Two-peptide bacteriocins produced by lactic acid bacteria

Biochimie

Volumn 84, Issue 5-6, 2002, Pages 577-592

  Garneau, Sylvie ^a   Martin, Nathaniel I ^a   Vederas, John C ^a  

^a UNIVERSITY OF ALBERTA   (Canada)

Author keywords

Antimicrobial peptide; Bacteriocin; Brochocin; Lactic acid bacteria; Lacticin; Lantibiotic; Nisin; Post translational modification

Indexed keywords

ABP 118; BACTERIOCIN; BROCHOCIN C; CYTOLYSIN; ENTEROCIN 1071; ENTEROCIN 1071A; ENTEROCIN 1071B; ENTEROCIN L50; LACTACIN F; LACTICIN 3147; LACTOCIN 705; LACTOCOCCIN G; LACTOCOCCIN G ALPHA; LACTOCOCCIN G BETA; LACTOCOCCIN MN; LANTIBIOTIC; LEUCOCIN H; MUTACIN IV; PLANTARICIN A ALPHA; PLANTARICIN E; PLANTARICIN EF; PLANTARICIN J; PLANTARICIN JK; PLANTARICIN K; PLANTARICIN S; PLANTARICIN W; POLYPEPTIDE ANTIBIOTIC AGENT; STAPHYLOCOCCIN C55; THERMOPHILIN 13; UNCLASSIFIED DRUG; UNINDEXED DRUG;

ANTIMICROBIAL ACTIVITY; BACTERIAL MEMBRANE; BACTERICIDAL ACTIVITY; DRUG CLASSIFICATION; DRUG POTENCY; DRUG STRUCTURE; DRUG SYNTHESIS; DRUG TARGETING; GRAM POSITIVE BACTERIUM; LACTIC ACID BACTERIUM; MOLECULE; NONHUMAN; REVIEW; RIBOSOME; STRUCTURE ANALYSIS; TERMINAL SEQUENCE; AMINO ACID SEQUENCE; BACTERIUM; CHEMISTRY; GENETICS; METABOLISM; MOLECULAR GENETICS; SEQUENCE HOMOLOGY;

POSIBACTERIA;

AMINO ACID SEQUENCE; BACTERIA; BACTERIOCINS; MOLECULAR SEQUENCE DATA; SEQUENCE HOMOLOGY;

EID: 0036589172     PISSN: 03009084     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0300-9084(02)01414-1     Document Type: Review

References (145)

1. J.R. Tagg, A.S. Dajani, L.W. Wannamaker, Bacteriocins of Gram-positive bacteria, Microbiol. Rev. 40 (1976) 722-756.
2. T.R. Klaenhammer, Bacteriocins of lactic acid bacteria, Biochimie 70 (1988) 337-349.
3. A. Gratia, C. R. Soc. Biol. 93 (1925) 1040.
4. J. Nissen-Meyer, I.F. Nes, Ribosomally synthesized antimicrobial peptides: their function, structure, biogenesis, and mechanism of action, Arch. Microbiol. 167 (1997) 67-77.
5. J.N. Hansen, S. Banerjee, L.W. Buchman, Potential of small ribosomally synthesized bacteriocins in the design of new food preservatives, J. Food Safety 10 (1989) 119-130.
6. I. Wiedemann, E. Breukink, C. van Kraaij, O.P. Kuipers, G. Bierbaum, B. de Kruiff, H.G. Sahl, Specific binding of nisin to the peptidoglycan precursor lipid II combines pore formation and the inhibition of cell wall biosynthesis for potent antibiotic activity, J. Biol. Chem. 276 (2001) 1772-1779.
7. E. Breukink, I. Wiedemann, C. van Kraaij, O.P. Kuipers, H.G. Sahl, B. de Kruiff, Use of the cell wall percursor lipid II by a pore-forming peptide antibiotic, Science 286 (1999) 2361-2364.
8. Y. Hechard, C. Pelletier, Y. Cenatiempo, J. Frere, Analysis of sigma(54)-dependent genes in Enterococcus faecalis: a mannose PTS permease (EIIMan) is involved in sensitivity to a bacteriocin, mersentericin Y105, Microbiol.-SGM 147 (2001) 1575-1580.
9. M. Ramnath, M. Beukes, K. Tamura, J.W. Hastings, 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 sodiuim dodecyl sulfate-polyacrylamide gel electrophoresis, Appl. Environ. Microbiol. 66 (2000) 3098-3101.
10. A. Guder, I. Wiedemann, H.G. Sahl, Posttranslationally modified bacteriocins - the lantibiotics, Biopolymers 55 (2000) 62-73.
11. N. Schnell, K.D. Entian, U. Schneider, F. Götz, H. Zähner, R. Kellner, G. Jung, Prepeptide sequence of epidermin, a riobosmally synthesized antibiotic with four sulphide rings, Nature 333 (1998) 276-278.
12. S. Ennahar, T. Sashihara, K. Somoto, A. Ishizaki, Class IIa bacteriocins: biosynthesis, structure and activity. FEMS Microbiol. Rev. 24 (2000) 85-106.
13. M.A. Riley, Molecular mechanisms of bacteriocin evolution. Annu, Rev. Gen. 32 (1998) 255-278.
14. M.A. Riley, D.M. Gordon, The ecology and evolution of bacteriocins, J. Industrial Microbiol. 17 (1996) 151-158.
15. I.F. Nes, D.B. Diep, L.S. Håvarstein, M.B. Brurberg, V. Eijsink, H. Holo, Biosynthesis of bacteriocins in lactic acid bacteria, Antonie van Leeuwenhoek 70 (1996) 113-128.
16. K.D. Entian, W.M. deVos, Genetics of subtilin and nisin biosyntheses - Biosynthesis of lantibiotics, Antonie van Leeuwenhoek Int. J. Gen. Mol. Microbiol. 69 (1996) 109-117.
17. J. Cleveland, T.J. Montville, I.F. Nes, M.L. Chikindas, Bacteriocins: safe, natural antimicrobials for food preservation, Int. J. Food Microbiol. 71 (2001) 1-20.
18. O. McAuliffe, R.R. Ross, C. Hill, Lantibiotics: structure, biosynthesis and mode and action, FEMS Microbiol. Rev. 25 (2001) 285-308.
19. M.J. van Belkum, M.E. Stiles, Nonlantibiotic antibacterial peptides from lactic acid bacterial, Natl. Prod. Rep. 17 (2000) 323-335.
20. I.G. Nes, H. Holo, Class II antimicrobial peptides from lactic acid bacteria, Biopolymers 55 (2000) 50-61.
21. T.J. Montville, Y. Chen, Mechanistic action of pediocin and nisin: recent progress and unresolved questions, Appl. Microbiol. Biotechnol. 50 (1998) 511-519.
22. M.A. Daw, F.R. Falkiner, Bacteriocins: nature, function and structure, Micron. 27 (1996) 467-479.
23. R.W. Jack, J.R. Tagg, B. Ray, Bacteriocins of Gram-positive bacteria, Microbiol. Rev. 59 (1995) 171-200.
24. T. Abee, Pore-forming bacteriocins of Gram-positive bacteria and self-protection mechanisms of producer organisms, FEMS Microbiol. Lett. 129 (1995) 1-10.
25. T.J. Montville, M.E.C. Bruno, Evidence that dissipation of proton motive force is a common mechanism of action for bacteriocins and other antimicrobial proteins, Int. J. Food Microbiol. 24 (1994) 53-74.
26. E. Parente, A. Ricciardi, Production, recovery and purification of bacteriocins from lactic acid bacteria, Appl. Microbiol. Biotechnol. 52 (1999) 628-638.
27. M.V. Carolissen, G. Arendse, Purification of bacteriocins of lactic acid bacteria: problems and pointers, Int. J. Food Microbiol. 34 (1997) 1-16.
28. S. Ennahar, K. Sonomoto, A. Ishizaki, Class IIa bacteriocins from lactic acid bacteria: antibacterial activity and food preservation, J. Biosci. Bioeng. 87 (1999) 705-716.
29. T. Requens, C. Pelaez, Review: antimicrobial activity of lactic acid bacteria. Bacteriocin production, Revista Espanola de ciencia y tecnologia de alimentos 35 (1995) 19-44.
30. E. Caplice, G.F. Fitzgerald, Food fermentations: role of microorganisms in food production and preservation, Int. J. Food Microbiol. 50 (1999) 131-149.
31. F.P. Rattray, P.F. Fox, Aspects of enzymology and biochemical properties of Brevibacterium linens relevant to cheese ripening: a review, J. Dairy Sci. 82 (1999) 891-909.
32. C.M.A.P. Franz, W.H. Holzapfel, M.E. Stiles, Enterococci at the crossroads of food safety? Int. J. Food Microbiol. 47 (1999) 1-24.
33. C. Daly, G.F. Fitzgerald, L. O'Connor, R. Davis, Technological and health benefits of dairy starter cultures, Int. Dairy J. 8 (1998) 195-205.
34. C.G. Kumar, S.K. Anand, Significance of microbial biofilms in food industry: A review, Int. J. Food Microbiol. 42 (1998) 9-27.
35. M.T. Aymerich, M. Hugas, J.M. Monfort, Bacteriocinogenic lactic acid bacteria associated with meat products. Food Sci. Technol. Int. 4 (1998) 141-158.
36. E. Ringo, F.J. Gatesoupe, Lactic acid bacteria in fish: a review, Aquaculture 160 (1998) 177-203.
37. M.R. Adams, L. Nicolaides, Review of the sensitivity of different foodborne pathogens to fermentation, Food Control 8 (1997) 227-239.
38. M.L. Chikindas, J. Novak, P.W. Caufield, K. Schilling, J.R. Tagg, Microbially-produced peptides having potential application to the prevention of dental caries, Int. J. Antimicrobial Agents 9 (1997) 95-105.
39. G. Giraffa, D. Carminati, E. Neviani, Enterococci isolated from dairy products: a review of risks and potential technological use, J. Food Protection 60 (1997) 732-737.
40. M.E. Stiles, W.H. Holzapfel, Lactic acid bacteria of foods and their current taxonomy, Int. J. Food Microbiol. 36 (1997) 1-29.
41. R.C. Post, Regulatory perspective of the USDA on the use of antimicrobials and inhibitors in foods, J. Food Protection Suppl. S (1996) 78-81.
42. G. Giraffa, Enterococcal bacteriocins: their potential as anti-Listeria factors in dairy technology, Food Microbiol. 12 (1995) 291-299.
43. T. Garcia, R. Martin, B. Sanz, P.E. Hernandez, Review: shelf life extension of fresh meat. 1. Modified atmosphere packaging, lactic acid bacteria and bacteriocins, Revista Espanola de ciencia y technologia de alimentos 35 (1995) 1-18.
44. W.H. Holzapfel, R. Geisen, U. Schillinger, Biological preservation of foods with reference to protective cultures, bacteriocins, and food-grade enzymes, Int. J. Food Microbiol. 24 (1995) 343-362.
45. I. Brook, Bacterial interference, Critical Rev. Microbiol. 25 (1999) 155-172.
46. S.M. Morgan, M. Galvin, R.P. Ross, C. Hill, Evaluation of a spray-dried Lacticin 3147 powder for the control of Listeria monocytogenes and Bacillus cereus in a range of food systems, Lett. Appl. Microbiol. 33 (2001) 387-391.
47. G.E.W. Gould, Preservation: past, present and future, British Med. Bull. 56 (2000) 84-96.
48. T.R. Klaenhammer, Genetics of bacteriocins produced by lactic acid bacteria, FEMS Microbiol. Rev. 12 (1993) 39-86.
49. S. Flynn, D. van Sinderen, G.M. Thornton, H. Holo, I.F. Nes, J.K. Collins, Characterization of the genetic locus responsible for the production of ABP-118, a novel bacteriocin produced by the probiotic bacterium Lactobacillus salivarius subsp. Salivarius UCC118, Microbiology 148 (2002) 973-984.
50. J.K. McCormick, A. Poon, M. Sailer, Y. Gao, K.L. Roy, L.M. McMullen, J.C. Vederas, M.E. Stiles, M.J. van Belkum, Genetic characterization and heterologous expression of brochocin-C, an antibotulinal, two-peptide bacteriocin produced by Brochothrix campestris ATCC 43754, Appl. Environ. Microbiol. 64 (1998) 4757-4766.
51. E. Balla, L.M.T. Dicks, M. Du Toit, M.J. Van Der Merwe, W.H. Holzapfel, Characterization and cloning of the genes encoding Enterocin 1071A and Enterocin 1071B, two antimicrobial peptides produced by enterococcus faecalis BFE 1071, Appl. Environ. Microbiol. 66 (2000) 1298-1304.
52. L.M. Cintas, P. Casaus, H. Holo, P.E. Hernandez, I.F. Nes, L.S. Håverstein, Enterocins L50A and L50B, two novel bacteriocins from Enterococcus faecium L50, are related to staphylococcal hemolysins, J. Bacteriol. 180 (1998) 1988-1994.
53. L.M. Cintas, P. Casaus, C. Herranz, L.Z. Håvarstein, H. Holo, P.E. Hernández, I.F. Nes, Biochemical and genetic evidence that Enterococcus faecium L50 produces Enterocins L50A and L50B, the sec-dependent Enterocin P, and a novel bacteriocin secreted without an N-terminal extension termed Enterocin Q, J. Bacteriol. 182 (2000) 6808-6814.
54. G.E. Allison, C. Fremaux, T.R. Klaenhammer, Expansion of bacteriocin activity and host range upon complementation of two peptides encoded within the Lactacin F operon, J. Bacteriol. 176 (1994) 2235-2241.
55. J. Palacios, G. Vignolo, M.E. Farías, A.P. Ruiz Holgado, G. de Oliver, F. Sesma, Purification and amino acid sequence of Lactocin 705, a bacteriocin produced by Lactobacillus casei CRL 705, Microbiol. Res. 154 (1999) 1-6.
56. S.A. Cuozzo, F. Sesma, J.M. Palacios, A.P. de Ruíz Holgado, R.R. Raya, Identification and nucleotide sequence of genes involved in the synthesis of Lactocin 705, a two-peptide bacteriocin from Lactobacillus casei CRL 705, FEMS Microbiol. Lett. 185 (2000) 157-161.
57. J. Nissen-Meyer, H. Holo, L.S. Håverstein, K. Sletten, I.F. Nes, A novel lactococcal bacteriocin whose activity depends on the complementary action of two peptides, J. Bacteriol. 174 (1992) 5686-5692.
58. M.J. van Belkum, B.J. Hayema, R.E. Jeeninga, J. Kok, G. Venema, Organization and nucleatide sequences of two lactococcal bacteriocin operons, Appl. Environ. Microbiol. 57 (1991) 492-498.
59. M.J. van Belkum, B.J. Hayema, A. Geis, J. Kok, G. Venema, Cloning of two bacteriocin genes from a lactococcal bacteriocin plasmid, Appl. Environ. Microbiol. 55 (1989) 1187-1191.
60. H. Blom, T. Katla, A. Holck, K. Sletten, L. Axelsson, H. Holo, Characterization, production, and purification of Leucocin H, a two-peptide bacteriocin from Leuconostic MF215B, Curr. Microbiol. 39 (1999) 43-48.
61. F. Qi, P. Chen, P.W. Caufield, The group I strain of Streptococcus mutans, UA140, produces both the lantibiotic mutacin I and nonlantibiotic bacteriocin, mutacin IV, Appl. Environ. Microbiol. 67 (2001) 15-21.
62. E.L. Anderssen, B.D. Diep, I.F. Nes, V.G.H. Eijsink, J. Nissen-Meyer, Antagonistic activity of Lactobacillus plantarum C11: two new two-peptide bacteriocins, plantaricins EF and JK, and the induction factor plantaricin A, Appl. Environ. Microbiol. 64 (1998) 2269-2272.
63. H.H. Hauge, D. Mantzilas, V.G.H. Eijsink, J. Nissen-Meyer, Membrane-mimicking entities induce structuring of the two-peptide bacteriocins plantaricin E/F and plantaricin J/K, J. Bacteriol. 181 (1999) 740-747.
64. G.N. Moll, van den Akker, H.H. Hauge, J. Nissen-Meyer, I.F. Nes, W.N. Konings, A.J.M. Driessen, Complementary and overlapping selectivity of the two-peptide bacteriocins plantaricin EF and JK, J. Bacteriol. 181 (1999) 4848-4852.
65. R. Jiménez-Díaz, J.L. Ruiz-Barba, D.P. Cathcart, H. Holo, I.F. Nes, K.H. Sletten, P.J. Warner, Purification and partial amino acid sequence of Plantaricin S, a bacteriocin produced by Lactobacillus plantarum LPCO10, the activity of which depends on the complementary action of two peptides, Appl. Environ. Microbiol. 61 (1995) 4459-4463.
66. O. Marciset, M.C. Jeronimus-Stratingh, B. Mollet, B. Poolman, Thermophilin 13, a nontypical antilisterial poration complex bacteriocin, that functions without a receptor, J. Biol. Chem. 272 (1997) 14277-14284.
67. M.C. Booth, C.P. Boogie, H.G. Sahl, R.J. Siezen, K.L. Hatter, M.S. Gilmore, Structural analysis and proteolytic activation of Enterococcus faecalis cytolysin, a novel lantibiotic, Mol. Microbiol. 21 (1996) 1175-1184.
68. M.P. Ryan, R.W. Jack, M. Josten, H.G. Sahl, G. Jung, R.P. Ross, C. Hill, Extensive post-translational modification, including serine to D-Alanine conversion, in the two-component lantiobiotic, Lacticin 3147, J. Biol. Chem. 274 (1999) 37544-37550.
69. H. Holo, Z. Jeknic, M. Daeschel, S. Stevanovic, I.F. Nes, Plantaricin W from Lactobacillus plantarum belongs to a new family of two-peptide lantiobiotics, Microbiology 147 (2001) 643-651.
70. M.A.D.B. Navaratna, H.G. Sahl, J.R. Tagg, Two-component anti-Staphylococcus aureus lantibiotic activity produced by Staphylococcus aureus C55, Appl. Environ. Microbiol. 64 (1998) 4803-4808.
71. C.F. Higgins, ABC transporters: from microorganisms to man, Annu. Rev. Cell Biol. 8 (1992) 67-113.
72. G.W. Buchman, S. Banerjee, J.N. Hansen, Structure, expression and evolution of a gene encoding the precursor of nisin, a small protein antibiotic, J. Biol. Chem. 263 (1988) 16260-16266.
73. S. Banerjee, J.N. Hansen, Structure and expression of the gene encoding the precursor of subtilin, a small protein antibiotic, J. Biol. Chem. 263 (1988) 9508-9514.
74. C. Kaletta, K.D. Entian, R. Kellner, G. Jung, M. Reis, H.G. Sahl, Pep5, A new lantibiotic: structural gene isolation and prepeptide sequence, Arch. Microbiol. 152 (1989) 16-19.
75. M. Slijper, C.W. Hilbers, R.N.H. Konings, F.J.M. van de Ven, NMR studies of lantiobitics, assignment of the 1H-NMR studies of lantibiotics, assignemnt of the 1H-NMR spectrum of nisin and identification of interresidual contacts, FEBS Lett. 252 (1989) 22-28.
76. S. Freund, G. Jung, O. Gutbrod, G. Folkers, W.A. Gibbons, H. Allgaier, R. Werner, The solution structure of the lantiobitic galidermin, Biopolymers 31 (1991) 803-811.
77. L.Y. Lian, W.C. Chan, S.D. Morley, G.C.K. Roberts, B.W. Bycroft, D. Jackson, NMR Studies of the solution structure of nisin A and related peptides, in: G. Jung, H.-G. Sahl (Eds.), Nisin and Novel Lantibiotics, 1991, pp. 43-58.
78. F.J.M. van den Ven, H.W. van den Hooven, R.N.H. Konings, C.W. Hilbers, NMR studies of lantiobiotics, the structure of nisin and aqueous solution, Eur. J. Biochem. 202 (1991) 1181-1188.
79. B. Bechinger, J.M. Ruysschaert, E. Goormaghtigh, Membrane helix orientation from linear dichroism of infrared attenuated total reflection spectra, Biophys. J. 76 (1999) 552-563.
80. B. Bechinger, M. Zasloff, S.J. Ophelia, Structure and orientation of the antibiotic peptide magainin in membranes by solid-state nuclear-magnetic-resonance spectroscopy, Protein Sci. 2 (1993) 2077-2084.
81. D.G. McCaffert, C. Predrag, M.K. Yu, D.C. Behenna, R. Kruger, Synergy and duality in peptide antibiotic mechanisms, Curr. Opin. Chem. Biol. 3 (1999) 672-680.
82. G.R. Siragusa, C. Nettles Cutter, Brochocin-C, a new bacteriocin produced by Brochothrix campestris, Appl. Environ. Microbiol. 59 (1993) 2326-2328.
83. L.M. Cintas, P. Casaus, C. Herranz, L.S. Håverstein, H. Holo, P.E. Hernandez, I.F. Nes, Biochemical and genetic evidence that Enterococcus faecium L50 produces Enterocins L50A and L50B, the sec-dependent Enterocin P, and a novel bacteriocin secreted without an N-terminal extension termed enterocin Q, J. Bacteriol. 182 (2000) 6806-6814.
84. T. Abee, T.R. Klaenhammer, L. Letellier, Kinetic studies of the action of Lactacin F, a Bacteriocin produced by Lactobacillus johnsonii that forms poration complexes in the cytoplasmic membrane, Appl. Environ. Microbiol. 60 (1994) 1006-1013.
85. C. Fremaux, C. Ahn, T.R. Klaenhammer, Molecular analysis of the Lactacin F Operon, App. Environ. Microbiol. 59 (1993) 1006-1013.
86. G.E. Allison, R.W. Worobo, ME. Stiles, T.R. Klaenhammer, Heterologous expression of the Lactacin F peptides by Carnobacterium piscicola LV17, Appl. Environ. Microbiol. 61 (1995) 1371-1377.
87. G.E. Allison, T.R. Klaenhammer, Functional analysis of the gene encoding immunity to Lactacin F, lafI, and its use as a Lactobacillus-specific, food-grade genetic marker, Appl. Environ. Microbiol. 62 (1996) 4450-4460.
88. G.E. Allison, C. Ahn, M.E. Stiles, T.R. Klaenhammer, Utilization of the Leucocin A export system in Leuconostoc gelidum for production of a Lactobacillus bacteriocin, FEMS Microbiol. Lett. 131 (1995) 87-93.
89. C. Fremaux, C. Ahn, T.R. Klaenhammer, Molecular analysis of the Lactacin F operon, Appl. Environ. Microbiol. 59 (1993) 3906-3915.
90. G. Moll, H. Hildeng-Hauge, J. Nissen-Meyer, I.F. Nes, W.N. Konings, J.M. Driessen, Mechanistic properties of the two-component Bacteriocin Lactococcin G, J. Bacteriol. 180 (1998) 96-99.
91. G. Moll, T. Ubbink-Kok, H. Hildeng-Hauge, J. Nissen-Meyer, I.F. Nes, W.N. Konings, J.M. Driessen, Lactococcin G is a potassium ion-conducting, two-component Bacteriocin, J. Bacteriol. 178 (1996) 600-605.
92. A. Fontana, Modification of tryptophan with BNPS-skatole (2-(2-nitrophenylsulphonyl)-3-methyl-3-bromoindolenine), Meth. Enzymol. 25 (1972) 419-423.
93. D.B. Diep, L.S. Håverstein, I.F. Nes, Characterization of the locus responsible for the Bacteriocin production in Lactobacillus plantarum C11, J. Bacteriol. 178 (1996) 4472-4483.
94. P.A. Risøen, O. Johnsborg, D.B. Diep, G. Hamoen, G. Venema, I.F. Nes, Regulation of bacteriocin production in Lactobacillus plantarum depends on a conserved promoter arrangement with consensus binding sequence, Mol. Genet. Genomics 265 (2001) 198-206.
95. P.A. Risøen, L.S. Håverstein, D.B. Diep, I.F. Nes, Identification of the DNA-binding sites for two response regulators involved in control of bacteriocin synthesis in Lactobacillus plantarum C11, Mol. Gen. Genet. 259 (1998) 224-232.
96. P. Klostermaier, C.H. Scheyhing, M. Ehrmann, R.F. Vogel, Mathematical evaluation of plantaricin formation supports an auto-induced production mechanism, Appl. Microbiol. Biotechnol. 51 (1999) 462-469.
97. S.K. Stephens, B. Floriano, D.P. Cathcart, S.A. Bayley, V.F. Witt, R. Jiménez-Diaz, P.J. Warner, J.L. Ruiz-Barba, Molecular analysis of the locus responsible for production of Plantaricin S, a two-peptide bacteriocin produced by Lactobacillus plantarum LPCO10, Appl. Environ. Microbiol. 64 (1998) 1871-1877.
98. L.C. Ingram, Synthesis of the antibiotic nisin: formation of lanthionine and β-methyllanthionine, Biochim. Biophys. Acta 184 (1969) 216-219.
99. G. Bierbaum, F. Götz, A. Peschel, T. Kupke, M. van de Kamp, H.G. Sahl, The biosynthesis of the lantibiotics epidermin, gallidermin, Pep5, and Epilancin K7, Antonie van Leeuwenhoek 69 (1996) 119-127.
100. H.G. Sahl, M. Reis, M. Eschbach, C. Szekat, A.G. Beck-Sickenger, J. Metzger, S. Stevanovic, G. Jung, Isolation of Pep5 prepeptides in different stages of modification, in: G. Jung, H.-G. Sahl (Eds.), Nisin and Novel Lantibiotics, 1991, pp. 332-346.
101. M. Skaugen, J. Nissen-Meyer, G. Jung, S. Stevanovic, K. Sletten, C.I.M. Abildgaard, I.F. Nes, In vivo conversion of L-serine to D-alanine in a ribosomally synthesized polypeptide. J. Biol. Chem. 269 (1994) 27183-27185.
102. H.G. Sahl, G. Bierbaum, Lantibiotics: biosynthesis and biological activities of uniquely modified peptides from Gram-positive bacteria, Annu. Rev. Microbiol. 52 (1998) 41-79.
103. O. McAuliffe, R.P. Ross, C. Hill, Lantibiotics: structure, biosynthesis and mode of action, FEMS Microbiol. Rev. 25 (2001) 285-308.
104. D.E. Palmer, D.F. Mierke, C. Pattaroni, M. Goodman, T. Wakamiya, K. Fukase, M. Kitazawa, H. Fujita, T. Shiba, Interactive NMR and computer simulation studies of lanthionine-ring structures, Biopolymers 28 (1989) 397-408.
105. R. Benz, G. Jung, H.-G. Sahl, Mechanism of channel-forming lantibiotics in black lipid membranes, in: G. Jung, H.-G. Sahl (Eds.), Nisin and Novel Lantibiotics, 1991, pp. 359-372.
106. M.E.C. Bruno, T.J. Montville, Common mechanistic action of bacteriocins from lactic acid bacteria. Appl. Environ. Microbiol. 59 (1993) 3003-3010.
107. M.J. Garcia-Garcera, M.G.L. Elfrink, A.J.M. Driessen, W.N. Konings, In vitro pore-forming activity of the lantibiotic nisin: role of protonmotive-force and lipid composition, Eur. J. Biochem. 212 (1993) 417-442.
108. M.C. Martinez-Cuesta, G. Buist, J. Kok, H.H. Hauge, J. Nissen-Meyer, C. Peláez, T. Requena, Biological and molecular characterization of a two-peptide lantibiotic produced by Lactococcus lactis IFP105. J. Appl. Microbiol. 89 (2000) 249-260.
109. B.A. Dougherty, C. Hill, J.F. Weidman, D.R. Richardson, J.C. Venter, R.P. Ross, Sequence and analysis of the 60 kb conjugative, bacteriocin-producing plasmid pMRC01 from Lactococcus lactis DPC3147, Mol. Microbiol. 29 (1998) 1029-1038.
110. O. McAuliffe , T. O'Keeffe, C. Hill, R.P. Ross, Regulation of immunity to the two-component lantibiotic, lacticin 3147, by the transcriptional repressor LtnR, Mol. Microbiol. 39 (2001) 982-993.
111. M.A.D.B. Navaratna, H.G. Sahl, J.R. Tagg, Identification of genes encoding two-component lantibiotic production in Staphylococcus aureus C55 and other phage group II S. aureus strains and demonstration of an association with the exfoliative toxin B gene, Infection and Immunity 67 (1999) 4268-4271.
112. I.G. Nes, H. Holo, Class II antimicrobial peptides from lactic acid bacteria. Biopolymers 55 (2000) 50-61.
113. R.A. Demel, T. Peelen, R.J. Siezen, B. de Kruiff, O.P. Kuipers, Z. Nisin, Mutant Nisin Z and Lacticin 481 interactions with anionic lipids correlate with antimicrobial activity - a monolayer study, Eur. J. Biochem. 235 (1996) 267-274.
114. Y.J. Wang, M.E. Henz, N.L. Fregeau-Gallagher, S.Y. Chai, A.C. Gibbs, L.Z. Yan, M.E. Stiles, D.S. Wishart, J.C. Vederas, Solution structure of carnobacteriocin B2 and implications for structure-activity relationships among type IIa bacteriocins from lactic acid bacteria, Biochemistry 38 (1999) 15438-15447.
115. N.L. Fregeau-Gallagher, M. Sailer, W.P. Niemczura, T.T. Nakashima, M.E. Stiles, J.C. Vederas, Three-dimensional structure of Leucocin A in trifluoroethanol and dodecylphosphocoline micelles: spatial location of residues critical for biological activity in type IIa bacteriocins from lactic acid bacteria, Biochemistry 36 (1997) 15062-15072.
116. G.N. Moll, G.C.K. Roberts, W.N. Konings, A.J.M. Driessen, Mechanism of lantibiotic-induced pore formation, Antonie van Leeuwenhoek 69 (1996) 185-191.
117. G. Boheim, W. Hanke, G. Jung, Alamethicin pore formation: voltage-dependent flip-flop of α-helix dipoles, Biophys. Struct. Mech. 9 (1983) 181-191.
118. S.J. Ludtke, K. He, W.T. Heller, T.A. Harroun, L. Yang, H.W. Huang, Membrane pores induced by magainin, Biochemistry 35 (1996) 13723-13728.
119. T. Abee, Pore-forming bacteriocins of Gram-positive bacteria and self-protection mechanisms of producer organisms, FEMS Microbiol. Lett. 129 (1995) 1-10.
120. M. Schiffer, A.B. Edmundson, Use of helical wheels to represent the structures of proteins and to identify segments with helical potential, Biophys. J. 7 (1967) 121-135.
121. H.H. Hauge, J. Nissen-Meyer, I.F. Nes, V.G. Eijsink, Amphiphilic alpha-helices are important structural motifs in the alpha and beta peptides that constitute the bacteriocin lactococcin G: enhancement of helix formation upon alpha-beta interaction, Eur. J. Biochem. 251 (1998) 565-572.
122. O. McAuliffe, M.P. Ryan, R.P. Ross, C. Hill, P. Breeuwer, T. Abee, Lacticin 3147, a broad spectrum bacteriocin which selectively dissipates the membrane potential, Appl. Environ. Microbiol. 64 (1998) 439-445.
123. J.R. Tagg, A.R. McGiven, Assay system for bacteriocins, Appl. Microbiol. 21 (1971) 943.
124. A. Hurst, Interaction of food starter cultures and food-borne pathogens: the antagonism between Streptococcus lactis and spore-forming microbes. J. Milk Food Technol. 35 (1972) 418-423.
125. Y. Gao, M.J. van Belkum, M.E. Stiles, The outer membrane of Gram-negative bacteria inhibits antibacterial activity of brochocin-C, Appl. Environ. Microbiol. 65 (1999) 4329-4333.
126. L.M. Cintas, J.M. Rodríguez, M.F. Fernández, K. Sletten, I.F. Nes, P.E. Hernández, H. Holo, Isolation and characterization of Pediocin L50, a new bacteriocin from Pediococcus acidilactici with a broad inhibitory spectrum, Appl. Environ. Microbiol. 61 (1995) 2643-2648.
127. L.M. Cintas, P. Casaus, M.F. Fernández, P.E. Hernández, Comparative antimicrobial activity of Enterocin L50, Pediocin PA-1, Nisin A and Lactocin S against spoilage and foodborne pathogenic bacteria, Food Microbiol. 15 (1998) 289-298.
128. P.M. Muriana, T.R. Klaenhammer, Conjugal transfer of plasmid-encoded determinants for bacteriocin production and immunity in Lactobacillus acidophilus 88, Appl. Environ. Microbiol. 53 (1987) 553-560.
129. N. Mulet-Powell, A.M. Lacoste-Armynot, M. Viñas, M. Simeon De Buochberg, Interaction between pairs of bacteriocins from lactic bacteria, J. Food. Prot. 61 (1998) 1210-1212.
130. M.P. Ryan, W.J. Meaney, R.P. Ross, C. Hill, Evaluation of Lacticin 3147 and a teat seal containing this bacteriocin for inhibition of mastitis pathogens, Appl. Environ. Microbiol. 64 (1998) 2287-2290.
131. M.R. Ryan, J. Flynn, C. Hill, R.P. Ross, W.J. Meaney, The natural food grade inhibitor, Lacticin 3147, reduced the incidence of mastitis after experimental challenge with Streptococcus dysgalactiae in nonlactating dairy cows, J. Dairy Sci. 82 (1999) 2108-2114.
132. M.P. Ryan, M.C. Rea, C. Hill, P. Ross, An application in cheddar cheese manufacture for a strain of Lactococcus lactis producing a novel broad-spectrum bacteriocin, Lacticin 3147, Appl. Environ. Microbiol. 62 (1996) 612-619.
133. O. McAuliffe, C. Hill, R.P. Ross, Inhibition of Listeria monocytogenes in cottage cheese manufactured with a Lacticin 3147-producing starter culture. J. Appl. Microbiol. 86 (1999) 251-256.
134. P.M. Davidson, A.L. Brannen (Eds.), Antimicrobials in Foods, Marcel Dekker, New York, 1993.
135. V.M. Dillon, R.G. Board (Eds.), Natural Antimicrobial Systems and Food Preservation, CAB International, Wallingford, Oxon, 1994.
136. Federal Register, Nisin Preparation: affirmation of GRAS status as a direct human food ingredient, Fed. Regist. 54 (1988) 11247-11251.
137. T. Aymerich, M. Garriga, J. Ylla, J. Vallier, J.M. Monfort, M. Hugas, Application of enterocins as biopreservatives against Listeria innocua in meat products, J. Food Prot. 63 (2000) 721-726.
138. T. Aymerich, M.G. Artigas, M. Garriga, J.M. Monfort, M. Hugas, Effect of sausage ingredients and additives on the production of enterocin A and B by Enterococcus faecium CT492, Optimization of in vitro production and anti-listerial effect in dry fermented sausages, J. Appl. Microbiol. 88 (2000) 686-694.
139. M.A. Fenelon, M.P. Ryan, M.C. Rea, T.P. Guinee, R.P. Ross, C. Hill, D. Harrington, Elevated temperature ripening of reduced fat cheddar made with or without Lacticin 3147-producing starter culture, J. Dairy Sci. 92 (1999) 10-22.
140. G. Vignolo, S. Fadda, M.N. de Kairuz, A.A. Ruis Holgado, G. Oliver, Control of Listeria monocytogenes in ground beef by 'Lactocin 705', a bacteriocin produced by Lactobacillus casei CRL 705, Int. J. Food. Microbiol. 29 (1996) 397-402.
141. J.L. Ruis-Barba, C.P. Cathcart, P.J. Warner, R. Jiménez-Díaz, Use of Lactobacillus plantarum LPCO10, a bacteriocin producer, as a starter culture in Spanish-style green olive fermentations, Appl. Environ. Microbiol. 60 (1994) 2059-2064.
142. S.L. Kesseler, A.S. Dajani, Listeria meningitis in infants and children, Pedia. Infect. Diseases J. 9 (1990) 61-63.
143. B.S. Azadian, G.T. Finnerty, A.D. Pearson, Cheese-borne Listeria meningitis in immunocompetent patient, Lancet i (1989) 322-323.
144. S.M. Morgan, M. Galvin, J. Delly, R.P. Ross, C. Hill, Development of a Lacticin 3147-enriched whey powder with inhibition activity against foodborne pathogens. J. Food. Prot. 62 (1999) 1011-1016.
145. A.G. Scannell, C. Hill, R.P. Ross, S. Marx, W. Hartmeier, E.K. Arendt, Development of bioactive food packaging materials using immobilized bacteriocins Lacticin 3147 and nisaplin, Int. J. Food Microbiol. 60 (2000) 241-249.