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J Biol Chem, Vol. 274, Issue 13, 8484-8490, March 26, 1999
Membrane Topology of the Lactococcal Bacteriocin ATP-binding
Cassette Transporter Protein LcnC
INVOLVEMENT OF LcnC IN LACTOCOCCIN A MATURATION
Christian M.
Franke,
Jan
Tiemersma,
Gerard
Venema, and
Jan
Kok
From the Department of Genetics, Groningen Biomolecular Sciences
and Biotechnology Institute, University of Groningen, Kerklaan 30, 9751 NN Haren, The Netherlands
Many non-lantibiotic bacteriocins of lactic acid
bacteria are produced as precursors with N-terminal leader peptides
different from those present in preproteins exported by the general
sec-dependent (type II) secretion pathway.
These bacteriocins utilize a dedicated (type I) secretion system for
externalization. The secretion apparatus for the lactococcins A, B, and
M/N (LcnA, B, and M/N) from Lactococcus lactis is composed
of the two membrane proteins LcnC and LcnD. LcnC belongs to the
ATP-binding cassette transporters, whereas LcnD is a protein with
similarities to other accessory proteins of type I secretion systems.
This paper shows that the N-terminal part of LcnC is involved in the
processing of the precursor of LcnA. By making translational fusions of
LcnC to the reporter proteins -galactosidase (LacZ) and alkaline
phosphatase (PhoA*), it was shown that both the N- and C-terminal parts
of LcnC are located in the cytoplasm. As the N terminus of LcnC is
required for LcnA maturation and is localized in the cytoplasm, we
conclude that the processing of the bacteriocin LcnA to its mature form takes place at the cytosolic side of the cytoplasmic membrane.
Copyright © 1999 by The American Society for Biochemistry and Molecular Biology, Inc.

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Copyright © 1999 by the American Society for Biochemistry and Molecular Biology.
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