This presentation focused on the transcriptional analysis of heterologous gene expression using the endogenous sD promoter from Bacillus halodurans. It concludes to a successful implementation of a high throughput mRNA sandwich hybridisation quantification assay. It also found that B. halodurans sD promoter regulated in a similar fashion in complex media as B. subtilis, that vector choice influences transcript levels, that flgM-null mutant improves transcript levels but not protein levels and that peptide production follows transcript profile for LB.
Reference:
Crampton, M.C. 2010. Transcriptional analysis of heterologous gene expression using the endogenous sD promoter from Bacillus halodurans. 11th International Symposium of the Genetics of Industrial Microorganisms, Melbourne, Australia, June 28- July 1, 2010, pp 18
Crampton, M. C. (2010). Transcriptional analysis of heterologous gene expression using the endogenous sD promoter from Bacillus halodurans. CSIR. http://hdl.handle.net/10204/4381
Crampton, Michael C. "Transcriptional analysis of heterologous gene expression using the endogenous sD promoter from Bacillus halodurans." (2010): http://hdl.handle.net/10204/4381
Crampton MC, Transcriptional analysis of heterologous gene expression using the endogenous sD promoter from Bacillus halodurans; CSIR; 2010. http://hdl.handle.net/10204/4381 .