Abstract
Expression of an esterase gene from Streptomyces scabies is regulated by zinc in both Streptomyces scabies and Streptomyces lividans. A specific protein-binding site was identified on an esterase promoter fragment by using an S-30 extract from S. scabies. The location of the protein-binding site was determined by gel shift assays of promoter deletion fragments and by DNase I footprinting analysis. The protein-binding site maps from nucleotides -59 to -81 relative to the start of transcription. An esterase gene construct cloned and expressed in S. lividans was used to assess the importance of the protein-binding site. Deletion of the 23-bp protein-binding site resulted in a 10-fold decrease in esterase production when cells were grown in zinc- inducing conditions. The protein-binding site may represent a region involved in positive regulation of the S. scabies esterase gene.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 4287-4293 |
| Number of pages | 7 |
| Journal | Journal of bacteriology |
| Volume | 174 |
| Issue number | 13 |
| DOIs | |
| State | Published - 1992 |
Fingerprint
Dive into the research topics of 'Identification of a protein-binding sequence involved in expression of an esterase gene from Streptomyces scabies'. Together they form a unique fingerprint.Cite this
- APA
- Standard
- Harvard
- Vancouver
- Author
- BIBTEX
- RIS