Please use this identifier to cite or link to this item: https://doi.org/10.1007/s11746-012-2099-6
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dc.titleBiocatalytic conversion of coconut oil to natural flavor esters optimized with response surface methodology
dc.contributor.authorSun, J.
dc.contributor.authorChin, J.H.
dc.contributor.authorZhou, W.
dc.contributor.authorYu, B.
dc.contributor.authorCurran, P.
dc.contributor.authorLiu, S.-Q.
dc.date.accessioned2014-10-16T08:21:19Z
dc.date.available2014-10-16T08:21:19Z
dc.date.issued2012-11
dc.identifier.citationSun, J., Chin, J.H., Zhou, W., Yu, B., Curran, P., Liu, S.-Q. (2012-11). Biocatalytic conversion of coconut oil to natural flavor esters optimized with response surface methodology. JAOCS, Journal of the American Oil Chemists' Society 89 (11) : 1991-1998. ScholarBank@NUS Repository. https://doi.org/10.1007/s11746-012-2099-6
dc.identifier.issn0003021X
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/93180
dc.description.abstractLipase (Lipozyme TL IM)-mediated biocatalysis in a solvent-free system was effectively employed to convert coconut oil and fusel oil to flavor-active octanoic acid esters (mainly ethyl-, butyl-, isobutyl- and (iso)amyl octanoate). Response surface methodology based on fivelevelthree-factor central composite design was applied to investigate the effects of single and multiple interactive factors on the conversion. Results indicated that the studied independent parameters including reactant molar ratio, enzyme loading and shaking speed were all significant factors that affected the formation of octanoic acid esters during transesterification reaction. According to the developed polynomial model (R2 = 0.947), the optimum transesterification conditions were determined as follows: molar ratio of 3.25:1 (alcohol/oil), enzyme loading of 16.7 % (wt%) and shaking speed of 160 rpm. Under the optimized reaction conditions an average conversion of 62.0 % was achieved which was in reasonable agreement with the predicted value of 64.1 % and about 9.4 mg of ethyl octanoate, 14.4 mg of isobutyl octanoate, 0.3 mg of butyl octanoate and 49.2 mg of (iso)amyl octanoate were produced per gram of coconut oil. © AOCS 2012.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1007/s11746-012-2099-6
dc.sourceScopus
dc.subjectBiocatalysis
dc.subjectCoconut oil
dc.subjectFlavor esters
dc.subjectFusel oil
dc.subjectLipase
dc.subjectSolvent-free transesterification
dc.typeArticle
dc.contributor.departmentCHEMISTRY
dc.description.doi10.1007/s11746-012-2099-6
dc.description.sourcetitleJAOCS, Journal of the American Oil Chemists' Society
dc.description.volume89
dc.description.issue11
dc.description.page1991-1998
dc.description.codenJAOCA
dc.identifier.isiut000310230200006
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