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Lipase-catalyzed acylation of naringin with palmitic acid in highly concentrated homogeneous solutions

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dc.contributor.author김현정-
dc.date.accessioned2014-12-21T16:51:29Z-
dc.date.available2014-12-21T16:51:29Z-
dc.date.issued2007-
dc.identifier.issn1381-1177-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/96483-
dc.description.abstractAcylation reactions of naringin with palmitic acid were performed by a lipase after formation of highly concentrated homogeneous solutions. Their initial naringin concentration was 840–950 mM, which is 20–60 times greater than that in organic solvent media. The overall productivity of highly concentrated solutions was more than 15 times greater than those of organic phase media. The addition of DMSO (20–40%, w/w) to substrate mixtures lowered the melting temperature of a naringin–palmitic acid mixture (1:1 molar ratio) to about 40 °C. Reactions at 80 °C apparently followed Michaelis–Menten kinetics despite extremely high substrate concentrations. As the temperature increased from 60 °C to 80 °C, the apparent viscosity of the highly concentrated solution decreased remarkably from 4.31 Pa s to 0.063 Pa s. An activation energy of 7.65 kcal/mol obtained in a range of 60–75 °C suggests a diffusion-control. On the other hand, an activation energy of 17.09 kcal/mol in a range of 75–90 °C indicates a reaction-control. The highest product conversion yield of 33% (mol/mol) was obtained in a 10 h reaction at 80 °C. Addition of activated molecular sieves to the highly concentrated solution increased the product conversion yield by 7% (mol/mol), suggesting that the original equilibrium was disrupted by removing water and then a new equilibrium was reached.-
dc.description.statementOfResponsibilityopen-
dc.format.extent26~31-
dc.relation.isPartOfJournal of Molecular Catalysis B-Ensymatic-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/2.0/kr/-
dc.titleLipase-catalyzed acylation of naringin with palmitic acid in highly concentrated homogeneous solutions-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentMedical Research Center (임상의학연구센터)-
dc.contributor.googleauthorSung Hun Youn-
dc.contributor.googleauthorHyun Jung Kim-
dc.contributor.googleauthorChul Soo Shin-
dc.contributor.googleauthorTae Han Kim-
dc.identifier.doi10.1016/j.molcatb.2007.02.002-
dc.admin.authorfalse-
dc.admin.mappingfalse-
dc.contributor.localIdA01131-
dc.relation.journalcodeJ01604-
dc.identifier.urlhttp://www.sciencedirect.com/science/article/pii/S1381117707000410-
dc.contributor.alternativeNameKim, Hyun Jung-
dc.contributor.affiliatedAuthorKim, Hyun Jung-
dc.rights.accessRightsnot free-
dc.citation.volume46-
dc.citation.number1-4-
dc.citation.startPage26-
dc.citation.endPage31-
dc.identifier.bibliographicCitationJournal of Molecular Catalysis B-Ensymatic, Vol.46(1-4) : 26-31, 2007-
Appears in Collections:
1. College of Medicine (의과대학) > Yonsei Biomedical Research Center (연세의생명연구원) > 1. Journal Papers

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