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Infection and Immunity, February 1999, p. 694-699, Vol. 67, No. 2
Department of Oral Biology, State University
of New York, Buffalo, New York 14214
Received 26 May 1998/Returned for modification 21 July
1998/Accepted 2 November 1998
Immediately downstream from the previously isolated Treponema
denticola ATCC 35405 prtB gene coding for a
chymotrypsinlike protease activity, an open reading frame, ORF3, was
identified which shared significant homology with the highly
conserved domains (HCDs) of bacterial methyl-accepting chemotaxis
proteins (MCPs). Nucleotide sequencing of this ORF revealed that the
gene would code for a protein with a size of approximately 41 kDa. In
addition, this sequence contained a domain which was virtually
identical to the HCD of a recently characterized MCP, DmcA, of strain
35405. Therefore, this ORF was named dmcB. Northern blot
analysis suggested that dmcB was part of an operon
structure containing prtB. Insertional inactivation of
dmcB utilizing an ermF-ermAM cassette resulted in a mutant with decreased chemoattraction toward nutrient supplements. In addition, the mutant displayed an altered pattern of methylated proteins under conditions of chemotaxis. Inactivation of the
dmcB gene also attenuated the methylation of the DmcA
protein. These results suggest that the dmcB gene codes for
an MCP in T. denticola which may interact with other MCPs
in these organisms.
0019-9567/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
Characterization of a Novel Methyl-Accepting Chemotaxis Gene,
dmcB, from the Oral Spirochete Treponema
denticola


*
Corresponding author. Mailing address: Department
of Oral Biology, SUNY, 3435 Main St., Buffalo, NY 14214. Phone: (716)
829-2068. Fax: (716) 829-3942. E-mail:
Kuramits{at}ACSU.BUFFALO.EDU.
Present address: Department of General Dentistry, Eastman Dental
Center, Rochester, NY 14642.
Present address: Department of Periodontology, Tokyo Medical and
Dental University, Tokyo, Japan.
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