Cloning, expression, crystallization and preliminary X-ray crystallographic analysis of glutamyl-tRNA synthetase (Xoo1504) from Xanthomonas oryzae pv. oryzae

被引:1
|
作者
Doan, Thanh Thi Ngoc [1 ]
Natarajan, Sampath [1 ]
Kim, Hyesoon [2 ]
Ahn, Yeh-Jin [2 ]
Kim, Jeong-Gu [3 ]
Lee, Byoung-Moo [3 ]
Kang, Lin-Woo [1 ]
机构
[1] Konkuk Univ, Dept Adv Technol Fus, Seoul 143701, South Korea
[2] Sangmyung Univ, Coll Nat Sci, Seoul 110743, South Korea
[3] RAD, NIAB, Microbial Genet Div, Suwon 441707, South Korea
来源
ACTA CRYSTALLOGRAPHICA SECTION F-STRUCTURAL BIOLOGY COMMUNICATIONS | 2009年 / 65卷
关键词
CRYSTAL-STRUCTURE; SEQUENCE;
D O I
10.1107/S1744309108039924
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The gltX gene from Xanthomonas oryzae pv. oryzae (Xoo1504) encodes glutamyl-tRNA synthetase (GluRS), one of the most important enzymes involved in bacterial blight (BB), which causes huge production losses of rice worldwide. GluRS is a class I-type aminoacyl-tRNA synthetase (aaRS) that is primarily responsible for the glutamylation of tRNA(Glu). It plays an essential role in protein synthesis, as well as the regulation of cells, in all organisms. As it represents an important target for the development of new antibacterial drugs against BB, determination of the three-dimensional structure of GluRS is essential in order to understand its catalytic mechanism. In order to analyze its structure and function, the gltX gene was cloned and the GluRS enzyme was expressed, purified and then crystallized. A GluRS crystal belonging to the monoclinic space group C2 diffracted to 2.8 angstrom resolution and had unit-cell parameters a = 186.8, b = 108.4, c = 166.1 angstrom, beta = 96.3 degrees. The unit-cell volume of the crystal allowed the presence of six to eight monomers in the asymmetric unit, with a corresponding Matthews coefficient (V-M) range of 2.70-2.02 angstrom(3) Da(-1) and a solvent-content range of 54.5-39.3%.
引用
收藏
页码:51 / 54
页数:4
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