首页 | 本学科首页   官方微博 | 高级检索  
     检索      

CryIA(c)和gna融合基因植物表达载体的构建
引用本文:冯翠莲,张树珍.CryIA(c)和gna融合基因植物表达载体的构建[J].热带作物学报,2010,31(2):224-228.
作者姓名:冯翠莲  张树珍
作者单位:1. 中国热带农业科学院热带生物技术研究所,海口571101;海南大学农学院,海南儋州,571737
2. 中国热带农业科学院热带生物技术研究所,海口,571101
基金项目:中央级公益性科研院所基本科研业务费,中国热带农业科学院院基金,现代农业产业技术体系建设专项基金 
摘    要:采用重叠延伸PCR技术(gene splicing by overlap extension PCR,简称SOE PCR),通过连接多肽FMDV2A序列将CryIA(c)和gna基因相融合,得到CryIA(c)-2A-gna抗虫融合基因。并进一步将玉米UBI启动子和融合基因(CryIA(c)-2A-gna)分别连接到植物表达载体pCAMBIA3300上,构建成由玉米UBI启动子驱动抗虫融合基因的植物表达载体pNUBG。经过限制性酶切分析鉴定,结果表明,含有融合基因的植物表达载体构建成功。

关 键 词:重叠延伸PCR  融合基因  表达载体

Construction of Expression Vector Harboring CryIA(c) and gna Fusion Gene
Feng Cuilian and Zhang Shuzhen.Construction of Expression Vector Harboring CryIA(c) and gna Fusion Gene[J].Chinese Journal of Tropical Crops,2010,31(2):224-228.
Authors:Feng Cuilian and Zhang Shuzhen
Institution:Feng Cuilian1,2,Zhang Shuzhen1 1 Institute of Tropical Bioscience , Biotechnology,CATAS,Haikou,Hainan 571101,2 College of Agronomy,Hainan University,Danzhou,Hainan 571737,China
Abstract:CryIA(c)and gna genes were ligated with FMDV2A by using the technique of gene splicing by overlap extension PCR(SOE PCR)to produce an insect-resistant fusion gene CryIA(c)-2A-gna.Then the maize's UBI promoter and the fusion gene were cloned into the plant expression vector pCAMBIA3300 to construct a plant expression vector pNUBG consisting of UBI promoter-driven insect-resistant fusion gene.These recombinant plasmids were confirmed by restriction enzyme and PCR analysis,and the results showed that these rec...
Keywords:FMDV2A  splicing by overlap extension PCR  FMDV2A  fusion gene  expression vector
本文献已被 CNKI 维普 万方数据 等数据库收录!
点击此处可从《热带作物学报》浏览原始摘要信息
点击此处可从《热带作物学报》下载免费的PDF全文
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号