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作 者:马中良[1] 史永昶[1] 姜涌明[1] 李艳利[1] 赵国俊[1]
出 处:《江苏农学院学报》1998年第4期89-92,共4页Jiangsu Agricultural Research
摘 要:以猪血为材料,采用等电点沉淀和724树脂离子交换柱层析分离提纯,得凝血酶原,经CaCl2激活后,通过DEAE-纤维素离子交换柱层析,获得比活为1200IU/mg的凝血酶制剂,其收率为32.1%。研究发现,NaCl浓度对猪凝血酶活力有较大的影响,加1mol/LNaCl于凝血酶溶液中,室温(25℃)放置3h后,活力丧失50%。猪凝血酶的最适温度和最适pH分别是37℃和pH7.0。猪凝血酶在pH7.0、40℃下放置27h,活力丧失84%。通过SephadexG-100凝胶层析,测出猪凝血酶的分子量为30kd。The porcine prothrombin was isolated by using isoelectric fractionation and 724 resin ion exchange column chromatography. The thrombin was obtained by DEAE cellulose ion exchange column chromatography form the prothrombin which was activated by CaCl 2. The purified thrombin had specific activity 1200 IU/mg and the recovery was 32.1%. The concentration of NaCl significantly affected the activity of porcine thrombin. In 0.6 mol/L NaCl at 25℃ for 3 h, it lost 50% activity. The optimum pH and temperature of porcine thrombin were pH 7 and 37℃ respectively. In pH7, 40℃, for 27 h, the enzyme lost 84% activity. The molecular weight of thrombin was 30 kd determined by Sephadex G 100 gel filtration.
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