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Purification of penicillin G acylase using immobilized metal affinity membranes

机译:使用固定化金属亲和膜纯化青霉素G酰基转移酶

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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 ℃, 0.5 M NaCl, 32.04 μmol Cu~(2+) per disk with 10 mM sodium phosphate buffer, pH 8.5, whereas elution conditions were: 1 M NH_4Cl 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.
机译:具有修饰的再生纤维素的固定化金属亲和膜(IMAM)用于纯化青霉素G酰基转移酶(PGA)。为了研究PGA在IMAM上的吸附能力,研究了螯合剂表面密度,螯合金属,负载温度,pH,NaCl浓度和洗脱液等因素。最佳的上样条件是在4℃,0.5 M NaCl,32.04μmolCu〜(2 +)/盘中用10 mM磷酸钠缓冲液,pH 8.5,而洗脱条件是:1 M NH_4Cl在10 mM磷酸钠缓冲液中,pH 6.8。通过将这些色谱条件应用于小柱中的流动实验,可获得比活性的9.11倍纯化,PGA纯化回收率为90.25%。同时,使用EDTA再生溶液可实现八倍以上的膜可重复使用性。

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