An overview of the mosaic bacteriocin pln loci from Lactobacillus plantarum

Peptides

Volumn 30, Issue 8, 2009, Pages 1562-1574

  Diep, Dzung B ^a   Straume, Daniel ^a   Kjos, Morten ^a   Torres, Carmen ^b   Nes, Ingolf F ^a  

^a NORWEGIAN UNIVERSITY OF LIFE SCIENCES   (Norway)

^b UNIVERSITY OF LA RIOJA   (Spain)

Author keywords

Antimicrobial peptide; Bacteriocin; Plantaricin; Probiotics

Indexed keywords

BACTERIAL PROTEIN; BACTERIOCIN; PHEROMONE; PLANTARICIN A; POLYPEPTIDE ANTIBIOTIC AGENT; REGULATOR PROTEIN; UNCLASSIFIED DRUG;

ANTIMICROBIAL ACTIVITY; CONTROLLED STUDY; GENE LOCUS; GENETIC CONSERVATION; GENETIC REGULATION; LACTOBACILLUS PLANTARUM; NONHUMAN; OPERON; PRIORITY JOURNAL; PROMOTER REGION; PROTEIN FAMILY; PROTEIN SECRETION; PROTEIN SYNTHESIS; QUORUM SENSING; REVIEW; STRAIN DIFFERENCE; TRANSPOSON;

ANTI-INFECTIVE AGENTS; BACTERIOCINS; LACTOBACILLUS PLANTARUM; MODELS, BIOLOGICAL;

LACTOBACILLUS PLANTARUM;

EID: 67650382228     PISSN: 01969781     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.peptides.2009.05.014     Document Type: Review

References (78)

1. Anderssen E.L., Diep D.B., Nes I.F., Eijsink V.G., and Nissen-Meyer J. 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
2. Babu M.M., Iyer L.M., Balaji S., and Aravind L. The natural history of the WRKY-GCM1 zinc fingers and the relationship between transcription factors and transposons. Nucleic Acids Res 34 (2006) 6505-6520
3. Ben Omar N., Abriouel H., Keleke S., Sanchez Valenzuela A., Martinez-Canamero M., Lucas Lopez R., et al. Bacteriocin-producing Lactobacillus strains isolated from poto poto, a Congolese fermented maize product, and genetic fingerprinting of their plantaricin operons. Int J Food Microbiol 127 (2008) 18-25
4. Breukink E., and de Kruijff B. Lipid II as a target for antibiotics. Nat Rev Drug Discov 5 (2006) 321-332
5. Bron P.A., Grangette C., Mercenier A., de Vos W.M., and Kleerebezem M. Identification of Lactobacillus plantarum genes that are induced in the gastrointestinal tract of mice. J Bacteriol 186 (2004) 5721-5729
6. Chatterjee C., Paul M., Xie L., and van der Donk W.A. Biosynthesis and mode of action of lantibiotics. Chem Rev 105 (2005) 633-684
7. Corr S.C., Li Y., Riedel C.U., O'Toole P.W., Hill C., and Gahan C.G. Bacteriocin production as a mechanism for the antiinfective activity of Lactobacillus salivarius UCC118. Proc Natl Acad Sci USA 104 (2007) 7617-7621
8. Cotter P.D., Hill C., and Ross R.P. Bacteriocins: developing innate immunity for food. Nat Rev Microbiol 3 (2005) 777-788
9. De Vuyst L., and Leroy F. Bacteriocins from lactic acid bacteria: production, purification, and food applications. J Mol Microbiol Biotechnol 13 (2007) 194-199
10. Diep D.B., Havarstein L.S., and Nes I.F. A bacteriocin-like peptide induces bacteriocin synthesis in Lactobacillus plantarum C11. Mol Microbiol 18 (1995) 631-639
11. Diep D.B., Havarstein L.S., and Nes I.F. Characterization of the locus responsible for the bacteriocin production in Lactobacillus plantarum C11. J Bacteriol 178 (1996) 4472-4483
12. Diep D.B., Havarstein L.S., Nissen-Meyer J., and Nes I.F. The gene encoding plantaricin A, a bacteriocin from Lactobacillus plantarum C11, is located on the same transcription unit as an agr-like regulatory system. Appl Environ Microbiol 60 (1994) 160-166
13. Diep D.B., Johnsborg O., Risøen P.A., and Nes I.F. Evidence for dual functionality of the operon plnABCD in the regulation of bacteriocin production in Lactobacillus plantarum. Mol Microbiol 41 (2001) 633-644
14. Diep D.B., Mathiesen G., Eijsink V.G., and Nes I.F. Use of lactobacilli and their pheromone-based regulatory mechanism in gene expression and drug delivery. Curr Pharm Biotechnol 10 (2009) 62-73
15. Diep D.B., Myhre R., Johnsborg O., Aakra A., and Nes I.F. Inducible bacteriocin production in Lactobacillus is regulated by differential expression of the pln operons and by two antagonizing response regulators, the activity of which is enhanced upon phosphorylation. Mol Microbiol 47 (2003) 483-494
16. Diep D.B., and Nes I.F. Ribosomally synthesized antibacterial peptides in Gram positive bacteria. Curr Drug Targets 3 (2002) 107-122
17. Diep D.B., Skaugen M., Salehian Z., Holo H., and Nes I.F. Common mechanisms of target cell recognition and immunity for class II bacteriocins. Proc Natl Acad Sci USA 104 (2007) 2384-2389
18. Drider D., Fimland G., Hechard Y., McMullen L.M., and Prevost H. The continuing story of class IIa bacteriocins. Microbiol Mol Biol Rev 70 (2006) 564-582
19. Eijsink V.G., Axelsson L., Diep D.B., Havarstein L.S., Holo H., and Nes I.F. Production of class II bacteriocins by lactic acid bacteria; an example of biological warfare and communication. Antonie van Leeuwenhoek 81 (2002) 639-654
20. Fimland N., Rogne P., Fimland G., Nissen-Meyer J., and Kristiansen P.E. Three-dimensional structure of the two peptides that constitute the two-peptide bacteriocin plantaricin EF. Biochim Biophys Acta 1784 (2008) 1711-1719
21. Forberg T. Lactic acid bacteria of different origin, production of antimicrobial substances and distribution of bacteriocin genes. Master Thesis; 2005.
22. Gerdes K., Christensen S.K., and Lobner-Olesen A. Prokaryotic toxin-antitoxin stress response loci. Nat Rev Microbiol 3 (2005) 371-382
23. Hancock R.E.W. Cationic peptides: effectors in innate immunity and novel antimicrobials. Lancet Infect Dis 1 (2001) 156-164
24. Hauge H.H., Mantzilas D., Eijsink V.G., and Nissen-Meyer J. Membrane-mimicking entities induce structuring of the two-peptide bacteriocins plantaricin E/F and plantaricin J/K. J Bacteriol 181 (1999) 740-747
25. Hauge H.H., Mantzilas D., Moll G.N., Konings W.N., Driessen A.J., Eijsink V.G., et al. Plantaricin A is an amphiphilic alpha-helical bacteriocin-like pheromone which exerts antimicrobial and pheromone activities through different mechanisms. Biochemistry 37 (1998) 16026-16032
26. Henderson J.T., Chopko A.L., and van Wassenaar P.D. Purification and primary structure of pediocin PA-1 produced by Pediococcus acidilactici PAC-1.0. Arch Biochem Biophys 295 (1992) 5-12
27. Holo H., Jeknic Z., Daeschel M., Stevanovic S., and Nes I.F. Plantaricin W from Lactobacillus plantarum belongs to a new family of two-peptide lantibiotics. Microbiology 147 (2001) 643-651
28. Hughes D. Exploiting genomics, genetics and chemistry to combat antibiotic resistance. Nat Rev Genet 4 (2003) 432-441
29. Håvarstein L.S., Diep D.B., and Nes I.F. A family of bacteriocin ABC transporters carry out proteolytic processing of their substrates concomitant with export. Mol Microbiol 16 (1995) 229-240
30. Jimenez-Diaz R., Rios-Sanchez R.M., Desmazeaud M., Ruiz-Barba J.L., and Piard J.C. Plantaricins S and T, two new bacteriocins produced by Lactobacillus plantarum LPCO10 isolated from a green olive fermentation. Appl Environ Microbiol 59 (1993) 1416-1424
31. Johnsborg O., Diep D.B., and Nes I.F. Structural analysis of the peptide pheromone receptor PlnB, a histidine protein kinase from Lactobacillus plantarum. J Bacteriol 185 (2003) 6913-6920
32. Johnsborg O., Godager L.H., and Nes I.F. Identification of a region involved in the pheromone receptor function of the histidine kinase PlnB. Arch Microbiol 182 (2004) 450-457
33. Klarin B., Johansson M.L., Molin G., Larsson A., and Jeppsson B. Adhesion of the probiotic bacterium Lactobacillus plantarum 299v onto the gut mucosa in critically ill patients: a randomised open trial. Crit Care 9 (2005) R285-R293
34. Kleerebezem M. Quorum sensing control of lantibiotic production; nisin and subtilin autoregulate their own biosynthesis. Peptides 25 (2004) 1405-1414
35. Kleerebezem M., Boekhorst J., van Kranenburg R., Molenaar D., Kuipers O.P., Leer R., et al. Complete genome sequence of Lactobacillus plantarum WCFS1. Proc Natl Acad Sci USA 100 (2003) 1990-1995
36. Knoll C., Divol B., and du Toit M. Genetic screening of lactic acid bacteria of oenological origin for bacteriocin-encoding genes. Food Microbiol 25 (2008) 983-991
37. Kristiansen P.E., Fimland G., Mantzilas D., and Nissen-Meyer J. Structure and mode of action of the membrane-permeabilizing antimicrobial peptide pheromone plantaricin A. J Biol Chem 280 (2005) 22945-22950
38. Kristiansen P.E., Fimland G., Mantzilas D., and Nissen-Meyer J. Structure and mode of action of the membrane-permeabilizing antimicrobial peptide pheromone plantaricin A. J Biol Chem (2005) M501620200
39. Kuipers O.P., Beerthuyzen M.M., de Ruyter P.G., Luesink E.J., and de Vos W.M. Autoregulation of nisin biosynthesis in Lactococcus lactis by signal transduction. J Biol Chem 270 (1995) 27299-27304
40. Levy S.B., and Marshall B. Antibacterial resistance worldwide: causes, challenges and responses. Nat Med 10 (2004) S122-S129
41. Maldonado-Barragan A., Ruiz-Barba J.L., and Jimenez-Diaz R. Knockout of three-component regulatory systems reveals that the apparently constitutive plantaricin-production phenotype shown by Lactobacillus plantarum on solid medium is regulated via quorum sensing. Int J Food Microbiol 130 (2009) 35-42
42. Maldonado A., Jimenez-Diaz R., and Ruiz-Barba J.L. Induction of plantaricin production in Lactobacillus plantarum NC8 after coculture with specific gram-positive bacteria is mediated by an autoinduction mechanism. J Bacteriol 186 (2004) 1556-1564
43. Maldonado A., Ruiz-Barba J.L., and Jimenez-Diaz R. Production of plantaricin NC8 by Lactobacillus plantarum NC8 is induced in the presence of different types of Gram-positive bacteria. Arch Microbiol 181 (2004) 8-16
44. Maldonado A., Ruiz-Barba J.L., and Jimenez-Diaz R. Purification and genetic characterization of plantaricin NC8, a novel coculture-inducible two-peptide bacteriocin from Lactobacillus plantarum NC8. Appl Environ Microbiol 69 (2003) 383-389
45. Marco M.L., Bongers R.S., de Vos W.M., and Kleerebezem M. Spatial and temporal expression of Lactobacillus plantarum genes in the gastrointestinal tracts of mice. Appl Environ Microbiol 73 (2007) 124-132
46. Marteau P. Living drugs for gastrointestinal diseases: the case for probiotics. Dig Dis 24 (2006) 137-147
47. McAuliffe O., Ross R.P., and Hill C. Lantibiotics: structure, biosynthesis and mode of action. FEMS Microbiol Rev 25 (2001) 285-308
48. Molenaar D., Bringel F., Schuren F.H., de Vos W.M., Siezen R.J., and Kleerebezem M. Exploring Lactobacillus plantarum genome diversity by using microarrays. J Bacteriol 187 (2005) 6119-6127
49. Molin G. Probiotics in foods not containing milk or milk constituents, with special reference to Lactobacillus plantarum 299v. Am J Clin Nutr 73 (2001) 380-385
50. Moll G.N., van den Akker E., Hauge H.H., Nissen-Meyer J., Nes I.F., Konings W.N., et al. Complementary and overlapping selectivity of the two-peptide bacteriocins plantaricin EF and JK. J Bacteriol 181 (1999) 4848-4852
51. Navarro L., Rojo-Bezares B., Saenz Y., Diez L., Zarazaga M., Ruiz-Larrea F., et al. Comparative study of the pln locus of the quorum-sensing regulated bacteriocin-producing L. plantarum J51 strain. Int J Food Microbiol 128 (2008) 390-394
52. Ndesendo V.M., Pillay V., Choonara Y.E., Buchmann E., Bayever D.N., and Meyer L.C. A review of current intravaginal drug delivery approaches employed for the prophylaxis of HIV/AIDS and prevention of sexually transmitted infections. AAPS PharmSciTech 9 (2008) 505-520
53. Nes I.F., Diep D.B., and Holo H. Bacteriocin diversity in Streptococcus and Enterococcus. J Bacteriol 189 (2007) 1189-1198
54. Nes I.F., Diep D.B., Håvarstein L.S., Brurberg M.B., Eijsink V.G.H., and Holo H. Biosynthesis of bacteriocins in lactic acid bacteria. Antonie Van Leeuwenhoek Int J Gen Mol Microbiol 70 (1996) 113-128
55. Nes I.F., Yoon S.S., and Diep D.B. Ribosomally synthesised antimicrobial peptides (bacteriocins) in lactic acid bacteria: a review. Food Sci Biotechnol 16 (2007) 675-690
56. Nieto Lozano J.C., Meyer J.N., Sletten K., Pelaz C., and Nes I.F. Purification and amino acid sequence of a bacteriocin produced by Pediococcus acidilactici. J Gen Microbiol 138 (1992) 1985-1990
57. Nissen-Meyer J., Larsen A.G., Sletten K., Daeschel M., and Nes I.F. Purification and characterization of plantaricin A, a Lactobacillus plantarum bacteriocin whose activity depends on the action of two peptides. J Gen Microbiol 139 (1993) 1973-1978
58. Nissen-Meyer J., Rogne P., Oppegard C., Haugen H.S., and Kristiansen P.E. Structure-function relationships of the non-lanthionine-containing peptide (class II) bacteriocins produced by Gram-positive bacteria. Curr Pharm Biotechnol 10 (2009) 19-37
59. Omar N.B., Abriouel H., Lucas R., Martinez-Canamero M., Guyot J.P., and Galvez A. Isolation of bacteriocinogenic Lactobacillus plantarum strains from ben saalga, a traditional fermented gruel from Burkina Faso. Int J Food Microbiol 112 (2006) 44-50
60. Oppegard C., Schmidt J., Kristiansen P.E., and Nissen-Meyer J. Mutational analysis of putative helix-helix interacting GxxxG-motifs and tryptophan residues in the two-peptide bacteriocin lactococcin G. Biochemistry 47 (2008) 5242-5249
61. Pei J., and Grishin N.V. Type II CAAX prenyl endopeptidases belong to a novel superfamily of putative membrane-bound metalloproteases. Trends Biochem Sci 26 (2001) 275-277
62. Risoen P.A., Brurberg M.B., Eijsink V.G., and Nes I.F. Functional analysis of promoters involved in quorum sensing-based regulation of bacteriocin production in Lactobacillus. Mol Microbiol 37 (2000) 619-628
63. Risoen P.A., Havarstein L.S., Diep D.B., and Nes I.F. 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
64. Risoen P.A., Johnsborg O., Diep D.B., Hamoen L., Venema G., and Nes I.F. Regulation of bacteriocin production in Lactobacillus plantarum depends on a conserved promoter arrangement with consensus binding sequence. Mol Genet Genomics 265 (2001) 198-206
65. Rojo-Bezares B., Saenz Y., Navarro L., Jimenez-Diaz R., Zarazaga M., Ruiz-Larrea F., et al. Characterization of a new organization of the plantaricin locus in the inducible bacteriocin-producing Lactobacillus plantarum J23 of grape must origin. Arch Microbiol 189 (2008) 491-499
66. Rojo-Bezares B., Saenz Y., Navarro L., Zarazaga M., Ruiz-Larrea F., and Torres C. Coculture-inducible bacteriocin activity of Lactobacillus plantarum strain J23 isolated from grape must. Food Microbiol 24 (2007) 482-491
67. Sáenz Y, Rojo-Bezares B, Navarro L, Díez L, Somalo S, Zarazaga M, et al. Genetic diversity of the pln locus among oenological Lactobacillus plantarum strains. Int J Food Microbiol., in press.
68. Sand S.L., Haug T.M., Nissen-Meyer J., and Sand O. The bacterial peptide pheromone plantaricin A permeabilizes cancerous, but not normal, rat pituitary cells and differentiates between the outer and inner membrane leaflet. J Membr Biol 216 (2007) 61-71
69. Saxelin M., Tynkkynen S., Mattila-Sandholm T., and de Vos W.M. Probiotic and other functional microbes: from markets to mechanisms. Curr Opin Biotechnol 16 (2005) 204-211
70. Seegers J.F. Lactobacilli as live vaccine delivery vectors: progress and prospects. Trends Biotechnol 20 (2002) 508-515
71. Sinensky M. Recent advances in the study of prenylated proteins. Biochim Biophys Acta 1484 (2000) 93-106
72. Singh A.K., and Ramesh A. Succession of dominant and antagonistic lactic acid bacteria in fermented cucumber: insights from a PCR-based approach. Food Microbiol 25 (2008) 278-287
73. Spiller R. Review article: probiotics and prebiotics in irritable bowel syndrome. Aliment Pharmacol Ther 28 (2008) 385-396
74. Straume D, Johansen RF, Bjørås M, Nes IF, Diep DB. DNA binding kinetics of two response regulators, PlnC and PlnD, from the bacteriocin regulon of Lactobacillus plantarum C11. BMC Biochem., in press.
75. Straume D., Kjos M., Nes I.F., and Diep D.B. Quorum-sensing based bacteriocin production is down-regulated by N-terminally truncated species of gene activators. Mol Genet Genomics 278 (2007) 283-293
76. Sturme M.H.J., Francke C., Siezen R.J., de Vos W.M., and Kleerebezem M. Making sense of quorum sensing in lactobacilli: a special focus on Lactobacillus plantarum WCFS1. Microbiology 153 (2007) 3939-3947
77. Trmcic A., Obermajer T., Rogelj I., and Bogovic Matijasic B. Short communication: culture-independent detection of lactic acid bacteria bacteriocin genes in two traditional slovenian raw milk cheeses and their microbial consortia. J Dairy Sci 91 (2008) 4535-4541
78. Wells J.M., and Mercenier A. Mucosal delivery of therapeutic and prophylactic molecules using lactic acid bacteria. Nat Rev Microbiol 6 (2008) 349-362