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| Content Provider | PubMed Central |
|---|---|
| Author | Orejas, Margarita Maccabe, Andrew P. Antonio, Pérez-gonzález José Kumar, Sudeep Ramón, Daniel |
| Copyright Year | 2001 |
| Abstract | The Aspergillus nidulans xlnB gene, which encodes the acidic endo-β-(1,4)-xylanase X24, is expressed when xylose is present as the sole carbon source and repressed in the presence of glucose. That the mutation creAd30 results in considerably elevated levels of xlnB mRNA indicates a role for the wide-domain repressor CreA in the repression of xlnB promoter (xlnBp) activity. Functional analyses of xlnBp::goxC reporter constructs show that none of the four CreA consensus target sites identified in xlnBp are functional in vivo. The CreA repressor is thus likely to exert carbon catabolite repression via an indirect mechanism rather than to influence xlnB expression by acting directly on xlnB. |
| Related Links | http://dx.doi.org/10.1128/jb.183.5.1517-1523.2001 |
| Ending Page | 1523 |
| Page Count | 7 |
| Starting Page | 1517 |
| File Format | |
| ISSN | 00219193 |
| e-ISSN | 10985530 |
| Journal | Journal of Bacteriology |
| Issue Number | 5 |
| Volume Number | 183 |
| Language | English |
| Publisher | American Society for Microbiology |
| Publisher Date | 2001-03-01 |
| Access Restriction | Open |
| Rights Holder | American Society for Microbiology |
| Subject Keyword | Molecular Biology Microbiology Research in Higher Education |
| Content Type | Text |
| Resource Type | Article |
| Subject | Molecular Biology Microbiology |
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