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噬菌体SPO1编码的RNA聚合酶σ因子的过量生产与纯化

Overproduction and purification of a bacteriophage SPO1-encoded RNA polymerase sigma factor.

作者信息

Costanzo M, Pero J

出版信息

J Biol Chem. 1984 May 25;259(10):6681-5.

PMID:6327692
Abstract

Gene 28 of bacteriophage SPO1 encodes an RNA polymerase sigma factor sigma gp28, which replaces the host Bacillus subtilis sigma subunit sigma 55, to alter the promoter recognition specificity of RNA polymerase. A fragment of SPO1 DNA containing gene 28 was placed under the control of the PL promoter of bacteriophage lambda in an Escherichia coli expression vector. When transcription of gene 28 was induced by derepression of PL, the sigma gp28 synthesized constituted several per cent of total cellular protein. Sigma gp28 purified from these cells was able to confer specificity for SPO1 middle gene promoters upon B. subtilis core RNA polymerase, and also enabled E. coli core RNA polymerase to recognize and initiate transcription from an SPO1 middle gene promoter.

摘要

噬菌体SPO1的基因28编码一种RNA聚合酶σ因子σ gp28,它取代宿主枯草芽孢杆菌的σ亚基σ 55,以改变RNA聚合酶的启动子识别特异性。将含有基因28的SPO1 DNA片段置于大肠杆菌表达载体中噬菌体λ的PL启动子控制之下。当通过PL的去阻遏诱导基因28转录时,合成的σ gp28占细胞总蛋白的百分之几。从这些细胞中纯化的σ gp28能够赋予枯草芽孢杆菌核心RNA聚合酶对SPO1中间基因启动子的特异性,也能使大肠杆菌核心RNA聚合酶识别SPO1中间基因启动子并从其起始转录。

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