
pmid: 21320555
The alcohol dehydrogenase gene adhA in Corynebacterium glutamicum is subject to a complex carbon source-dependent regulation mediated by RamA, RamB and GlxR. In this study we identified SucR as the fourth transcriptional regulator involved in expression control of the adhA gene. SucR specifically binds to the adhA promoter and acts as transcriptional repressor independent of the carbon source used. Furthermore, we found that SucR negatively controls the expression of its own gene. This negative autoregulation is mediated by binding of SucR to at least one of four identified binding sites located in the promoter region of sucR. EMSA experiments and subsequent sequence analysis led to the identification of the SucR consensus binding sequence YYAACAWMAW. This binding motif is different from the binding site (ACTCTAGGGG) recently described for SucR in the promoter region of the sucCD operon. However, we were not able to detect a specific interaction of purified SucR protein with this motif present in the sucCD promoter region.
DNA, Bacterial, Binding Sites, Base Sequence, Transcription, Genetic, Alcohol dehydrogenase, Molecular Sequence Data, Alcohol Dehydrogenase, Gene Expression Regulation, Bacterial, Ethanol metabolism, Corynebacterium glutamicum, Transcriptional regulation, Bacterial Proteins, Genes, Bacterial, Genetic Loci, SucR transcriptional regulator, Gene Silencing, Promoter Regions, Genetic, Plasmids, Protein Binding
DNA, Bacterial, Binding Sites, Base Sequence, Transcription, Genetic, Alcohol dehydrogenase, Molecular Sequence Data, Alcohol Dehydrogenase, Gene Expression Regulation, Bacterial, Ethanol metabolism, Corynebacterium glutamicum, Transcriptional regulation, Bacterial Proteins, Genes, Bacterial, Genetic Loci, SucR transcriptional regulator, Gene Silencing, Promoter Regions, Genetic, Plasmids, Protein Binding
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