Novel polymeric microspheres: Synthesis, enzyme immobilization, antimutagenic activity, and antimicrobial evaluation against pathogenic microorganisms
dc.contributor.author | Nartop, Dilek | |
dc.contributor.author | Demirel, Birtane | |
dc.contributor.author | Güleç, Murat | |
dc.contributor.author | Özkan, Elvan Hasanoğlu | |
dc.contributor.author | Yetim, Nurdan Kurnaz | |
dc.contributor.author | Sarı, Nurşen | |
dc.contributor.author | Ağar, Güleray | |
dc.date.accessioned | 2020-04-30T13:32:54Z | |
dc.date.available | 2020-04-30T13:32:54Z | |
dc.date.issued | 2020 | |
dc.department | DÜ, Teknoloji Fakültesi, Polimer Mühendisliği Bölümü | en_US |
dc.description | PubMed ID: 31851403 | en_US |
dc.description.abstract | New polymeric microspheres containing azomethine (1a-1c and 2a-2c) were synthesized by condensation to compare the enzymatic properties of the enzyme glucose oxidase (GOx) and to investigate antimutagenic and antimicrobial activities. The polymeric microspheres were characterized by elemental analysis, infrared spectra (FT-IR), proton nuclear magnetic resonance spectra, thermal gravimetric analysis, and scanning electron microscopy analysis. The catalytic activity of the glucose oxidase enzyme follows Michaelis-Menten kinetics. Influence of temperature, reusability, and storage capacity of the free and immobilized glucose oxidase enzyme were investigated. It is determined that immobilized enzymes exhibit good storage stability and reusability. After immobilization of GOx in polymeric supports, the thermal stability of the enzyme increased and the maximum reaction rate (Vmax) decreased. The activity of the immobilized enzymes was preserved even after 5 months. The antibacterial and antifungal activity of the polymeric microspheres were evaluated by well-diffusion method against some selected pathogenic microorganisms. The antimutagenic properties of all compounds were also examined against sodium azide in human lymphocyte cells by micronuclei and sister chromatid exchange tests. © 2019 Wiley Periodicals, Inc. | en_US |
dc.identifier.doi | 10.1002/jbt.22432 | en_US |
dc.identifier.issn | 1095-6670 | |
dc.identifier.issue | 2 | en_US |
dc.identifier.scopusquality | Q2 | en_US |
dc.identifier.uri | https://dx.doi.org/10.1002/jbt.22432 | |
dc.identifier.uri | https://hdl.handle.net/20.500.12684/476 | |
dc.identifier.volume | 34 | en_US |
dc.indekslendigikaynak | Scopus | en_US |
dc.indekslendigikaynak | PubMed | en_US |
dc.language.iso | en | en_US |
dc.publisher | John Wiley and Sons Inc. | en_US |
dc.relation.ispartof | Journal of Biochemical and Molecular Toxicology | en_US |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.subject | antimicrobial property; antimutagenic effect; glucose oxidase; Polymeric microsphere; Pt4+-azomethine | en_US |
dc.title | Novel polymeric microspheres: Synthesis, enzyme immobilization, antimutagenic activity, and antimicrobial evaluation against pathogenic microorganisms | en_US |
dc.type | Article | en_US |
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