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Journal of Bacteriology, December 1999, p. 7373-7380, Vol. 181, No. 23
Department of Biology, Biotechnical Faculty,
University of Ljubljana, Ve
Received 26 May 1999/Accepted 23 September 1999
Colicin-producing strains occur frequently in natural populations
of Escherichia coli, and colicinogenicity seems to provide a competitive advantage in the natural habitat. A cka-lacZ
fusion was used to study the regulation of expression of the colicin K
structural gene. Expression is growth phase dependent, with high
activity in the late stationary phase. Nutrient depletion induces the
expression of cka due to an increase in ppGpp. Temperature is a strong signal for cka expression, since only
basal-level activity was detected at 22°C. Mitomycin C induction
demonstrates that cka expression is regulated to a lesser
extent by the SOS response independently of ppGpp. Increased osmolarity
induces a partial increase, while the global regulator integration host factor inhibits expression in the late stationary phase. Induction of
cka was demonstrated to be independent of the cyclic
AMP-Crp complex, carbon source, RpoS, Lrp, H-NS, pH, and short-chain
fatty acids. In contrast to colicin E1, cka expression is
independent of catabolite repression and is partially affected by
anaerobiosis only upon SOS induction. These results indicate that while
different colicins are expressed in response to some common signals
such as nutrient depletion, the expression of individual colicins could be further influenced by specific environmental cues.
0021-9193/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
Transcription Regulation of the Colicin K
cka Gene Reveals Induction of Colicin Synthesis by
Differential Responses to Environmental Signals
gur-Bertok*
na pot 111, 1000 Ljubljana, Slovenia
*
Corresponding author. Mailing address: Department of
Biology, Biotechnical Faculty, University of Ljubljana, Ve
na pot
111, 1000 Ljubljana, Slovenia. Phone: 386 61 123 33 88. Fax: 386 61 273 390. E-mail: Darja.Zgur{at}uni-Lj.Si.
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