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PMID: 190211 Published · ppublish English Journal Article Research Support, U.S. Gov't, Non-P.H.S.

Constitutive mutations in the controlling site region of the araBAD operon of Escherichia coli B/r that decrease sensitivity to catabolite repression.

Journal of bacteriology ·Vol. 129 ·No. 2 ·1977-02-00 ·Pages 948-58

Colomé J, Wilcox G, Englesberg E

Abstract

Strains of Escherichia coli B/r containing a deletion of the regulatory gene araC are Ara-. Slow-growing revertants of these strains were isolated and designated aralc because they contain a second mutation in a controlling site, aral, that allows for a low level of constitutive expression of the araBAD operon (Englesbert et al., 1969). We mutagenized aralc delta C strains and selected mutants that grow faster in mineral L-arabinose medium. The new mutations, called araXc, map very close to the original aralc mutations and are in the controlling site region between araB and araC. The aralcXc delta C strains have a higher constitutive level of expression of the araBAD operon than the aralc delta C parents. The araXc mutations are cis acting and decrease the araBAD operon's sensitivity to catabolite repression. The araBAD operon is expressed equally well in ara delta C and ara C cya crp backgrounds. The repressor form of ara C protein is able to repress the constitutive synthesis due to the ara Xc allele.

MeSH Terms
Arabinose/metabolism Carbohydrate Epimerases/metabolism Chromosome Mapping Enzyme Repression Escherichia coli/enzymology,metabolism Genes Genes, Regulator Glucose/metabolism Glycerol/metabolism Mutation Operon Phosphotransferases/metabolism
Chemicals
Arabinose Phosphotransferases Carbohydrate Epimerases Glucose Glycerol
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Colomé J
Wilcox G
Englesberg E
References (14)
14 references, click to expand
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Article Info
Journal
Journal of bacteriology
Abbr.
J Bacteriol
ISSN
0021-9193
Published
1977-02-00
Pages
948-58
Language
English
Region
United States
NLM ID
2985120R
PMCID
PMC235033
Subset
IM
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