Pai S B
Biochem Biophys Res Commun. 1983 Jan 27;110(2):412-6. doi: 10.1016/0006-291x(83)91164-6.
A phosphatase catalysing the hydrolysis of organophosphorus pesticides was purified to homogeneity using Cibacron 3GA-Sepharose CL 6B affinity chromatography. The enzyme which is localized in the periplasm of the bacterium Alcaligenes NC5 was extracted by treating with 0.2M MgCl2, pH 8.4. The enzyme was adsorbed to the Cibacron-Sepharose at pH 7.0 and eluted with Tris-HCl buffer at pH 8.0, with 47 per cent recovery. The enzyme thus obtained was electrophoretically homogeneous. This simple affinity purification procedure enhances the potential for its use in large scale detoxification systems.
使用汽巴克隆3GA-琼脂糖凝胶CL 6B亲和色谱法将一种催化有机磷农药水解的磷酸酶纯化至同质。通过用0.2M氯化镁(pH 8.4)处理,提取位于产碱菌NC5周质中的该酶。该酶在pH 7.0时吸附到汽巴克隆-琼脂糖凝胶上,并在pH 8.0的Tris-HCl缓冲液中洗脱,回收率为47%。由此获得的酶在电泳上是同质的。这种简单的亲和纯化方法提高了其在大规模解毒系统中应用的潜力。