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PMID: 2521619 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Effect of mutations in the cyclic AMP receptor protein-binding site on araBAD and araC expression.

Journal of bacteriology ·Vol. 171 ·No. 2 ·1989-02-00 ·Pages 1178-84

Stoltzfus L, Wilcox G

Abstract

Maximum expression of the adjacent but divergently transcribed araBAD operon and araC gene requires the presence of cyclic AMP (cAMP) and the cAMP receptor protein (CRP). DNase I protection studies have previously revealed a high-affinity CRP-binding site in the ara regulatory region. Deletion mutations introduced into this site resulted in reduced expression of araBAD and araC. However, other experiments have demonstrated that spacing changes in the ara regulatory region may have multiple effects due to disruption of a DNA loop. Thus, the deletions could have destroyed the CRP-binding site, the ability to form a loop, or both. In the present study, substitution mutations were introduced into the CRP site in order to avoid creating spacing changes. We found that a 3-base-pair substitution resulted in a 30% reduction in araBAD expression, whereas a 6-base-pair substitution resulted in an 80% reduction. Both of these substitution mutations reduced araC expression threefold. We conclude that CRP bound to this site regulates expression in both directions. We found that a spacing change in the CRP site does not alter araBAD expression any more than does a substitution mutation.

MeSH Terms
Arabinose/metabolism Base Sequence Escherichia coli/genetics Genes Genes, Bacterial Genes, Regulator Genes, araC Molecular Sequence Data Mutation Plasmids Receptors, Cyclic AMP/genetics Transcription, Genetic
Chemicals
Receptors, Cyclic AMP Arabinose
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Stoltzfus L
Department of Microbiology, University of California, Los Angeles 90024.
Wilcox G
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42 references, click to expand
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Article Info
Journal
Journal of bacteriology
Abbr.
J Bacteriol
ISSN
0021-9193
Published
1989-02-00
Pages
1178-84
Language
English
Region
United States
NLM ID
2985120R
PMCID
PMC209717
Subset
IM
Grants
NIGMS NIH HHS · GM07185 · United States
NIGMS NIH HHS · GM30896 · United States
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