Vinyl imidazole carrying metal-chelated beads for reversible use in yeast invertase adsorption


Osman B., Kara A., Uzun L., Besirli N., Denizli A.

JOURNAL OF MOLECULAR CATALYSIS B-ENZYMATIC, cilt.37, ss.88-94, 2005 (SCI-Expanded) identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 37
  • Basım Tarihi: 2005
  • Doi Numarası: 10.1016/j.molcatb.2005.09.007
  • Dergi Adı: JOURNAL OF MOLECULAR CATALYSIS B-ENZYMATIC
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.88-94
  • Anahtar Kelimeler: enzyme immobilization, invertase, chelating beads, N-vinyl imidazole, affinity beads, COVALENT IMMOBILIZATION, CATALASE ADSORPTION, AFFINITY ADSORBENTS, GLUCOSE-OXIDASE, HOLLOW-FIBERS, GLUCOAMYLASE, MEMBRANE, POLYETHYLENEIMINE, MICROSPHERES, HYDROLYSIS
  • Bursa Uludağ Üniversitesi Adresli: Evet

Özet

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. (c) 2005 Elsevier B.V. All rights reserved.