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Journal of Bacteriology, September 2000, p. 4926-4933, Vol. 182, No. 17
0021-9193/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
Cell-Associated Pheromone Peptide (cCF10)
Production and Pheromone Inhibition in Enterococcus
faecalis
B. A. (Leonard)
Buttaro,
M. H.
Antiporta, and
G. M.
Dunny*
Department of Microbiology, University of
Minnesota Medical School, Minneapolis, Minnesota 55455
Received 28 December 1999/Accepted 8 June 2000
In Enterococcus faecalis, the peptide cCF10 acts as a
pheromone, inducing transfer of the conjugative plasmid pCF10 from
plasmid-containing donor cells to plasmid-free recipient cells. In
these studies, it was found that a substantial amount of cCF10
associates with the envelope of the producing cell. Pheromone activity
was detected in both wall and membrane fractions, with the highest
activity associated with the wall. Experiments examining the effects of protease inhibitor treatments either prior to or following cell fractionation suggested the presence of a cell envelope-associated pro-cCF10 that can be processed to mature cCF10 by a maturase or
protease. A pCF10-encoded membrane protein, PrgY, was shown to prevent
self-induction of donor cells by reducing the level of pheromone
activity in the cell wall fraction.
*
Corresponding author. Mailing address: Department of
Microbiology, University of Minnesota Medical School, 1420 Delaware St. SE, Minneapolis, MN 55455. Phone: (612) 625-9930. Fax: (612) 626-0623. E-mail: gary-d{at}biosci.cbs.umn.edu.

Present address: Department of Microbiology and Immunology, Temple
University School of Medicine, Philadelphia, PA
19140.
Journal of Bacteriology, September 2000, p. 4926-4933, Vol. 182, No. 17
0021-9193/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
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