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Merck
모든 사진(1)

주요 문서

79847

Sigma-Aldrich

Hydroxynitrile Lyase, Arabidopsis thaliana, recombinant from E. coli

≥500 U/mL

동의어(들):

Hydroxymandelonitrile Lyase, Arabidopsis thaliana, recombinant from E. coli

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About This Item

CAS Number:
MDL number:
UNSPSC 코드:
12352204
NACRES:
NA.54

재조합

expressed in E. coli

양식

liquid

특이 활성도

≥500 U/mL

저장 온도

−20°C

애플리케이션

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 [1].

생화학적/생리학적 작용

Hydroxynitrile lyases (Oxynitrilases) catalyze the addition of HCN to aldehydes and ketones thereby forming α-hydroxynitriles, also known as cyanohydrins [1]. Product 79847, Hydroxynitrile Lyase from Arabidopsis thaliana , is used to hydrolyze mandelonitrile.

단위 정의

1 U corresponds to the amount of enzyme which converts 1 μmol mandelonitrile per minte at pH 5.0 and 25°C.

픽토그램

Health hazard

신호어

Danger

유해 및 위험 성명서

예방조치 성명서

Hazard Classifications

Resp. Sens. 1

Storage Class Code

11 - Combustible Solids

WGK

WGK 1

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable

개인 보호 장비

Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)


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문서 라이브러리 방문

Screening for hydroxynitrile lyases in plants
Hickel, A., Heinrich, G., et al.
Biotechnol. Tech., 11, 55-58 (1997)
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
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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