lb674 and LTH673 is regulated by a typical peptide pheromone-based QS mechanism [40,93].

The genetic organization of divercin V41 presents an unusual organization [92]. The dvn locus encodes a 66-amino-acid divercin V41 precursor, an ATP dependent transporter, two immunity-like proteins and two components of a lantibiotic-type signal-transducing system [92] (see Figure 2). Interestingly, a so-called transport accessory protein was absent from the locus. Generally, the genes encoding the HPK are located upstream of the genes encoding RR in anti-listeria bacteriocin operon [100]. However, in the dvn locus of divercin V41, the HPK gene followed the RR gene, which is a characteristic of lantibiotic operons. The genetic organization of the fragment suggests important gene rearrangements [92].

Sometimes one locus can include productions of two bacteriocins. L. sakei 5 produces a plasmid-encoded bacteriocin sakacin P, as well as two chromosomally encoded bacteriocins, i.e., sakacin T, which is a class IIb two-peptide bacteriocin and sakacin X, which is a class IIa bacteriocin [101]. The sakacin TX locus encodes structural genes of sakacin T and sakacin X, including two adjacent but divergently oriented gene clusters (See Figure 2). The first gene cluster stxPRKT is believed to encode an inducing peptide, three proteins involved in regulation and secretion of these bacteriocins. The second gene cluster includes sakTa, sakTß, sakIT, sakX and sakIX, which encode the structural and immunity genes for sakacin T and sakacin X [101].

L. mesenteroides FR52 produces both mesentericin 52A and 52B [102]. Mesentericin 52A is a 37-amino-acid class IIa bacteriocin, identical to mesentericin Y105 from L. mesenteroides Y105 [103]. Mesentericin 52B is a 32-amino-acid atypical class II bacteriocin, identical to mesentericin B105 from L. mesenteroides Y105 [104]. The mes locus of L. mesenteroides FR52 is involved in productions of mesentericin 52A and 52B [104]. The previous study revealed that ATP dependent transporter MesD and transport accessory protein MesE were involved in secretion and transport of these bacteriocins [104]. Mesentericin 52A and mesentericin 52B have own immunity genes mesI and mesH, respectively.

The sakacin G gene cluster (skg locus) from L. sake 2512, R1333 and CWBI-B1365 was very interesting because it contained duplicated structural genes skgA1 and skgA2 [105-107]. There is only a two-amino-acid difference in sequence occurs in leader peptides of these prebacteriocins which makes these mature peptides, SkgA1 and SkgA2, essentially identical [106,107].

The genetic organization of avicin A gene cluster (avc locus) from E. avium has been established [21]. It is the first bacteriocin locus identified in E. avium to be characterized at the molecular level [21]. The locus showed a particular gene organization. The accessory gene avcD associated with bacteriocin transport did not occur immediately downstream of the gene avcT (which encodes an ABC transporter), but two regulatory genes avcK (which encodes a HPK) and avcR (which encodes a RR) followed the gene avcT [21]. The avcK, avcR, and induction peptide pheromone-encoding gene avcF, constituted a three-component regulatory system in the avicin locus.

This indicated that the production of avicin A was regulated by the peptide pheromone-inducible regulatory system [21]. For most class IIa bacteriocins, three genes responsible for regulation are located in the same operon, but avcK, avcR, and avcF were located in two different operons (See Figure 2). In this locus includes two bacteriocins structural genes avcA and avcB. Avicin B is a divergincin-like bacteriocin, but it didn't show antimicrobial activity and is probably a relic of a previous functional bacteriocin [21].

5. Structure-Function Relationship and Target Recognition of Class IIa Bacteriocins

To date, the 3D structures of leucocin A [74], carnobacteriocin B2 [108], sakacin P [109] and curvacin A [110] have been characterized by nuclear magnetic resonance (NMR) spectroscopy. The 3D analysis revealed that class IIa bacteriocins consist of a hydrophilic, cationic and highly conserved N-terminal P-sheet domain, and a flexible, diverse hydrophobic/amphiphilic C-terminal domain [3,74,108-110]. The former is structurally stabilized by a conserved disulfide bridge; the latter contains a central amphiphilic a-helix, ending with a structurally extended C-terminal tail. The amphipathic a-helix was critical for antimicrobial specificity and temperature-dependent activity of these class IIa bacteriocins [74,108,111-114]. The C-terminal part of some class IIa bacteriocins, such as enterocin A, divergicin M35, divercin V41, coagulin, pediocin PA-1, sakacin G and plantaricin 423, formed a hairpin structure which was stabilized by a disulfide bridge between a cysteine residue in the middle of the a-helix and a cysteine residue at the C-terminus [3].

Two cysteines that come from the conserved N-terminal region (YGNGVxCxK/NxxC) of class IIa bacteriocins formed a conserved disulfide bond. In most class IIa bacteriocins, the disulfide bond is formed between cysteine9 and cysteine14. Extensive studies indicate that this conserved disulfide bond is required for antimicrobial activity for class IIa bacteriocins [115-117]. Mutants of mesentericin Y105 (cysteine9 ^-serine9, cysteine14^serine14) showed a marked loss in antimicrobial effects [115]. The antimicrobial activity of pediocin PA-1 was abrogated by the substitution of 11 different amino acids at cysteine14 based on NNK scanning [116]. Substitution of the cysteines with serines in leucocin A (LeuA) abolished antimicrobial effects [117].

However, some results from Derksen et al. indicated that the disulfide bond in leucocin A (LeuA) could be replaced by a noncyclic diallyl moiety without significant loss in activity [117]. The leucocin A (C9F, C14F), bis-allyglycine-leucocin A, and norvaline-leucocin A retained activities comparable to that of the natural leucocin A [75,114]. The researchers speculated that hydrophobic or n-stacking interactions can compensate for the absence of the disulfide in this molecule and assist receptor binding [75,114,117].

Three analogues of leucocin A (LeuA) and six analogues of pediocin PA-1(Ped) were synthesized by replacing the conserved cysteines that form a disulfide bond with pairs of hydrophobic amino acids [114]. Noncovalent hydrophobic interactions in all of the leucocin A (LeuA) derivatives effectively replaced the disulfide and afforded peptides with full antimicrobial activity [114]. Apparently the propensity of the intraloop sequence of leucocin A (LeuA) to induce P-turns in combination with the hydrophobic interaction of the two Phe residues is sufficient to achieve the appropriate conformation for bioactivity [114,118].

Sit et al. presented the 3D solution structures of the inactive (C9S, C14S)-leucocin A and the active (C9L, C14L)-leucocin A peptides [75]. Mutation of the two cysteine residues to serines or leucines did not affect the overall charge of the peptide, and therefore is highly unlikely to interfere with the electrostatic interactionsbetween the peptide and the bacterial cell surfaces. It was speculated that the N terminus may be serving a more crucial function, such as forming intermolecular contacts with other leucocin A-EIItman complexes during pore formation [75].

Receptor binding might occur on the surface of a three-strand antiparallel P-sheet at the N terminus of the peptide as well as by recognition of the hydrophobic face of the amphipathic C-terminal a- helix, which is known to be required and determines specificity for particular organisms [112,119,120]. These results indicate that although the N-terminal loop has a vital influence on the activity of the peptide, additional interactions at the C terminus with the receptor must match and contribute to the overall activity [115,119-121].

Most class IIa bacteriocins present a single intramolecular disulfide bond between cysteine9 and cysteine14. The C-terminal part of a few class IIa bacteriocins, contains an additional C-terminal disulfide bridge, such as sakacin G (between cysteine24 and cysteine37), plantaricin 423 (between

24 37 24 44

cysteine and cysteine ), pediocin PA-1/AcH (between cysteine and cysteine ), divercin V41

25 43 29 47

(between cysteine and cysteine ), and enterocin A (between cysteine and cysteine ). The second disulfide bridge not only plays an important role in stabilizing the 3D structure of the C-terminal domain, but also correlates strongly with spectrum of activity [2,20,109,113,122,123]. The previous studies indicated that the second disulfide bridge in the class IIabacteriocins contributes to widening of the antimicrobial spectrum as well as to higher potency at elevated temperatures [113].

It is well known that class IIa bacteriocins kill target cells by forming pores and disrupting the integrity of target cell membranes, causing dissipation of proton motive force, depletion of interacellular ATP and leakage of amino acids and ions [2,19]. Numerous mode-of-action studies have demonstrated that the sugar transporter mannose phosphotransferase system (Man-PTS) serve as target receptors for class IIa bacteriocins on sensitive cells [124-131]. The Man-PTS, which is a complex sugar uptake system in the Gram-positive Firmicutes and Gram-negative Gammaproteobacteria, includes a general PTS protein enzyme I (EI), a histidine containing phosphocarrier protein (HPr) and a carbohydrate-specific protein complex (enzyme II, EII) [132].

The enzyme II consists of four subunits: IIA, IIB, IIC and IID [132]. Subunits IIA and IIB are located in the cytoplasm and are responsible for phosphorylation. They are often found together on one protein. The IIC subunit is an integral membrane protein involved in sugar transport. The IID subunit is also a transmembrane protein [132]. The membrane proteins IIC and IID together form a membrane-located complex. IIA and IIB are in reversible contact with the membrane-located complex [129,133]. Other studies indicated that a single extracellular loop of the membrane-located protein IIC (MptC) was involved in specific target recognition by the class IIa bacteriocins, and was the major determinant responsible for species-specificity [125,130].

The proposed mechanism of action for IIa bacteriocins is as follows: first, the N-terminal P-sheet domain of bacteriocin binds to the extracellular loop of IIC in the Man-PTS. Then, C-terminal a-helix-containing hairpin or hairpin-like domain of the bacteriocin interacts with the transmembrane helices of the Man-PTS, leading to conformational changes in the Man-PTS proteins in a manner that renders the transporter irreversibly open thereby causing uncontrolled efflux of essential molecules,

disruption of the membrane integrity and in effect, cell death [131,134]. In bacteriocin producing cells, a cognate immunity protein tightly binds the receptor in a bacteriocin-dependent manner, to prevent killing by the bacteriocin [129]. However some class IIa bacteriocins, including enterocin P and sakacin A, showed a different mode of receptor recognition. They employ the IIC and IID complex as a receptor on target cells and then the cognate immunity protein (LciA) is tightly associated with the bacteriocin-receptor complex to render producer cells immune [129,135].

Most class IIa bacteriocins have a relatively narrow inhibitory spectrum, inhibiting predominantly genera or species closely related to the bacteriocin producers. In order to reveal the mechanism of the receptor function specificity, a phylogenetic analysis of membrane-located proteins (IIC and IID) of 86 Man-PTSs from a wide range of bacterial genera was performed [136]. These man-PTSs are clustered into three distinct groups, named groups I, II and III. Fourteen man-PTSs distributed all over the phylogenetic tree were selected for heterologous expression in L. lactis indigenous man-PTS-deletion mutant [136]. Bacteriocin sensitivity of the different L. lactis clones was determined with four class IIa bacteriocins, including pediocin PA-1, enterocin P, sakacin P, and penocin A [136]. The results indicated that only members of group I could serve as receptors for class IIa bacteriocins. A multiple sequence alignment analysis of IIC and IID proteins revealed three sequence regions (two in IIC and one in IID) that distinguish members of the group from those of the other groups, suggesting that these amino acid regions confer the specific bacteriocin receptor function [136].

The receptor efficiencies of Listeria, Enterococcus, Lactobacillus, Leuconostoc, Carnobacterium, Clostridium, Pediococcus and Streptococcus varied in a pattern directly related to their phylogenetic position [136]. The species of Enterococcus, Listeria and Carnobacterium showed most active receptors and were highly sensitive to four IIa bacteriocins; the species of Lactobacillus, Pediococcus and Clostridium are also frequently inhibited by these bacteriocins, although they are often less sensitive; and the strains of Streptococcus and Leuconostoc are occasionally reported to be sensitive to class IIa bacteriocins at a low level. These results are in line with previous comparative analyses of the inhibitory spectra of class IIa bacteriocins [122,137]. Different strains of the same bacterial species can vary greatly in sensitivity to a given bacteriocin [122,138]. The variation in sensitivity might be due to differential expression levels of the receptor [136].

Generally, the conserved N-terminal region of class IIa bacteriocin was speculated to be involved in the receptor interaction, and the diverse C-terminal region was responsible for target cell species-specificity [136]. But some studies strongly suggest that the C-terminal region of class IIa bacteriocin might be involved in interaction between bacteriocin and its receptor [119,121,139,140]. Therefore it was speculated that N-terminal and C-terminal regions take part in the interaction with target cell receptor and that, they have different function during different stage of interaction. Synthesis of bacteriocin mutants and analogues provides valuable structure-activity relationships and tools to obtain further information on the peptide-receptor complex [117,119].

Resistance of Listeria spp. and other Gram-positive bacteria to class IIa bacteriocins was correlated with loss or reduction of expression of Man-PTS, inthe following phenotypes [132,135,141-143]: (i) absence of the IIAB subunit of Man-PTS in the proteomes of resistant bacteria [125,143]; (ii) mutations in the sigma transcription factor o54 (rpoN) and the G54-dependent transcription activator ManR of the mpt operon [124,126,127,144-146], (iii) a mutation in the promoter proximal mptA (IIA) cistron [125], and (iv) in-frame deletions in the mptD (IID) gene (which may have compromised the

folding and stability of IID and IIC) [144]. Recently natural food isolates of L. monocytogenes with different susceptibilities to class IIa bacteriocins were investigated [135]. The results also identified Man-PTS as a key player in the mechanisms of resistance. At the same time, downregulation of the mpoABCD (mannose permease one) operon in L. monocytogenes was shown to promote resistance to class IIa bacteriocins [147]. The mpoABCD operon putatively encodes a PTS permease of the mannose family similar to that encoded by the mpt operon. In silico analysis indicated that mpo transcription might be dependent on o54.

Bacterial strains sensitive to class IIa bacteriocins readily give rise to resistant mutants upon bacteriocin exposure. The development of highly tolerant and/or resistant strains may decrease the efficiency of bacteriocins as biopreservatives. The acquiring of resistance to bacteriocins can significantly affect physiological activity profile of bacteria, alter cell-envelope lipid composition, and also modify the antibiotic susceptibility/resistance profile of bacteria [148].

6. Discovery of Class IIa Bacteriocins

To date, traditional screening strategies have relied on detection of antimicrobial activity as the basis for discovery of new and potent bacteriocins [131]. New bacteriocins are detected and identified by screening large number of potential bacteriocin-producing bacteria for antimicrobial activity. The screened bacteriocins are then purified and characterized. These classic screening strategies are time-consuming and labor-intensive, so researchers need to explore and develop more rapid and higher-throughput approaches for identification of bacteriocins potential [149-152]. The PCR assays that target bacteriocin-coding genes or bacteriocin regulation-related genes for rapid detection of bacteriocins have been developed [152-156]. Most PCR assays can only detect known bacteriocins because they use specific primers which were designed according to previously characterized bacteriocins [154,155,157]. Wi^ckowicz et al. have developed a rapid PCR assay with primers which were designed on the basis of a large scale alignment of class IIa bacteriocin genes. Several potentially novel bacteriocin-coding sequences were found by means of this high-throughput PCR assay [152].

A large number of LAB genomes have been published during the last decade [158,159]. At the same time, bioinformatics as well as new technologies such as transcriptomics, proteomics and metabolomic analysis have expanded tremendously in past decade. All of the above mentioned technologies have provided a basis for detection of bacteriocins by means of silico analysis [160]. Recently, there has been a trend from classical screening strategies for antimicrobial activity towards silico analysis of genomic data as computational approaches are able toaccelerate the process of novel antimicrobial peptides (AMPs) discovery and design [131,137,161,162].

Dirix et al. identified over 50 bacteriocins or bacteriocin-like peptides by screening for peptides containing a double-glycine leader sequence and the corresponding ABC transports in 165 fully sequenced bacterial genomes (including 45 Gram-positive bacteria and 120 Gram-negative bacteria) [161,162]. Diep et al. identified a new class IIa bacteriocin penocin A in the genome of P. pentosaceus ATCC 25745 by means of silico-based analysis. The antimicrobial activity of penocin A has been determined by experiments [137]. The silico analysis for prediction of bacteriocins, is a challenging task due to the small sizes and diversity in sequence, structure and function of bacteriocins [131].

Some databases and bioinformatics tools have been developed and designed for prediction of AMPs production by both Gram-positive and Gram-negative bacteria. For example, an antimicrobial peptide database (APD) was developed by means of sequence similarity and certain known principles of AMPs [163]. The database was updated in 2009 [164]. AMPer database provided hidden Markov models (HMMs) to automatically discover AMPs [165]. An integrated open-access database BACTIBASE ( [166], and a genome mining software BAGEL2 ( [167] were specifically designed for AMPs discovery [168,169]. Wang et al. constructed a new method by means of sequence alignment and feature selection methods to predict AMPs [170]. Recently Fernandes et al. employed adaptive neuro-Fuzzy inference system (ANFIS) as a pattern recognition tool to classify a putative peptide as an AMP or non-AMP [171].

Quantitative structure-activity relationship (QSAR) modeling is one of the most broadly used chemoinformatics approaches. It can be defined as quantitative models that correlate the variation in measured biological activity with the variation in molecular structure among a series of chemical compounds. QSAR has been applied successfully to AMPs discovery [172-175]. The CAMEL database employed QSAR and artificial neural networks (ANN) to predict AMPs function [176]. Recently a novel quantitative prediction method of AMP was established by QSAR modeling based on the physicochemical properties of amino acids [177].

The activity of an AMP is commonly expressed as the threshold concentration (minimum inhibitory concentration, MIC) upon which bacterial growth is inhibited. Biophysical studies with model phospholipid membranes often identify concentration thresholds upon which the peptide behavior becomes disruptive through pore formation or membrane lysis [178-183]. The connections between in vivo MICs and thresholds in model membranes have been recently proposed [183,184]. Recently, Melo et al. developed an interaction model of antimicrobial peptides with biological membranes [178]. A straightforward and robust method was presented and used to implement this relationship. The methodology provides a basis for fast, cost-effective alternatives for screening AMPs, with potential application to high-throughput screening approaches. These tools will accelerate and optimize the discovery and identification of novel bacteriocins. Howerverthese bacteriocins still have to be verified by measuring their antimicrobial activities according to excepted experimental procedures.

7. Conclusions

A large number of new class IIa bacteriocins have been detected and purified in the last decade. Some class IIa bacteriocins with wide-spectrum antimicrobial activity have been reported and new discovery methods have been introduced. Acuña et al. presented a novel procedure for designing hybrid bacteriocins through fusion of microcins with class IIa bacteriocins in order to produce new wide-spectrum bacteriocins with high specific activity [185]. All of these advancements will accelerate the developments of class IIa bacteriocins.


This work was supported by a grant from the State Key Laboratory of Veterinary Biotechnology (No. SKLVBF201202), and a project in the Postdoctoral Science-Research Foundation of Heilongjiang province (LBH-Q11119).

Int. J. Mol. Sci. 2012, 13 Supplementary Information

Table S1. Some characteristics of the class IIa bacteriocins.

Bacteriocin Account Nucleotide Account Protein Prepeptie size (aa) MP size (aa) MP Mass (Da) PI Producer Origin References

Group I

Sub-group I-1

Avicin A FJ851402.1 ACZ36002.1 61 43 4291.9 9.32 E. avium XA83 Feces of healthy infants [21]

Bavaricin A/SppA AF526262 AAM88858.1 61 43 4435.9 8.76 L. sakei MI401 Sourdough [22]

Curvaticin L442# P84886.1 L. curvatus L442 Greek fermented sausage [23]

Enterocin CRL35 AY398693 AAQ95741.1 58 43 4287 9.82 E. mundtii CRL35 Argentinian artisanal cheese [24]

Enterocin HF P86183 43 4333 9.37 E. faecium HS and TA29 Humans and fish

Listeriocin 743A AF330821.1 AAK19401.1 71 43 4484 9.98 L. innocua 743 Food [186, 4]

Mundticin P80925.1 43 4287 E. mundtii ATO6 Fresh chicory endive [187]

Mundticin CRL35 AY444743 AAR26473.1 58 43 4287 9.82 E. mundtii CRL35/AT06 Artisanal cheese [24]

Mundticin KS AB066267 BAB88211.1 50 43 4287 9.82 E. mundtii NFRI 7393/AT06 Fresh chicory endive [188]

Mundticin L FJ899708.1 ACQ77507.1 58 43 4301.8 9.82 E. mundtii CUGF08 Alfalfa sprouts [32]

Mundticin QU2 43 * 4287 E. mundtii QU 2 Fermented soybean [189]

Pediocin ACCEL* P. pentosaceus ACCEL

Piscicocin CS526 * C. piscicola CS526 Cold-smoked salmon [190]

Piscicolin 126 AY812745 AAX21354.1 62 44 4417 9.32 C.maltaromaticum UAL26 Vacuum-packaged beef [191]

Piscicolin 126 AF275938.1 AAK69419.1 62 44 4417 9.32 C. piscicola JG126 Spoiled ham [192]

Piscicocin Via 44 4417 9.32 C. piscicola V1 Fish [193]

Sakacin P DQ019413.1 AAY44078.1 61 43 4461.9 8.74 L.curvatus LTH1174 Meat fermentation [38]

Sakacin P DQ019414.1 AAY44080.1 61 43 4461.9 8.74 L.curvatus L442 Greek fermented sausage [39]

Sakacin P AY875983 AAW79057.1 61 43 4435.9 8.76 L.sakei I151 Sausage [41]

Sakacin P AF002276.1 AAB93970.1 61 43 4435.9 8.76 L.sakei LTH673 Meat fermentation [40]

Table S1. Cont.

Bacteriocin Account Nucleotide Account Protein Prepeptie size (aa) MP size (aa) MP Mass (Da) pI Producer Origin References

Sakacin P NZ AGBU01000084.1 ZP 09041901.1 61 43 4435.9 8.76 L. curvatus CRL 705 Fermented sausage

Sakacin X AY206863 AAP44569.1 61 43 4364 9.32 L. sakei 5 Malted barley [101]

Sakacin X ZP 09041912.1 61 43 4364 9.32 L. curvatus CRL 705 Fermented sausage

Sub-group I-2

Bifidocin B # 36 3801.5 8.05 B. bifidum NCFB 1454 Human isolate [10,11]

CoaA/Coagulin/CoaA AF300457.1 AAG28763.1 62 44 4614.2 8.66 B. coagulans I4 Cattle feces [194,13]

Mutacin F-59.1 P86386.1 25 * S. mutans 59.1 [9]

PapA NC 004832.1 NP 857602.1 62 44 4627.2 8.66 P. acidilactici H [195]

Pediocin EU826148.1 ACF32966.1 62 44 4627.2 8.66 P. acidilactici MTCC 5101

Pediocin A 44 4628 8.66 P. pentosaceus FBB61 Cucumber fementations [51]

Pediocin AcH S74PEDACH AAA98337.1 62 44 4627.2 8.66 P. acidilactici H Fermented sausage [44]

Pediocin AcH 44 4627.2 8.66 L. plantarum WHE92 Soft cheese in France [52]

Pediocin PA-1 HQ876214.1 AEH68223.1 62 44 4627.2 8.66 E. faecium Acr4

Pediocin PA-1 AAB23877.1 44 * P. acidilactici [196]

Pediocin PA-1 M83924.1 AAA25559.1 62 44 4627.2 8.66 P. acidilactici PAC1.0. Sorghum beer [197,42]

Pediocin PA-1 44 4628 8.66 L. plantarum DDEN 11007 [53,66]

Pediocin PA-1 44 4628 8.66 P. acidilactici MM33 Human stool [49]

Pediocin PP-1 44 4602.2 8.66 P. pentosaceus CBT8 Kimchi [198]

Pediocin SJ-1 P. acidilactici SJ-1 Meat [57]

Prepediocin AcH S44537.1 AAC60413.2 62 44 4605.2 8.33 P. acidila I ctici Lb42-923 [44]

Prepediocin PA-1 AY705375.1 AAT95422.1 62 44 4627.2 8.66 P. acidilactici K10 Kimchi [47]


Leucocin C LCCC LEUME P81053.2 43 4595 8.76 L. mesenteroides 6 Malted barley [67]

Leucocin C-TA33a 36 * 4598 L. mesenteroides TA33a Vacuum-packaged meat [69]

Weissellin A 43 4450 9.32 W. paramesenteroides DX [25]

Table S1. Cont.

Bacteriocin Account Nucleotide Account Protein Prepeptie size (aa) MP size (aa) MP Mass (Da) PI Producer Origin References


Bacteriocin 602 P86393.1 39 3864 7.2 P. polymyxa NRRLB-30509 Broiler chicken, crop [26]

Bavaricin MN P80493.2 42 4769 10.0 L. sakei MN Meat [27]

Divercin V41 AJ224003 CAA11804.1 66 43 4512.3 8.65 C. divergens V41 Fish viscera [92,199]

Divergicin M35 P84962.1 43 4518.75 8.3 C. divergens M35 Smoked salmon [200]

Duracin GL HQ696461.1 ADW93772.1 71 43 4966.7 8.74 E. durans 41D Cheese product

Enterocin A X94181.1 CAA63890.1 65 47 4829 8.98 E. faecium CTC492 Fermented sausage [91]

Enterocin A 65 47 4833 8.98 E. faecium WHE 81 Cheese [201]

Enterocin A NZ GG692545.1 ZP 05660016.1 65 47 4831.6 8.98 E. faecium 1,230,933

Enterocin A AB038464.1 BAA92138.1 65 47 4831.6 8.98 E. faecium N15 Japanese rice-bran paste [153]

Enterocin A/ EntA AF099088.1 AAD29132 65 47 4831.6 8.98 E. faecium DPC1146 [202]

Enterocin BC25 AF240561.1 AAF44686.1 65 47 4831.6 8.98 E. faecium BC25 [203]

Group II

Bacteriocin 31 /BacA D78257.1 BAA11329.1 67 43 5007.8 9.72 E. faecalis YI717 Clinical sample [72]

Bacteriocin 1580 P86394.1 35 3486 7.8 B. circulans NRRLB-30644 Broiler chicken, crop [26]

Carnobacteriocin B2 L47121.1 AAB81310.1 66 48 4969.9 9.97 C. piscicola LV17B Pork [77,108]

Bacteriocin 43 AB178871 BAF36626.1 74 44 5092.9 9.26 E. faecium [204]

Bacteriocin RC714 43 4936.7 8.74 E. faecium RC714 Human fecal [205]

Bacteriocin T8 74 44 5092.9 9.26 E. faecium T8 Children Infected with HIV [206]

Enterocin SE-K4 AB092692.1 BAC20326.1 76 48 5356.2 9.93 E. faecalis K-4 Grass silage in Thailand [207,71]

Hiracin JM79 DQ664500 ABG47453.1 74 44 5092.9 9.26 E. hirae DCH5 Mallard ducks [70]

Penocin A/PenA YP_803635 60 42 4688.4 9.72 P. pentosaceus ATCC 25745 [137]

Table S1. Cont.

Bacteriocin Account Nucleotide Account Protein Prepeptie size (aa) MP size (aa) MP Mass (Da) pI Producer Origin References

Group III

Sub-group III-1

Bacteriocin MC4-1 EU047916 ABW08100.1 71 43 4890.6 9.27 E. faecalis MC4 [34]

Carnocin CP52 CPU76763 AAB18989.1 66 48 4969.9 9.97 C. piscicola CP32 Cheese [208]

Leucocin A M64371.1/LEULAIP AAA68003.1 61 37 3932.3 8.78 L. gelidum UAL 187 Vacuum-packaged meat [209,33]

Leucocin B-Ta11a S72922.1 AAC60488.1 61 37 3931.6 8.78 L. carnosum Talla Vacuum-packaged meat [33]

Mesentericin 52A AY286003 AAP37395.1 61 37 3869.3 8.78 L. mesenteroides subsp. mesenteroides FR32 Raw milk [102]

Mesentericin Y105 X81803.1 CAA57405.1 61 37 3869.3 8.78 L.mesenteroides Y103 Goat's milk in France [103]

Plantaricin 423 AF304384 AAL09346.1 36 37 3934.6 8.67 L. plantarum 423 Sorghum beer [73, 210-212]

Plantaricin C19 36 3843.3 9.88 L. plantarum C19 Fermented cucumbers [213,214]

Prebacteriocin SkgA2 ZP 08080540.1 36 38 4139.8 9.03 L. ruminis ATCC 23644 Human gastrointestinal tract

Sakacin G AF393333.1 AAM73712.1 33 37 3837.4 7.96 L. sakei 2312 Rhodia food collection [103]

Sakacin G FJ621368.1 ACM68469.1 33 37 3837.4 7.96 L. sakei R1333 Smoked salmon [107]

Sakacin G EU370233 ACB72724.1 33 37 3837.4 7.96 L. sakei CWBI-B1363 Raw poultry meat [106]

Sakacin G EU370233 ACB72725.1 33 37 3837.4 7.96 L. sakei CWBI-B1363 Raw poultry meat [106]

Sub-group III-2

Lactococcin MMFII P83002.1 37 4144.6 7.23 L. lactis MMFII Tunisian cheese [76]

Bacteriocin P86291.1 41 4601.3 7.23 Lactococcus sp.

Group IV

Carnobacteriocin BM1 L29038.1 AAA23014.1 61 43 4324.6 8.76 C. piscicola LV17B Fresh pork [77]

Curvacin A S67323.1 AAB28845.1 39 41 4308.0 9.37 L.curvatus LTH 1174 Fermented sausage [78]

Ubericin A EF203933.1 ABQ23939.1 70 49 3270.3 9.33 S. uberis E [8]

Enterocin P GQ369322.1 ACU28817.1 71 44 4701.3 7.23 E. faecium IJ-31 Dairy products in Islamabad [84]

Enterocin P AF003726 AAC45870 71 44 4493 8.22 E. faecium P13 Spanish fermented sausage [79]

Enterocin P AY728263 AAU29394.1 44 4714.3 3.31 E. faecium GM-1 Feces of a newborn infant [81]

Table S1. Cont.

Bacteriocin Account Nucleotide Account Protein Prepeptie size (aa) MP size (aa) MP Mass (Da) pI Producer Origin References

Enterocin P-like AY633748 AAT58220.1 44 4701.3 7.25 E. faecium ATB 197a

Enterocin P-like AB075741 BAC00780.1 40* E. faecium JCM5804T [80]

Enterocin P DQ867125 ABI29857.1 44 4629.3 8.22 E. faecium LHICA 51 Nonfermented animal foods [82]

Enterocin P DQ867124 ABI29856.1 44 4629.3 8.22 E. faecium LHICA 28-4 Nonfermented animal foods [82]

Enterocin P FJ416487 ACJ46053.1 44 4629.3 8.22 E. faecium LHICA 40-4 Nonfermented animal foods [83]

Piscicocin V1b 43 4526 8.76 C. piscicola V1 Fish [193]

Sakacin A Z46867 CAA86942.1 59 41 4308.0 9.37 L. sakei Lb706 Meat [215-217]

Group V

Bacteriocin E50-52 P85148.1 39 4124.9 8.12 E. faecium NRRL B-30746 [28]

Group VI

Bacteriocin L-1077 37 3454 9.1 L. salivarius 1077 Healthy broiler chickens [31]

Group VII

Bacteriocin 37 P86395.1 30 3465.4 10.1 P. polymyxa NRRL B-30507 Broiler chicken, crop [26]

Group VIII

Acidocin A BAA07120 81 58 6501.5 10.93 L. acidophilus TK9201 [29]

Bacteriocin OR-7 54 6214 10.32 L. salivarius NRRL B-30514 Cecal contents of chickens [30]

aa, Amino acids; MP, Mature peptide; #, the whole sequence of bacteriocin has not been determined, including Curvaticin L442 and bifidocin B; *, some amino acids of bacteriocin has not been determined;

B. circulans, Bacillus circulans; B. coagulans, Bacillus coagulans; B.bifidum, Bifidobacterium bifidum; C. divergens, Carnobacterium divergens; C. maltaromaticum, Carnobacterium maltaromaticum; C. piscícola, Carnobacterium piscicola; E. avium, Enterococcus avium; E. durans, Enterococcus durans; E. faecalis, Enterococcus faecalis; E. faecium, Enterococcus faecium; E. hirae, Enterococcus hirae; E. mundtii, Enterococcus mundtii; L. acidophilus, Lactobacillus acidophilus; L. carnosum, Leuconostoc carnosum; L. curvatus, Lactobacillus curvatus; L. gelidum, Leuconostoc gelidum; L. innocua, Listeria innocua; L. lactis, Lactococcus lactis; L. mesenteroides, Leuconostoc mesenteroides; L. pentosus, Lactobacillus pentosus; L. plantarum, Lactobacillus plantarum; L. ruminis, Lactobacillus ruminis; L. sakei, Lactobacillus sakei; L. salivarius, Lactobacillus salivarius; P. acidilactici, Pediococcus acidilactici; P. parvulus, Pediococcus parvulus; P. pentosaceus, Pediococcus pentosaceus; P. polymyxa, Paenibacillus polymyxa; S. mutans, Streptococcus mutans; S. uberis, Streptococcus uberis; W. paramesenteroides, Weissellaparamesenteroides; HIV, Human Immunodeficiency Virus.


1. Klaenhammer, T.R. Genetics of bacteriocins produced by lactic bacteria. FEMS Microbiol. Rev. 1993, 12, 39-86.

2. Drider, D.; Fimland, G.; Héchard, Y.; McMullen, L.M.; Prévost, H. The continuing story of class IIa bacteriocins. Microbiol. Mol. Biol. Rev. 2006, 70, 564-582.

3. Nissen-Meyer, J.; Rogne, P.; Oppegârd, C.; Haugen, H.S.; Kristiansen, P.E. Structure-function relationships of the non-Lanthionine-containing peptide (class II) bacteriocins produced by Gram-positive bacteria. Curr. Pharm. Biotechnol. 2009, 10, 19-37.

4. Ennahar, S.; Sonomoto, K.; Ishizaki, A. Class IIa bacteriocins from lactic acid bacteria: Antibacterial activity and food preservation. J. Biosci. Bioeng. 1999, 87, 705-716.

5. Gâlvez, A.; Abriouel, H.; Lopez, R.L.; Ben Omar, N. Bacteriocin-based strategies for food biopreservation. Int. J. Food Microbiol. 2007, 120, 51-70.

6. Garcia, P.; Rodriguez, L.; Rodriguez, A.; Martinez, B. Food biopreservation: Promising strategies using bacteriocins, bacteriophages and endolysins. Trends Food Sci. Technol. 2010, 21, 373-382.

7. Mills, S.; Stanton, C.; Hill, C.; Ross, R.P. New developments and applications of bacteriocins and peptides in foods. Annu. Rev. Food Sci. Technol. 2011, 2, 299-329.

8. Heng, N.C.K.; Burtenshaw, G.A.; Jack, R.W.; Tagg, J.R. Ubericin A, a Class IIa bacteriocin produced by Streptococcus uberis. Appl. Environ. Microbiol. 2007, 73, 7763-7766.

9. Nicolas, G.G.; LaPointe, G.; Lavoie, M.C. Production, purification, sequencing and activity spectra of mutacins D-123.1 and F-59.1. BMC Microbiol. 2011, 11, 69.

10. Yildirim, Z.; Johnson, M.G. Characterization and antimicrobial spectrum of bifidocin B, a bacteriocin produced by Bifidobacterium bifidum NCFB 1454. J. Food Prot. 1998, 61, 47-51.

11. Yildirim, Z.; Winters, D.K.; Johnson, M.G. Purification, amino acid sequence and mode of action of bifidocin B produced by Bifidobacterium bifidum NCFB 1454. J. Appl. Microbiol. 1999, 86, 45-54.

12. Cheikhyoussef, A.; Cheikhyoussef, N.; Chen, H.Q.; Zhao, J.X.; Tang, J.; Zhang, H. Bifidin I—A new bacteriocin produced by Bifidobacterium infantis BCRC 14602: Purification and partial amino acid sequence. Food Control. 2010, 21, 746-753.

13. Le Marrec, C.; Hyronimus, B.; Bressollier, P.; Verneuil, B.; Urdaci, M.C. Biochemical and genetic characterization of coagulin, a new antilisterial bacteriocin in the pediocin family of bacteriocins, produced by Bacillus coagulans I4. Appl. Environ. Microbiol. 2000, 66, 5213-5220.

14. Kalmokoff, M.L.; Banerjee, S.K.; Cyr, T.; Hefford, M.A.; Gleeson, T. Identification of a new plasmid-encoded sec-dependent bacteriocin produced by Listeria innocua 743. Appl. Environ. Microbiol. 2001, 67, 4041-4047.

15. Hâvarstein, L.S.; Diep, D.B.; Nes, I.F. A family of bacteriocin ABC transporters carry out proteolytic processing of their substrates concomitant with export. Mol. Microbiol. 1995, 16, 229-240.

16. Zouhir, A.; Hammami, R.; Fliss, I.; Hamida, J.B. A new structure-based classification of Gram-positive bacteriocins. Protein J. 2010, 29, 432-439.

17. Rea, M.C.; Ross, R.P.; Cotter, P.D.; Hill, C. Classification of Bacteriocins from Gram-Positive Bacteria. In Prokaryotic Antimicrobial Peptides: From Genes to Applications; Drider, D., Rebuffat, S., Eds.; Springer Publishing Inc: New York, NY, USA, 2011; pp. 29-53.

18. Diep, D.B.; Nes, I.F. Ribosomally synthesized antibacterial peptides in Gram positive bacteria. Curr. Drug Targets 2002, 3, 107-122.

19. Belguesmia, Y.; Naghmouchi, K.; Chihib, N.-E.; Drider, D. Class IIa Bacteriocins: Current Knowledge and Perspectives. In Prokaryotic Antimicrobial Peptides: From Genes to Applications; Drider, D., Rebuffat, S., Eds.; Springer Publishing, Inc.: New York, NY, USA, 2011; pp. 171-195.

20. Fimland, G.; Johnsen, L.; Dalhus, B.; Nissen-Meyer, J. Pediocinlike antimicrobial peptides (class IIa bacteriocins) and their immunity proteins: Biosynthesis, structure and mode of action. J. Pept. Sci. 2005, 11, 688-696.

21. Birri, D.J.; Brede, D.A.; Forberg, T.; Holo, H.; Nes, I.F. Molecular and genetic characterization of a novel bacteriocin locus in Enterococcus avium isolates from infants. Appl. Environ. Microbiol. 2010, 76, 483-492.

22. Larsen, A.G.; Vogensen, F.K.; Josephsen, J. Antimicrobial activity of lactic acid bacteria isolated from sour doughs: Purification and characterization of bavaricin A, a bacteriocin produced by Lactobacillus bavaricus MI401. J. Appl. Microbiol. 1993, 75, 113-122.

23. Xiraphi, N.; Georgalaki, M.; van Driessche, G.; Devreese, B.; van Beeumen, J.; Tsakalidou, E.; Metaxopoulos, J.; Drosinos, E.H. Purification and characterization of curvaticin L442, a bacteriocin produced by Lactobacillus curvatus L442. Antonie Van Leeuwenhoek 2006, 89, 19-26.

24. Saavedra, L.; Minahk, C.; de Ruiz Holgado, A.P.; Sesma, F. Enhancement of the enterocin CRL35 activity by a synthetic peptide derived from the NH2-terminal sequence. Antimicrob. Agents Chemother. 2004, 48, 2778-2781.

25. Papagianni, M.; Papamichae, E.M. Purification, amino acid sequence and characterization of the class IIa bacteriocin weissellin A, produced by Weissella paramesenteroides DX. Bioresour. Technol. 2011, 102, 6730-6734.

26. Svetoch, E.A.; Stern, N.J.; Eruslanov, B.V.; Kovalev, Y.N.; Volodina, L.I.; Perelygin, V.V.; Mitsevich, E.V.; Mitsevich, I.P.; Pokhilenko, V.D.; Borzenkov, V.N.; et al. Isolation of Bacillus circulans and Paenibacillus polymyxa strains inhibitory to Campylobacter jejuni and characterization of associated bacteriocins. J. Food Prot. 2005, 68, 11-17.

27. Kaiser, A.L.; Montville, T.J. Purification of the bacteriocin bavaricin MN and characterization of its mode of action against Listeria monocytogenes Scott A cells and lipid vesicles. J. Appl. Microbiol. 1996, 62, 4529-4535.

28. Svetoch, E.A.; Eruslanov, B.V.; Perelygin, V.V.; Mitsevich, E.V.; Mitsevich, I.P.; Borzenkov, V.N.; Levchuk, V.P.; Svetoch, O.E.; Kovalev, Y.N.; Stepanshin, Y.G.; et al. Diverse antimicrobial killing by Enterococcus faecium E 50-52 bacteriocin. J. Agric. Food Chem. 2008, 56, 1942-1948.

29. Kanatani, K.; Oshimura, M.; Sano, K. Isolation and characterization of acidocin A and cloning of the bacteriocin gene from Lactobacillus acidophilus. Appl. Environ. Microbiol. 1995, 61, 1061-1067.

30. Stern, N.J.; Svetoch, E.A.; Eruslanov, B.V.; Perelygin,V.V.; Mitsevich, E.V.; Mitsevich, I.P.; Pokhilenko, V.D.; Levchuk, V.P.; Svetoch, O.E.; Seal, B.S. Isolation of a Lactobacillus salivarius strain and purification of its bacteriocin, which is inhibitory to Campylobacter jejuni in the chicken gastrointestinal system. Antimicrob. Agents Chemother. 2006, 50, 3111-3116.

31. Svetoch, E.A.; Eruslanov, B.V.; Levchuk, V.P.; Perelygin, V.V.; Mitsevich, E.V.; Mitsevich, I.P.; Stepanshin, J.; Dyatlov, I.; Seal, B.S.; Stern, N.J. Isolation of Lactobacillus salivarius 1077 (NRRL B-50053) and characterization of its bacteriocin, including the antimicrobial activity spectrum. Appl. Environ. Microbiol. 2011, 77, 2749-2754.

32. Feng, G.; Guron, G.K.; Churey, J.J.; Worobo, R.W. Characterization of mundticin L, a class IIa anti-Listeria bacteriocin from Enterococcus mundtii CUGF08. Appl. Environ. Microbiol. 2009, 75, 5708-5713.

33. Felix, J.V.; Papathanasopoulos, M.A.; Smith, A.A.; von Holy, A.; Hastings, J.W. Characterization of leucocin B-Ta11a, a bacteriocin from Leuconostoc carnosum Ta11a isolated from meat. Curr. Microbiol. 1994, 29, 207-212.

34. Flannagan, S.E.; Clewell, D.B.; Sedgley, C.M. A "retrocidal" plasmid in Enterococcus faecalis, passage and protection. Plasmid 2008, 59, 217-230.

35. Arnold, K.; Bordoli, L.; Kopp, J.; Schwede, T. The SWISS-MODEL Workspace: A web-based environment for protein structure homology modelling. Bioinformatics 2006, 22, 195-201.

36. Schwede, T.; Kopp, J.; Guex, N.; Peitsch, M.C. SWISS-MODEL: An automated protein homology-modeling server. Nucleic Acids Res. 2003, 31, 3381-3385.

37. Guex, N.; Peitsch, M.C. SWISS-MODEL and the Swiss-PdbViewer: An environment for comparative protein modelling. Electrophoresis 1997, 18, 2714-2723.

38. Tichaczek, P.S.; Nissen-Meyer, J.; Nes, I.F.; Vogel, R.F.; Hammes, W.P. Characterization of the bacteriocins curvacin A from Lactobacillus curvatus LTH1174 and sakacin P from L. sake LTH673. Syst. Appl. Microbiol. 1992, 15, 460-468.

39. Cocolin, L.; Rantsiou, K. Sequencing and expression analysis of sakacin genes in Lactobacillus curvatus strains. Appl. Environ. Microbiol. 2007, 76, 1403-1411.

40. Tichaczek, P.S.; Vogel, R.F.; Hammes, W.P. Cloning and sequencing of sakP encoding sakacin P, the bacteriocin produced by Lactobacillus sake LTH 673. Microbiology 1994, 140, 361-367.

41. Urso, R.; Rantsiou, K.; Cantoni, C.; Comi, G.; Cocolin, L. Sequencing and expression analysis of the sakacin P bacteriocin produced by a Lactobacillus sakei strain isolated from naturally fermented sausages. Appl. Environ. Microbiology 2006, 71, 480-485.

42. Gonzalez, C.F.; Kunka, B.S. Plasmid-associated bacteriocin production and sucrose fermentation in Pediococcus acidilactici. Appl. Environ. Microbiol. 1987, 53, 2534-2538.

43. Bhunia, A.K.; Johnson, M.C.; Ray, B. Direct detection of an antimicrobial peptide of Pediococcus acidilactici in SDS-PAGE. J. Ind. Microbiol. 1987, 2, 319-322.

44. Motlagh, A.M.; Bhunia, A.K.; Szostek, F.; Hansen, T.R.; Johnson, M.C.; Ray, B. Nucleotide and amino acid sequence of pap-gene (pediocin AcH production) in Pediococcus acidilactici H. Lett. Appl. Microbiol. 1992, 15, 45-48.

45. Ray, S.K.; Johnson, M.C.; Ray, B. Bacteriocin plasmids of Pediococcus acidilactici. J. Ind. Microbiol. 1989, 4, 163-171.

46. Kim, W.J.; Ray, B.; Johnson, M.C. Plasmid transfers by conjugation and electroporation in Pediococcus acidilactici. J. Appl. Bacteriol. 1992, 72, 2G1-2G7.

47. Kwon, D.Y.; Koo, M.; Ryoo, C.R.; Kang, C.H.; Min, K.H.; Kim, W.J. Bacteriocin produced by Pediococcus sp. in kimchi and its characteristics. J. Microbiol. Biot. 2GG2, 12, 9б-Ю3.

48. Albano, H.; Todorov, S.D.; van Reenen, C.A.; Hogg, T.; Dicks, L.M.T.; Teixeira, P. Characterization of two bacteriocins produced by Pediococcus acidilactici isolated from "Alheira", a fermented sausage traditionally produced in Portugal. Int. J. Food Microbiol. 2GG7, 11б, 239-247.

49. Millette, M.; Dupont, C.; Shareck, F.; Ruiz, M.T.; Archambault, D.; Lacroix, M. Purification and identification of the pediocin produced by Pediococcus acidilactici MM33, a new human intestinal strain. J. Appl. Microbiol. 2GGS, 104, 2б9-273.

3G. Bennik, M.H.J.; Verheul, A.; Abee, T.; Naaktgeboren-Stoffels, G.; Gorris, L.G.M.; Smid, E.J. Interactions of nisin and pediocin PA-1 with closely related lactic acid bacteria that manifest over 1GG-fold differences in bacteriocin sensitivity. Appl. Environ. Microbiol. 1997, бЗ, 3б28-3б3б.

31. Casadei, G.; Grilli, E.; Piva, A. Pediocin A modulates intestinal microflora metabolism in swine in vitro intestinal fermentations. J. Anim. Sci. 2GG9, S7, 2G2G-2G28.

32. Ennahar, S.; Aoude-Werner, D.; Sorokine, O.; van Dorsselaer, A.; Bringel, F.; Hubert, J.C.; Hasselmann, C. Production of pediocin AcH by Lactobacillus plantarum WHE92 isolated from cheese. Appl. Environ. Microbiol. 199б, б2, 4381-4387.

33. Bernbom, N.; Licht, T.R.; Saadbye, P.; Vogensen, F.K.; Norrung, B. Lactobacillus plantarum inhibits growth of Listeria monocytogenes in an in vitro continuous flow gut model, but promotes invasion of L. monocytogenes in the gut of gnotobiotic rats. Int. J. Food Microbiol. 2GG6, 10S, 1G-14.

34. Hoover, D.G.; Walsh, P.M.; Kolaetis, K.M.; Daly, M.M. A bacteriocin produced by Pediococcus species associated with a 3.3 megadalton plasmid. J. Food Prot. 19SS, З9, 29-31.

33. Jager, K.; Harlander, S. Characterization of a bacteriocin from Pediococcus acidilactici PC and comparison of bacteriocin-producing strains using molecular typing procedures. Appl. Environ. Microbiol. 1992, З7, б31-б37.

36. Ray, B.; Motlagh, A.M.; Johnson, M.C.; Bozoglu, F. Mapping of pSMB74, a plasmid encoding bacteriocin AcH production (Pap ) trait in Pediococcus acidilactici H. Lett. Appl. Microbiol.

1992, 1З, 33-37.

37. Schved, F.; Lalazar, A.; Henis, Y.; Juven, B.J. Purification, partial characterization and plasmid linkage of pediocin SJ-1, a bacteriocin produced by Pediococcus acidilactici. J. Appl. Bacteriol.

1993, 74, б7-77.

38. Bhunia, A.K.; Bhowmik, T.K.; Johnson, M.G. Determination of bacteriocin-encoding plasmids of Pediococcus acidilactici strains by southern hybridization. Lett. Appl. Microbiol. 1994, 1S, 168-17G.

39. Rodríguez, J.M.; Cintas, L.M.; Casaus, P.; Martínez, M.I.; Suárez, A.; Hernández, P.E. Detection of pediocin PA-1 producing pediococci by rapid molecular producing by rapid molecular biology techniques. Food Microbiol. 1997, 14, 3б3-371.

6g. Ray, S.K.; Kim, W.J.; Johnson, M.C.; Ray, B. Conjugal transfer of a plasmid encoding bacteriocin production and immunity in Pediococcus acidilactici H. J. Appl. Bacteriol. 19S9, бб, 393-399.

61. Rodríguez, J.M.; Martínez, M.I.; Kok, J. Pediocin PA-1, a wide-spectrum bacteriocin from lactic acid bacteria. Crit. Rev. Food Sci. Nutr. 2002, 42, 91-121.

62. Miller, K.W.; Ray, P.; Steinmetz, T.; Hanekamp, T.; Ray, B. Gene organization and sequences of pediocin AcH/PA-1, production operons in Pediococcus and Lactococcus plasmids. Lett. Appl. Microbiol. 2005, 40, 32-62.

63. Meijer, W.J.J.; Wisman, G.B.A.; Terpstra, P.; Thorsted, P.B.; Thomas, C.M.; Holsappel, S.; Venema, G.; Bron, S. Rolling-circle plasmids from B. subtilis: Complete nucleotide sequences and analyses of genes of pTAl0l3, pTAl040, pTAl030 and pTAl060, and comparisons with related plasmids from Gram-positive bacteria. FEMSMicrobiol. Rev. 1998, 21, 337-368.

64. Nicolas, G.G.; Lavoie, M.C.; Lapointe, G. Molecular genetics, genomics and biochemistry of mutacins. Genes Genomes Genomics 2007, 1, 193-208.

63. Collado, M. C.; Hernández, M.; Sanz, Y. Production of bacteriocin-like compounds by human faecal Bifidobacterium strains. J. Food Prot. 2005, 68, 1034-1040.

66. Bernbom, N.; Jelle, B.; Brogren, C.H.; Vogensen, F.K.; Norrung, B.; Licht, T.R. Pediocin PA-1 and a pediocin producing Lactobacillus plantarum strain do not change the HMA rat microbiota. Int. J. Food Microbiol. 2009, 130, 231-237.

67. Fimland, G.; Sletten, K.; Nissen-Meyer, J. The complete aminoacid sequence of the pediocin-like antimicrobial peptide leucocin C. Biochem. Biophys. Res. Commun. 2002, 295, 826-827.

68. Papathanasopoulos, M.A.; Krier, F.; Revol-Junelles, A.-M.; Lefebvre, G.; le Caer, J.P.; von Holy, A.; Hastings, J.W. Multiple bacteriocin production by Leuconostoc mesenteroides TA33a and other Leuconostoc/Weissella strains. Curr. Microbiol. 1997, 35, 331-333.

69. Papathanasopoulos, M.A.; Dykes, G.A.; Revol-Junelles, A.-M.; Delfour, A.; von Holy, A.; Hastings J.W. Sequence and structural relationships of leucocins A-, B- and C-TA33a from Leuconostoc mesenteroides TA33a. Microbiology 1998, 144, 1343-1348.

70. Sánchez, J.; Die, D. B.; Herranz, C.; Nes, I.F.; Cintas, L.M.; Hernandez, P.E. Amino acid and nucleotide sequence, adjacent genes, and heterologous expression of hiracin JM79, a sec-dependent bacteriocin produced by Enterococcus hirae DCH3, isolated from Mallard ducks (Anas platyrhynchos). FEMS Microbiol. Lett. 2007, 270, 227-236.

71. Doi, K.; Eguchi, T.; Choi, S.-H.; Iwatake, A.; Ohmomo, S.; Ogata, S. Isolation of enterocin SE-K4-encoding plasmid and a high enterocin SE-K4 producing strain of Enterococcus faecalis K-4. J. Biosci. Bioeng. 2002, 93, 434-436.

72. Tomita, H.; Fujimoto, S.; Tanimoto, K.; Ike, Y. Cloning and genetic organization of the bacteriocin 31 determinant encoded on the Enterococcus faecalis pheromone-responsive conjugative plasmid pYIl7. J. Bacteriol. 1996, 178, 3383-3393.

73. Van Reenen, C.A.; Dicks, L.M.T.; Chikindas, M.L. Isolation, purification and partial characterization of plantaricin 423, a bacteriocin produced by Lactobacillus plantarum. J. Appl. Microbiol. 1998, 84, 1131-1137.

74. Gallager, N.L.F.; Sailer, V.; Niemczura, W.P.; Nakashima, T.T.; Stiles, M.E.; Vederas, J.C. Three-dimensional structure of leucocin A in trifluoroethanol and dodecylphosphocholine micelles: Spatial location of residues critical for biological activity in type IIa bacteriocins from lactic acid bacteria. Biochemistry 1997, 36, 13062-13072.

73. Sit, C.S.; Lohans, C.T.; van Belkum, M.J.; Campbell, C.D.; Miskolzie, M.; Vederas, J.C. Substitution of a conserved disulfide in the type IIa bacteriocin, leucocin A, with L-leucine and L-serine residues: Effects on activity and three-dimensional structure. ChemBioChem 2G12, 1З, 33-38.

76. Ferchichi, M.; Frère, J.; Mabrouk, K.; Manai, M. Lactococcin MMFII, a novel class IIa bacteriocin produced by Lactococcus lactis MMFII, isolated from a Tunisian dairy product. FEMSMicrobiol. Lett. 2GG1, 20З, 49-33.

77. Quadri, L.E.; Sailer, M.; Roy, K.L.; Vederas, J.C.; Stiles, M.E. Chemical and genetic characterization of bacteriocins produced by Carnobacterium piscicola LV17B. J. Biol. Chem. 1994, 2б9, 122G4-12211.

78. Verluyten, J.; Messens, W.; de Vuyst, L. Sodium chloride reduces production of Curvacin A, a bacteriocin produced by Lactobacillus curvatus strain LTH 1174, originating from fermented sausage. Appl. Environ. Microbiol. 2GG4, 70, 2271-2278.

79. Cintas, L.M.; Casaus, P.; Havarstein, L.S.; Hernandez, P.E.; Nes, I.F. Biochemical and genetic characterization of enterocin P, a novel sec-dependent bacteriocin from Enterococcus faecium P13 with a broad antimicrobial spectrum. Appl. Environ. Microbiol. 1997, бЗ, 4321-433G.

8G. Park, S.H.; Itoh, K.; Fujisawa, T. Characteristics and identification of enterocins produced by Enterococcus faecium JCM 38G4T. J. Appl. Microbiol. 2GG3, 9З, 294-3GG.

81. Kang, J.H.; Lee, M.S. Characterization of a bacteriocin produced by Enterococcus faecium GM-1 isolated from an infant. J. Appl. Microbiol. 2GG5, 9S, 1169-1176.

82. Samuel, A.; Calo, P.; Franco, C.M.; Prado, M.; Cepeda, A.; Barros-Velazquez, J. Single nucleotide polymorphism analysis of the enterocin P structural gene of Enterococcus faecium strains isolated from nonfermented animal foods. Mol. Nutr. Food Res. 2GG6, 20, 1229-1238.

83. Hosseini, S.V.; Arlindo, S.; Böhme, K.; Fernández-No, C.; Calo-Mata, P.; Barros-Velázquez, J. Molecular and probiotic characterization of bacteriocin-producing Enterococcus faecium strains isolated from nonfermented animal foods. J. Appl. Microbiol. 2GG9, 107, 1392-14G3.

84. Javed, I.; Ahmed, S.; Manam, S.; Riaz, M.; Ahmad, B.; Ali, M.I.; Hameed, A.; Chaudry, G.J. Production, characterization, and antimicrobial activity of a bacteriocin from newly isolated Enterococcus faecium IJ-31. J. Food Prot. 2G1G, 7З, 44-32.

83. Waters, C.M.; Bassler, B.L. Quorum sensing: Cell-to-cell communication in bacteria. Annu. Rev. Cell Dev. Biol. 2GG5, 21, 319-346.

86. Kleerebezem, M.; Quadri, L.E.N.; Kuipers, O.P.; de Vos, W.M. Quorum sensing by peptide pheromones and two-component signal-transduction systems in Gram-positive bacteria. Mol. Microbiol. 1997, 24, 893-9G4.

87. Atkinson, S.; Williams, P. Quorum sensing and social networking in the microbial world. J. R. Soc. Interface 2GG9, б, 939-978.

88. Nes, I.F.; Eijsink, V.G.H. Regulation of Group II Peptide Bacteriocin Synthesis by Quorum-Sensing Mechanisms. In Cell-Cell Signalling in Bacteria; Dunny, G.M., Winans, S.C., Eds.; American Society for Microbiology: Washington, DC, USA, 1999; pp. 173-192.

89. Ennahar, S.; Sashihara, T.; Sonomoto, K.; Ishizaki, A. Class IIa bacteriocins: Biosynthesis, structure and activity. FEMS Microbiol. Rev. 2GGG, 24, 83-1G6.

90. Cho, H.S.; Pelton, J.G.; Yan, D.; Kustu, S.; Wemmer, D.E. Phosphoaspartates in bacterial signal transduction. Curr. Opin. Struct. Biol. 2001, 11, 679-684.

91. Aymerich, T.; Holo, H.; Havarstein, L.S.; Hugas, M.; Garriga, M.; Nes, I.F. Biochemical and genetic characterization of enterocin A from Enterococcus faecium, a new antilisterial bacteriocin in the pediocin family of bacteriocins. Appl. Environ. Microbiol. 1996, 62, 1676-1682.

92. Métivier, A.; Pilet, M.-F.; Dousset, X.; Sorokine, O.; Anglade, P.; Zagorec, M.; Piard, J.-C.; Marion, D.; Cenatiempo, Y.; Fremaux, C. Divercin V41, a new bacteriocin with two disulphide bonds produced by Carnobacterium divergens V41: Primary structure and genomic organization. Microbiology 1998, 144, 2837-2844.

93. Hühne, K.; Axelsson, L.; Holck, A.; Kröckel, L. Analysis of the sakacin P gene cluster from Lactobacillus sake Lb674 and its expression in sakacin-negative Lb. sake strains. Microbiology 1996, 142, 1437-1448.

94. Quadri, L.E.N.; Kleerebezem, M.; Kuipers, O.P.; de Vos, W.M.; Roy, K.L.; Vederas, J.C.; Stiles, M.E. Characterization of a locus from Carnobacterium piscicola LV17B involved in bacteriocin production and immunity: Evidence for global inducer-mediated transcriptional regulation. J. Bacteriol. 1997, 179, 6163-6171.

95. Herranz, C.; Driessen, A.J.M. Sec-mediated secretion of bacteriocin enterocin P by Lactococcus lactis. Appl. Environ. Microbiol. 2005, 71, 1959-1963.

96. Gierasch, L.M. Signal sequences. Biochemistry 1989, 28, 923-930.

97. Pugsley, A.P. The complete general secretory pathway in Gram-negative bacteria. Microbiol. Rev. 1993, 57, 50-108.

98. Izard, J.W.; Kendall, D.A. Signal peptides: Exquisitely designed transport promoters. Microbiol. Biotechnol. 1994, 13, 765-773.

99. Van Belkum, M.J.; Stiles, M.E. Molecular characterization of genes involved in the production of the bacteriocin leucocin A from Leuconostoc gelidum. Appl. Environ. Microbiol. 1995, 61, 3573-3579.

100. Nes, I.F.; Diep, D.B.; Hâvarstein, L.S.; Brurberg, M.B.; Eijsink, V.; Holo, H. Biosynthesis of bacteriocins in lactic acid bacteria. Antonie Van Leeuwenhoek 1996, 70, 113-128.

101. Vaughan, A.; Eijsink, V.G.; van Sinderen, D. Functional characterization of a composite bacteriocin locus from malt isolate Lactobacillus sakei 5. Appl. Environ. Microbiol. 2003, 69, 7194-7203.

102. Revol-Junelles, A.M.; Mathis, R.; Krier, F.; Fleury, Y.; Delfour, A.; Lefebvre, G. Leuconostoc mesenteroides subsp. mesenteroides FR52 synthesizes two distinct bacteriocins. Lett. Appl. Microbiol. 1996, 23, 120-124.

103. Fremaux, C.; Héchard, Y.; Cenatiempo, Y. Mesentericin Y105 gene clusters in Leuconostoc rnesenteroides Y 105. Microbiology 1995, 14, 1637-1645.

104. Aucher, W.; Simonet, V.; Fremaux, C.; Dalet, K.; Simon, L.; Cenatiempo, Y.; Frère, J.; Berjeaud, J.M. Differences in mesentericin secretion systems from two Leuconostoc strains. FEMS Microbiol. Lett. 2004, 232, 15-22.

105. Simon, L.; Fremaux, C.; Cenatiempo, Y.; Berjeaud, J.M. Sakacin G, a new type of antilisterial bacteriocin. Appl. Environ. Microbiol. 2002, 68, 6416-6420.

106. Dortu, C.; Huch, M.; Holzapfel, W.H.; Franz, C.M.A.P.; Thonart, P. Anti-listerial activity of bacteriocin-producing Lactobacillus curvatus CWBI-B28 and Lactobacillus sakei CWBI-B1365 on raw beef and poultry meat. Lett. Appl. Microbiol. 2008, 47, 581-586.

107. Todorov, S.D.; Rachman, C.; Fourrier, A.; Dicks, L.M.T.; van Reenen, C.A.; Prévost, H.; Dousset, X. Characterization of a bacteriocin produced by Lactobacillus sakei R1333 isolated from smoked salmon. Anaerobe 2011, 17, 23-31.

108. Wang, Y.; Henz, M.E.; Gallagher, N.L.; Chai, S.; Gibbs, A.C.; Yan, L.Z.; Stiles, M.E.; Wishart, D.S.; Vederas, J.C. Solution structure of carnobacteriocin B2 and implications for structure-activity relationships among type IIa bacteriocins from lactic acid bacteria. Biochemistry 1999, 38, 15438-15447.

109. Uteng, M.; Hauge, H.H.; Markwick, P.R.; Fimland, G.; Mantzilas, D.; Nissen-Meyer, J.; Muhle-Goll, C. Three-dimensional structure in lipid micelles of the pediocin-like antimicrobial peptide sakacin P and a sakacin P variant that is structurally stabilized by an inserted C-terminal disulfide bridge. Biochemistry 2003, 42, 11417-11426.

110. Haugen, H.S.; Fimland, G.; Nissen-Meyer, J.; Kristiansen, P.E. Three-dimensional structure in lipid micelles of the pediocin-like antimicrobial peptide curvacin A. Biochemistry 2005, 44, 16149-16157.

111. Kaur, K.; Andrew, L.C.; Wishart, D.S.; Vederas, J.C. Dynamic relationships among type IIa bacteriocins: Temperature effects on antimicrobial activity and on structure of the C-terminal amphipathic a-helix as a receptor binding region. Biochemistry 2004, 43, 9009-9020.

112. Fimland, G.; Blingsmo, O.R.; Sletten, K.; Jung, G.; Nes, I.F.; Nissen-Meyer, J. New biologically active hybrid bacteriocins constructed by combining regions from various pediocin-like bacteriocins: The C-terminal region is important for determining specificity. Appl. Environ. Microbiol. 1996, 62, 3313-3318.

113. Fimland, G.; Johnsen, L.; Axelsson, L.; Brurberg, M.B.; Nes, I.F.; Eijsink, V.G.H.; Nissen-Meyer, J. A C-terminal disulfide bridge in pediocin-like bacteriocins renders bacteriocin activity less temperature dependent and is a major determinant of the antimicrobial spectrum. J. Bacteriol. 2000, 182, 2643-2648.

114. Derksen, D.J.; Boudreau, M.A.; Vederas, J.C. Hydrophobic interactions as substitutes for a conserved disulfide linkage in the type IIa bacteriocins, leucocin A and pediocin PA-1. ChemBioChem 2008, 9, 1898-1901.

115. Fleury, Y.; Dayem, M.A.; Montagne, J.J.; Chaboisseau, E.; le Caer, J.P.; Nicolas, P.; Delfour, A. Covalent structure, synthesis, and structure-function studies of mesentericin Y 105(37), a defensive peptide from gram-positive bacteria Leuconostoc mesenteroides. J. Biol. Chem. 1996, 271, 14421-14429.

116. Tominaga, T.; Hatakeyama, Y. Determination of essential and variable residues in pediocin PA-1 by NNK scanning. Appl. Environ. Microbiol. 2006, 72, 1141-1147.

117. Derksen, D.J.; Stymiest, J.L.; Vederas, J.C. Antimicrobial leucocin analogues with a disulfide bridge replaced by a carbocycle or by noncovalent interactions of allyl glycine residues. J. Am. Chem. Soc. 2006, 128, 14252-14253.

118. Hutchinson, E.G.; Thornton, J.M. A revised set of potentials for beta-turn formation in proteins. Protein Sci. 1994, 3, 2207-2216.

119. Yan, L.Z.; Gibbs, A.C.; Stiles, M.E.; Wishart, D.S.; Vederas, J.C. Analogues of bacteriocins: antimicrobial specificity and interactions of leucocin A with its enantiomer, carnobacteriocin B2, and truncated derivatives. J. Med. Chem. 2000, 43, 4379-4381.

120. Quadri, L.E.N.; Yan, L.Z.; Stiles, M.E.; Vederas, J.C. Overproduction of the antimicrobial peptide, its engineered variants, and its precursor in Escherichia coli. J. Biol. Chem. 1997, 272, 3384-3388.

121. Fimland, G.; Jack, R.; Jung, G.; Nes, I.F.; Nissen-Meyer, J. The bactericidal activity of pediocin PA-1 is specifically inhibited by a 13-mer fragment that spans the bacteriocin from the center toward the C terminus. Appl. Environ. Microbiol. 1998, 64, 3037-3060.

122. Eijsink, V.G.; Skeie, M.; Middelhoven, P.H.; Brurberg, M.B.; Nes, I.F. Comparative studies of class IIa bacteriocins of lactic acid bacteria. Appl. Environ. Microbiol. 1998, 64, 3273-3281.

123. Richard, C.; Cañon, R.; Naghmouchi, K.; Bertrand, D.; Prévosta, H.; Drider, D. Evidence on correlation between number ofdisulfide bridge and toxicity of class IIa bacteriocins. Food Microbiol. 2006, 23, 173-183.

124. Robichon, D.; Gouin, E.; Débarbouillé, M.; Cossart, P.; Cenatiempo, Y.; Héchard, Y. The rpoN (g34) gene from Listeria monocytogenes is involved in resistance to mesentericin Y103, an antibacterial peptide from Leuconostoc mesenteroides. J. Bacteriol. 1997, 179, 7391-7394.

123. Ramnath, M.; Beukes, M.; Tamura, K.; Hastings, J.W. Absence of a putative mannose-specific phosphotransferase system enzyme IIAB component in a leucocin A-resistant strain of Listeria monocytogenes, as shown by two-dimensional sodium dodecyl sulfatepolyacrylamide gel electrophoresis. Appl. Environ. Microbiol. 2000, 66, 3098-3101.

126. Dalet, K.; Briand, C.; Cenatiempo, Y.; Héchard, Y. The rpoN gene of Enterococcus faecalis directs sensitivity to subclass IIa bacteriocins. Curr. Microbiol. 2000, 41, 441-443.

127. Héchard, Y.; Pelletier, C.; Cenatiempo, Y.; Frère, J. Analysis of G34-dependent genes in Enterococcus faecalis: A mannose PTS permease (EIIMan) is involved in sensitivity to a bacteriocin, mesentericin Y103. Microbiology 2001, 147, 1373-1380.

128. Ramnath, M.; Arous, S.; Gravesen, A.; Hastings, J.W.; Héchard, Y. Expression of mptC of Listeria monocytogenes induces sensitivity to class IIa bacteriocins in Lactococcus lactis. Microbiology 2004, 150, 2663-2668.

129. Diep, D.B.; Skaugen, M.; Salehian, Z.; Holo, H.; Nes, I.F. Common mechanisms of target cell recognition and immunity for class II bacteriocins. Proc. Natl. Acad. Sci. USA 2007, 104, 2384-2389.

130. Kjos, M.; Salehian, Z.; Nes, I.F.; Diep, D.B. An extracellular loop of the mannose phosphotransferase system component IIC is responsible for specific targeting by class IIa bacteriocins. J. Bacteriol. 2010, 192, 3906-3913.

131. Kjos, M.; Borrero, J.; Opsata, M.; Birri, D.J.; Holo, H.; Cintas, L.M, Snipen, L.; Hernández, P.E; Nes, I.F.; Diep, D.B. Target recognition, resistance, immunity and genome mining of class II bacteriocins from Gram-positive bacteria. Microbiology 2011, 157, 3236-3267.

132. Postma, P.W.; Lengeler, J.W.; Jacobson, G.R. Phosphoenol pyruvate: Carbohydrate phosphotransferase systems of bacteria. Microbiol. Rev. 1993, 57, 343-394.

133. Mao, Q.; Schunk, T.; Flukiger, K.; Erni, B. Functional reconstitution of the purified mannose phosphotransferase system of Escherichia coli into phospholipid vesicles. J. Biol. Chem. 1995, 270, 3238-3263.

134. Hassan, M.; Kjos, M.; Nes, I.F.; Diep, D.B.; Lotfipour, F. Natural antimicrobial peptides from bacteria: Characteristics and potential applications to fight against antibiotic resistance. J. Appl. Microbiol. 2012, 113, 723-736.

135. Kjos, M.; Nes I.F.; Diep, D.B. Mechanisms of resistance to bacteriocins targeting the mannose phosphotransferase system. Appl. Environ. Microbiol. 2011, 77, 3335-3342.

136. Kjos, M.; Nes, I.F.; Diep, D.B. Class II one-peptide bacteriocins target a phylogenetically defined subgroup of mannose phosphotransferase systems on sensitive cells. Microbiology 2009, 155, 2949-2961.

137. Diep, D.B.; Godager, L.; Brede, D.; Nes, I.F. Data mining and characterization of a novel pediocin-like bacteriocin system from the genome of Pediococcus pentosaceus ATCC 25745. Microbiology 2006, 152, 1649-1659.

138. Katla, T.; Naterstad, K.; Vancanneyt, M.; Swings, J.; Axelsson, L. Differences in susceptibility of Listeria monocytogenes strains to sakacin P, sakacin A, pediocin PA-1, and nisin. Appl. Environ. Microbiol. 2003, 69, 4431-4437.

139. Johnsen, L.; Fimland, G.; Nissen-Meyer, J. The C-terminal domain of pediocin-like antimicrobial peptides (class IIa bacteriocins) is involved in specific recognition of the C-terminal part of cognate immunity proteins and in determining the antimicrobial spectrum. J. Biol. Chem. 2005, 280, 9243-9250.

140. Haugen, H.S.; Fimland, G.; Nissen-Meyer, J. Mutational analysis of residues in the helical region of the class IIa bacteriocin pediocin PA-1. Appl. Environ. Microbiol. 2011, 77, 1966-1972.

141. Erni, B. The mannose transporter complex: An open door for the macromolecular invasion of bacteria. J. Bacteriol. 2006, 188, 7036-7038.

142. Gravesen, A.; Ramnath, M.; Rechinger, K.B.; Andersen, N.; Jansch, L.; Hechard, Y.; Hastings, J.W.; Knöchel, S. High-level resistance to class IIa bacteriocins is associated with one general mechanism in Listeria monocytogenes. Microbiology 2002, 148, 2361-2369.

143. Tessema, G.T.; Moretro, T.; Kohler, A.; Axelsson, L.; Naterstad, K. Complex phenotypic and genotypic responses of Listeria monocytogenes strains exposed to the class IIa bacteriocin sakacin P. Appl. Environ. Microbiol. 2009, 75, 6973-6980.

144. Dalet, K.; Cenatiempo, Y.; Cossart, P.; Hechard, Y. A sigma (o54)-dependent PTS permease of the mannose family is responsible for sensitivity of Listeria monocytogenes to mesentericin Y105. Microbiology 2001, 147, 3263-3269.

145. Duffes, F.; Jenoe, P.; Boyaval, P. Use of two-dimensional electrophoresis to study differential protein expression in divercin V41-resistant and wild-type strains of Listeria monocytogenes. Appl. Environ. Microbiol. 2000, 66, 4318-4324.

146. Xue, J.; Hunter, I.; Steinmetz, T.; Peters, A.; Ray, B.; Miller, K.W. Novel activator of mannose-specific phosphotransferase system permease expression in Listeria innocua, identified by screening for pediocin AcH resistance. Appl. Environ. Microbiol. 2005, 71, 1283-1290.

147. Arous, S.; Dalet, K.; Hechard, Y. Involvement of the mpo operon in resistance to class IIa bacteriocins in Listeria monocytogenes. FEMS Microbiol. Lett. 2004, 238, 37-41.

148. Kaur, G.; Malik, R.K.; Mishra, S.K.; Singh, T.P.; Bhardwaj, A.; Singroha, G.; Vij, S.; Kumar, N. Nisin and class IIa bacteriocin resistance among Listeria and other foodborne pathogens and spoilage bacteria. Microb. Drug Resist. 2011, 17, 197-205.

149. Simon, L.; Fremaux, C.; Cenatiempo, Y.; Berjeaud, J.-M. Luminescent method for the detection of antibacterial activities. Appl. Microbiol. Biotechnol. 2001, 57, 757-763.

150. Eijsink, V.G.H.; Axelsson, L.; Diep, D.B.; Hávarstein, L.S.; Holo, H.; Nes, I.F. Production of class II bacteriocins by lactic acid bacteria: An example of biological warfare and communication. Antonie Van Leeuwenhoek 2002, 81, 639-654.

151. Rouse, S.; Sun, F.; Vaughan, A.; van Sinderen, D. High-throughput isolation of bacteriocin-producing lactic acid bacteria, with potential application in the brewing industry. J. Inst. Brew. 2007, 113, 256-262.

152. Wi^ckowicz, M.; Schmidt, M.; Sip, A.; Grajek, W. Development of a PCR-based assay for rapid detection of class IIa bacteriocin genes. Lett. Appl. Microbiol. 2011, 52, 281-289.

153. Losteinkit, C.; Uchiyama, K.; Ochi, S.; Takaoka, T.; Nagahisa, K.; Shioya, S. Characterization of bacteriocin N15 produced by Enterococcus faecium N15 and cloning of the related genes. J. Biosci. Bioeng. 2001, 91, 390-395.

154. Choho, G.; Abriouel, H.; Omar, N.; López, R.; Ortega, E.; Martínez-Cañamero, M.; Laglaoui, A.; Barrijal, S.; Gálvez, A. Characterization of a bacteriocin-producing strain of Enterococcus faecalis from cow's milk used in the production of Moroccan traditional dairy foods. World J. Microbiol. Biotechnol. 2008, 24, 997-1001.

155. Belgacem, Z.B.; Abriouel, H.; Omar, N.B.; Lucas, R.; Martínez-Canamero, M.; Gálvez, A.; Manai, M. Antimicrobial activity, safety aspects, and some technological properties of bacteriocinogenic Enterococcus faecium from artisanal Tunisian fermented meat. Food Control 2010, 21, 462-470.

156. Yi, H.; Zhang, L.; Tuo, Y.; Han, X.; Du, M. A novel method for rapid detection of class IIa bacteriocin-producing lactic acid bacteria. Food Control 2010, 21, 426-430.

157. Knoll, C.; Divol, B.; Toit, M. Genetic screening of lactic acid bacteria of oenological origin for bacteriocin-encoding genes. Food Microbiol. 2008, 25, 983-991.

158. Liu, M.J.; van Enckevort, F.H.J.; Siezen, R.J. Genome update: Lactic acid bacteria genome sequencing is booming. Microbiology 2005, 151, 3811-3814.

159. Pfeiler, E.A.; Klaenhammer, T.R. The genomics of lactic acid bacteria. Trends Microbiol. 2007, 15, 546-553.

160. Nes, I.F.; Johnsborg, O. Exploration of antimicrobial potential in LAB by genomics. Curr. Opin. Biotechnol. 2004, 15, 100-104.

161. Dirix, G.; Monsieurs, P.; Dombrecht, B.; Daniels, R.; Marchalb, K.; Vanderleydena, J.; Michielsa, J. Peptide signal molecules and bacteriocins in Gram-negative bacteria: A genome-wide in silico screening for peptides containing a double-glycine leader sequence and their cognate transporters. Peptides 2004, 25, 1425-1440.

162. Dirix, G.; Monsieurs, P.; Marchal, K.; Vanderleyden, J.; Michiels, J. Screening genomes of Gram-positive bacteria for double-glycine-motif containing peptides. Microbiology 2004, 150, 1121-1126.

163. Wang, Z.; Wang, G. APD: The antimicrobial peptide database. Nucleic Acids Res. 2004, 32, D590-D592.

164. Fjell, CD.; Jenssen, H.; Hilpert, K.; Cheung, W.A.; Pante, N.; Hancock, R.E.; Cherkasov, A. Identification of novel antibacterial peptides by chemoinformatics and machine learning. J. Med. Chem. 2009, 52, 2006-2015.

165. Fjell, C.D.; Hancock, R.E.; Cherkasov, A. AMPer: A database and an automated discovery tool for antimicrobial peptides. Bioinformatics 2007, 23, 1148-1155.

166. Bactibase: Database dedicated to bacteriocins. Available online: (accessed on 20 November 2012).

167. Bagel2: The bacteriocin mining tool. Available online: (accessed on 20 November 2012).

168. Hammami, R.; Zouhir, A.; Lay, C.L.; Hamida, J.B.; Fliss, I. BACTIBASE second release: A database and tool platform for bacteriocin characterization. BMC Microbiol. 2010, 10, 22.

169. De Jong, A.; van Heel, A.J.; Kok, J.; Kuipers, O.P. BAGEL2: Mining for bacteriocins in genomic data. Nucleic Acids Res. 2010, 38, W647-W651.

170. Wang, P.; Hu, L.; Liu, G.Y.; Jiang, N.; Chen, X.Y.; Xu, J.Y.; Zheng, W.; Li, L.; Tan, M.; Chen, Z.; et al. Prediction of antimicrobial peptides based on sequence alignment and feature selection methods. PLoS One 2011, 6, e18476.

171. Fernandes, F.C.; Rigden, D.J.; Franco, O.L. Prediction of antimicrobial peptides based on the adaptive neuro-Fuzzy inference system application. Pept. Sci. 2012, 98, 280-287.

172. Hammami, R.; Fliss, I. Current trends in antimicrobial agent research: Chemo- and bioinformatics approaches. DrugDiscov. Today 2010, 15, 540-546.

173. Hilpert, K.; Elliott, M.R.; Volkmer-Engert, R.; Henklein, P.; Donini, O.; Zhou, Q.; Winkler, D.F.; Hancock, R.E. Sequence requirements and an optimization strategy for short antimicrobial peptides. Chem. Biol. 2006, 13, 1101-1107.

174. Jenssen, H.; Fjell, C.D.; Cherkasov, A.; Hancock, R.E. QSAR modeling and computer-aided design of antimicrobial peptides. J. Pept. Sci. 2008, 14, 110-114.

175. Frecer, V.; Ho, B.; Ding, J.L. De novo design of potent antimicrobial peptides. Antimicrob. Agents Chemother. 2004, 48, 3349-3357.

176. Cherkasov, A.; Jankovic, B. Application of 'inductive' QSAR descriptors for quantification of antibacterial activity of cationic polypeptides. Molecules 2004, 9, 1034-1052.

177. Wang, Y.Q.; Ding, Y.; Wen, H.X.; Lin, Y.; Hu, Y.; Zhang, Y.; Xia, Q.Y.; Li, Z.H. QSAR modeling and design of cationic antimicrobial peptides based on structural properties of amino acids. Comb. Chem. High Throughput Screening 2012, 15, 347-353.

178. Melo, M.N.; Ferre, R.; Feliu, L.; Bardaji, E.; Planas, M.; Castanho, M.A.R.B. Prediction of antibacterial activity from physicochemical properties of antimicrobial peptides. PLoS One 2011, 6, e28549.

179. Huang, H.W. Molecular mechanism of antimicrobial peptides: The origin of cooperativity. Biochim. Biophys. Acta 2006, 1758, 1292-1302.

180. Leontiadou, H.; Mark, A.E.; Marrink, S.J. Antimicrobial peptides in action. J. Am. Chem. Soc. 2006, 128, 12156-12161.

181. Melo, M.N.; Castanho, M.A. Omiganan interaction with bacterial membranes and cell wall models. Assigning a biological role to saturation. Biochim. Biophys. Acta 2007, 1768, 1277-1290.

182. Pistolesi, S.; Pogni, R.; Feix, J.B. Membrane insertion and bilayer perturbation by antimicrobial peptide CM13. Biophys. J. 2007, 93, 1631-1660.

183. Melo, M.N.; Ferre, R.; Castanho, M.A. Antimicrobial peptides: Linking partition, activity and high membrane-bound concentrations. Nat. Rev. Microbiol. 2009, 7, 243-230.

184. Alves, C.S.; Melo, M.N.; Franquelim, H.G.; Ferre, R.; Planas, M.; Feliu, L.; Bardají, E.; Kowalczyk, W.; Andreu, D.; Santos, N.C.; et al. Escherichia coli cell surface perturbation and disruption induced by antimicrobial peptides BP100 and pepR. J. Biol. Chem. 2010, 285, 27336-27344.

183. Acuña, L.; Morero, R.D.; Bellomio, A. Development of wide-spectrum hybrid bacteriocins for food biopreservation. FoodBioprocess Technol. 2011, 4, 1029-1049.

186. Kalmokoff, M.L.; Daley, E.; Austin, J.W.; Farber, J.M. Bacteriocin-like inhibitory activities among various species of Listeria. Int. J. Food Microbiol. 1999, 50, 191-201.

187. Bennik, M.H.J.; Vanloo, B.; Brasseur, R.; Gorris, L.G.M.; Smid, E.J. A novel bacteriocin with a YGNGV motif from vegetable-associated Enterococcus mundtii: full characterization and interaction with target organisms. Biochim. Biophys. Acta 1998, 1373, 47-38.

188. Kawamoto, S.; Shima, J.; Sato, R.; Eguchi, T.; Ohmomo, S.; Shibato, J.; Horikoshi, N.; Takeshita, K.; Sameshima, T. Biochemical and genetic characterization of mundticin KS, an antilisterial peptide produced by Enterococcus mundtii NFRI 7393. J. Appl. Microbiol. 2002, 68, 3830-3840.

189. Zendo, T.; Eungruttanagorn, N.; Fujioka, S.; Tashiro, Y.; Nomura, K.; Sera, Y.; Kobayashi, G.; Nakayama, J.; Ishizaki, A.; Sonomoto, K. Identification and production of a bacteriocin from Enterococcus mundtii QU2 isolated from soybean. J. Appl. Microbiol. 2005, 99, 1181-1190.

190. Yamazaki, K.; Suzuki, M.; Kawai, Y.; Inoue, N.; Montville, T.J. Purification and characterization of a novel class IIa bacteriocin, piscicocin CS326, from Surimi-associated Carnobacterium piscicola CS326. Appl. Environ. Microbiol. 2005, 71, 334-337.

191. Gursky, L.J.; Martin, N.I.; Derksen, D.J.; van Belkum, M.J.; Kaur, K.; Vederas, J.C.; Stiles, M.E.; McMullen, L.M. Production of piscicolin 126 by Carnobacterium maltaromaticum UAL26 is controlled by temperature and induction peptide concentration. Arch. Microbiol. 2006, 186, 317-323.

192. Jack, R.W.; Wan, J.; Gordon, J.; Harmark, K.; Davidson, B.E.; Hillier, A.J.; Wettenhall, R.E.; Hickey, M.W.; Coventry, M.J. Characterization of the chemical and antimicrobial properties of piscicolin 126, a bacteriocin produced by Carnobacterium piscicola JG126. Appl. Environ. Microbiol. 1996, 62, 2897-2903.

193. Bhugaloo-Vial, P.; Dousset, X.; Metivier, A.; Sorokine, O.; Anglade, P.; Boyaval, P.; Marion, D. Purification and amino acid sequences of piscicocins Vla and Vlb, two class IIa bacteriocins secreted by Carnobacterium piscicola V1 that display significantly different levels of specific inhibitory activity. Appl. Environ. Microbiol. 1996, 62, 4410-4416.

194. Hyronimus, B.; Le Marrec, C.; Urdaci, M.C. Coagulin, a bacteriocin-like inhibitory substance produced by Bacillus coagulans I4. J. Appl. Microbiol. 1998, 85, 42-30.

193. Motlagh, A.; Bukhtiyarova, M.; Ray, B. Complete nucleotide sequence of pSMB 74, a plasmid encoding the production of pediocin AcH in Pediococcus acidilactici. Lett. Appl. Microbiol. 1994, 18, 303-312.

196. Nieto, L.J.C.; Meyer, J.N.; Sletten, K.; Pelâz, C.; Nes, I.F. Purification and amino acid sequence of a bacteriocin produced by Pediococcus acidilactici. J. Gen. Microbiol. 1992, 138, 1985-1990.

197. Marugg, J.D.; Gonzalez, C.F.; Kunka, B.S.; Ledeboer, A.M.; Pucci, M.J.; Toonen, M.Y.; Walker, S.A.; Zoetmulder, L.C.M.; Vandenbergh, P.A. Cloning, expression, and nucleotide-sequence of genes involved in production of pediocin PA-1, a bacteriocin from Pediococcus acidilactici PAC1.0. Appl. Environ. Microbiol. 1992, 58, 2360-2367.

198. Kim, I.K.; Kim, M.K.; Kim, J.Y.; Yim, H.S.; Cha, S.S.; Kang, S.O. High resolution crystal structure of PedB: A structural basis for the classification of pediocin-like immunity proteins. BMC Struct. Biol. 2007, 7, 35.

199. Rihakova, J.; Petit, V.W.; Demnerova, K.; Prévost, H.; Rebuffat, S.; Drider, D. Insights into structure-activity relationships in the c-terminal region of divercin V41, a class IIa bacteriocin with high-level antilisterial activity. Appl. Environ. Microbiol. 2009, 75, 1811-1819.

200. Tahiri, I.; Desbiens, M.; Benech, R.; Kheadr, E.; Lacroix, C.; Thibault, S.; Ouellet, D.; Fliss, I. Purification, characterization and amino acid sequencing of divergicin M35: a novel class IIa bacteriocin produced by Carnobacterium divergens M35. Int. J. Food Microbiol. 2004, 97, 123-136.

201. Ennahar, S.; Asou, Y.; Zendo, T.; Sonomoto, K.; Ishizaki, A. Biochemical and genetic evidence for production of enterocins A and B by Enterococcus faecium WHE 81. Int. J. Food Microbiol. 2001, 70, 291-301.

202. O'Keeffe, T.; Hill, C.; Ross, R.P. Characterization and heterologous expression of the genes encoding enterocin a production, immunity, and regulation in Enterococcus faecium DPC1146. Appl. Environ. Microbiol. 1999, 65, 1506-1515.

203. Morovsky, M.; Pristas, P.; Javorsky, P.; Nes, I.F.; Holo, H. Isolation and characterization of enterocin BC25 and occurrence of the entA gene among ruminal gram-positive cocci. Microbiol. Res. 2001, 156, 133-138.

204. Todokoro, D.; Tomita, H.; Inoue, T.; Ike, Y. Genetic analysis of bacteriocin 43 of vancomycin-resistant Enterococcus faecium. Appl. Environ. Microbiol. 2006, 72, 6955-6964.

205. Del Campo, R.; Tenorio, C.; Jiménez-diaz, R.; Rubio, C.; Gomez-Lui, R.; Baquero, F.; Torres, C. Bacteriocin production in vancomycin-resistant and vancomycin-susceptible Enterococcus isolates of different origins. Antimicrob. Agents Chemother. 2001, 45, 905-912.

206. De Kwaadsteniet, M.; Fraser, T.; van Reenen, C.A.; Dicks, L.M. Bacteriocin T8, a novel class IIa sec-dependent bacteriocin produced by Enterococcus faecium T8, isolated from vaginal secretions of children infected with human immunodeficiency virus. Appl. Environ. Microbiol. 2006, 72, 4761-4766.

207. Eguchi, T.; Kaminaka, K.; Shima, J.; Kawamoto, S.; Mori, K.; Choi, S. H.; Doi, K.; Ohmomo, S.; Ogata, S. Isolation and characterization of enterocin SE-K4 produced by thermophilic enterococci, Enterococcus faecalis K-4. Biosc. Biotechnol. Biochem. 2001, 65, 247-253.

208. Herbin, S.; Mathieu, F.; Brule, F.; Branlant, C.; Lefebvre, G.; Lebrihi, A. Characteristics and genetic determinants of bacteriocin activities produced by Carnobacterium piscicola CP5 isolated from cheese. Curr. Microbiol. 1997, 35, 319-326.

209. Hastings, J.W.; Sailer, M.; Johnson, K.; Roy, K.L.; Vederas, J.C.; Stiles, M.E. Characterization of leucocin A-UAL 187 and cloning of the bacteriocin gene from Leuconostoc gelidum. J. Bacteriol. 1991, 173, 7491-7500.

210. Van Reenen, C.A.; Chikindas, M.L.; van Zyl, W.H.; Dicks, L.M. Characterization and heterologous expression of a class IIa bacteriocin, plantaricin 423 from Lactobacillus plantarum 423, in Saccharomyces cerevisiae. Int. J. Food Microbiol. 2003, 81, 29-40.

211. Van Reenen, C.A.; van Zyl, W.H.; Dicks, L.M. Expression of the immunity protein of plantaricin 423, produced by Lactobacillus plantarum 423, and analysis of the plasmid encoding the bacteriocin. Appl. Environ. Microbiol. 2006, 72, 7644-7651.

212. Maré, L.; Wolfaardt, G.M.; Dicks, L.M.T. Adhesion of Lactobacillus plantarum 423 and Lactobacillus salivarius 241 to the intestinal tract of piglets, as recorded with fluorescent in situ hybridization (FISH), and production of plantaricin 423 by cells colonized to the ileum. J. Appl. Microbiol. 2006, 100, 838-845.

213. Atrih, A.; Rekhif, N.; Michel, M.; Lefebvre, G. Detection of bacteriocins produced by Lactobacillus plantarum isolated from different foods. Microbiology 1993, 75, 117-123.

214. Atrih, A.; Rekhif, N.; Moir, A.J.; Lebrihi, A.; Lefebvre, G. Mode of action, purification and amino acid sequence of plantaricin C19, an anti-Listeria bacteriocin produced by Lactobacillus plantarum C19. Int. J. Food Microbiol. 2001, 68, 93-104.

215. Holck, A.; Axelsson, L.; Birkeland, S.E.; Aukrust, T.; Blom, H. Purification and amino acid sequence of sakacin A, a bacteriocin from Lactobacillus sake Lb706. J. Gen. Microbiol. 1992, 138, 2715-2720.

216. Axelsson, L.; Holck, A.; Birkeland, S.E.; Aukrust, T.; Blom, H. Cloning and nucleotide sequence of a gene from Lactobacillus sake Lb706 necessary for sakacin A production and immunity. Appl. Environ. Microbiol. 1993, 59, 2868-2875.

217. Axelsson, L.; Holck, A. The genes involved in production of and immunity to sakacin A, a bacteriocin from Lactobacillus sake Lb706. J. Bacteriol. 1995, 177, 2125-2137.

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