Cloning, expression, purification, crystallization and preliminary X-ray analysis of EaLsc, a levansucrase from Erwinia amylovora

被引:18
|
作者
Caputi, Lorenzo [1 ]
Cianci, Michele [2 ]
Benini, Stefano [1 ]
机构
[1] Free Univ Bolzano, Fac Sci & Technol, Lab Bioorgan Chem & Crystallog, I-39100 Bolzano, Italy
[2] EMBL, D-22607 Hamburg, Germany
关键词
BACILLUS-SUBTILIS LEVANSUCRASE; ZYMOMONAS-MOBILIS; CRYSTAL-STRUCTURE; INULOSUCRASE; STABILITY; ENZYMES; LEVAN;
D O I
10.1107/S1744309113010750
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The Gram-negative bacterium Erwinia amylovora is a destructive pathogen of Rosaceae. During infection, E. amylovora produces the exopolysaccharide levan, which contributes to the occlusion of plant vessels, causing the wilting of shoots. Levan is a fructose polymer that is synthesized by multifunctional enzymes called levansucrases. The levansucrase from E. amylovora (EaLsc) was heterologously expressed as a GST-fusion protein in Escherichia coli, purified and crystallized after tag removal. The protein crystallized in space group P2(1)2(1)2. X-ray diffraction data were acquired to 2.77 angstrom resolution. The structure of the enzyme was solved by molecular replacement. The asymmetric unit contains eight enzyme molecules, giving a solvent content of 58.74% and a Matthews coefficient of 2.98 angstrom(3) Da(-1).
引用
收藏
页码:570 / 573
页数:4
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