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菜心中高等电点高活性的乙醇酸氧化酶同工酶的纯化和特性
引用本文:尹汉萍,徐杰,曾秋莲,王再花,叶庆生,董宇亮,黄美意,韩雪,苏燕琼,庄莹莹.菜心中高等电点高活性的乙醇酸氧化酶同工酶的纯化和特性[J].中国生物化学与分子生物学报,2004,20(5):690-695.
作者姓名:尹汉萍  徐杰  曾秋莲  王再花  叶庆生  董宇亮  黄美意  韩雪  苏燕琼  庄莹莹
作者单位:1. 华南师范大学生命科学学院,广东省植物发育生物工程重点实验室,广州,510631;中国农业大学植物生理学与生物化学国家重点开放实验室,北京,100094
2. 华南师范大学生命科学学院,广东省植物发育生物工程重点实验室,广州,510631
基金项目:国家自然科学基金 (No .3 980 0 0 0 9),中国农业大学植物生理学与生物化学国家重点开放实验室基金 (G19980 10 10 0 8和G19990 1170 0 4),广东省自然科学基金 (No.0 2 110 5 )资助~~
摘    要:乙醇酸氧化酶 (EC 1 1 3 15 ,GO)被认为只含4 0kD一种碱性亚基 ,是因为从多种植物中获得了具GO活性的蛋白 ,SDS PAGE后呈约 4 0kD单带1] .菠菜GOcDNA编码约 370个氨基酸 ,即 4 0kD多肽 ,其碱 酸性氨基酸的比例高达 0 96 ,富含碱性氨基酸2 ] .已克隆的GOcDNA在E .coli中表达

收稿时间:2004-10-20
修稿时间:2003年12月11

Purification and Characterization of Glycolate Oxidase Isozyme with High Isoelectric Point and High Activity from Green Leaves of Brassica parachinensis Bailey
YIN Han-ping,XU Jie,ZENG Qiu-lian ,WANG Zai-hua ,YE Qing-sheng ,DONG Yu-liang ,HUANG Mei-yi ,HAN Xue ,SU Yan-qiong ,ZHUANG Yin-yin.Purification and Characterization of Glycolate Oxidase Isozyme with High Isoelectric Point and High Activity from Green Leaves of Brassica parachinensis Bailey[J].Chinese Journal of Biochemistry and Molecular Biology,2004,20(5):690-695.
Authors:YIN Han-ping    XU Jie    ZENG Qiu-lian  WANG Zai-hua  YE Qing-sheng  DONG Yu-liang  HUANG Mei-yi  HAN Xue  SU Yan-qiong  ZHUANG Yin-yin
Institution:( 1) College of Life Sciences, South China Normal University, Guangdong Key Laboratory of Biotechnology for Plant Development, Guangzhou 510631,China; 2) State Key Laboratory of Plant Physiology and Biochemistry, China Agricultural University, Beijing 100094,China
Abstract:Glycolate oxidase (GO) isozyme with high specific activity (75.0~279.0 U/mg) is purified quickly on DEAE- Cellulose column from Brassica parachinensis Bailey. Its pI is greater than 10.0 assayed by acetate cellulose membrane electrophoresis for 1 hour. In view of about ten kinds of pI varied from 4.5 to 10.0 are observed when the same GO isozyme is assayed in IEF for 14 hours, it is obvious that its pI decreases in IEF. Its pI also decreases when this GO isozyme is assayed in PAGE for 14 hours. Based on the results in SDS-PAGE, CGE-SDS, and IEF, it is most likely that this GO isozyme comprises two noncovalently associated 66 kD basic subunit and 40 kD acidic subunit, the phenomenon of pI change is related to subunit dissociation. The basic/acidic amino acid residues ratios in GO isozyme and its 40 kD acidic subunit are detected to be 0.66 and 0.54, respectively, a value much lower than that (0.96) in 40 kD peptide encoded by GO cDNA reported previously, indicating neither M r nor charge characteristic of this 40 kD peptide is similar to that of GO isozyme subunits, two subunits of GO isozyme may be the modified products of the same GO gene after post-translation.
Keywords:pI  glycolate oxidase isozyme  purification  subunit component
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