Abstract
Derivatives of lambda pF13 phage in which lacZ expression (beta-galactosidase synthesis) is directed by transcription initiated at a heat-shock promoter (PrpoDhs or PgroE) were constructed and used for analysis of the heat-shock response in Escherichia coli. A wild-type strain (MC4100) lysogenic for either of these phages exhibited typical transient induction of beta-galactosidase synthesis upon a temperature shift from 30 degrees to 42 degrees C or after addition of ethanol to the medium (4% to 5%) at 30 degrees C. In contrast, most amber rpoH (htpR) mutants tested (in a Su- background) failed to respond to a temperature shift, though some mutants affected in the carboxy-terminal region exhibited a partial response. All rpoH mutants tested showed a weak but significant response to ethanol. F' plasmids carrying each of six known nonsense suppressors were then introduced into each of four rpoH amber mutants lysogenic for lambda pF13-(Phs-lacZ), creating a set of F' strains that produce sigma 32 protein with a specific amino acid substitution at a known site. Some of these strains showed an essentially normal heat-shock response while others showed little response with either or both of the promoters. In some instances, the response was significantly delayed. These results point to the usefulness of the lambda pF13-derivative phages for quantitative and systematic analysis of heat-shock response in E. coli.
MeSH Terms
Bacterial Proteins/genetics
Escherichia coli/genetics
Gene Expression Regulation
Genes, Bacterial
Heat-Shock Proteins/genetics
Operon
Promoter Regions, Genetic
Recombinant Fusion Proteins/biosynthesis,genetics
Sigma Factor/genetics
Transcription Factors/genetics
Chemicals
Bacterial Proteins
Heat-Shock Proteins
Recombinant Fusion Proteins
Sigma Factor
Transcription Factors
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Yano R
Imai M
Yura T
References (21)
21 references, click to expand
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