Analysis of the Corynebacterium glutamicum dapA promoter
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Updated: Oct 19, 2026

Methods to Discover Alternative Promoter Usage and Transcriptional Regulation of Murine Bcrp1
Published on: May 27, 2016
P Vasicová1, M Pátek, J Nesvera
1Institute of Microbiology, Academy of Sciences of the Czech Republic, CZ-14220 Praha 4, Czech Republic.
Abstract:
Deletion and mutational analysis of the promoter P-dapA from Corynebacterium glutamicum was performed to identify regions and particular nucleotides important for its function. An extended -10 region and a stretch of six T's at positions -55 to -50 were found to be the most important elements in the promoter function. The results of mutational analysis of P-dapA are consistent with the conclusions of statistical computer-aided analysis of 44 C. glutamicum promoter sequences.
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