摘要
采用CTAB法提取玉米及其制品的总DNA,用PCR方法检测其中的转基因成分如花椰菜花叶病毒(Cauliflowermosaicvirus,CaMV)35S启动子、根癌农杆菌(Agrobacteriumtumefaciens)胭脂碱合成酶基因(nos)终止子、根癌农杆菌CP4菌株的EPSPS基因、吸水链霉菌(Treptomyceshygroscopicus)bar基因及苏云金芽孢杆菌库尔斯塔克亚种(Bacillusthuringiensissubsp.kurstaki)cryIA(b)基因,筛选到阳性样品,并建立了几组玉米内源zein基因和转基因成分之间的多重PCR检测方法。结果表明,建立的多重PCR方法用于同时检测玉米内源基因和转基因成分是可行的,值得推广;虽然我国还未有已获准商品化生产的转基因玉米,但国外转基因玉米已流入福建省。
The total DNAs of maize and its products were extracted by CTAB method. The positive samples were screened by detecting of several genetically modified components such as Cauliflower mosaic virus(CaMV) 35S promoter, Agrobacterium tumefaciens nopaline synthase(nos) terminator, A.tumefaciens strain CP4 EPSPS gene, Treptomyces hygroscopicus bar gene and Bacillus thuringiensis subsp, kurstaki cryIA(b) gene with single PCR. The multiplex PCR methods detecting synchronously of maize endogenous zein gene and several genetically modified components were developed. The results showed that the multiplex PCR methods developed for detecting synchronously of endogenous gene and genetically modified components were practical and worthy of being popularized, and there is no commercial genetically modified maize in our country, but foreign commercial transgenic maizes were inpoured into fujian province.
出处
《食品科学》
EI
CAS
CSCD
北大核心
2005年第9期380-384,共5页
Food Science
基金
福建省青年科技人才创新项目(2001J040)
国家质检总局科技项目(2003IK046)
福建出入境检验检疫局科研项目(FK2003-02)
关键词
玉米
转基因成分
PCR
多重PCR
maize
genetically modified component
PCR
multiplex PCR