Durante-Rodríguez Gonzalo, Zamarro M Teresa, García José L, Díaz Eduardo, Carmona Manuel
Departamento de Microbiología Molecular, Centro de Investigaciones Biológicas-CSIC, Ramiro de Maeztu 9, 28040 Madrid, Spain.
Microbiology (Reading). 2008 Jan;154(Pt 1):306-316. doi: 10.1099/mic.0.2007/011361-0.
The expression of the bzd genes involved in the anaerobic degradation of benzoate in Azoarcus sp. CIB is controlled by the specific BzdR transcriptional repressor at the P(N) promoter. This catabolic promoter is also subject to catabolite repression by some organic acids. In vivo and in vitro experiments have shown that BzdR behaves as a repressor of the P(R) promoter by overlapping the transcription initiation site as well as the -35 and -10 boxes, benzoyl-CoA being the inducer molecule. In addition, by using a P(N) : : lacZ fusion both in Azoarcus sp. CIB and in an isogenic strain lacking the bzdR gene, we have shown that the succinate-dependent catabolite repression requires participation of the BzdR repressor.
偶氮弧菌属CIB菌株中参与苯甲酸厌氧降解的bzd基因的表达受P(N)启动子处特异性BzdR转录阻遏物的控制。该分解代谢启动子也受到某些有机酸的分解代谢物阻遏。体内和体外实验表明,BzdR通过与转录起始位点以及-35和-10框重叠而作为P(R)启动子的阻遏物,苯甲酰辅酶A为诱导分子。此外,通过在偶氮弧菌属CIB菌株和缺乏bzdR基因的同基因菌株中使用P(N)::lacZ融合,我们已经表明琥珀酸依赖性分解代谢物阻遏需要BzdR阻遏物的参与。