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Mutational analysis of upstream sequences required for transcriptional activation of the Klebsiella pneumoniae nifH promoter.

机译:肺炎克雷伯氏菌nifH启动子转录激活所需上游序列的突变分析。

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摘要

Upstream sequences of the Klebsiella pneumoniae nifH promoter were mutagenised and activation of the mutated promoters by the nif-specific transcriptional activator protein NifA examined in vivo. Of the sixteen mutations analysed, only those within the nifH upstream activator sequence (UAS), characterised by a TGT-N10-ACA motif, influenced nifH promoter activity. Mutations altering the two-fold rotational symmetry of the UAS or the spacing between the TGT and ACA motifs reduced promoter activity, consistent with the UAS functioning as a NifA binding site. The bases flanking the TGT-ACA motif of the UAS also appear to influence activation by NifA. Substituting the nifH UAS with a binding site for the transcriptional activator NtrC resulted in improved NtrC-dependent activation of the nifH promoter demonstrating that the activator specificity of the nifH promoter is dependent upon the presence of the appropriate upstream sequences to which the activator binds.
机译:诱变肺炎克雷伯氏菌nifH启动子的上游序列,并在体内检查nif特异性转录激活蛋白NifA对突变启动子的激活。在分析的16个突变中,只有nifH上游激活子序列(UAS)中以TGT-N10-ACA基序为特征的那些突变影响nifH启动子活性。改变UAS的两倍旋转对称性或TGT和ACA基序之间的间隔的突变降低了启动子活性,这与UAS发挥NifA结合位点的作用是一致的。 UAS的TGT-ACA主题两侧的碱基也似乎会影响NifA的激活。用具有转录激活因子NtrC结合位点的nifH UAS替代导致nifH启动子的NtrC依赖性增强的激活,表明nifH启动子的激活子特异性取决于该激活子结合的合适上游序列的存在。

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