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PMID: 2014002 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S. Review

The molecular basis of carbon-starvation-induced general resistance in Escherichia coli.

Molecular microbiology ·Vol. 5 ·No. 1 ·1991-01-00 ·Pages 3-10

Matin A

Abstract

At the onset of starvation Escherichia coli undergoes a temporally ordered program of starvation gene expression involving 40-80 genes which some four hours later yields cells possessing an enhanced general resistance. Two classes of genes are induced upon carbon starvation: the cst genes, requiring cyclic AMP, and the pex genes, not requiring this nucleotide for induction. The cst genes are not involved in the development of the resistant state and are concerned with escape from starvation, while the pex gene induction appears to be associated with resistance. Many of the latter are induced in response to a variety of starvation conditions. They include heat shock and oxidation resistance genes, and some utilize minor, stationary-phase-specific sigma factors for induction during starvation. The protective role of stress proteins may be due to their ability to rescue misfolded macromolecules. The starvation promoters can be potentially useful for selective expression of desired genes in metabolically sluggish populations, e.g. in high-density industrial fermentations and in situ bioremediation.

Related Genes
MeSH Terms
Bacterial Proteins/biosynthesis,genetics Base Sequence Carbon/metabolism DNA, Bacterial Escherichia coli/genetics,growth & development,metabolism Gene Expression Regulation, Bacterial Molecular Sequence Data Promoter Regions, Genetic Transcriptional Activation
Chemicals
Bacterial Proteins DNA, Bacterial Carbon
Authors & Affiliations
1 authors, click to expand affiliations / ORCID
Matin A
Department of Microbiology and Immunology, Stanford University, California 94305-5402.
Article Info
Journal
Molecular microbiology
Abbr.
Mol Microbiol
ISSN
0950-382X
Published
1991-01-00
Pages
3-10
Language
English
Region
England
NLM ID
8712028
Subset
IM
Grants
NIGMS NIH HHS · 1R01-GM42159 · United States
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