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PMID: 1490614 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

The PurR binding site in the glyA promoter region of Escherichia coli.

FEMS microbiology letters ·Vol. 78 ·No. 2-3 ·1992-12-01 ·Pages 299-304

Steiert JG, Kubu C, Stauffer GV

Abstract

Site-directed mutagenesis was used to change the PurR binding site in the control region of a glyA-lac gene fusion. Mutations that changed the PurR binding sequence away from the consensus sequence reduced PurR binding, which correlated with reduced purine-mediated repression. Mutations that changed the binding sequence toward the consensus sequence had no significant effect on either PurR binding or purine-mediated repression. Hypoxanthine and guanine, co-repressors for PurR-mediated regulation of the pur regulon, increased binding of PurR to glyA operator DNA.

Related Genes
MeSH Terms
Bacterial Proteins/metabolism Base Sequence Binding Sites DNA, Bacterial/genetics DNA-Binding Proteins/metabolism Escherichia coli/genetics,metabolism Escherichia coli Proteins Genes, Bacterial Molecular Sequence Data Mutagenesis, Site-Directed Promoter Regions, Genetic Repressor Proteins/metabolism
Chemicals
Bacterial Proteins DNA, Bacterial DNA-Binding Proteins Escherichia coli Proteins PurR protein, Bacteria PurR protein, E coli Repressor Proteins
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Steiert J G
Department of Microbiology, University of Iowa, Iowa City 52242.
Kubu C
Stauffer G V
Article Info
Journal
FEMS microbiology letters
Abbr.
FEMS Microbiol Lett
ISSN
0378-1097
Published
1992-12-01
Pages
299-304
Language
English
Region
England
NLM ID
7705721
Subset
IM
Grants
NIGMS NIH HHS · GM26876 · United States
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