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首页> 外文期刊>Journal of bacteriology >Cross talk between catabolic pathways in Pseudomonas putida: XylS-dependent and -independent activation of the TOL meta operon requires the same cis-acting sequences within the Pm promoter.
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Cross talk between catabolic pathways in Pseudomonas putida: XylS-dependent and -independent activation of the TOL meta operon requires the same cis-acting sequences within the Pm promoter.

机译:恶臭假单胞菌分解代谢途径之间的串扰:TOL操纵子的XylS依赖性和非依赖性活化需要在Pm启动子内具有相同的顺式作用序列。

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摘要

The Pm promoter of the meta cleavage operon in the TOL (toluene degradation) plasmid pWW0 of Pseudomonas putida becomes activated by the plasmid-encoded XylS regulator in the presence of benzoate and certain substituted analogs such as 3-methylbenzoate. In the absence of XylS, Pm was still responsive to unsubstituted benzoate but with induction kinetics and a range of transcriptional activity which differed substantially from those for the XylS-mediated activation. XylS-independent induction by benzoate did not occur in a rpoN genetic background. Pm was also silent while cells were actively growing in rich medium. However, XylS-dependent transcription and XylS-independent transcription were initiated at the same nucleotide, as determined with primer extension mapping. Furthermore, a series of deletions and mutations at the Pm promoter sequence showed the same overall pattern of responsiveness to benzoate with and without XylS, thus providing genetic evidence that the same promoter structure is recognized and activated by at least two different regulators. One of them is XylS, while the other, provided by the host bacterium, could be related to the chromosome-encoded benzoate degradation pathway.
机译:在苯甲酸酯和某些取代的类似物(例如3-甲基苯甲酸酯)的存在下,恶臭假单胞菌TOL(甲苯降解)质粒pWW0中的间位裂解操纵子的Pm启动子被质粒编码的XylS调节剂激活。在不存在XylS的情况下,Pm仍对未取代的苯甲酸酯有反应,但其诱导动力学和一系列转录活性与XylS介导的活化反应大不相同。在rpoN遗传背景中未发生苯甲酸酯的XylS独立诱导。当细胞在丰富的培养基中活跃生长时,Pm也保持沉默。但是,如引物延伸图谱所确定的,XylS依赖的转录和XylS依赖的转录在相同的核苷酸处起始。此外,在Pm启动子序列上的一系列缺失和突变显示了在有和没有XylS的情况下对苯甲酸酯的响应的总体模式相同,从而提供了遗传学证据,表明相同的启动子结构被至少两个不同的调节剂识别和激活。其中一个是XylS,而另一个是由宿主细菌提供的,可能与染色体编码的苯甲酸酯降解途径有关。

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