提出了一种从基因工程毕赤酵母(Pichia pastoris)培养液中分离纯化重组巴西日圆线虫(Nippostrongylus brasiliensis)乙酰胆碱酯酶(NbAChE)的方法.采用Q-Sepharose Fast Flow强阴离子交换色谱柱对重组NbAChE进行了分离纯化.十二烷基硫酸钠聚丙烯酰胺凝胶电泳分析表明,纯化物的活性峰为单一蛋白质带,其相对分子质量约为66000.该方法的活性回收率为52.6%,纯化因子为3.87;纯化后AChE的比活为2 837 U/mg.结果表明,该法是一种理想的分离纯化重组NbAChE的方法.
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