Development of the magnetic beads for dye ligand affinity chromatography and application to magnetically stabilized fluidized bed system

被引:17
作者
Tuzmen, Nalan [1 ]
Akdogan, Funda
Kalburcu, Tuelden
Akgol, Sinan [2 ]
Denizli, Adil [3 ]
机构
[1] Dokuz Eylul Univ, Dept Chem, Fac Sci & Arts, TR-35600 Izmir, Turkey
[2] Adnan Menderes Univ, Dept Chem, Aydin, Turkey
[3] Hacettepe Univ, Dept Chem, TR-06532 Ankara, Turkey
关键词
Dye-affinity beads; Magnetic polymers; Protein purification; beta-Casein; Magnetic beads; BETA-CASEIN; ANTIBODY PURIFICATION; HUMAN SERUM; ADSORBENT; ADSORPTION; FIELD; REMOVAL; ALBUMIN;
D O I
10.1016/j.procbio.2009.12.001
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Magnetic poly(2-hydroxyethylmethacrylate) [mPHEMA] beads were prepared by suspension polymerization of HEMA in the presence of Fe(3)O(4) nano-powder. Cibacron Blue F3GA was covalently immobilized to the mPHEMA beads via nucleophilic substitution reaction between chloride of its triazine ring and hydroxyl groups of HEMA under alkaline conditions. The mPHEMA/Cibacron Blue F3GA beads (100-140 mu m in diameter) carrying 68.3 mu mol Cibacron Blue F3GA per gram polymer were used for beta-casein adsorption studies. Adsorption studies were performed under different conditions in a batch system (i.e., pH beta-casein initial concentration, temperature, and ionic strength) and then in a magnetically stabilized fluidized bed (MSFB) system. The swelling ratio of the mPHEMA was 62.1%. The maximum adsorption capacity for batch system was 20.2% lower as compared to the value obtained in MSFB. The mPHEMA/Cibacron Blue F3GA beads could be repeatedly applied for beta-casein adsorption without significant losses in the adsorption capacity. (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:556 / 562
页数:7
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