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豌豆肌动蛋白异型体PEAc3的原核表达及其聚合特性分析

Prokaryotic expression and polymerization properties analysis of a pea actin isoform3(PEAc3)

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【作者】 张少斌刘曦刘国琴

【Author】 ZHANG Shao-bin1,LIU Xi1,LIU Guo-qin2(1.Biological Science and Technology College,Shenyang Agricultural University,Shenyang 110161,China;2.National Key Laboratory of Plant Physiology and Biochemistry,China Agricultural University,Beijing 100193,China)

【机构】 沈阳农业大学生物科学技术学院中国农业大学植物生理生化国家重点实验室

【摘要】 植物肌动蛋白在植物顶端生长、细胞分裂分化和细胞信号转导等多种生命活动中发挥着重要作用。豌豆中存在多种肌动蛋白异型体。研究豌豆肌动蛋白异型体PEAc3与组氨酸标签(His-tag)及绿色荧光蛋白(GFP)的融合表达,并分析了融合蛋白的聚合特性。采用RT-PCR的方法克隆PEAc3基因,构建原核表达载体pET30 a-His-PEAc3-GFP。用DNAman生物学软件分析表明,PEAc3融合蛋白全长675个氨基酸,分子量74.74 ku,等电点5.81。将pET30 a-His-PEAc3-GFP转入大肠杆菌BL21中,优化的诱导表达条件为:25℃,当菌液OD600达到0.8时加入IPTG(浓度0.1 mmol/L),诱导表达4 h。采用尿素变性复性、镍柱亲和层析的方法从包涵体中纯化获得高纯度融合蛋白。融合蛋白His-PEAc3-GFP能够体外聚合,聚合临界浓度为0.5μmol/L。单体His-PEAc3-GFP对DNaseⅠ有抑制作用,聚合后对肌球蛋白Mg-ATPase活性有一定的激活作用。上述结果表明,原核表达的His-PEAc3-GFP可能具有类似于一般肌动蛋白的聚合特性。

【Abstract】 Plant actins play very important role in many living process,such as apical growth,cell division or differentiation,signal transduction.There are many actin isoforms in pea.In this paper,PEAc3 fused with His-tag and green fluorescence protein(GFP) was expressed in E.Coli,and the polymerization properties of the fusion protein were analyzed.The gene of PEAc3 was cloned by RT-PCR,and a prokaryotic expression vector of pET30a-His-PEAc3-GFP was constructed.The fusion protein has 674 amino acids,the molecular weight(MW) of fusion protein is 74.74 ku,and its isoelectric point is 5.81(predicted by DNAman).The plasmid of pET30a-His-PEAc3-GFP was transformed into E.coli strain of BL21,the induction expression conditions for the fusion protein is as following:the E.coli BL21 with plasmid was cultured at 25 ℃,followed by addition of IPTG(0.1 mmol/L) in the culture liquid when its OD600 was about 0.8.The induction was performed for four hours.The fusion protein of His-PEAc3-GFP was purified from inclusion body by Ni-resins chromatography after denaturation and renaturation in urea.The polymerization property analysis in vitro indicated that His-PEAc3-GFP could be polymerized.The critical concentration for polymerizing was 0.5 μmol/L.The His-PEAc3-GFP monomers could inhiit the activity of DNaseⅠ.The polymerized His-PEAc3-GFP had the ability of activating the Mg-ATPase of myosin.So,we could probably draw a conclusion that the His-PEAc3-GFP purified from E.coli.has the similar polymerization characteristics with that of normal actins.

【基金】 植物生理生化国家重点实验室开放课题(PPB003);辽宁省教育厅项目(20080663);沈阳农业大学中青年导师基金项目(2007001)
  • 【文献出处】 中国农业大学学报 ,Journal of China Agricultural University , 编辑部邮箱 ,2010年03期
  • 【分类号】Q786
  • 【下载频次】90
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