Affiliation:
1. Department of Microbiology and Molecular Genetics, Harvard Medical School, Boston, Massachusetts 02115
Abstract
ABSTRACT
Previously an
Escherichia coli
mutant that had acquired the ability to grow on propanediol as the sole carbon and energy source was isolated. This phenotype is the result of the constitutive expression of the
fucO
gene (in the
fucAO
operon), which encodes one of the enzymes in the fucose metabolic pathway. The mutant was found to bear an IS
5
insertion in the intergenic regulatory region between the divergently oriented
fucAO
and
fucPIK
operons. Though expression of the
fucAO
operon was constitutive, the
fucPIK
operon became noninducible such that the mutant could no longer grow on fucose. A fucose-positive revertant which was found to contain a suppressor mutation in the
crp
gene was selected. Here we identify this
crp
mutation, which results in a single amino acid substitution (K52N) that has been proposed previously to uncover a cryptic activating region in the cyclic AMP receptor protein (CRP). We show that the mutant CRP constitutively activates transcription from both the IS
5
-disrupted and the wild-type
fucPIK
promoters, and we identify the CRP-binding site that is required for this activity. Our results show that the
fucPIK
promoter, a complex promoter which ordinarily depends on both CRP and the fucose-specific regulator FucR for its activation, can be activated in the absence of FucR by a mutant CRP that uses three, rather than two, activating regions to contact RNA polymerase. For the IS
5
-disrupted promoter, which retains a single CRP-binding site, the additional activating region of the mutant CRP evidently compensates for the lack of upstream regulatory sequences.
Publisher
American Society for Microbiology
Subject
Molecular Biology,Microbiology
Cited by
10 articles.
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