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dc.contributor.authorKeçili, Rüstem
dc.contributor.authorSay, Rıdvan
dc.contributor.authorYavuz, Handan
dc.date.accessioned2019-10-20T09:30:47Z
dc.date.available2019-10-20T09:30:47Z
dc.date.issued2006
dc.identifier.issn0141-8130
dc.identifier.urihttps://dx.doi.org/10.1016/j.ijbiomac.2006.04.001
dc.identifier.urihttps://hdl.handle.net/11421/17463
dc.descriptionWOS: 000242525200014en_US
dc.descriptionPubMed ID: 16712925en_US
dc.description.abstractThe aim of this work was to test a chromatographic affinity support containing methacryloyl antipyrine (MAAP) for penicillin acylase (PA) purification by using pure penicillin acylase and crude extract. First, MAAP as a pseudo-specific ligand was synthesized by using methacryloyl chloride and 4-aminoantipyrine. Polymer beads (average size diameter: 40-120 mu m) were prepared by suspension polymerization of ethylene glycol dimethacrylate (EGDMA) and MAAP. This approach for the preparation of adsorbent has several advantages over conventional preparation protocols. An expensive and time consuming step in the preparation of adsorbent is immobilization of a ligand to the adsorption matrix. In this procedure, affinity ligand MAAP acts as comonomer without further modification steps. Poly(EGDMA-MAAP) beads were characterized by FTIR, NMR and screen analysis. Elemental analysis of MAAP for nitrogen was estimated as 89.3 mu mol/g. The prepared adsorbent was then used for the capture of penicillin acylase in batch system. The maximum penicillin acylase adsorption capacity of the poly(EGDMA-MAAP) beads was found to be 82.2 mg/g at pH 5.0. Chromatography with crude feedstock resulted in 23.2-fold purification and 93% recovery with 1.0 M NaOHen_US
dc.language.isoengen_US
dc.publisherElsevier Science BVen_US
dc.relation.isversionof10.1016/j.ijbiomac.2006.04.001en_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectPseudo-Affinity Liganden_US
dc.subjectPenicillin Acylaseen_US
dc.subjectMethacryloyl Antipyrine (Maap)en_US
dc.titleSynthesis and characterization of pseudo-affinity ligand for penicillin acylase purificationen_US
dc.typearticleen_US
dc.relation.journalInternational Journal of Biological Macromoleculesen_US
dc.contributor.departmentAnadolu Üniversitesi, Fen Fakültesi, Fizik Bölümüen_US
dc.identifier.volume39en_US
dc.identifier.issue4.Mayen_US
dc.identifier.startpage250en_US
dc.identifier.endpage255en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.contributor.institutionauthorKeçili, Rüstem
dc.contributor.institutionauthorSay, Rıdvan


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