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PMID: 2163388 Published · ppublish English Journal Article Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S.

Cloning and in vivo and in vitro regulation of cyclic AMP-dependent carbon starvation genes from Escherichia coli.

Journal of bacteriology ·Vol. 172 ·No. 7 ·1990-07-00 ·Pages 3813-20

Blum PH, Jovanovich SB, McCann MP, Schultz JE, Lesley SA, Burgess RR, Matin A

Abstract

The regulation of three Escherichia coli carbon starvation (cst) genes fused to lacZ was examined. Expression of these genes is induced by starvation for a carbon source. The role of carbon and cyclic AMP (cAMP) availability and of an altered-function crp mutation were investigated for their effect on cst expression in vivo. The experiments indicated that cAMP concentrations controlled the absolute expression of one cst fusion, but the other two cst fusions were dependent upon some component not present in exponentially growing cells under conditions of glucose excess, even when cAMP was added. To examine the regulation of these genes in further detail, the three cst::lacZ fusions were cloned on multicopy plasmids. All three cst::lacZ fusions retained their inducible regulatory phenotype in the multicopy state. Analysis of the expression of the cloned cst::lacZ fusions in an in vitro-coupled transcription-translation cell-free system demonstrated that the predominant promoter(s) present on each cloned DNA was dependent on sigma 70 for expression. In vitro cAMP titration curves indicated that this molecule was necessary and sufficient for the expression of one fusion but not sufficient for the second fusion, while the third fusion exhibited constitutive levels of expression in vitro. The results are discussed in the context of the E. coli carbon starvation response.

MeSH Terms
Antibodies, Monoclonal Carbon/metabolism Cloning, Molecular/methods Cyclic AMP/metabolism,pharmacology Escherichia coli/drug effects,genetics,metabolism Gene Expression Regulation, Bacterial Genes, Bacterial Genotype Mutation Promoter Regions, Genetic Protein Biosynthesis Recombinant Fusion Proteins/metabolism Sigma Factor/immunology,metabolism Transcription, Genetic beta-Galactosidase/genetics,metabolism
Chemicals
Antibodies, Monoclonal Recombinant Fusion Proteins Sigma Factor Carbon Cyclic AMP beta-Galactosidase
Authors & Affiliations
7 authors, click to expand affiliations / ORCID
Blum P H
Department of Microbiology and Immunology, Stanford University, California 94305-5402.
Jovanovich S B
McCann M P
Schultz J E
Lesley S A
Burgess R R
Matin A
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Article Info
Journal
Journal of bacteriology
Abbr.
J Bacteriol
ISSN
0021-9193
Published
1990-07-00
Pages
3813-20
Language
English
Region
United States
NLM ID
2985120R
PMCID
PMC213360
Subset
IM
Grants
NIGMS NIH HHS · GM42159 · United States
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