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张春香1△ 罗学刚2 童锦禄3 蒋声海1 符玉梅1 杨道文1.牛肠激酶催化亚基工程菌的构建[J].现代生物医学进展英文版,2011,11(3):489-492.
牛肠激酶催化亚基工程菌的构建
Building Bovine Enterokinase Catalytic Subunit Engineering Bacteria
  
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中文关键词: 牛肠激酶催化亚基  工程菌  构建
英文关键词: Bovine enterokinase catalytic subunit  Engineering bacteria  Building
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Author NameAffiliation
ZHANG Chun-xiang1△, LUO Xue-gang2, TONG Jin-lu3, JIANG Sheng-hai1, FU Yu-mei1, YANG Dao-wen1 南京医科大学附属江宁医院药剂科 
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中文摘要:
      目的:构建牛肠激酶催化亚基工程菌。方法:将带有牛肠激酶催化亚基(bEKL)的结构基因进行克隆,将克隆产物纯化后,构 建bEKL克隆质粒,后构建bEKL表达质粒,并将表达质粒制导入备感受态细胞,进行蛋白表达。结果:琼脂糖电泳验证牛肠激酶 催化亚基基因已经成功地插入表达载体,序列与预期设计一致。结论:表达质粒构建成功。
英文摘要:
      Objective: To build a Bovine Enterokinase Catalytic Subunit Engineering Bacteria. Methods: Clone the structural gene of Enterokinase Catalytic Subunit, and construct bEKL clonic plasmid. Then construct bEKL expressive plasmid, and translate the expressive plasmid into competent cell. Results: The agarose electrophoresis revealed that Bovine Enterokinase Catalytic Subunit gene had been successfully inserted expressive plasmid and the sequence was same with primary design. Conclusion: The expressive plasmids was successfully builded.
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