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首页> 外文期刊>Gene: An International Journal Focusing on Gene Cloning and Gene Structure and Function >Functional analysis of cus operon promoter of Klebsiella pneumoniae using E. coli lacZ assay
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Functional analysis of cus operon promoter of Klebsiella pneumoniae using E. coli lacZ assay

机译:大肠杆菌lacZ法检测肺炎克雷伯菌cus操纵子启动子的功能。

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The transcriptional fusion of reporter lacZ gene with cusRS regulatory promoter of cus operon of Klebsiella pneumoniae enabled us to analyze the inductive effect of copper on promoter via lacZ assay. The stimulus response curve of promoter to a range of copper metal concentrations indicated a normal sigmoidal response profile with apparent Hill coefficient 1.0. There was a positive correlation of promoter response to the increasing concentration of copper in the medium. AC 50 value of copper was calculated to be 1mM, whereas the promoter response was exponential beyond 1mM and up to 2.5mM concentration. The promoter activity did not increase exponentially in copper concentration higher than 2.5mM. The promoter PcusRS requires two chromosomally encoded regulatory proteins, CusS and CusR, in trans for maximal in vitro activation. The PcusRS regulatory promoter sequence also contained regulatory -10 and -35 boxes along with CusR binding motif. The results supported the concept of cus operon regulation as an essential mechanism for maintaining the cellular homeostasis at very high (e.g. 3mM), and even toxic copper concentrations.
机译:报告基因lacZ基因与肺炎克雷伯菌的cus操纵子的cusRS调控启动子的转录融合使我们能够通过lacZ分析来分析铜对启动子的诱导作用。启动子对一系列铜金属浓度的刺激反应曲线表明其正常的S形反应曲线具有明显的希尔系数1.0。启动子响应与培养基中铜浓度的增加呈正相关。铜的AC 50值经计算为1mM,而启动子响应超过1mM且高达2.5mM浓度呈指数关系。在高于2.5mM的铜浓度下,启动子活性没有指数增加。启动子PcusRS需要两个染色体编码的调节蛋白CusS和CusR反式才能获得最大的体外活化。 PcusRS调控启动子序列还包含-10和-35调控框以及CusR结合基序。结果支持cus operon调节的概念,将其作为维持细胞体内稳态非常高(例如3mM)甚至有毒铜浓度的基本机制。

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