Crystallization of type I chloramphenicol acetyltransferase: an approach based on the concept of ionic strength reducers

被引:2
作者
Andreeva, AE
Borissova, BE
Mironova, R
Glykos, NM
Kotsifaki, D
Ivanov, I
Krysteva, M
Kokkinidis, M
机构
[1] Inst Mol Biol & Biotechnol, GR-71110 Iraklion, Greece
[2] Univ Sofia, Dept Biotechnol, Sofia 1756, Bulgaria
[3] Bulgarian Acad Sci, Inst Mol Biol, BU-1113 Sofia, Bulgaria
[4] Univ Crete, Dept Biol, GR-71409 Iraklion, Greece
来源
ACTA CRYSTALLOGRAPHICA SECTION D-BIOLOGICAL CRYSTALLOGRAPHY | 2000年 / 56卷
关键词
D O I
10.1107/S090744499901481X
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Chloramphenicol acetyltransferase (CAT) is responsible for bacterial resistance to chloramphenicol. It catalyzes inactivation of the antibiotic by acetyl-group transfer from acetyl CoA to one or both hydroxyl groups of chloramphenicol, Type I CAT possesses some unique properties which are not observed in other CAT variants. Type I CAT overexpressed in Escherichia coli was purified and crystals with a resolution limit of 2.22 Angstrom have been obtained using a novel procedure which is based on the concept of 'ionic strength reducers'. The crystals have the symmetry of space group P1 and unit-cell parameters a = 96.46, b = 113.86, c = 114.21 Angstrom, alpha = 119.9, beta = 94.1, gamma = 98.6 degrees. These dimensions are consistent with four to six trimers per unit cell, corresponding to a solvent fraction ranging from 65 to 47%.
引用
收藏
页码:101 / 103
页数:3
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