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http://hdl.handle.net/11452/21261
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DC Field | Value | Language |
---|---|---|
dc.contributor.author | Uzun, Lokman | - |
dc.contributor.author | Denizli, Adil | - |
dc.date.accessioned | 2021-07-14T07:18:01Z | - |
dc.date.available | 2021-07-14T07:18:01Z | - |
dc.date.issued | 2005-12-01 | - |
dc.identifier.citation | Osman, B. vd. (2005). "Vinyl imidazole carrying metal-chelated beads for reversible use in yeast invertase adsorption". Journal of Molecular Catalysis B-Enzymatic, 37(1-6), 88-94. | en_US |
dc.identifier.issn | 1381-1177 | - |
dc.identifier.uri | https://doi.org/10.1016/j.molcatb.2005.09.007 | - |
dc.identifier.uri | http://hdl.handle.net/11452/21261 | - |
dc.description.abstract | Poly(ethylene glycol dimethacrylate-n-vinyl imidazole) [poly(EGDMA-VIM)] hydrogel (average diameter 150-200 mu m) was prepared copolymerizing ethylene glycol dimethacrylate (EGDMA) with n-vinyl imidazole (VIM). Poly(EGDMA-VIM) beads had a specific surface area of 59.8 M-2/g. Poly(EGDMA-VIM) beads were characterized by swelling studies and scanning electron microscope (SEM). Cu2+ ions were chelated on the poly(EGDMA-VIM) beads (452 mu mol Cu2+/g), then the metal-chelated beads were used in the adsorption of yeast invertase in a batch system. The maximum invertase adsorption capacity of the poly(EGDMA-VIM)-Cu2+ beads was observed as 35.2 mg/g at pH 4.5. The adsorption isotherm of the poly(EGDMA-VIM)-Cu2+ beads can be well fitted to the Langmuir model. Adsorption kinetics data were tested using pseudo-first- and -second-order models. Kinetic studies showed that the adsorption followed a pseudo- second-order reaction. The value of the Michaelis constant K-m of invertase was significantly larger upon adsorption, indicating decreased affinity by the enzyme for its substrate, whereas V-max was smaller for the adsorbed invertase. The optimum temperature for the adsorbed preparation of poly(EGDMA-VIM)-CU2+- invertase at 50 degrees C, 10 degrees C higher than that of the free enzyme at 40 degrees C. Storage stability was found to increase with adsorption. Adsorbed invertase retains an activity of 82% after 10 batch successive reactions, demonstrating the usefulness of the enzyme-loaded beads in biocatalytic applications. | en_US |
dc.language.iso | en | en_US |
dc.publisher | Elsevier Science BV | en_US |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.subject | Enzyme immobilization | en_US |
dc.subject | N-vinyl imidazole | en_US |
dc.subject | Invertase | en_US |
dc.subject | Chelating beads | en_US |
dc.subject | Affinity beads | en_US |
dc.subject | Covalent immobilization | en_US |
dc.subject | Microspheres | en_US |
dc.subject | Catalase adsorption | en_US |
dc.subject | Affinity adsorbents | en_US |
dc.subject | Glucose-oxidase | en_US |
dc.subject | Hollow-fibers | en_US |
dc.subject | Glucoamylase | en_US |
dc.subject | Membrane | en_US |
dc.subject | Polyethyleneimine | en_US |
dc.subject | Hydrolysis | en_US |
dc.title | Vinyl imidazole carrying metal-chelated beads for reversible use in yeast invertase adsorption | en_US |
dc.type | Article | en_US |
dc.identifier.wos | 000234026100014 | tr_TR |
dc.identifier.scopus | 2-s2.0-27944482512 | tr_TR |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi | tr_TR |
dc.contributor.department | Uludağ Üniversitesi/Fen Edebiyat Fakültesi/Kimya Bölümü. | tr_TR |
dc.identifier.startpage | 88 | tr_TR |
dc.identifier.endpage | 94 | tr_TR |
dc.identifier.volume | 37 | tr_TR |
dc.identifier.issue | 1-6 | tr_TR |
dc.relation.journal | Journal of Molecular Catalysis B-Enzymatic | en_US |
dc.contributor.buuauthor | Osman, Bilgen | - |
dc.contributor.buuauthor | Kara, Ali | - |
dc.contributor.buuauthor | Beşirli, Necati | - |
dc.contributor.researcherid | AAG-6271-2019 | tr_TR |
dc.contributor.researcherid | ABI-3951-2020 | tr_TR |
dc.relation.collaboration | Yurt içi | tr_TR |
dc.subject.wos | Biochemistry & molecular biology | en_US |
dc.subject.wos | Chemistry, physical | en_US |
dc.indexed.wos | SCIE | en_US |
dc.wos.quartile | Q2 (Chemistry, physical) | en_US |
dc.wos.quartile | Q3 | en_US |
dc.contributor.scopusid | 15221651200 | tr_TR |
dc.contributor.scopusid | 7102824859 | tr_TR |
dc.contributor.scopusid | 6507924888 | tr_TR |
dc.subject.scopus | Cibacron Blue F 3Ga | tr_TR |
dc.subject.scopus | Cryogels | en_US |
dc.subject.scopus | Muramidase | en_US |
dc.subject.emtree | Beta fructofuranosidase | en_US |
dc.subject.emtree | Copper ion | en_US |
dc.subject.emtree | Ethylene glycol dimethacrylate | en_US |
dc.subject.emtree | Imidazole | en_US |
dc.subject.emtree | Imidazole derivative | en_US |
dc.subject.emtree | Macrogol | en_US |
dc.subject.emtree | Metal | en_US |
dc.subject.emtree | Adsorption | en_US |
dc.subject.emtree | Binding affinity | en_US |
dc.subject.emtree | Catalysis | en_US |
dc.subject.emtree | Chelation | en_US |
dc.subject.emtree | Chemical reaction | en_US |
dc.subject.emtree | Hydrogel | en_US |
dc.subject.emtree | Iron chelation | en_US |
dc.subject.emtree | Kinetics | en_US |
dc.subject.emtree | Michaelis constant | en_US |
dc.subject.emtree | Scanning electron microscopy | en_US |
dc.subject.emtree | Temperature measurement | en_US |
dc.subject.emtree | Yeast | en_US |
Appears in Collections: | Scopus Web of Science |
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