Efficient Production of Naringin Acetate with Different Acyl Donors via Enzymatic Transesterification by Lipases

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dc.contributor.authorBaek, Yesolko
dc.contributor.authorLee, Seungmeeko
dc.contributor.authorSon, Jeminko
dc.contributor.authorLee, Taekko
dc.contributor.authorOh, Jong-Minko
dc.contributor.authorLee, Sang Hunko
dc.contributor.authorKim, Hyun Ukko
dc.contributor.authorSeo, Sang Wooko
dc.contributor.authorPark, Si Jaeko
dc.contributor.authorYoo, Hah Youngko
dc.contributor.authorPark, Chulhwanko
dc.date.accessioned2022-04-13T06:52:22Z-
dc.date.available2022-04-13T06:52:22Z-
dc.date.created2022-04-10-
dc.date.created2022-04-10-
dc.date.created2022-04-10-
dc.date.created2022-04-10-
dc.date.issued2022-03-
dc.identifier.citationINTERNATIONAL JOURNAL OF ENVIRONMENTAL RESEARCH AND PUBLIC HEALTH, v.19, no.5, pp.2972-
dc.identifier.issn1661-7827-
dc.identifier.urihttp://hdl.handle.net/10203/292594-
dc.description.abstractNaringin, one of the citrus flavonoids and known as a natural antioxidant, has limited bioavailability owing to its low stability and solubility. However, naringin esters formed via acylation have recently been reported to possess improved physical and chemical properties. The development of these compounds has a great potential in the food, cosmetic and pharmaceutical industries, but low conversion and productivity are barriers to industrial applications. This study aimed to improve the conversion of naringin acetate, which is formed via the enzymatic reaction between naringin and an acyl donor. An optimal reaction condition was determined by evaluating the effect of various variables (enzyme type, enzyme concentration, acyl donor, molar ratio of reactants, reaction temperature, and solvent) on the synthesis of naringin acetate. The optimal condition was as follows: 3 g/L of Lipozyme TL IM, molar ratio of 1:5 (naringin:acyl donor), reaction temperature of 40-
dc.languageEnglish-
dc.publisherMDPI-
dc.titleEfficient Production of Naringin Acetate with Different Acyl Donors via Enzymatic Transesterification by Lipases-
dc.typeArticle-
dc.identifier.wosid000774199700001-
dc.identifier.scopusid2-s2.0-85125588461-
dc.type.rimsART-
dc.citation.volume19-
dc.citation.issue5-
dc.citation.beginningpage2972-
dc.citation.publicationnameINTERNATIONAL JOURNAL OF ENVIRONMENTAL RESEARCH AND PUBLIC HEALTH-
dc.identifier.doi10.3390/ijerph19052972-
dc.contributor.localauthorKim, Hyun Uk-
dc.contributor.nonIdAuthorBaek, Yesol-
dc.contributor.nonIdAuthorLee, Seungmee-
dc.contributor.nonIdAuthorSon, Jemin-
dc.contributor.nonIdAuthorLee, Taek-
dc.contributor.nonIdAuthorOh, Jong-Min-
dc.contributor.nonIdAuthorLee, Sang Hun-
dc.contributor.nonIdAuthorSeo, Sang Woo-
dc.contributor.nonIdAuthorPark, Si Jae-
dc.contributor.nonIdAuthorYoo, Hah Young-
dc.contributor.nonIdAuthorPark, Chulhwan-
dc.description.isOpenAccessN-
dc.type.journalArticleArticle-
dc.subject.keywordAuthorantioxidant-
dc.subject.keywordAuthorflavonoid-
dc.subject.keywordAuthornaringin-
dc.subject.keywordAuthorflavonoid ester-
dc.subject.keywordAuthorflavonoid acetate-
dc.subject.keywordAuthoracylation-
dc.subject.keywordAuthorlipase-
dc.subject.keywordAuthortransesterification-
dc.subject.keywordAuthorenzymatic synthesis-
dc.subject.keywordPlusCANDIDA-ANTARCTICA LIPASEFATTY-ACID ESTERSREGIOSELECTIVE ACYLATIONCATALYZED ESTERIFICATIONBIOCATALYTIC PREPARATIONIMMOBILIZED LIPASEFLAVONOID ESTERSISOAMYL ACETATEMEDIATED SYNTHESISLIPOPHILIC RUTIN-
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CBE-Journal Papers(저널논문)
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