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XA21和PI-D2激酶蛋白质在酿酒酵母中的表达及其自我磷酸化研究
引用本文:王书利,李莉云,尚俊军,王静,刘国振.XA21和PI-D2激酶蛋白质在酿酒酵母中的表达及其自我磷酸化研究[J].微生物学报,2007,47(6):1009-1012.
作者姓名:王书利  李莉云  尚俊军  王静  刘国振
作者单位:1. 河北农业大学生命科学学院,保定,071001
2. 中国科学院遗传与发育生物学研究所,北京,100101
摘    要:白叶枯病和稻瘟病是最主要的水稻病害。Xa21是水稻白叶枯病抗性基因,Pi-d2是稻瘟病抗性基因,二者都编码类受体激酶蛋白质。在前期研究中,曾系统地研究了细菌中表达XA21激酶蛋白质的生化活性。在此实验中利用真核表达系统酿酒酵母对Xa21和Pi-d2编码的蛋白激酶进行了表达、纯化及自我磷酸化活性分析,为进一步的生化分析、蛋白质-蛋白质相互作用研究、底物筛选等奠定了基础。

关 键 词:水稻  白叶枯病  稻瘟病  抗病基因  酿酒酵母
文章编号:0001-6209(2007)06-1009-04
收稿时间:2007/3/23 0:00:00
修稿时间:2007-03-23

Expression and autophosphorylation analysis of XA21 and PI-D2 protein kinases in Saccharomyces cerevisiae
WANG Shu-li,LI Li-yun,SHANG Jun-jun,WANG Jing and LIU Guo-zhen.Expression and autophosphorylation analysis of XA21 and PI-D2 protein kinases in Saccharomyces cerevisiae[J].Acta Microbiologica Sinica,2007,47(6):1009-1012.
Authors:WANG Shu-li  LI Li-yun  SHANG Jun-jun  WANG Jing and LIU Guo-zhen
Institution:College of Life Sciences; Agricultural University of Hebei; Baoding 071001; China;College of Life Sciences; Agricultural University of Hebei; Baoding 071001; China;Institute of Genetics and Developmental Biology; Chinese Academy of Sciences; Beijing 100101; China;Institute of Genetics and Developmental Biology; Chinese Academy of Sciences; Beijing 100101; China;College of Life Sciences; Agricultural University of Hebei; Baoding 071001; China
Abstract:Rice bacterial blight and blast are the most crucial rice disease. Xa21 confers resistance to bacterial blight,while Pi-d2 confers resistance to rice blast. Both Xa21 and Pi-d2 encode receptor kinase-like proteins. Biochemical properties of XA21 kinase expressed in bacterial were characterized in our previous report. In this study,both XA21 and PI-D2 kinase domain were PCR amplified and cloned into yeast expression vector pEGH via recombinational cloning strategy,kinase proteins expressed in eukaryotic yeast system was purified and autophosphorylation assay was carried out. The results indicated that XA21 and PI-D2 protein can be detected by SDS-PAGE and showed expected molecular weight. Autophosphorylation assay indicated that yeast expressed XA21 and PI-D2 were active when incubated with P~ 32 labelled ATP. The experiment provided basic materials for biochemical prosperity analysis,protein-protein interaction and substrate screening research.
Keywords:rice  bacterial blight  rice blast  disease resistance gene  Saccharomyces cerevisiae
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