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J Bacteriol, May 1998, p. 2402-2408, Vol. 180, No. 9
HSP Research Institute, Kyoto Research Park,
Kyoto 600, Japan
Received 10 November 1997/Accepted 27 February 1998
The heat shock response in Escherichia coli is mediated
primarily by the rpoH gene, encoding
0021-9193/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
Regulatory Conservation and Divergence of
32 Homologs from Gram-Negative Bacteria: Serratia
marcescens, Proteus mirabilis, Pseudomonas
aeruginosa, and Agrobacterium tumefaciens
32,
which is specifically required for transcription of heat shock genes. A
number of
32 homologs have recently been cloned from
gram-negative bacteria that belong to the gamma or alpha subdivisions
of the proteobacteria. We report here some of the regulatory features
of several such homologs (RpoH) expressed in E. coli as
well as in respective cognate bacteria. When expressed in an E. coli
rpoH strain lacking its own
32, these homologs activated the transcription of heat
shock genes (groE and dnaK) from the start
sites normally used in E. coli. The level of RpoH in
Serratia marcescens and Pseudomonas aeruginosa cells was very low at 30°C but was elevated markedly upon a shift to
42°C, as found previously with E. coli. The increased
RpoH levels upon heat shock resulted from both increased synthesis and
stabilization of the normally unstable RpoH protein. In contrast, the
RpoH level in Proteus mirabilis was relatively high at
30°C and increased less markedly upon heat shock, mostly by increased synthesis; this
32 homolog was already stable at 30°C,
and little further stabilization occurred upon the shift to 42°C. The
increased synthesis of RpoH homologs in all these gamma proteobacteria
was observed even in the presence of rifampin, suggesting that the
induction occurred at the level of translation. Thus, the basic
regulatory strategy of the heat shock response by enhancing the RpoH
level is well conserved in the gamma proteobacteria, but some
divergence in the actual mechanisms used occurred during evolution.
*
Corresponding author. Mailing address: HSP Research
Institute, Kyoto Research Park, Kyoto 600, Japan. Phone:
(81)-75-315-8619. Fax: (81)-75-315-8659. E-mail:
tyura{at}hsp.co.jp.
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