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结核分枝杆菌DNA拓扑异构酶I的克隆、表达、纯化及特性分析

Cloning, expression, purification and characterization of DNA topoisomerase I of Mycobacterium tuberculosis.

作者信息

Yang F, Lu G, Rubin H

机构信息

Department of Medicine, University of Pennsylvania, Philadelphia 19104, USA.

出版信息

Gene. 1996 Oct 31;178(1-2):63-9. doi: 10.1016/0378-1119(96)00335-6.

Abstract

The complete gene encoding Topoisomerase 1 (Topo I) from Mycobacterium tuberculosis (MTb), Erdman strain, has been isolated and sequenced. The coding region of this gene is 2700 nt encoding a polypeptide of 900 amino acids with a calculated molecular mass of 99353 Da. The amino-acid sequence identity compared to E. coli and Synechococcus Topo I is 22 and 30%, respectively. The gene was expressed in E. coli BL21(DE3) and purified to near homogeneity. Recombinant MTb Topo I is enzymatically active, relaxing negatively supercoiled DNA in a magnesium-dependent, ATP-independent reaction. Spermidine, a typical inhibitor of prokaryotic type I DNA topoisomerase, inhibits the activity. Unlike the more well-characterized E. coli Topo I, MTb Topo I does not contain a zinc-finger DNA-binding motif in the C-terminal domain of the protein.

摘要

已从结核分枝杆菌(MTb)埃尔德曼菌株中分离并测序了编码拓扑异构酶1(Topo I)的完整基因。该基因的编码区为2700个核苷酸,编码一个由900个氨基酸组成的多肽,计算分子量为99353道尔顿。与大肠杆菌和集胞藻Topo I相比,氨基酸序列同一性分别为22%和30%。该基因在大肠杆菌BL21(DE3)中表达并纯化至接近均一。重组MTb Topo I具有酶活性,在依赖镁、不依赖ATP的反应中使负超螺旋DNA松弛。亚精胺是原核I型DNA拓扑异构酶的典型抑制剂,可抑制其活性。与特征更明确的大肠杆菌Topo I不同,MTb Topo I在蛋白质的C末端结构域中不包含锌指DNA结合基序。

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