Expression, purification, crystallization and preliminary X-ray diffraction analysis of carbonyl reductase from Candida parapsilosis ATCC 7330

被引:12
|
作者
Aggarwal, Nidhi [1 ]
Mandal, P. K. [2 ]
Gautham, Namasivayam [2 ]
Chadha, Anju [1 ,3 ]
机构
[1] Indian Inst Technol, Dept Biotechnol, Madras 600036, Tamil Nadu, India
[2] Univ Madras, CAS Crystallog & Biophys, Madras 600025, Tamil Nadu, India
[3] Indian Inst Technol, Natl Ctr Catalysis Res, Madras 600036, Tamil Nadu, India
来源
ACTA CRYSTALLOGRAPHICA SECTION F-STRUCTURAL BIOLOGY COMMUNICATIONS | 2013年 / 69卷
关键词
carbonyl reductase; alcohol dehydrogenase; enantioselectivity; Candida parapsilosis; ALCOHOL-DEHYDROGENASE; ASYMMETRIC REDUCTION;
D O I
10.1107/S1744309113003667
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The NAD(P)H-dependent carbonyl reductase from Candida parapsilosis ATCC 7330 catalyses the asymmetric reduction of ethyl 4-phenyl-2-oxobutanoate to ethyl (R)-4-phenyl-2-hydroxybutanoate, a precursor of angiotensin-converting enzyme inhibitors such as Cilazapril and Benazepril. The carbonyl reductase was expressed in Escherichia coli and purified by GST-affinity and size-exclusion chromatography. Crystals were obtained by the hanging-drop vapour-diffusion method and diffracted to 1.86 angstrom resolution. The asymmetric unit contained two molecules of carbonyl reductase, with a solvent content of 48%. The structure was solved by molecular replacement using cinnamyl alcohol dehydrogenase from Saccharomyces cerevisiae as a search model.
引用
收藏
页码:313 / 315
页数:3
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