Enzymatic synthesis of citronellol laurate in organic media and in supercritical carbon dioxide

Short-chain esters of carboxylic acids and monoterpene alcohols are very important compounds in food, cosmetic and pharmaceutical industries. Lipase-catalyzed esterification of β-citronellol and lauric acid was performed in organic solvents and in supercritical carbon dioxide (SC CO 2). The optimal...

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Bibliographic Details
Published in:Biochemical engineering journal Vol. 42; no. 1; pp. 6 - 12
Main Authors: Habulin, Maja, Šabeder, Saša, Sampedro, Miguel Acebes, Knez, Željko
Format: Journal Article
Language:English
Published: Lausanne Elsevier B.V 15-10-2008
Amsterdam Elsevier Science
New York, NY
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Summary:Short-chain esters of carboxylic acids and monoterpene alcohols are very important compounds in food, cosmetic and pharmaceutical industries. Lipase-catalyzed esterification of β-citronellol and lauric acid was performed in organic solvents and in supercritical carbon dioxide (SC CO 2). The optimal conditions found in organic solvents at atmospheric pressure were: an equimolar ratio of substrates, a temperature of 60 °C, an agitation speed of 500 rpm, 12% (w/w of substrates) enzyme preparation of lipase B from Candida antarctica. The highest conversion in SC CO 2 was obtained at 60 °C and 10 MPa with ethyl methylketone serving as a co-solvent.
ISSN:1369-703X
1873-295X
DOI:10.1016/j.bej.2008.05.012