体外合成的NifA蛋白结合克雷伯菌氧化克雷伯菌nifB基因启动子上游激活子序列。

Y. M. Kim, M. Hidaka, H. Masaki, T. Beppu, T. Uozumi
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引用次数: 3

摘要

各种细菌的固氮(nif)基因是由NifA蛋白激活的替代rna聚合酶调控的。1*对肺炎克雷伯菌nifYL启动子(2'3)的分析表明,NifA蛋白与上游激活子序列整合宿主因子(IHF)在启动子区域的结合对于完全转录激活是必不可少的。本文研究了体外合成的氧化克雷伯菌NifA蛋白与ni/B启动子的uaso结合以及IHF与nifB启动子的相互作用。NifA蛋白是用从Amersham购买的Escherichia coli mre600的S30提取物,在pNOA1015上由氯霉素乙酰转移酶基因启动子控制的人工NifA基因偶联转录和翻译4*合成的。为了测定其dna结合活性,该翻译混合物直接与dna探针孵育
本文章由计算机程序翻译,如有差异,请以英文原文为准。
NifA protein synthesized in vitro binds to the upstream activator sequence in the promoter of the Klebsiella oxytoca nifB gene.
The nitrogen fixation (nif) genes of various bacteria are transcribed with an RNApolymerase modulated by the alternative activated by the NifA protein.1* Several analyses of the Klebsiella pneumoniae nifYL promoter2'3) showed that not only binding of the NifA protein to the upstream activator sequence integration host factor (IHF) to the promoter region was essential for completetranscriptional activation. Here we demonstrate the binding ofKlebsiella oxytoca NifA protein synthesized in vitro to the UASof ni/B promoter and the interaction of IHF with the nifB promoter. The NifA protein was synthesized by a coupled transcription and translation4* of an artificial nifA gene, whose expression wascontrolled by the promoter of the chlor-amphenicol acetyl transferase gene, on pNOA1015)using S30 extract of Escherichia coli MRE600purchased from Amersham. To assay its DNAbinding activity, this trans-lation mixture was directly incubated with a DNAprobe
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