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蓝藻Synechococcus sp.PCC 7942穿梭表达质粒的构建及胸腺素α1基因的表达

CONSTRUCTION OF SHUTTLE EXPRESSION VECTOR AND EXPRESSION OF THYMOSIN α1 IN SYNECHOCOCCUS SP.PCC7942

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【作者】 章军秦燕欧阳青徐虹周克夫刘仁海楼士林

【Author】 ZHANG Jun QIN Yan OUYANG Qing XU Hong ZHOU Ke Fu LIU Ren Hai LOU Shi Lin(The Key Laboratory of Ministry of Education for Cell Biology and Tumor Ce/l Engineering School of Life Science, Xiamen University, Xiamen 361005)

【机构】 细胞生物学与肿瘤细胞工程教育部重点实验室厦门大学生命科学学院细胞生物学与肿瘤细胞工程教育部重点实验室厦门大学生命科学学院 厦门 361005厦门 361005厦门 361005

【摘要】 利用本实验室构建的含蓝藻Plectonema boryanum内源小质粒的穿梭质粒pPRS-1,改建成含热诱导启动子、泛素融合的胸腺素α1(UB-Tα1)目的基因、卡那霉素抗性选择标记、rbcs终止子的新的穿梭表达重组质粒pPRFUT。将这种重组质粒转化蓝藻Synechococcus sp.PCC7942,通过抗性筛选获得了具卡那霉素抗性的转化藻株。经Southern-blot杂交证实,穿梭表达质粒已转入蓝藻Synechococcus sp. PCC7942细胞中;在42℃热诱导30min后,目的基因UB-Tα1得到较高水平表达,表达量约占总蛋白量的7.5%。

【Abstract】 The shutter expression vector pPREUT was constructed from the plasmid pPRS-1 containing the en dogenous snail plasmid of Plectonema boryanum. The expression elements such as heat shock gene groESL promoter, foreign gene Ub-thymosin α1, rbcS polyA terminator and Kanamycin resistance gene were all included. The shutter plasmid pPREUT was direcdy transferred into Synechococcus sp. PCC7942. The transformants were obtained through Kanamycin screening. Southern blotting analysis showed that the shutter plasmid have been transferred into Synechococcus sp. PCC7942. After induction by heat shock(42℃) for 30 min, the foreign protein LIR-Tα1 was ex pressed efficiently, which reacted 7.5% of total amount protein.

【基金】 国家863资助项目(863-819-04-03)
  • 【文献出处】 实验生物学报 ,Acta Biologiae Experimentalis Sinica , 编辑部邮箱 ,2003年01期
  • 【分类号】Q786
  • 【被引频次】7
  • 【下载频次】163
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