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Infection and Immunity, September 1999, p. 4510-4516, Vol. 67, No. 9
0019-9567/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
Stress-Induced Membrane Association of the Streptococcus
mutans GTP-Binding Protein, an Essential G Protein, and
Investigation of Its Physiological Role by Utilizing an Antisense
RNA Strategy
Didi
Baev,1
Reg
England,2 and
Howard
K.
Kuramitsu1,*
Department of Oral Biology, State University
of New York, Buffalo, New York 14214,1 and
Department of Biological Sciences, University of Central
Lancashire, Preston PR1 2HE, United Kingdom2
Received 26 April 1999/Returned for modification 19 May
1999/Accepted 7 June 1999
SGP (for Streptococcus GTP-binding protein) is a
Streptococcus mutans essential GTPase which has significant
sequence identity to the previously identified Escherichia
coli Era protein and to numerous other prokaryotic GTPase
proteins of unknown function. Recent studies in our laboratory have
addressed the possible role of SGP in the stress response of the oral
pathogen S. mutans. Here we report that during growth in
the early stationary phase, and in response to elevated temperatures or
acidic pH, the distribution of SGP between the cytoplasm and the
membranes of S. mutans cells varies. Immunoblot analysis of
soluble and membrane protein fractions collected from the mid-log and
early stationary growth phases of bacterial populations grown at normal
temperature (37°C) and at the elevated temperature of 43°C, or at
acidic pH, demonstrated that the total amount of SGP increased with the
age of the bacterial culture, elevated temperature, or acidic pH.
Furthermore, it was established that a substantial amount of SGP is
associated with the membrane fraction under stress conditions. In order
to investigate the physiological role of SGP, we constructed an
S. mutans strain capable of chromosomal
sgp antisense RNA expression, which interferes with the
normal information processing of the sgp gene. Utilizing this strain, we determined conditions whereby the streptococcal cells
can be depleted of SGP, thus avoiding the problem of constructing a
conditional lethal system. From the results of measurements of the
nucleotide pools extracted from the antisense strain and its isogenic
counterpart, we propose that one of the physiological roles of SGP is
regulation and modulation of the GTP/GDP ratio under different growth
conditions. Moreover, we observed that in SGP-depleted cells the levels
of glucan-binding protein A (GbpA) substantially increased, suggesting
that GbpA may have stress response-related physiological functions.
Finally, the potential applications of the antisense RNA approach that
we employed are discussed.
*
Corresponding author. Mailing address: SUNY at Buffalo,
Department of Oral Biology, 3435 Main St., Buffalo, NY 14214. Phone: (716) 829-2068. Fax: (716) 829-3942. E-mail:
kuramits{at}acsu.buffalo.edu.
Infection and Immunity, September 1999, p. 4510-4516, Vol. 67, No. 9
0019-9567/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
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