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PMID: 6378888 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Mutation causing reverse osmoregulation of synthesis of OmpF, a major outer membrane protein of Escherichia coli.

Journal of bacteriology ·Vol. 159 ·No. 2 ·1984-08-00 ·Pages 688-92

Nara F, Inokuchi K, Matsuyama S, Mizushima S

Abstract

Supplementation of growth media with high concentrations of substances like sucrose results in the induction of OmpC synthesis and the suppression of OmpF synthesis. We isolated a novel mutant in which OmpF synthesis is in the opposite direction from normal osmoregulation. By transductional mapping, the mutation was localized at 75 min between malA and aroB on the Escherichia coli chromosome map where the ompR-envZ region is. The mutation was suppressed by a plasmid carrying the ompR gene but not by a plasmid carrying the envZ gene alone. The mutation also resulted in the almost complete suppression of OmpC synthesis. However, the remaining OmpC synthesis was osmoregulated normally. Based on these observations, the mechanism of osmoregulation of OmpF-OmpC synthesis is discussed.

MeSH Terms
Bacterial Outer Membrane Proteins Bacterial Proteins/biosynthesis Conjugation, Genetic Escherichia coli/genetics,metabolism Genetic Complementation Test Membrane Proteins/biosynthesis,genetics Mutation Plasmids Species Specificity Transduction, Genetic Water-Electrolyte Balance
Chemicals
Bacterial Outer Membrane Proteins Bacterial Proteins Membrane Proteins
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Nara F
Inokuchi K
Matsuyama S
Mizushima S
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34 references, click to expand
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Article Info
Journal
Journal of bacteriology
Abbr.
J Bacteriol
ISSN
0021-9193
Published
1984-08-00
Pages
688-92
Language
English
Region
United States
NLM ID
2985120R
PMCID
PMC215699
Subset
IM
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