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Journal of Bacteriology, July 2001, p. 3903-3909, Vol. 183, No. 13
0021-9193/01/$04.00+0 DOI: 10.1128/JB.183.13.3903-3909.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.
Signaling System in Porphyromonas gingivalis
Based on a LuxS Protein
Whasun O.
Chung,1
Yoonsuk
Park,1,*
Richard J.
Lamont,1
Rod
McNab,2
Bruno
Barbieri,2 and
Donald
R.
Demuth3
Department of Oral Biology, University of
Washington, Seattle, Washington 981951;
Department of Microbiology, Eastman Dental Institute, London,
United Kingdom2; and
Department of Biochemistry, University of Pennsylvania,
Philadelphia, Pennsylvania 191043
Received 3 January 2001/Accepted 12 April 2001
The luxS gene of quorum-sensing Vibrio
harveyi is required for type 2 autoinducer production. We
identified a Porphyromonas gingivalis open reading
frame encoding a predicted peptide of 161 aa that shares 29%
identity with the amino acid sequence of the LuxS protein of V.
harveyi. Conditioned medium from a late-log-phase P.
gingivalis culture induced the luciferase operon of V.
harveyi, but that from a luxS insertional mutant
did not. In P. gingivalis, the expression of
luxS mRNA was environmentally controlled and varied
according to the cell density and the osmolarity of the culture medium.
In addition, differential display PCR showed that the inactivation of
P. gingivalis luxS resulted in up-regulation of a hemin
acquisition protein and an arginine-specific protease and reduced
expression of a hemin-regulated protein, a TonB homologue, and an
excinuclease. The data suggest that the luxS gene in
P. gingivalis may function to control the expression of
genes involved in the acquisition of hemin.
*
Corresponding author. Mailing address: Mail Stop
357132, Department of Oral Biology, University of Washington, Seattle,
WA 98195-7132. Phone: (206) 543-5477. Fax: (206) 685-3162. E-mail: yoonpark{at}u.washington.edu.
Journal of Bacteriology, July 2001, p. 3903-3909, Vol. 183, No. 13
0021-9193/01/$04.00+0 DOI: 10.1128/JB.183.13.3903-3909.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.
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