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Title: | Vinyl imidazole carrying metal-chelated beads for reversible use in yeast invertase adsorption |
Authors: | Uzun, Lokman Denizli, Adil Uludağ Üniversitesi/Fen Edebiyat Fakültesi/Kimya Bölümü. Osman, Bilgen Kara, Ali Beşirli, Necati AAG-6271-2019 ABI-3951-2020 15221651200 7102824859 6507924888 |
Keywords: | Enzyme immobilization N-vinyl imidazole Invertase Chelating beads Affinity beads Covalent immobilization Microspheres Catalase adsorption Affinity adsorbents Glucose-oxidase Hollow-fibers Glucoamylase Membrane Polyethyleneimine Hydrolysis |
Issue Date: | 1-Dec-2005 |
Publisher: | Elsevier Science BV |
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. |
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. |
URI: | https://doi.org/10.1016/j.molcatb.2005.09.007 http://hdl.handle.net/11452/21261 |
ISSN: | 1381-1177 |
Appears in Collections: | Scopus Web of Science |
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