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来自水稻白叶枯病菌的DNA促旋酶GyrB亚基的结晶及初步X射线晶体学分析

Crystallization and preliminary X-ray crystallographic analysis of DNA gyrase GyrB subunit from Xanthomonas oryzae pv. oryzae.

作者信息

Jung Ha Yun, Lee Ki Jeung, Kim Kyung Ha, Hyoung Ji Hye, Han Mi Ra, Kim Hyun Kyoung, Kang Lin-Woo, Ahn Yeh-Jin, Heo Yong-Seok

机构信息

Department of Chemistry, Konkuk University, Hwayang-dong, Gwangjin-gu, Seoul 143-701, Republic of Korea.

出版信息

Acta Crystallogr Sect F Struct Biol Cryst Commun. 2010 Jan 1;66(Pt 1):48-50. doi: 10.1107/S1744309109047721. Epub 2009 Dec 25.

Abstract

DNA gyrase is a type II topoisomerase that is essential for chromosome segregation and cell division owing to its ability to modify the topological forms of bacterial DNA. In this study, the N-terminal fragment of the GyrB subunit of DNA gyrase from Xanthomonas oryzae pv. oryzae was overexpressed in Escherichia coli, purified and crystallized. Diffraction data were collected to 2.10 A resolution using a synchrotron-radiation source. The crystal belonged to space group I4(1), with unit-cell parameters a = b = 110.27, c = 70.75 A. The asymmetric unit contained one molecule, with a V(M) of 2.57 A(3) Da(-1) and a solvent content of 50.2%.

摘要

DNA促旋酶是一种II型拓扑异构酶,由于其能够改变细菌DNA的拓扑形式,对于染色体分离和细胞分裂至关重要。在本研究中,来自水稻黄单胞菌稻瘟病菌株的DNA促旋酶GyrB亚基的N端片段在大肠杆菌中过表达、纯化并结晶。使用同步辐射源收集了分辨率为2.10 Å的衍射数据。晶体属于空间群I4(1),晶胞参数a = b = 110.27,c = 70.75 Å。不对称单元包含一个分子,V(M)为2.57 ų Da⁻¹,溶剂含量为50.2%。

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