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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.
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页码:33 / 39
页数:7
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