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以聚乙二醇为层析伴侣同时制备SOD、过氧化氢酶和血红蛋白
引用本文:王永权, 路秀玲, 苏志国,.以聚乙二醇为层析伴侣同时制备SOD、过氧化氢酶和血红蛋白[J].生物工程学报,2005,21(3):466-472.
作者姓名:王永权  路秀玲  苏志国  
作者单位:中国科学院过程工程研究所生化工程国家重点实验室,北京,100080
基金项目:国家自然科学基金重点基金项目 (No.2 0 13 60 2 0 ),中国科学院知识创新重点方向项目~~
摘    要:发展了一条从红细胞裂解液中同时制备超氧化物歧化酶(SOD)、过氧化氢酶和血红蛋白的新工艺。采用0 75 %的聚乙二醇600作为层析伴侣,使血红蛋白直接流过阴离子交换层析柱,同时吸附SOD和过氧化氢酶。经过梯度洗脱获得SOD和过氧化氢酶组分,再经过疏水性相互作用层析与凝胶过滤层析相串联,使SOD和过氧化氢酶得到纯化。纯化后的SOD和过氧化氢酶的比活力分别达到15932u/mg和65918u/mg ,血红蛋白的纯度达到99.9%以上。总回收率为:SOD ,47.4% ;过氧化氢酶,29.6% ;血红蛋白,88.7%。

关 键 词:超氧化物歧化酶    过氧化氢酶    血红蛋白    离子交换层析    疏水性相互作用层析  
文章编号:1000-3061(2005)03-0466-07
修稿时间:2005年1月10日

Simultaneous Purification of Superoxide Dismutase, Catalase and Hemoglobin from Bovine Erythrocyte Lysate with PEG 600 as Chaperon
WANG Yong-quan,LU Xiu-ling,SU Zhi-guo.Simultaneous Purification of Superoxide Dismutase, Catalase and Hemoglobin from Bovine Erythrocyte Lysate with PEG 600 as Chaperon[J].Chinese Journal of Biotechnology,2005,21(3):466-472.
Authors:WANG Yong-quan  LU Xiu-ling  SU Zhi-guo
Institution:State Key Laboratory of Biochemical Engineering, Institute of Process Engineering, Chinese Academy of Sciences, Beijing 100080, China.
Abstract:Superoxide dismutase, catalase and hemoglobin were purified simultaneously from the same batch of bovine erythrocyte lysate. The process involves an initial anion exchange chromatography, followed by a hydrophobic interaction chromatography and gel filtration chromatography. 0.75% polyethylene glycol 600 was added as a purification chaperon before the anion exchange chromatography. The hemoglobin fraction passed through the ion exchange column without being retained. The superoxide dismutase and catalase were adsorbed by the column and were eluted separately during elution. The two eluted fractions containing crude superoxide dismutase and catalase were further purified with hydrophobic interaction chromatography and gel filtration chromatography in sequence. The specific activities of superoxide dismutase and catalase were 15932u/mg and 65918u/mg, respectively. SDS-polyacrylamide gel electrophoresis and gel filtration chromatography were used to analyze the purity of the proteins. The purity of superoxide dismutase, catalase and hemoglobin were 77.6%, 81.9% and 99.9%, respectively. The total recoveries for superoxide dismutase, catalase and hemoglobin were 47.4%, 29.6% and 88.7%, respectively.
Keywords:superoxide dismutase  catalase  hemoglobin  ion exchange chromatography  hydrophobic interaction chromatography
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