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PMID: 2842291 Published · ppublish English Journal Article Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S.

Differential regulation by cyclic AMP of starvation protein synthesis in Escherichia coli.

Journal of bacteriology ·Vol. 170 ·No. 9 ·1988-09-00 ·Pages 3903-9

Schultz JE, Latter GI, Matin A

Abstract

Of the 30 carbon starvation proteins whose induction has been previously shown to be important for starvation survival of Escherichia coli, two-thirds were not induced in cya or crp deletion mutants of E. coli at the onset of carbon starvation. The rest were induced, although not necessarily with the same temporal pattern as exhibited in the wild type. The starvation proteins that were homologous to previously identified heat shock proteins belonged to the latter class and were hyperinduced in delta cya or delta crp mutants during starvation. Most of the cyclic AMP-dependent proteins were synthesized in the delta cya mutant if exogenous cyclic AMP was added at the onset of starvation. Furthermore, beta-galactosidase induction of several carbon starvation response gene fusions occurred only in a cya+ genetic background. Thus, two-thirds of the carbon starvation proteins of E. coli require cyclic AMP and its receptor protein for induction; the rest do not. The former class evidently has no role in starvation survival, since delta cya or delta crp mutants of either E. coli or Salmonella typhimurium survived starvation as well as their wild-type parents did. The latter class, therefore, is likely to have a direct role in starvation survival. This possibility is strengthened by the finding that nearly all of the cya- and crp-independent proteins were also induced during nitrogen starvation and, as shown previously, during phosphate starvation. Proteins whose synthesis is independent of cya- and crp control are referred to as Pex (postexponential).

MeSH Terms
Bacterial Proteins/biosynthesis Cloning, Molecular Cyclic AMP/physiology Escherichia coli/genetics,growth & development,metabolism Genes, Bacterial Kinetics Mutation Nitrogen/metabolism Transduction, Genetic
Chemicals
Bacterial Proteins Cyclic AMP Nitrogen
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Schultz J E
Department of Microbiology and Immunology, Stanford University School of Medicine, California 94305-5402.
Latter G I
Matin A
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Article Info
Journal
Journal of bacteriology
Abbr.
J Bacteriol
ISSN
0021-9193
Published
1988-09-00
Pages
3903-9
Language
English
Region
United States
NLM ID
2985120R
PMCID
PMC211388
Subset
IM
Grants
NIGMS NIH HHS · GM 07276-13 · United States
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