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dc.contributor.authorYigitoglu, Mustafa
dc.contributor.authorTemocin, Zuelfikar
dc.date.accessioned2020-06-25T17:49:18Z
dc.date.available2020-06-25T17:49:18Z
dc.date.issued2010
dc.identifier.issn1381-1177
dc.identifier.issn1873-3158
dc.identifier.urihttps://doi.org/10.1016/j.molcatb.2010.04.007
dc.identifier.urihttps://hdl.handle.net/20.500.12587/4685
dc.descriptionTemocin, Zulfikar/0000-0001-7151-9772en_US
dc.descriptionWOS: 000280928200017en_US
dc.description.abstractCandida rugosa lipase was effectively immobilized on the poly(ethylene terephthalate) grafted acrylamide (PET-g-AAm) fiber which was prepared through Hofmann reaction. The activities of the immobilized enzyme and the free enzyme were investigated in the hydrolysis reaction of olive oil in isooctane-water biphasic medium. The activities of the free and the immobilized lipases were measured at different pH values, and temperatures. The thermal stability and storage stability of them were also determined. The kinetic parameters of the free and the immobilized lipases, K-m and V-max were calculated, as well. Moreover, the application of immobilized lipase to the hydrolysis of different vegetable oils was realized. The effect of organic solvents on olive oil hydrolysis was examined and time course of the oil hydrolysis was studied. The optimum pH was shifted from 6 to 7 by immobilization of the enzyme. The maximum activity of the free and the immobilized enzymes occurred at 40 degrees C. It was found that the immobilized lipase stored at 4 degrees C retained 90% of its original activity after 60 days, whereas the free lipase stored at 4 degrees C retained 75% of its activity after the same period. In addition, the immobilized lipase exhibited as 0.06 U of the remaining activity even after 10 times reuses. Kinetics studies show that the corresponding values of K-m and V-max were 47.2 mg ml(-1) and 48.1 U mg(-1) protein for free lipase and 151.6 mg ml(-1) and 10.9 U mg(-1) protein for immobilized lipase. The immobilized and free enzymes showed similar behavior with respect to the different oil hydrolysis. The time course of the immobilized lipase on canola and olive oils hydrolysis used as substrate was much better than that of the free lipase. A high rate of oil hydrolysis was obtained when isooctane was used as solvent. (C) 2010 Elsevier B.V. All rights reserved.en_US
dc.description.sponsorshipKirikkale UniversityKirikkale Universityen_US
dc.description.sponsorshipWe are grateful to the Kirikkale University Research Fund for the financial support of this work.en_US
dc.language.isoengen_US
dc.publisherElsevier Science Bven_US
dc.relation.isversionof10.1016/j.molcatb.2010.04.007en_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectAcrylamideen_US
dc.subjectImmobilizationen_US
dc.subjectLipaseen_US
dc.subjectOil hydrolysisen_US
dc.subjectPET fiberen_US
dc.titleImmobilization of Candida rugosa lipase on glutaraldehyde-activated polyester fiber and its application for hydrolysis of some vegetable oilsen_US
dc.typearticleen_US
dc.contributor.departmentKırıkkale Üniversitesien_US
dc.identifier.volume66en_US
dc.identifier.issue1-2en_US
dc.identifier.startpage130en_US
dc.identifier.endpage135en_US
dc.relation.journalJournal Of Molecular Catalysis B-Enzymaticen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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