Development of the reversible PGA immobilization by using the immobilized metal ion affinity membrane

被引:13
|
作者
Chen, Chih-I [1 ]
Ko, Yi-Miao [2 ]
Lien, Wei-Ling [2 ]
Lin, Yi-Hsuan [2 ]
Li, I-Tsang [2 ]
Chen, Chien-Hsun [2 ]
Shieh, Chwen-Jen [3 ]
Liu, Yung-Chuan [2 ]
机构
[1] Hsiuping Univ Sci & Technol, Dept Chem Engn, Taichung 41280, Taiwan
[2] Natl Chung Hsing Univ, Dept Chem Engn, Taichung 40227, Taiwan
[3] Natl Chung Hsing Univ, Ctr Biotechnol, Taichung 40227, Taiwan
关键词
Immobilized metal affinity membrane; Enzyme immobilization; Penicillin G acylase; Regeneration process; Coordination immobilization; PENICILLIN-G ACYLASE; PROTEIN ADSORPTION; ESCHERICHIA-COLI; PURIFICATION; CHROMATOGRAPHY; SUPPORTS;
D O I
10.1016/j.memsci.2012.01.022
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
In this study, an immobilized metal ion affinity membrane (IMAM) was prepared and used to immobilize penicillin G acylase (PGA). The stability of storage of the immobilized PGA membrane (IPM) was tested. When stored in deionized water (DI) at 4 degrees C, only 19% residual activity of IPM was retained for 10 days. However, when stored in 10 mM phosphate buffer (PB, pH 8) with 0.1% NaN3, the IPM can retain 99% of its activity for a 10-day reaction and storage test. The feasibility of the IPM regeneration after a long period of reaction was investigated. When using 100 mM EDTA as the stripping solution, the re-immobilized capacity for PGA is only 52% of the original one after 4 regenerations. When the regeneration process was modified by using the stripping solution (300 mM NaCl, 25 mM EDTA, 20 mM PB, pH 8) for 30 min, then immersed in 0.5 M HCl and 0.5 M NaOH respectively for 10 min, the resulting IMAM can reserve 99% PGA immobilized activity after 5 regenerations. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:33 / 39
页数:7
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