Microbiology
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


Microbiology 146 (2000), 2147-2154
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via CrossRef
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by McAuliffe, O.
Right arrow Articles by Ross, R. P.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by McAuliffe, O.
Right arrow Articles by Ross, R. P.
Agricola
Right arrow Articles by McAuliffe, O.
Right arrow Articles by Ross, R. P.
Microbiology (2000), 146, 2147-2154.
© 2000 Society for General Microbiology


Genetics and Molecular Biology

Each peptide of the two-component lantibiotic lacticin 3147 requires a separate modification enzyme for activity

Olivia McAuliffe1, Colin Hill1 and R. Paul Ross2

Department of Microbiology and National Food Biotechnology Centre, University College Cork, Ireland1
National Dairy Products Research Centre, Moorepark, Fermoy, Co. Cork, Ireland2

Author for correspondence: Colin Hill. Tel: +353 21 902397. Fax: +353 21 903101. e-mail: c.hill{at}ucc.ie

The genetic determinants for production and immunity to the two-component lantibiotic lacticin 3147 are encoded by a 12·6 kb region of the plasmid pMRC01. This region contains ten genes arranged in two divergent clusters; these include the structural genes and a number of genes whose products show significant similarity to proteins involved in the biosynthesis of other lantibiotics. Using a strategy of deletion and mutational analysis, the effect of disruption of a number of these genes was investigated. Inactivation of either of the structural genes, ltnA1 or ltnA2, resulted in mutants that were incapable of producing active lacticin 3147; however, the combination of the cell-free supernatant from both mutants resulted in a restoration of bacteriocin activity, confirming that processing and export of the structural peptides can occur independently. An unusual feature of the lacticin 3147 gene cluster is the presence of two lanM homologues, whose gene products are proposed to be involved in the dehydration and thioether-forming reactions which result in lanthionine bridge formation. Mutants created in the ltnM1 and ltnM2 genes were also incapable of lantibiotic production, confirming an essential role for these enzymes in the lacticin 3147 biosynthetic pathway and supporting the assertion that these proteins are modification enzymes. Interestingly, addition of purified LtnA1, but not purified LtnA2, to the cell-free supernatant of the ltnM1 mutant restored bacteriocin activity; in contrast, only purified LtnA2 could complement the cell-free supernatant of the ltnM2 mutant. Creation of a number of double mutants supported these findings, and confirmed that LtnM1 is required to produce mature LtnA1, while LtnM2 is required to produce mature LtnA2.

Keywords: lacticin 3147, lantibiotic production, immunity, modification enzymes

Abbreviations: ABC, ATP-binding cassette; AU, arbitrary units; CFS, cell-free supernatant




This article has been cited by other articles:


Home page
Appl. Environ. Microbiol.Home page
C. M. Guinane, P. D. Cotter, E. M. Lawton, C. Hill, and R. P. Ross
Insertional Mutagenesis To Generate Lantibiotic Resistance in Lactococcus lactis
Appl. Envir. Microbiol., July 15, 2007; 73(14): 4677 - 4680.
[Abstract] [Full Text] [PDF]


Home page
J Med MicrobiolHome page
M. C. Rea, E. Clayton, P. M. O'Connor, F. Shanahan, B. Kiely, R. P. Ross, and C. Hill
Antimicrobial activity of lacticin 3147 against clinical Clostridium difficile strains
J. Med. Microbiol., July 1, 2007; 56(7): 940 - 946.
[Abstract] [Full Text] [PDF]


Home page
Proc. Natl. Acad. Sci. USAHome page
A. L. McClerren, L. E. Cooper, C. Quan, P. M. Thomas, N. L. Kelleher, and W. A. van der Donk
Discovery and in vitro biosynthesis of haloduracin, a two-component lantibiotic
PNAS, November 14, 2006; 103(46): 17243 - 17248.
[Abstract] [Full Text] [PDF]


Home page
Appl. Environ. Microbiol.Home page
P. D. Cotter, L. A. Draper, E. M. Lawton, O. McAuliffe, C. Hill, and R. P. Ross
Overproduction of wild-type and bioengineered derivatives of the lantibiotic lacticin 3147.
Appl. Envir. Microbiol., June 1, 2006; 72(6): 4492 - 4496.
[Abstract] [Full Text] [PDF]


Home page
Proc. Natl. Acad. Sci. USAHome page
P. D. Cotter, P. M. O'Connor, L. A. Draper, E. M. Lawton, L. H. Deegan, C. Hill, and R. P. Ross
Posttranslational conversion of L-serines to D-alanines is vital for optimal production and activity of the lantibiotic lacticin 3147
PNAS, December 20, 2005; 102(51): 18584 - 18589.
[Abstract] [Full Text] [PDF]


Home page
Appl. Environ. Microbiol.Home page
P. D. Cotter, C. Hill, and R. P. Ross
A Food-Grade Approach for Functional Analysis and Modification of Native Plasmids in Lactococcus lactis
Appl. Envir. Microbiol., January 1, 2003; 69(1): 702 - 706.
[Abstract] [Full Text] [PDF]


Home page
J. Bacteriol.Home page
T. Stein, S. Borchert, B. Conrad, J. Feesche, B. Hofemeister, J. Hofemeister, and K.-D. Entian
Two Different Lantibiotic-Like Peptides Originate from the Ericin Gene Cluster of Bacillus subtilis A1/3
J. Bacteriol., March 15, 2002; 184(6): 1703 - 1711.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
INT J SYST EVOL MICROBIOL MICROBIOLOGY J GEN VIROL
J MED MICROBIOL ALL SGM JOURNALS
Copyright © 2000 Society for General Microbiology.