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钝顶螺旋藻FtsZ在大肠杆菌中的表达和定位

吴娟, 邹路阳, 曾群安, 徐虹

吴娟, 邹路阳, 曾群安, 徐虹. 钝顶螺旋藻FtsZ在大肠杆菌中的表达和定位[J]. 植物科学学报, 2013, 31(2): 171-177. DOI: 10.3724/SP.J.1142.2013.20171
引用本文: 吴娟, 邹路阳, 曾群安, 徐虹. 钝顶螺旋藻FtsZ在大肠杆菌中的表达和定位[J]. 植物科学学报, 2013, 31(2): 171-177. DOI: 10.3724/SP.J.1142.2013.20171
WU Juan, ZOU Lu-Yang, ZENG Qun-An, XU Hong. Expression and Localization of FtsZ from Spirulina platensis in Escherichia coli[J]. Plant Science Journal, 2013, 31(2): 171-177. DOI: 10.3724/SP.J.1142.2013.20171
Citation: WU Juan, ZOU Lu-Yang, ZENG Qun-An, XU Hong. Expression and Localization of FtsZ from Spirulina platensis in Escherichia coli[J]. Plant Science Journal, 2013, 31(2): 171-177. DOI: 10.3724/SP.J.1142.2013.20171
吴娟, 邹路阳, 曾群安, 徐虹. 钝顶螺旋藻FtsZ在大肠杆菌中的表达和定位[J]. 植物科学学报, 2013, 31(2): 171-177. CSTR: 32231.14.SP.J.1142.2013.20171
引用本文: 吴娟, 邹路阳, 曾群安, 徐虹. 钝顶螺旋藻FtsZ在大肠杆菌中的表达和定位[J]. 植物科学学报, 2013, 31(2): 171-177. CSTR: 32231.14.SP.J.1142.2013.20171
WU Juan, ZOU Lu-Yang, ZENG Qun-An, XU Hong. Expression and Localization of FtsZ from Spirulina platensis in Escherichia coli[J]. Plant Science Journal, 2013, 31(2): 171-177. CSTR: 32231.14.SP.J.1142.2013.20171
Citation: WU Juan, ZOU Lu-Yang, ZENG Qun-An, XU Hong. Expression and Localization of FtsZ from Spirulina platensis in Escherichia coli[J]. Plant Science Journal, 2013, 31(2): 171-177. CSTR: 32231.14.SP.J.1142.2013.20171

钝顶螺旋藻FtsZ在大肠杆菌中的表达和定位

基金项目: 国家自然科学基金资助项目(30571446);福建省自然科学基金资助项目(2009J01193)。
详细信息
    作者简介:

    吴娟(1984-),女,硕士研究生,主要从事海洋分子生物学的研究。

    通讯作者:

    徐虹, E-mail: hxu@xmu.edu.cn

  • 中图分类号: Q949.22+1

Expression and Localization of FtsZ from Spirulina platensis in Escherichia coli

  • 摘要: FtsZ是与真核微管蛋白类似的原核骨架蛋白,能在细胞分裂位点聚合组装成环状结构而调控细胞分裂过程。为了研究钝顶螺旋藻(Spirulina platensis)FtsZ蛋白的功能,构建了钝顶螺旋藻FtsZ与绿色荧光蛋白GFP融合表达的质粒,并在大肠杆菌中进行了表达和定位研究,结果发现,表达融合蛋白GFP-FtsZ的大肠杆菌细胞由短杆状变为长丝状,且菌丝体长度与融合蛋白的表达量呈正比。在荧光显微镜下观察到融合蛋白GFP-FtsZ在长丝状体细菌中呈有规律的点状分布,这说明FtsZ蛋白功能高度保守,钝顶螺旋藻FtsZ蛋白能识别大肠杆菌分裂位点并装配成环状结构调控大肠杆菌细胞分裂,FtsZ蛋白的过量表达能抑制大肠杆菌正常的细胞分裂而导致长丝状体细胞的形成。
    Abstract: Prokaryotic cytoskeletal protein FtsZ, a microtubule homolog, assembles into a compact circular structure at the mid-cell and plays an important role in cytokinesis. To explore the function of FtsZ in Spirulina platensis morphogenesis, we cloned the ftsZ gene from S.platensis and constructed its fusion tag of GFP expression plasmid pGFP-FtsZ. The recombined expression vector was transformed to Escherichia coli BL21. Western blot analysis showed that the GFP-FtsZ fusion gene was successfully expressed in the transformant. The transformed bacteria that expressed the GFP-FtsZ protein changed from normal short-rod shapes and formed long filaments. The length of the filamentation cells was proportional to the expression amount of FtsZ in cells. Regular-dot distribution of the GFP-FtsZ fusion protein in transformed bacteria was observed by fluorescent light microscopy. The data demonstrated that FtsZ was a highly conserved functional protein. The FtsZ of S.platensis assembled the complete cytokinesis apparatus and formed a Z-ring structure at the future division site to regulate cell division in E.coli.The overexpression of FtsZ blocked the normal cell cycle and led to cell filamentation.
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出版历程
  • 收稿日期:  2012-06-20
  • 修回日期:  2013-01-03
  • 发布日期:  2013-04-29

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