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Originally published In Press as doi:10.1074/jbc.M211100200 on June 11, 2003
J. Biol. Chem., Vol. 278, Issue 36, 34291-34298, September 5, 2003
Novel Mechanism of Bacteriocin Secretion and Immunity Carried Out by Lactococcal Multidrug Resistance Proteins*
Olivera Gajic ,
Girbe Buist ,
Milan Kojic ,
Ljubisa Topisirovic ,
Oscar P. Kuipers and
Jan Kok ¶
From the
Department of Genetics, Groningen
Biomolecular Sciences and Biotechnology Institute, University of Groningen,
Kerklaan 30, 9751 NN Haren, The Netherlands and
Institute for Molecular Genetics and Genetic
Engineering, Vojvode Stepe 444a, 11000 Belgrade, Yugoslavia
A natural isolate of Lactococcus lactis was shown to produce two
narrow spectrum class II bacteriocins, designated LsbA and LsbB. The cognate
genes are located on a 5.6-kb plasmid within a gene cluster specifying LmrB,
an ATP-binding cassette-type multidrug resistance transporter protein. LsbA is
a hydrophobic peptide that is initially synthesized with an N-terminal
extension. The housekeeping surface proteinase HtrA was shown to be
responsible for the cleavage of precursor peptide to yield the active
bacteriocin. LsbB is a relatively hydrophilic protein synthesized without an
N-terminal leader sequence or signal peptide. The secretion of both
polypeptides was shown to be mediated by LmrB. An L. lactis strain
lacking plasmid-encoded LmrB and the chromosomally encoded LmrA is unable to
secrete either of the two bacteriocins. Complementation of the strain with an
active LmrB protein resulted in restored export of the two polypeptides across
the cytoplasmic membrane. When expressed in an L. lactis strain that
is sensitive to LsbA and LsbB, LmrB was shown to confer resistance toward both
bacteriocins. It does so, most likely, by removing the two polypeptides from
the cytoplasmic membrane. This is the first report in which a multidrug
transporter protein is shown to be involved in both secretion and immunity of
antimicrobial peptides.
Received for publication, October 30, 2002
, and in revised form, June 11, 2003.
* The costs of publication of this article were defrayed in part by the
payment of page charges. This article must therefore be hereby marked
"advertisement" in accordance with 18 U.S.C. Section 1734
solely to indicate this fact.
¶
To whom correspondence should be addressed. Tel.: 31-50-3632111; Fax:
31-50-3632348; E-mail:
j.kok{at}biol.rug.nl.

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Copyright © 2003 by the American Society for Biochemistry and Molecular Biology.
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