dc.contributor.author | Doğaç, Yasemin İspirli | |
dc.contributor.author | Deveci, İlyas | |
dc.contributor.author | Teke, Mustafa | |
dc.contributor.author | Mercimek, Bedrettin | |
dc.date.accessioned | 2020-11-20T16:17:55Z | |
dc.date.available | 2020-11-20T16:17:55Z | |
dc.date.issued | 2014 | |
dc.identifier.issn | 0928-4931 | |
dc.identifier.issn | 1873-0191 | |
dc.identifier.uri | https://doi.org/10.1016/j.msec.2014.05.058 | |
dc.identifier.uri | https://hdl.handle.net/20.500.12809/3417 | |
dc.description | WOS: 000340687400055 | en_US |
dc.description.abstract | The aim of the present study is to synthesize TiO2 beads for urease immobilization. Two different strategies were used to immobilize the urease on TiO2 beads. In the first method (A), urease enzyme was immobilized onto TiO2 beads by adsorption and then crosslinking. In the second method (B), TiO2 beads were coated with chitosan-urease mixture. To determine optimum conditions of immobilization, different parameters were investigated. The parameters of optimization were initial enzyme concentration (0.5; 1; 1.5; 2 mg/ml), alginate concentration (1; 2; 3%), glutaraldehyde concentration (1; 2; 3% v/v) and chitosan concentration (2; 3; 4 mg/ml). The optimum enzyme concentrations were determined as 1.5 mg/ml for A and 1.0 mg/ml for B. The other optimum conditions were found 2.0% (w/v) for alginate concentration (both A and B); 3.0 mg/ml for chitosan concentration (B) and 2.0% (v/v) for glutaraldehyde concentration (A). The optimum temperature (20-60 degrees C), optimum pH (3.0-10.0), kinetic parameters, thermal stability (4-70 degrees C), pH stability (4.0-9.0), operational stability (0-230 min) and reusability (20 times) were investigated for characterization. The optimum temperatures were 30 degrees C (A), 40 degrees C (B) and 35 degrees C (soluble). The temperature profiles of the immobilized ureases were spread over a large area. The optimum pH values for the soluble urease and immobilized urease prepared by using methods (A) and (B) were found to be 7.5, 7.0, 7.0, respectively. The thermal stabilities of immobilized enzyme sets were studied and they maintained 50% activity at 65 degrees C. However, at this temperature free urease protected only 15% activity. (C) 2014 Elsevier B.V. All rights reserved. | en_US |
dc.item-language.iso | eng | en_US |
dc.publisher | Elsevier Science Bv | en_US |
dc.item-rights | info:eu-repo/semantics/closedAccess | en_US |
dc.subject | Urease | en_US |
dc.subject | Immobilization | en_US |
dc.subject | Tio2 | en_US |
dc.subject | Chitosan | en_US |
dc.subject | Sol Gel Templating Method | en_US |
dc.title | TiO2 beads and TiO2-chitosan beads for urease immobilization | en_US |
dc.item-type | article | en_US |
dc.contributor.department | MÜ, Muğla Meslek Yüksekokulu, Kimya Ve Kimyasal İşleme Teknolojileri Bölümü | en_US |
dc.contributor.authorID | 0000-0002-2753-2301 | |
dc.contributor.authorID | 0000-0001-8616-0280 | |
dc.contributor.institutionauthor | Doğaç, Yasemin İspirli | |
dc.contributor.institutionauthor | Deveci, İlyas | |
dc.contributor.institutionauthor | Teke, Mustafa | |
dc.contributor.institutionauthor | Mercimek, Bedrettin | |
dc.identifier.doi | 10.1016/j.msec.2014.05.058 | |
dc.identifier.volume | 42 | en_US |
dc.identifier.startpage | 429 | en_US |
dc.identifier.endpage | 435 | en_US |
dc.relation.journal | Materials Science & Engineering C-Materials For Biological Applications | en_US |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |