Belitsky Boris R, Kim Hyun-Jin, Sonenshein Abraham L
Department of Molecular Biology and Microbiology, Tufts University School of Medicine, Boston, Massachusetts 02111, USA.
J Bacteriol. 2004 Jun;186(11):3392-8. doi: 10.1128/JB.186.11.3392-3398.2004.
The Bacillus subtilis rocG gene, encoding catabolic glutamate dehydrogenase, was found to be subject to direct CcpA-dependent glucose repression. The effect of CcpA required the presence of both the HPr and Crh proteins. The primary CcpA binding site was identified by mutational analysis and DNase I footprinting. In the absence of inducers of the Roc pathway, rocG was still expressed at a low level due to readthrough transcription. CcpA-dependent repression of rocG readthrough transcription proved to contribute to the slow growth rate of B. subtilis cells in glucose-glutamate medium. Increased readthrough expression of rocG was shown to be partially responsible for the growth defect of ccpA strains in glucose-ammonium medium.
编码分解代谢型谷氨酸脱氢酶的枯草芽孢杆菌rocG基因被发现受到直接的CcpA依赖性葡萄糖阻遏作用。CcpA的作用需要HPr和Crh蛋白同时存在。通过突变分析和DNase I足迹法确定了主要的CcpA结合位点。在没有Roc途径诱导物的情况下,由于通读转录,rocG仍以低水平表达。事实证明,CcpA对rocG通读转录的阻遏作用导致枯草芽孢杆菌细胞在葡萄糖-谷氨酸培养基中的生长速率缓慢。rocG通读表达的增加被证明部分导致了ccpA菌株在葡萄糖-铵培养基中的生长缺陷。