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Effects of structural changes in the dsdA-dsdC intergenic region on D-serine deaminase synthesis
- Publication Year :
- 1991
-
Abstract
- Single-base-pair changes well upstream of its transcription initiation site resulted in partially to fully constitutive expression of the D-serine deaminase structural gene, dsdA, independently of the cyclic AMP-cyclic AMP-binding protein complex and of the specific D-serine deaminase activator protein. These promoter mutations appear to define a consensus sequence that is repeated several times. Basal expression of dsdA+ was also strongly enhanced by subcloning on multicopy plasmids, by the DNA gyrase inhibitor novobiocin, and in dsdC(Con) mutants by increasing growth temperature. These results suggest that activation of dsdA+ expression by the dsdC-encoded protein involves distortion of promoter DNA. A dsdA translation start at bp -731 was verified by subcloning of dsdC+. Plasmid-specified activator at a high concentration interfered with chromosomal dsdC(Con) expression, and the interference was enhanced by deletion of most of the intergenic region from the plasmid. Even at a high concentration, however, plasmid-specified activator did not activate expression of chromosomal dsdA+, and in one case it was actually repressive. These results confirm the strong cis tropism of plasmid-specified dsdC-encoded protein and suggest that it is mediated by multiple sites in the dsdA-dsdC intergenic region.
- Subjects :
- Isopropyl Thiogalactoside
L-Serine Dehydratase
Transcription, Genetic
Molecular Sequence Data
Restriction Mapping
Biology
Microbiology
Plasmid
Gene expression
Consensus Sequence
Consensus sequence
Escherichia coli
Serine
Cloning, Molecular
Promoter Regions, Genetic
Molecular Biology
Gene
Repetitive Sequences, Nucleic Acid
Base Sequence
Activator (genetics)
Structural gene
Temperature
Promoter
Gene Expression Regulation, Bacterial
Molecular biology
Introns
Subcloning
Genes, Bacterial
Protein Biosynthesis
Novobiocin
Research Article
Subjects
Details
- Language :
- English
- Database :
- OpenAIRE
- Accession number :
- edsair.doi.dedup.....c2e290bd47e76de983ddfb43d2fa49ea