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在大肠杆菌无细胞系统中,两个不需要EnvZ磷酸化的转录活性OmpR突变体。

Two transcriptionally active OmpR mutants that do not require phosphorylation by EnvZ in an Escherichia coli cell-free system.

作者信息

Bowrin V, Brissette R, Inouye M

机构信息

Department of Biochemistry, Robert Wood Johnson Medical School, University of Medicine and Dentistry of New Jersey at Rutgers, Piscataway 08854.

出版信息

J Bacteriol. 1992 Oct;174(20):6685-7. doi: 10.1128/jb.174.20.6685-6687.1992.

Abstract

D55Q-T83A and D55Q-G94S, two pseudorevertants of the D55Q mutant OmpR, an Escherichia coli transcriptional activator, were isolated previously by R. Brissette, K. Tsung, and M. Inouye (J. Bacteriol. 173:3749-3755, 1991). These pseudorevertant OmpR proteins were purified and examined for their function as transcriptional activators in a cell-free system with an ompF DNA fragment. These proteins were transcriptionally active, even after acid treatment, whereas the wild-type OmpR was completely inactive after the same treatment. Phosphorylation of acid-treated wild-type OmpR with an EnvZ11 membrane fraction and ATP restored transcriptional activity, whereas the activities of the mutant OmpR proteins did not change after phosphorylation.

摘要

D55Q-T83A和D55Q-G94S是大肠杆菌转录激活因子D55Q突变体OmpR的两个假回复突变体,先前由R. 布里塞特、K. 宗和M. 井上分离得到(《细菌学杂志》173:3749 - 3755, 1991)。这些假回复突变体OmpR蛋白被纯化,并在无细胞体系中用ompF DNA片段检测其作为转录激活因子的功能。这些蛋白即使经过酸处理仍具有转录活性,而野生型OmpR在相同处理后则完全无活性。用EnvZ11膜组分和ATP对酸处理后的野生型OmpR进行磷酸化可恢复转录活性,而突变体OmpR蛋白磷酸化后活性不变。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bda3/207654/1c6abec43c81/jbacter00086-0378-a.jpg

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