79847
Hydroxynitrile Lyase, Arabidopsis thaliana, recombinant from E. coli
≥500 U/mL
别名:
Hydroxymandelonitrile Lyase, Arabidopsis thaliana, recombinant from E. coli
重组
expressed in E. coli
表单
liquid
比活
≥500 U/mL
储存温度
−20°C
应用
Hydroxynitrile lyases (Oxynitrilases) are used for various biotransformation processes and to convert a broad range of substrates. They may be used with bacterial nitrilases to generate biocatalysts .
生化/生理作用
Hydroxynitrile lyases (Oxynitrilases) catalyze the addition of HCN to aldehydes and ketones thereby forming α-hydroxynitriles, also known as cyanohydrins . Product 79847, Hydroxynitrile Lyase from Arabidopsis thaliana , is used to hydrolyze mandelonitrile.
其他说明
1 U corresponds to the amount of enzyme which converts 1 μmol mandelonitrile per minte at pH 5.0 and 25°C.
警示用语：
Danger
危险声明
预防措施声明
危险分类
Resp. Sens. 1
储存分类代码
11 - Combustible Solids
WGK
WGK 1
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)
法规信息
新产品
此项目有
White et al.
Plant physiology, 116(4), 1219-1225 (1998-04-29)
In the cyanogenic crop cassava (Manihot esculenta, Crantz), the final step in cyanide production is the conversion of acetone cyanohydrin, the deglycosylation product of linamarin, to cyanide plus acetone. This process occurs spontaneously at pH greater than 5. 0 or
Screening for hydroxynitrile lyases in plants
Hickel, A., Heinrich, G., et al.
Biotechnol. Tech., 11, 55-58 (1997)
Kathrin Emmi Scholz et al.
Applied and environmental microbiology, 78(14), 5025-5027 (2012-05-01)
Synthesis of chiral cyanohydrins is performed in a monophasic micro-aqueous reaction system using whole recombinant Escherichia coli cells expressing the Arabidopsis thaliana hydroxynitrile lyase (AtHNL). Microscopy studies employing a fusion of AtHNL with a flavin-based fluorescent protein (FbFP) reveal that
Stefanie Baum et al.
Applied and environmental microbiology, 78(1), 48-57 (2011-10-25)
The nitrilase from Pseudomonas fluorescens EBC191 converted 2-methyl-2-phenylpropionitrile, which contains a quaternary carbon atom in the α-position toward the nitrile group, and also similar sterically demanding substrates, such as 2-hydroxy-2-phenylpropionitrile (acetophenone cyanohydrin) or 2-acetyloxy-2-methylphenylacetonitrile. 2-Methyl-2-phenylpropionitrile was hydrolyzed to almost stoichiometric
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