水稻rab5B基因在大肠杆菌中的表达、纯化和GTP结合分析
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国家高技术“863”计划资助项目(BH-01-02-03);中国科学院华南植物研究所所长基金资助项目(10-00-312).


Prokaryotic Expression , Purification and GTP-binding Assay of rab5B Gene From Rice(Oryza sativa L.)
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This research was supported by State 863 High Technology R&D Project of China (BH-01-02-03) and The Dean Foundation of South China Institute of Botany, The Chinese Academy of Sciences (10-00-312).

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    摘要:

    Rab5B类蛋白因为其编码产物的N端具有特殊结构而被认为是一类特殊的蛋白质.水稻rab5B基因Osrab5B是这类蛋白质基因在单子叶植物中的首例发现.将Osrab5B基因的编码序列按正确读码框重组到具有谷胱甘肽硫转移酶(glutathione S-transferase, GST)融合标签的pGEX-4T1表达载体中,转化大肠杆菌,获得了稳定表达目标融合蛋白的菌株,经GSTrapTM柱纯化,获得了纯化的目标融合蛋白.GTP结合试验表明,在原核细胞中表达出的GST-OsRab5B融合蛋白具有体外结合GTP的能力.

    Abstract:

    Rab protein family belongs to the superfamily of ras-like GTP-binding protein. Osrab5B,designated for rab5B gene from rice, encodes a putative Rab protein. In order to investigate the physiological and biochemical functions of this protein OsRab5B, the complete coding sequence (CDS) of Osrab5B was amplified and inserted into a prokaryotic GluGST expression vector, pGEX-4T1, thus constructing the prokaryotic expression vector. The in-frame recombinant plasmid was confirmed by sequencing and was named pG-5BE. Then the vector pG-5BE was transformed into prokaryotic cell E.coli strain BL21 (DE3). The GST fusion protein expressed by this positive strain was purified with GSTrapTM column. The result from GTP-binding assay proved that the fusion protein has GTP-binding ability.

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林慧贤,刘筱斌,梁承邺,刘良式.水稻rab5B基因在大肠杆菌中的表达、纯化和GTP结合分析[J].生物化学与生物物理进展,2002,29(3):434-438

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  • 收稿日期:2001-10-12
  • 最后修改日期:2001-12-03
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