Title of article
Purification of penicillin G acylase using immobilized metal affinity membranes
Author/Authors
Liu، نويسنده , , Yung-Chuan and ChangChien، نويسنده , , Chih-Chiang and Suen، نويسنده , , Shing-Yi، نويسنده ,
Issue Information
روزنامه با شماره پیاپی سال 2003
Pages
10
From page
67
To page
76
Abstract
The immobilized metal affinity membrane (IMAM) with modified regeneration cellulose was employed for purification of penicillin G acylase (PGA). For studying PGA adsorption capacity on the IMAM, factors such as chelator surface density, chelating metal, loading temperature, pH, NaCl concentration and elution solutions were investigated. The optimal loading conditions were found at 4 °C, 0.5 M NaCl, 32.04 μmol Cu2+ per disk with 10 mM sodium phosphate buffer, pH 8.5, whereas elution conditions were: 1 M NH4Cl with 10 mM sodium phosphate buffer, pH 6.8. By applying these chromatographic conditions to the flow experiments in a cartridge, a 9.11-fold purification in specific activity with 90.25% recovery for PGA purification was obtained. Meanwhile, more than eight-times reusability of the membrane was achieved with the EDTA regeneration solutions.
Keywords
enzymes , Penicillin G acylase
Journal title
Journal of Chromatography B
Serial Year
2003
Journal title
Journal of Chromatography B
Record number
1455749
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