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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Published in: | Biochemical engineering journal Vol. 42; no. 1; pp. 6 - 12 |
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Main Authors: | , , , |
Format: | Journal Article |
Language: | English |
Published: |
Lausanne
Elsevier B.V
15-10-2008
Amsterdam Elsevier Science New York, NY |
Subjects: | |
Online Access: | Get full text |
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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. |
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ISSN: | 1369-703X 1873-295X |
DOI: | 10.1016/j.bej.2008.05.012 |