Optimized synthesis of lipase-catalyzed l-ascorbyl laurate by Novozym® 435

Journal of Molecular Catalysis B: Enzymatic

Volumn 56, Issue 1, 2009, Pages 7-12

  Chang, S W ^a   Yang, C J ^a   Chen, F Y ^a   Akoh, C C ^b   Shieh, C J ^a,c  

^a DA YEH UNIVERSITY   (Taiwan)

^b UNIVERSITY OF GEORGIA   (United States)

^c NATIONAL CHUNG HSING UNIVERSITY   (Taiwan)

Author keywords

Antioxidant; Ascorbyl esters; Lipase; Optimization; Response surface methodology

Indexed keywords

ENZYMES; ESTERIFICATION; ESTERS; FATTY ACIDS; KETONES; ORGANIC ACIDS; ORGANIC COMPOUNDS; PSYCHOPHYSIOLOGY; SURFACE PROPERTIES;

ANALYSIS RESULTS; ANTIOXIDANT; APPLICATIONS.; ASCORBIC ACIDS; ASCORBYL ESTERS; CANDIDA ANTARCTICA; CENTRAL COMPOSITE ROTATABLE DESIGNS; CHEMICALLY SYNTHESIZED; CONSUMER DEMANDS; DIRECT ESTERIFICATIONS; ENZYMATIC SYNTHESES; FATTY ACID DERIVATIVES; HARMFUL EFFECTS; IMMOBILIZED LIPASES; LAURATE; LAURIC ACIDS; MOLAR CONVERSIONS; MOLAR RATIOS; NATURAL ANTIOXIDANTS; NOVOZYM; OPTIMIZED SYNTHESES; REACTION TIMES; RESPONSE SURFACE METHODOLOGIES; RESPONSE SURFACE METHODOLOGY; SYNTHESIS PARAMETERS;

ACIDS;

ANTIOXIDANT; ASCORBIC ACID; ASCORBIC ACID LAURATE; LAURIC ACID; NOVOZYM; TRIACYLGLYCEROL LIPASE; UNCLASSIFIED DRUG;

ANALYSIS OF VARIANCE; ARTICLE; CANDIDA ANTARCTICA; CATALYST; CHEMICAL ANALYSIS; CHEMICAL REACTION; CHEMICAL STRUCTURE; DRUG STRUCTURE; DRUG SYNTHESIS; ENZYME SYNTHESIS; ESTERIFICATION; NONHUMAN; REACTION TIME; RESPONSE SURFACE METHOD; TEMPERATURE;

CANDIDA ANTARCTICA;

EID: 56049085397     PISSN: 13811177     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.molcatb.2008.04.001     Document Type: Article

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