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Pseudomonas cepacia lipase - Mediated transesterification reactions of hydrocinnamates
Kuttikode Priya,
Published in
2002
PMID: 22908416
Volume: 39
   
Issue: 4
Pages: 259 - 263
Abstract
Use of lipase from Pseudomonas cepacia in transesterifcation reactions of ethyl hydrocinnamate with different alcohols has been examined. Among the alcohols tested, viz., n-butanol, iso-amyl alcohol, benzyl alcohol, n-octanol and 1-phenylethanol, only n-butanol yielded the transesterified product. Among the solvents tested, viz., n-heptane, n-hexane, cyclohexane, toluene, diisopropylether and n-butanol, the initial rate of transesterification proceeded in the order cyclohexane > n-heptane > n-hexane > diisopropylether > n-butanol > toluene. Using hexane as the solvent and a substrate to enzyme ratio of 1:5, the substrate to alcohol ratio was varied to maximize the yield, n-Butyl hydrocinnamate was obtained in 92% yield in 48 hr by employing a 1:1 (wt/wt) ratio of ethyl hydrocinnamate to lipase and a 1:5 (vol/vol) ratio of ethyl hydrocinnamate to n-butanol in hexane.
About the journal
JournalIndian Journal of Biochemistry and Biophysics
ISSN03011208
Open AccessNo
Concepts (40)
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    1 PHENYLETHANOL
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    Alcohol derivative
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    Benzyl alcohol
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    Butanol
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    Cinnamic acid derivative
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    Cyclohexane
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    DIISOPROPYLETHER
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    Enzyme
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    Ether derivative
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    ETHYL HYDROCINNAMATE
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    Heptane
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    Hexane
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    OCTANOL
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    Solvent
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    Toluene
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    TRIACYLGLYCEROL LIPASE
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    Unclassified drug
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    Article
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    BURKHOLDERIA CEPACIA
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    Chemical reaction
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    Nonhuman
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    Transesterification
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    Alcohols
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    BURKHOLDERIA CEPACIA
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    Butanols
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    Catalysis
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    Esterification
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    Hexanes
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    Kinetics
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    Lipase
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    Models, chemical
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    PHENYLPROPIONATES
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    Solvents
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    Sonication
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    Substrate specificity
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    Temperature
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    Time factors
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    Burkholderia
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    BURKHOLDERIA CEPACIA
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    Pseudomonas