生物技术进展 ›› 2018, Vol. 8 ›› Issue (1): 41-45.DOI: 10.19586/j.2095-2341.2017.0152

• 研究论文 • 上一篇    下一篇

CryNGc蛋白在转基因玉米和大肠杆菌中表达的等同性研究

赵方方1,刘洋2,井乐刚1,尹悦佳2,冯树丹1*,刘相国2*   

  1. 1.哈尔滨师范大学生命科学与技术学院, 哈尔滨 150025; 2.吉林省农业科学院农业生物技术研究所, 吉林省农业生物技术重点实验室, 长春 130033
  • 收稿日期:2017-11-17 出版日期:2018-01-25 发布日期:2017-12-07
  • 通讯作者: 冯树丹,教授,主要从事天然产物的开发与研究。E-mail:sdf6616@163.com;刘相国,副研究员,研究方向为功能基因的挖掘。E-mail:liu9983@163.com
  • 作者简介:赵方方,硕士研究生,研究方向为抗虫转基因玉米。E-mail:307890882@qq.com。
  • 基金资助:
    国家转基因生物新品种培育重大专项(2015ZX8013002-007);吉林省农业创新工程(CXGC2017ZY026)资助。

Equivalence Study of CryNGc Protein Expressed in Transgenic Maize and Escherichia coli

ZHAO Fangfang, LIU Yang, JING Legang, YIN Yuejia, FENG Shudan, LIU Xiangguo   

  1. 1.College of Life Science and Technology, Harbin Normal University, Harbin 150025, China; 2.Jilin Provincial Key Laboratory of Agricultural Biotechnology, Institute of Agricultural Biotechnology, Jilin Academy of Agricultural Sciences, Changchun 130033, China
  • Received:2017-11-17 Online:2018-01-25 Published:2017-12-07

摘要: 转基因玉米表达蛋白的身份鉴定和对玉米表达蛋白与大肠杆菌表达蛋白的等同性研究是进行蛋白安全性评价的重要前提。以人工合成的新型重组抗虫蛋白CryNGc 为研究材料,通过密码子优化、cryNGc杀虫蛋白编码基因化学合成、原核表达载体构建、大肠杆菌表达条件优化等方法原核表达 CryNGc 蛋白。在此基础上,利用SDS-PAGE电泳、免疫杂交分析和液相色谱-串联质谱鉴定技术对玉米转化体 HiII-NGc-1和大肠杆菌表达的CryNGc重组蛋白进行了特性分析和一致性评价。研究结果表明,抗虫基因cryNGc在转基因玉米和大肠杆菌中表达的蛋白电泳迁移率、免疫活性和氨基酸组成具有一致性,证实玉米转化体HiII-NGc-1中产生的CryNGc蛋白的特性与理论预测相符,且与大肠杆菌表达的CryNGc蛋白实质等同。研究结果为进一步开展新型抗虫重组蛋白CryNGc 玉米转化体的生物安全性评价提供了理论基础和数据支持。

关键词: 抗虫蛋白, cryNGc基因, 原核表达, 等同性, 转基因

Abstract: The important precondition of safety evaluation of protein in genetically engineered maize is protein identification and equivalence study of proteins expressed in genetically engineered maize and Escherichia coli. CryNGc protein was expressed in E. coli through optimized methods such as codon optimization, cryNGc insecticidal protein gene synthesis, prokaryotic expression vector construction and E. coli expression conditions optimizition. On this basis, the characteristics and consistency of the recombinant protein HiII-NGc-1 in maize and CryNGc expressed in E. coli were analyzed by SDS-PAGE, immunoblot analysis and liquid chromatography-tandem mass spectrometry. The results showed that there was consistent in the expression of cryNGc gene in transgenic maize and E. coli by electrophoresis mobility, immune competence and amino acid composition consistent. The results confirmed that the CryNGc protein characteristics of maize transformants HiII-NGc-1 was consistent with the theoretical prediction, and was substantially equivalent to the CryNGc protein expressed in E. coli. The results provided the theoretical basis and data support for further biosafety evaluation of the new insect-resistant recombinant protein CryNGc maize transformants.

Key words: insect-resistant protein, cryNGc gene, prokaryotic expression, equivalence, transgenic maize