Synthesis of (R)-β-nitro alcohols catalyzed by R-selective hydroxynitrile lyase from Arabidopsis thaliana in the aqueous-organic biphasic system

Journal of Biotechnology

Volumn 153, Issue 3-4, 2011, Pages 153-159

  Fuhshuku, Ken Ichi ^a   Asano, Yasuhisa ^a  

^a TOYAMA PREFECTURAL UNIVERSITY   (Japan)

Author keywords

Arabidopsis thaliana; Asymmetric Henry reaction; Carbon carbon bond formation; Enzyme catalyzed reaction; Hydroxynitrile lyase; Optically active nitro alcohol

Indexed keywords

ARABIDOPSIS THALIANA; ASYMMETRIC HENRY REACTION; CARBON-CARBON BOND FORMATION; ENZYME-CATALYZED REACTIONS; HYDROXYNITRILE LYASES; OPTICALLY ACTIVE;

ALDEHYDES; CATALYSIS; CATALYSTS; CONDENSATION REACTIONS; ENANTIOSELECTIVITY; ENZYMES; ORGANIC SOLVENTS;

SYNTHESIS (CHEMICAL);

ACETIC ACID; ALDEHYDE; HYDROLASE; HYDROXYNITRILE LYASE; NITROMETHANE; ORGANIC SOLVENT;

ALCOHOL PRODUCTION; ALDOL REACTION; AQUEOUS SOLUTION; ARABIDOPSIS; ARTICLE; CATALYSIS; ENANTIOSELECTIVITY; HEVEA BRASILIENSIS; NONHUMAN; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL;

ALDEHYDE-LYASES; ARABIDOPSIS PROTEINS; CATALYSIS; ETHANOL; HYDROGEN-ION CONCENTRATION; METHANE; NITRO COMPOUNDS; NITROPARAFFINS; RECOMBINANT FUSION PROTEINS; SUBSTRATE SPECIFICITY;

ARABIDOPSIS THALIANA; HEVEA BRASILIENSIS;

EID: 79955766024     PISSN: 01681656     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jbiotec.2011.03.011     Document Type: Article

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