Comparative studies of immunity proteins of pediocin-like bacteriocins

Microbiology

Volumn 148, Issue 11, 2002, Pages 3661-3670

  Fimland, Gunnar ^a   Eijsink, Vincent G H ^b   Nissen Meyer, Jon ^a  

^a UNIVERSITY OF OSLO   (Norway)

^b NORWEGIAN UNIVERSITY OF LIFE SCIENCES   (Norway)

Author keywords

Bacteriocin resistance; Lactic acid bacteria

Indexed keywords

BACTERIAL PROTEIN; BACTERIOCIN; CURVACIN A; ENTEROCIN A; ENTEROCIN P; LACTOCOCCIN; LEUCOCIN A; PEDIOCIN; PEDIOCIN PA 1; RECEPTOR PROTEIN; SAKACIN P; UNCLASSIFIED DRUG;

BACTERIAL MEMBRANE; BACTERIAL STRAIN; CARNOBACTERIUM MALTAROMATICUM; COMPARATIVE STUDY; CONTROLLED STUDY; CROSS REACTION; ENTEROCOCCUS FAECALIS; GENE EXPRESSION; GENETIC TRANSCRIPTION; IMMUNITY; LACTIC ACID BACTERIUM; LACTOBACILLUS SAKEI; MEMBRANE COMPONENT; NONHUMAN; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; PROTEIN FUNCTION; PROTEIN PROTEIN INTERACTION; PROTEIN PURIFICATION; PROTEIN SYNTHESIS; REVIEW; SENSITIVITY ANALYSIS; SEQUENCE HOMOLOGY;

BACTERIA (MICROORGANISMS); CARNOBACTERIUM MALTAROMATICUM; CARNOBACTERIUM PISCICOLA; ENTEROCOCCUS FAECALIS; LACTOBACILLUS SAKE; LACTOBACILLUS SAKEI; PISCICOLA; POSIBACTERIA;

EID: 0041848440     PISSN: 13500872     EISSN: None     Source Type: Journal    
DOI: 10.1099/00221287-148-11-3661     Document Type: Review

References (53)

1. Atrih, A., Rekhif, N., Moir, A. J., Lebrihi, A. & Lefebvre, G. (2001). Mode of action, purification and amino acid sequence of plantaricin C19, an anti-Listeria bacteriocin produced by Lactobacillus plantarum C19. Int J Food Microbiol 68, 93-104.
2. Aukrust, T. W., Brurberg, M. B. & Nes, I. F. (1995). Transformation of Lactobacillus by electroporation. In Methods in Molecular Biology, vol. 47, Electroporation Protocols for Microorganisms, pp. 201-208. Edited by J. A. Nickoloff. Totowa, NJ: Humana Press.
3. Axelsson, L. & Holck, A. (1995). The genes involved in production of and immunity to sakacin A, a bacteriocin from Lactobacillus sake Lb706. J Bacteriol 177, 2125-2137.
4. Axelsson, L., Katla, T., Bjørnslett, M., Eijsink, V. G. H. & Holck, A. (1998). A system for heterologous expression of bacteriocins in Lactobacillus sake. FEMS Microbiol Lett 168, 137-143.
5. Aymerich, T., Holo, H., Håvarstein, L. S., Hugas, M., Garriga, M. & Nes, I. F. (1996). Biochemical and genetic characterization of enterocin A from Enterococcus faecium, a new antilisterial bacteriocin in the pediocin family of bacteriocins. Appl Environ Microbiol 62, 1676-1682.
6. Brurberg, M. B., Nes, I. F. & Eijsink, V. G. H. (1997). Pheromone-induced production of antimicrobial peptides in Lactobacillus. Mol Microbiol 26, 347-360.
7. Chikindas, M. L., Garcia-Garcera, M. J., Driessen, A. J. M., Ledeboer, A. M., Nissen-Meyer, J., Nes, I. F., Abee, T., Konings, W. N. & Venema, G. (1993). Pediocin PA-1, a bacteriocin from Pediococcus acidilactici PAC1.0, forms hydrophilic pores in the cytoplasmic membrane of target cells. Appl Environ Microbiol 59, 3577-3584.
8. Cintas, L. M., Casaus, P., Håvarstein, L. S., Hernández, P. E. & Nes, I. F. (1997). Biochemical and genetical characterization of enterocin P, a novel sec-dependent bacteriocin from Enterococcus faecium P13 with a broad antimicrobial spectrum. Appl Environ Microbiol 63, 4321-4330.
9. Crandal, A. D. & Montville, T. (1998). Nisin resistance in Listeria monocytogenes ATCC700302 is a complex phenotype. Appl Environ Microbiol 64, 231-237.
10. Dalet, K., Briand, C., Cenatiempo, Y. & Héchard, Y. (2000). The rpoN gene of Enterococcus faecalis directs sensitivity to subclass IIa bacteriocins. Curr Microbiol 41, 441-443.
11. 54-dependent PTS permease of the mannose family is responsible for sensitivity of Listeria monocytogenes to mesentericin Y105. Microbiology 147, 3263-3269.
12. Dayem, M. A., Fleury, Y., Devilliers, G., Chaboisseau, E., Girard, R., Nicolas, P. & Delfor, A. (1996). The putative immunity protein of the Gram-positive bacterium Leuconostoc mesenteroides is preferentially located in the cytoplasm compartment. FEMS Microbiol Lett 138, 251-259.
13. Dower, D. J., Miller, J. F. & Ragsdale, C. W. (1998). High efficiency transformation of Escherichia coli by high voltage electroporation. Nucleic Acids Res 16, 6127-6145.
14. Eijsink, V. G. H., Brurberg, M. B., Midelhoven, P. J. & Nes, I. F. (1996). Induction of bacteriocin production in Lactobacillus sake by a secreted peptide. J Bacteriol 178, 2232-2237.
15. Eijsink, V. G. H., Skeie, M., Middelhoven, H., Brurberg, M. B. & Nes, I. F. (1998). Comparative studies of pediocin-like bacteriocins. Appl Environ Microbiol 64, 3275-3281.
16. Ennahar, S., Sashihara, T., Sonomoto, K. & Ishizaki, A. (2000). Class IIa bacteriocins: biosynthesis, structure and activity. FEMS Microbiol Rev 24, 85-106.
17. Fimland, G., Blingsmo, O. R., Sletten, K., Jung, G., Nes, I. F. & Nissen-Meyer, J. (1996). 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 62, 3313-3318.
18. Fimland, G., Johnsen, L., Axelsson, L., Brurberg, M. B., Nes, I. F., Eijsink, V. G. H. & Nissen-Meyer, J. (2000). 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 182, 2643-2648.
19. Fimland, G., Eijsink, V. G. H. & Nissen-Meyer, J. (2002a). Mutational analysis of the role of tryptophan residues in the antimicrobial peptide sakacin P. Biochemistry 41, 9508-9515.
20. Fimland, G., Sletten, K. & Nissen-Meyer, J. (2002b). The complete amino acid sequence of the pediocin-like antimicrobial peptide leucocin C. Biochem Biophys Res Commun 295, 826-827.
21. Fregeau Gallagher, N. L., Sailer, M., Niemczura, W. P., Nakashima, T. T., Stiles, M. E. & Vederas, J. C. (1997). 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 36, 15062-15072.
22. Fremaux, C., Héchard, Y. & Cenatiempo, Y. (1995). Mesentericin Y105 gene clusters in Leuconostoc mesenteroides Y105. Microbiology 141, 1637-1645.
23. Hastings, J. W., Sailer, M., Johnson, K., Roy, K. L., Vederas, J. C. & Stiles, M. (1991). Characterization of leucocin A-UAL 187 and cloning of the bacteriocin gene from Leuconostoc gelidium. J Bacteriol 173, 7491-7500.
24. man) is involved in sensitivity to a bacteriocin, mesentericin Y105. Microbiology 147, 1575-1580.
25. Holo, H. & Nes, I. F. (1995). Transformation of Lactococcus by electroporation. In Methods in Molecular Biology, vol. 47, Electroporation Protocols for Microorganisms, pp. 195-199. Edited by J. A. Nickoloff. Totowa, NJ: Humana Press.
26. Hühne, K., Axelsson, L., Holck, A. & Kröckel, L. (1996). Analysis of the sakacin P gene cluster from Lactobacillus sake Lb674 and its expression in sakacin-negative Lb. sake strains. Microbiology 142, 1437-1448.
27. Jack, R. W., Wan, J., Gordon, J., Harmark, K., Davidson, B. E., Hillier, A. J., Wettenhall, R. E. H., Hickey, M. W. & Coventry, M. J. (1996). Characterization of the chemical and antimicrobial properties of piscicolin 126, a bacteriocin produced by Carnobacterium piscicola JG126. Appl Environ Microbiol 62, 2897-2903.
28. Kalmokoff, M. L., Banerjee, S. K., Cyr, T., Hefford, M. A. & Gleeson, T. (2001). Identification of a new plasmid-encoded sec-dependent bacteriocin produced by Listeria innocua 743. Appl Environ Microbiol 67, 4041-4047.
29. 4. Appl Environ Microbiol 66, 5213-5220.
30. Marugg, J. D., Gonzalez, C. F., Kunka, B. S., Lederboer, A. M., Pucci, M. J., Toonen, M. Y., Walker, S. A., Zoetmulder, L. C. M. & Vandenbergh, P. A. (1992). Cloning, expression, and nucleotide sequence of genes involved in production of pediocin PA-1, a bacteriocin from Pediococcus acidilactici PAC1.0. Appl Environ Microbiol 58, 2360-2367.
31. Métivier, A., Pilet, M.-F., Dousset, X., Sorokine, O., Anglade, P., Zagorec, M., Piard, J.-C., Marion, D., Cenatiempo, Y. & Fremaux, C. (1998). Divercin V41, a new bacteriocin with two disulphide bonds produced by Carnobacterium divergens V41: primary structure and genomic organization. Microbiology 144, 2837-2844.
32. Miller, K. W., Schamber, R., Osmanagaoglu, O. & Ray, B. (1998). Isolation and characterization of pediocin AcH chimeric protein mutants with altered bactericidal activity. Appl Environ Microbiol 64, 1997-2005.
33. Nes, I. F. & Holo, H. (2000). Class II antimicrobial peptides from lactic acid bacteria. Biopolymers 55, 50-61.
34. Nes, I. F., Holo, H., Fimland, G., Hauge, H. H. & Nissen-Meyer, J. (2002). Unmodified peptide-bacteriocins (class II) produced by lactic acid bacteria. In Peptide Antibiotics, Discovery, Modes of Action and Application. Edited by C. J. Dutton, M. A. Haxell, H. A. I. McArthur & R. G. Wax. New York: Marcel Decker.
35. Nieto Lozano, J. C., Nissen-Meyer, J., Sletten, K., Peláz, C. & Nes, I. F. (1992). Purification and amino acid sequences of a bacteriocin produced by Pediococcus acidilactici. J Gen Microbiol 138, 1985-1990.
36. Nissen-Meyer, J., Holo, H., Håvarstein, L. S., Sletten, K. & Nes, I. F. (1992). A novel lactococcal bacteriocin whose activity depends on the complementary action of two peptides. J Bacteriol 174, 5686-5692.
37. Nissen-Meyer, J., Håvarstein, L. S., Holo, H., Sletten, K. & Nes, I. F. (1993). Association of the lactococcin A immunity factor with the cell membrane: purification and characterization of the immunity factor. J Gen Microbiol 139, 1503-1509.
38. Quadri, L. E. N., Sailer, M., Roy, K. L., Vederas, J. C. & Stiles, M. E. (1994). Chemical and genetic characterization of bacteriocins produced by Carnobacterium piscicola LV17B. J Biol Chem 269, 12204-12211.
39. Quadri, L. E. N., Sailer, M., Terbiznik, M. R., Roy, K. L., Vederas, J. C. & Stiles, M. E. (1995). Characterization of the protein conferring immunity to the antimicrobial peptide carnobacteriocin B2 and expression of carnobacteriocins B2 and BM1. J Bacteriol 177, 1144-1151.
40. Quadri, L. E. N., Kleerebezem, M., Kuipers, O. P., de Vos, W. M., Roy, K. L., Vederas, J. C. & Stiles, M. E. (1997). Characterization of a locus from Carnobacterium piscicola LV17B involved in bacteriocin production and immunity: evidence for global inducer-mediated transcription regulation. J Bacteriol 179, 6163-6171.
41. Ramnath, M., Beukes, M., Tamura, K. & Hastings, J. W. (2000). 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 sulfate-polyacrylamide gel electrophoresis. Appl Environ Microbiol 66, 3098-3101.
42. Shepard, D. B. & Gilmore, M. S. (1995). Electroporation and efficient transformation of Enterococcus faecalis grown in high concentration of glycine. In Methods in Molecular Biology, vol. 47, Electroporation Protocols for Microorganisms, pp. 217-226. Edited by J. A. Nickoloff. Totowa, NJ: Humana Press.
43. Stoffels, G., Nissen-Meyer, J., Gudmundsdottir, A., Sletten, K., Holo, H. & Nes, I. F. (1992). Purification and characterization of a new bacteriocin isolated from a Carnobacterium sp. Appl Environ Microbiol 58, 1417-1422.
44. Tichaczek, P. S., Vogel, R. F. & Hammes, W. P. (1993). Cloning and sequencing of curA encoding curvacin A, the bacteriocin produced by Lactobacillus curvatus LTH1174. Arch Microbiol 160, 279-283.
45. Tichaczek, P. S., Vogel, R. F. & Hammes, W. P. (1994). Cloning and sequencing of sakP encoding sakacin P, the bacteriocin produced by Lactobacillus sake LTH673. Microbiology 140, 361-367.
46. Tomita, H., Fujimoto, S., Tanimoto, K. & Yasuyoshi, I. (1996). Cloning and genetic organization of the bacteriocin 31 determinant encoded on the Enterococcus faecalis pheromone-responsive conjugative plasmid pY117. J Bacteriol 178, 3585-3593.
47. van de Guchte, M., van der Vossen, J. M. B. M., Kok, J. & Venema, G. (1989). Construction of a lactococcal expression vector: expression of hen egg white lysozyme in Lactococcus lactis subsp. lactis. Appl Environ Microbiol 55, 224-228.
48. Vaughan, A., Eijsink, V. G. H., O'Sullivan, T. F., O'Hanlon, K. & van Sinderen, D. (2001). An analysis of bacteriocins produced by lactic acid bacteria isolated from malted barley. J Appl Microbiol 91, 131-138.
49. Venema, K., Haverkort, R. E., Abee, T., Haandrikman, A. J., Leenhouts, K. J., de Leij, L., Venema, G. & Kok, J. (1994). Mode of action of LciA, the lactococcin A immunity protein. Mol Microbiol 14, 521-532.
50. Venema, K., Kok, J., Marugg, J. D., Toonen, M. Y., Ledeboer, A. M., Venema, G. & Chikindas, M. L. (1995). Functional analysis of the pediocin operon of Pediococcus acidilactici PAC1.0: PedB is the immunity protein and PedD is the precursor processing enzyme. Mol Microbiol 17, 515-522.
51. Wang, Y., Henz, M. E., Fregeau Gallagher, N. L., Chai, S., Gibbs, A. C., Liang, Z. Y., Stiles, M. E., Wishart, D. S. & Vederas, J. C. (1999). Solution structure of carnobacteriocin B2 and implications for structure-activity relationships among type IIa bacteriocins from lactic acid bacteria. Biochemistry 38, 15438-15447.
52. Watson, R. M., Woody, R. W., Lewis, R. V., Bohle, D. S., Andreotti, A. H., Ray, B. & Miller, K. W. (2001). Conformational changes in pediocin AcH upon vesicle binding and approximation of the membrane-bound structure in detergent micelles. Biochemistry 40, 14037-14046.
53. Yan, L. Z., Gibbs, A. C., Stiles, M. E., Wishart, D. S. & Vederas, J. C. (2000). Analogues of bacteriocins: antimicrobial specificity and interactions of leucocin A with its enantiomer, carnobacteriocin B2, and truncated derivatives. J Med Chem 43, 4579-4581.