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dc.contributor.authorDemirci, Gökhan
dc.contributor.authorDoğac, Yasemin İspirli
dc.contributor.authorTeke, Mustafa
dc.date.accessioned2020-11-20T15:04:30Z
dc.date.available2020-11-20T15:04:30Z
dc.date.issued2015
dc.identifier.issn0952-3499
dc.identifier.issn1099-1352
dc.identifier.urihttps://doi.org/10.1002/jmr.2475
dc.identifier.urihttps://hdl.handle.net/20.500.12809/2890
dc.descriptionWOS: 000362906400001en_US
dc.descriptionPubMed ID: 25857716en_US
dc.description.abstractIn the present study, we immobilized acetylcholinesterase (AChE) enzyme onto acetylcholine removed imprinted polymer and acetylcholine containing polymer. First, the polymers were produced with acetylcholine, substrate of AChE, by dispersion polymerization. Then, the enzyme was immobilized onto the polymers by using two different methods: In the first method (method A), acetylcholine was removed from the polymer, and then AChE was immobilized onto this polymer (acetylcholine removed imprinted polymer). In the second method (method B), AChE was immobilized onto acetylcholine containing polymer by affinity. In method A, enzyme-specific species (binding sites) occurred by removing acetylcholine from the polymer. The immobilized AChE reached 240% relative specific activity comparison with free AChE because the active enzyme molecules bounded onto the polymer. Transmission electron microscopy results were taken before and after immobilization of AChE for the assessment of morphological structure of polymer. Also, the experiments, which include optimum temperature (25-65 degrees C), optimum pH (3-10), thermal stability (4-70 degrees C), kinetic parameters, operational stability and reusability, were performed to determine the characteristic of the immobilized AChE. Copyright (c) 2015 John Wiley & Sons, Ltd.en_US
dc.description.sponsorshipMugla Sitki Kocman University Scientific Research ProjectMugla Sitki Kocman University [12/119]en_US
dc.description.sponsorshipThis work was supported by a grant from the Mugla Sitki Kocman University Scientific Research Project (no: 12/119).en_US
dc.item-language.isoengen_US
dc.publisherWiley-Blackwellen_US
dc.item-rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectSelective Immobilizationen_US
dc.subjectMolecular Recognitionen_US
dc.subjectAcetylcholinesteraseen_US
dc.subjectMolecularly Imprinted Polymeren_US
dc.titleA selective molecularly imprinted polymer for immobilization of acetylcholinesterase (AChE): an active enzyme targeted and efficient methoden_US
dc.item-typearticleen_US
dc.contributor.departmentMÜ, Fen Fakültesi, Kimya Bölümüen_US
dc.contributor.authorID0000-0001-8616-0280
dc.contributor.institutionauthorDoğac, Yasemin İspirli
dc.contributor.institutionauthorTeke, Mustafa
dc.identifier.doi10.1002/jmr.2475
dc.identifier.volume28en_US
dc.identifier.issue11en_US
dc.identifier.startpage645en_US
dc.identifier.endpage650en_US
dc.relation.journalJournal of Molecular Recognitionen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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