The penicillin G acylase from Alcaligenes faecalis was covalently immobilized to epoxy-type carrier Eurpergit C.The immobilization conditions including the ratio of the enzyme to the support,reaction time,pH and temperature were studied.The optimized immobilization conditions are 375 mg recombinantAlcaligenes faecalis penicillin G acylase of 5 000 U/g specific activi-ty to per gram Eupergit C,pH 8.0 and 30 ℃.After stirring for 120 h,the activity of immobilized penicillin G acylase is up to 220 U/g and the efficiency is 10.7%.The immobilized enzyme can completely hydrolysis penicillin G potassium salt in saturated butyl-acetate phosphate buffer.After hydrolyzing penicillin G potassium salt 15 times in a reactor,the immobilized enzyme still remains 95% activity and it shows a good operational stability.%粪产碱杆菌来源的青霉素 G 酰化酶通过共价结合在环氧型载体 Eupergit C 上,通过对酶质量浓度、固定化反应时间、pH 值以及反应温度等条件的考察,确定了最优固定化条件:375 mg 比活力5000 U/g 的重组粪产碱杆菌青霉素 G 酰化酶蛋白对应1 g 载体,最适 pH 8.0,反应温度30℃。反应120 h 后制得固定化青霉素 G 酰化酶活力达到220 U/g,固定化酶效率为10.7%。该固定化酶可在含饱和乙酸丁酯磷酸缓冲液中彻底水解青霉素 G 钾盐。经过15批连续水解反应,固定化酶仍保持95%的活力,展现出良好的稳定性。
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