Literature DB >> 7603408

Bacteriocins of gram-positive bacteria.

R W Jack1, J R Tagg, B Ray.   

Abstract

In recent years, a group of antibacterial proteins produced by gram-positive bacteria have attracted great interest in their potential use as food preservatives and as antibacterial agents to combat certain infections due to gram-positive pathogenic bacteria. They are ribosomally synthesized peptides of 30 to less than 60 amino acids, with a narrow to wide antibacterial spectrum against gram-positive bacteria; the antibacterial property is heat stable, and a producer strain displays a degree of specific self-protection against its own antibacterial peptide. In many respects, these proteins are quite different from the colicins and other bacteriocins produced by gram-negative bacteria, yet customarily they also are grouped as bacteriocins. Although a large number of these bacteriocins (or bacteriocin-like inhibitory substances) have been reported, only a few have been studied in detail for their mode of action, amino acid sequence, genetic characteristics, and biosynthesis mechanisms. Nevertheless, in general, they appear to be translated as inactive prepeptides containing an N-terminal leader sequence and a C-terminal propeptide component. During posttranslational modifications, the leader peptide is removed. In addition, depending on the particular type, some amino acids in the propeptide components may undergo either dehydration and thioether ring formation to produce lanthionine and beta-methyl lanthionine (as in lantibiotics) or thio ester ring formation to form cystine (as in thiolbiotics). Some of these steps, as well as the translocation of the molecules through the cytoplasmic membrane and producer self-protection against the homologous bacteriocin, are mediated through specific proteins (enzymes). Limited genetic studies have shown that the structural gene for such a bacteriocin and the genes encoding proteins associated with immunity, translocation, and processing are present in a cluster in either a plasmid, the chromosome, or a transposon. Following posttranslational modification and depending on the pH, the molecules may either be released into the environment or remain bound to the cell wall. The antibacterial action against a sensitive cell of a gram-positive strain is produced principally by destabilization of membrane functions. Under certain conditions, gram-negative bacterial cells can also be sensitive to some of these molecules. By application of site-specific mutagenesis, bacteriocin variants which may differ in their antimicrobial spectrum and physicochemical characteristics can be produced. Research activity in this field has grown remarkably but sometimes with an undisciplined regard for conformity in the definition, naming, and categorization of these molecules and their genetic effectors. Some suggestions for improved standardization of nomenclature are offered.

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Year:  1995        PMID: 7603408      PMCID: PMC239359          DOI: 10.1128/mr.59.2.171-200.1995

Source DB:  PubMed          Journal:  Microbiol Rev        ISSN: 0146-0749


  166 in total

1.  Some chemical and physical properties of nisin, a small-protein antibiotic produced by Lactococcus lactis.

Authors:  W Liu; J N Hansen
Journal:  Appl Environ Microbiol       Date:  1990-08       Impact factor: 4.792

2.  Cloning of two bacteriocin genes from a lactococcal bacteriocin plasmid.

Authors:  M J van Belkum; B J Hayema; A Geis; J Kok; G Venema
Journal:  Appl Environ Microbiol       Date:  1989-05       Impact factor: 4.792

3.  Interaction of the pore forming-peptide antibiotics Pep 5, nisin and subtilin with non-energized liposomes.

Authors:  M Kordel; F Schüller; H G Sahl
Journal:  FEBS Lett       Date:  1989-02-13       Impact factor: 4.124

4.  Some possible autoimmune mechanisms in rheumatic carditis.

Authors:  J R Tagg; A R McGiven
Journal:  Lancet       Date:  1972-09-30       Impact factor: 79.321

5.  Mode of action of the peptide antibiotic nisin and influence on the membrane potential of whole cells and on cytoplasmic and artificial membrane vesicles.

Authors:  E Ruhr; H G Sahl
Journal:  Antimicrob Agents Chemother       Date:  1985-05       Impact factor: 5.191

Review 6.  Control of antibiotic biosynthesis.

Authors:  J F Martin; A L Demain
Journal:  Microbiol Rev       Date:  1980-06

7.  Characterization and purification of helveticin J and evidence for a chromosomally determined bacteriocin produced by Lactobacillus helveticus 481.

Authors:  M C Joerger; T R Klaenhammer
Journal:  J Bacteriol       Date:  1986-08       Impact factor: 3.490

8.  The effect of nisin on murein synthesis.

Authors:  P Reisinger; H Seidel; H Tschesche; W P Hammes
Journal:  Arch Microbiol       Date:  1980-10       Impact factor: 2.552

9.  Interaction of the staphylococcin-like peptide Pep 5 with cell walls and isolated cell wall components of Gram-positive bacteria.

Authors:  H G Sahl; C Hahn; H Brandis
Journal:  Zentralbl Bakteriol Mikrobiol Hyg A       Date:  1985-10

Review 10.  Lantibiotics--unusually modified bacteriocin-like peptides from gram-positive bacteria.

Authors:  G Bierbaum; H G Sahl
Journal:  Zentralbl Bakteriol       Date:  1993-02
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  326 in total

1.  Biological activities and structural properties of the atypical bacteriocins mesenterocin 52b and leucocin b-ta33a.

Authors:  C Corbier; F Krier; G Mulliert; B Vitoux; A M Revol-Junelles
Journal:  Appl Environ Microbiol       Date:  2001-04       Impact factor: 4.792

2.  MICs of mutacin B-Ny266, nisin A, vancomycin, and oxacillin against bacterial pathogens.

Authors:  M Mota-Meira; G LaPointe; C Lacroix; M C Lavoie
Journal:  Antimicrob Agents Chemother       Date:  2000-01       Impact factor: 5.191

3.  Bacteriocin production with Lactobacillus amylovorus DCE 471 is improved and stabilized by fed-batch fermentation.

Authors:  R Callewaert; L De Vuyst
Journal:  Appl Environ Microbiol       Date:  2000-02       Impact factor: 4.792

4.  Mutational analysis of the sbo-alb locus of Bacillus subtilis: identification of genes required for subtilosin production and immunity.

Authors:  G Zheng; R Hehn; P Zuber
Journal:  J Bacteriol       Date:  2000-06       Impact factor: 3.490

5.  In vitro activities of polycationic peptides alone and in combination with clinically used antimicrobial agents against Rhodococcus equi.

Authors:  A Giacometti; O Cirioni; F Ancarani; M S Del Prete; M Fortuna; G Scalise
Journal:  Antimicrob Agents Chemother       Date:  1999-08       Impact factor: 5.191

6.  Pulsed-electric field treatment enhances the bactericidal action of nisin against Bacillus cereus.

Authors:  I E Pol; H C Mastwijk; P V Bartels; E J Smid
Journal:  Appl Environ Microbiol       Date:  2000-01       Impact factor: 4.792

7.  Bacteriocin production by Lactobacillus salivarius of animal origin.

Authors:  B Robredo; C Torres
Journal:  J Clin Microbiol       Date:  2000-10       Impact factor: 5.948

8.  Detection of bacteriocins by matrix-assisted laser Desorption/Ionization time-of-flight mass spectrometry

Authors: 
Journal:  Appl Environ Microbiol       Date:  1999-05       Impact factor: 4.792

9.  Production of bacteriocins by different enterococcal isolates.

Authors:  A Lauková; M Mareková
Journal:  Folia Microbiol (Praha)       Date:  2001       Impact factor: 2.099

10.  Microcin E492, a channel-forming bacteriocin from Klebsiella pneumoniae, induces apoptosis in some human cell lines.

Authors:  Claudio Hetz; María Rosa Bono; Luis Felipe Barros; Rosalba Lagos
Journal:  Proc Natl Acad Sci U S A       Date:  2002-03-05       Impact factor: 11.205

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