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Journal of Bacteriology, March 2009, p. 1695-1702, Vol. 191, No. 5
0021-9193/09/$08.00+0 doi:10.1128/JB.01536-08
Copyright © 2009, American Society for Microbiology. All Rights Reserved.
32 Regulon in Escherichia coli
,
Gernot Rieser, and
Günther Koraimann*
Institut für Molekulare Biowissenschaften, Karl-Franzens-Universität Graz, Humboldtstrasse 50, A-8010 Graz, Austria
Received 30 October 2008/ Accepted 16 December 2008
Alternative sigma factors allow bacteria to reprogram global transcription rapidly and to adapt to changes in the environment. Here we report on growth- and cell division-dependent
32 regulon activity in Escherichia coli in batch culture. By analyzing
32 expression in growing cells, an increase in
32 protein levels is observed during the first round of cell division after exit from stationary phase. Increased
32 protein levels result from transcriptional activation of the rpoH gene. After the first round of bulk cell division, rpoH transcript levels and
32 protein levels decrease again. The late-logarithmic phase and the transition to stationary phase are accompanied by a second increase in
32 levels and enhanced stability of
32 protein but not by enhanced transcription of rpoH. Throughout growth,
32 target genes show expression patterns consistent with oscillating
32 protein levels. However, during the transition to early-stationary phase, despite high
32 protein levels, the transcription of
32 target genes is downregulated, suggesting functional inactivation of
32. It is deduced from these data that there may be a link between
32 regulon activity and cell division events. Further support for this hypothesis is provided by the observation that in cells in which FtsZ is depleted,
32 regulon activation is suppressed.
Published ahead of print on 29 December 2008.
Supplemental material for this article may be found at http://jb.asm.org/.
Present address: Roche Diagnostics Graz GmbH, Kratkystrasse 2, A-8020 Graz, Austria.
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