Cinnamyl acetate synthesis by lipase-catalyzed transesterification in a solvent-free system

Biotechnology and Applied Biochemistry

Volumn 59, Issue 4, 2012, Pages 270-275

  Geng, Bo ^a   Wang, Mengfan ^a   Qi, Wei ^a   Su, Rongxin ^a   He, Zhimin ^a  

^a TIANJIN UNIVERSITY   (China)

Author keywords

flavor ester; kinetic model; Novozym 435; solvent free system; transesterification

Indexed keywords

ACYL DONORS; CINNAMYL ALCOHOLS; ETHYL ACETATES; FLAVOR ESTERS; IMMOBILIZED LIPASE; INHIBITION CONSTANTS; KINETIC MODELS; KINETIC STUDY; LIPASE-CATALYZED; MICHAELIS CONSTANTS; NOVOZYM435; PING-PONG BI-BI MECHANISM; REACTION SYSTEM; SOLVENT-FREE SYSTEM;

KINETIC THEORY; LOADING; REUSABILITY; SOLVENTS; SYNTHESIS (CHEMICAL); VOLATILE FATTY ACIDS;

TRANSESTERIFICATION;

ACETIC ACID DERIVATIVE; CINNAMYL ACETATE; ESTER; FLAVORING AGENT; SOLVENT; TRIACYLGLYCEROL LIPASE; UNCLASSIFIED DRUG;

ARTICLE; CANDIDA ANTARCTICA; CATALYSIS; CHEMICAL REACTION; CHEMICAL REACTION KINETICS; ENZYME ACTIVITY; ENZYME SUBSTRATE; FLAVOR; NONHUMAN; QUANTITATIVE ANALYSIS; SYNTHESIS; TEMPERATURE; TRANSESTERIFICATION;

BIOCATALYSIS; CANDIDA; CHEMISTRY TECHNIQUES, SYNTHETIC; ESTERIFICATION; KINETICS; LIPASE; MODELS, CHEMICAL; PROPANOLS; TEMPERATURE;

EID: 84865246904     PISSN: 08854513     EISSN: 14708744     Source Type: Journal    
DOI: 10.1002/bab.1023     Document Type: Article

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