Abstract
The Escherichia coli MelR protein binds to two sites at the melAB promoter and activates transcription in response to melibiose. The binding of purified MelR to the melAB promoter and to a number of derivatives carrying point mutations has been studied. A melAB promoter fragment that is very weakly activated by the melR gene product has been made by creating multiple symmetrical changes in both MelR-binding sites. A library of random substitutions in MelR was screened to find mutants that were able to activate this mutant promoter. One of these mutants contained a substitution in a proposed helix-turn-helix region that most likely relaxes the sequence-specificity of MelR binding. The other mutants contain substitutions throughout the central part of MelR and appear to alter the conformation of MelR, such that activity is triggered at lower melibiose concentrations and by arabinose.
MeSH Terms
Base Sequence
Binding Sites
DNA-Binding Proteins/metabolism
Escherichia coli/genetics
Escherichia coli Proteins
Gene Expression Regulation, Bacterial
Genes, Suppressor
Melibiose/metabolism
Molecular Sequence Data
Operator Regions, Genetic
Operon
Promoter Regions, Genetic
Structure-Activity Relationship
Trans-Activators/metabolism
Chemicals
DNA-Binding Proteins
Escherichia coli Proteins
MelR protein, E coli
Trans-Activators
Melibiose
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Williams J
School of Biochemistry, University of Birmingham, U.K.
Michan C
Webster C
Busby S
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