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大肠杆菌RNA聚合酶β亚基的遗传学研究。VIII. 参与启动子选择性的区域定位。

Genetic studies on the beta subunit of Escherichia coli RNA polymerase. VIII. Localisation of a region involved in promoter selectivity.

作者信息

Glass R E, Jones S T, Nene V, Nomura T, Fujita N, Ishihama A

出版信息

Mol Gen Genet. 1986 Jun;203(3):487-91. doi: 10.1007/BF00422074.

Abstract

We have previously isolated an E. coli derivative carrying a small internal deletion (delta(rpoB)1570-1) of the beta structural gene. This RNA polymerase deletion mutant has no noticeable phenotype other than a slightly increased generation time in minimal medium. The deletion, which removes about 165 bp, has been localised to between codons 965 and 1,083, indicating it excises part of a tandem repeat structure present in the C-terminal region of beta. Analysis in vitro of purified RNA polymerase from the deletion mutant indicates that this enzyme has an altered promoter selectivity. These observations allow localisation of a site on the beta polypeptide of E. coli RNA polymerase involved in transcriptional initiation.

摘要

我们之前分离出了一种大肠杆菌衍生物,它携带β结构基因的一个小的内部缺失(delta(rpoB)1570 - 1)。这个RNA聚合酶缺失突变体除了在基本培养基中的代时略有增加外,没有明显的表型。该缺失去除了约165 bp,已定位在密码子965和1083之间,表明它切除了β C末端区域存在的部分串联重复结构。对缺失突变体纯化的RNA聚合酶进行的体外分析表明,这种酶的启动子选择性发生了改变。这些观察结果使得能够定位大肠杆菌RNA聚合酶β多肽上参与转录起始的位点。

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