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rNM23-H1/NDPK-A中试纯化工艺研究
引用本文:钱垂文,罗勇,张美英,林锋,王一飞.rNM23-H1/NDPK-A中试纯化工艺研究[J].生物技术,2002,12(1):23-24.
作者姓名:钱垂文  罗勇  张美英  林锋  王一飞
作者单位:广州暨南生物医药研究开发基地,广东, 广州 510632
基金项目:“8 6 3”科研基金项目 (10 2 - 0 8- 0 7- 0 5 ),广州市科委 基金资助项目 (1999-Z - 0 0 7- 0 1)
摘    要:为比较3种DEAE填料对rNM23-H1/NDPK-A的纯化效果,利用同一批中试发酵样品在相同的条件下进行离子交换层析,分别收集P0.2和P1.0两个洗脱峰。通过对洗脱峰中蛋白质含量、目标蛋白相对含量以及酶比活的测定,计算得出Matrex Cellufine A-200,DEAE Sephadex A-25,Macro-Prep DEAE Support三种填料相对应的NDPK-A得率及纯化倍数分别为74.5%、40.8%、92.6%、2.4、1.9、3.1倍。综合分析表明Macro-Prep DEAE Support填料对rNM23-H1/NDPK-A的纯化效果最好。

关 键 词:rNM23-H1/NDPK-A  填料  纯化工艺  目标蛋白  抑癌基因
文章编号:1004-311X(2002)01-0023-02
修稿时间:2001年8月29日

Purification of rNM23-H1/NDPK-A in middle-scale
QIAN Chui-wen,LUO Yong,ZHANG Mei-ying,LIN Feng,WANG Yi-fei.Purification of rNM23-H1/NDPK-A in middle-scale[J].Biotechnology,2002,12(1):23-24.
Authors:QIAN Chui-wen  LUO Yong  ZHANG Mei-ying  LIN Feng  WANG Yi-fei
Abstract:To compare purification of rNM23-H1/NDPK-A with three DEAE media,ion exchange chromatography experiments were made using a batch of fermentation samples at the same operating conditions Fractions of P 0 2 and P 1 0 were collected solely By analysis of parameters of fractions of P 0 2 and P 1 0 in all experiments,efficient of NDPK-A and purification times of enzyme activity of one microgram protein is 74 5%,40 8%,92 6%,2 4,1 9,3 1 times corresponding to Matrex Cellufine A-200,DEAE Sephadex A-25,Macro-Prep DEAE support media From these above,a conclusion can be drawn that Macro-Prep DEAE support media is the best one in three media
Keywords:media  DEAE  purification
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