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重组RNA聚合酶:大肠杆菌rpo基因产物的诱导型过表达、纯化及组装

Recombinant RNA polymerase: inducible overexpression, purification and assembly of Escherichia coli rpo gene products.

作者信息

Zalenskaya K, Lee J, Gujuluva C N, Shin Y K, Slutsky M, Goldfarb A

机构信息

Department of Microbiology, Columbia University College of Physicians and Surgeons, New York, NY 10032.

出版信息

Gene. 1990 Apr 30;89(1):7-12. doi: 10.1016/0378-1119(90)90199-2.

Abstract

The genes, rpoA, rpoB and rpoC of Escherichia coli, which encode the RNA polymerase alpha-, beta- and beta'-subunits, respectively, have been individually placed on expression plasmids under the control of the bacteriophage T7 promoter. Induction of the T7 RNA polymerase gene in host cells harboring each of the three plasmids resulted in the extensive overproduction of the three polypeptides. The overproduced subunits were purified and assembled into a functional enzyme, whose specific activity and dependence on the sigma-factor were indistinguishable from native RNA polymerase purified by conventional methods.

摘要

大肠杆菌的rpoA、rpoB和rpoC基因分别编码RNA聚合酶的α-、β-和β'-亚基,它们已被分别置于噬菌体T7启动子控制下的表达质粒上。在含有这三种质粒的宿主细胞中诱导T7 RNA聚合酶基因,导致这三种多肽大量过量产生。过量产生的亚基被纯化并组装成一种功能性酶,其比活性和对σ因子的依赖性与用传统方法纯化的天然RNA聚合酶没有区别。

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