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Growth medium composition-determined regulatory mechanisms are superimposed on CatR-mediated transcription from the pheBA and catBCA promoters in Pseudomonas putida

机译:生长培养基的成分确定的调节机制叠加在普韦达帕皮达(Pseudomonassvida)的Catr介导的转录上

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Expression of the phenol degradation pathway in Pseudomonas putida strain PaW85 requires coordinated transcription of the plasmid-borne pheBA operon encoding catechol 1,2-dioxygenase and phenol monooxygenase, respectively, and the chromosomally encoded catechol degradation catBCA operon. Transcriptional activation from the pheBA and catBCA promoters is regulated by CatR and the catechol degradation pathway intermediate cis,cis-muconate. Here it is shown that physiological control mechanisms are superimposed on this regulatory system. Transcriptional activation from the pheBA and catBCA promoters is growth-phase-regulated in P. putida cells grown on rich medium (LB medium). CatR-mediated transcription from these promoters is silenced on rich medium until the transition from exponential to stationary phase. A slight positive effect (threefold) of stationary-phase-specific sigma factor σS on transcription from the pheBA promoter was observed. Expression of the catBCA promoter was not influenced by the activity of this sigma factor. In contrast to rich growth medium, transcription from the pheBA and catBCA promoters in minimal medium containing a mixture of glucose and sodium benzoate was rapidly induced in exponential culture. It was shown that the presence of amino acids in the culture medium causes exponential silencing of the pheBA and catBCA promoters. The possibility that a hypothetical repressor protein could be involved in physiological control of transcription from the pheBA and catBCA promoters is discussed.
机译:PSEUDOMONAS PIDIDA菌株PAW85中酚类降解途径的表达需要分别编码儿茶酚1,2-二氧合酶和苯酚单氧化酶的质粒传播的PHEBA型和苯酚单氧酶的协调转录,以及染色体编码的儿茶酚降解CATBCA操纵子。来自PHEBA和CATBCA启动子的转录活化由CATR和儿茶酚降解途径中间体顺式调节,顺式粘液酸酯。在这里,结果表明,生理控制机制叠加在该监管系统上。来自Pheba和CATBCA启动子的转录激活是在富含介质(LB培养基)上生长的P. Putida细胞中生长相位调节的。 Catr介导的来自这些促进剂的转录在富含培养基上沉默,直至从指数转变为固定相。观察到植物启动子转录的静态相位特异性Sigma因子σs的轻微效应(三倍)。 CATBCA启动子的表达不受这种Σ因素的活性的影响。与富生长培养基相反,在指数培养中迅速诱导含有葡萄糖和苯甲酸钠混合物的PHEBA和CATBCA启动子的转录。结果表明,培养基中存在氨基酸导致磷虾和CATBCA启动子的指数沉默。讨论了假设的阻遏蛋白可以参与来自PHEBA和CATBCA启动子的转录的生理控制的可能性。

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