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The Escherichia coli MeIR transcription activator: production of a stable fragment containing the DNA-binding domain

机译:大肠杆菌MeIR转录激活剂:产生包含DNA结合域的稳定片段

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摘要

A set of nested deletions has been made In the Escherichia coll melR gene, encoding the MelR transcription activator protein. Expression of the resulting meIR derivatives led to the production of nine MeIR proteins with N-termlnal deletions of different lengths. The properties of the shortened proteins have been studied both In vivo and in vitro None of the truncated proteins activate transcription from the E.coll melAB promoter but three; MelR220, MelR183 and MelR173, Inhibit activation of the melAB promoter by chromoso-mally-encoded full-length MeIR. In gel retardation assays, both MeIR 183 and MelR173 clearly retard DNA fragments carrying the melAB promoter. MeIR 173 has been overproduced In a T7 expression system and shown to be stable In vivo for up to 2 h. DNAase I footprintlng assays of partially purified protein show that it binds to the melAB promoter, protecting the same sites as the full-length protein. This fragment may be suitable for further structure/function studies of this class of transcription activator.
机译:在大肠杆菌coll melR基因中已完成了一系列嵌套的缺失,编码MelR转录激活蛋白。所得meIR衍生物的表达导致产生9种具有不同长度N末端缺失的MeIR蛋白。已经在体内和体外研究了缩短的蛋白的特性。没有一个被截短的蛋白能激活E.coll melAB启动子的转录,只有三个能激活。 MelR220,MelR183和MelR173,通过染色体编码的全长MeIR抑制melAB启动子的激活。在凝胶阻滞测定中,MeIR 183和MelR173均明显阻滞了携带melAB启动子的DNA片段。 MeIR 173已在T7表达系统中过量生产,并显示在体内长达2小时稳定。部分纯化的蛋白质的DNAase I足迹测定表明,它与melAB启动子结合,保护了与全长蛋白质相同的位点。此片段可能适合此类转录激活子的进一步结构/功能研究。

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