Suppr超能文献

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。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验