[1]邢宇俊,陆丹丹,吴季荣,等.用于检测转基因作物中调控元件的质粒标准分子的构建[J].江苏农业学报,2018,(06):1392-1400.[doi:doi:10.3969/j.issn.1000-4440.2018.06.027]
 XING Yu-jun,LU Dan-dan,WU Ji-rong,et al.Construction of standard plasmid molecules of regulatory elements to detect genetically modified crop[J].,2018,(06):1392-1400.[doi:doi:10.3969/j.issn.1000-4440.2018.06.027]
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用于检测转基因作物中调控元件的质粒标准分子的构建()
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江苏农业学报[ISSN:1006-6977/CN:61-1281/TN]

卷:
期数:
2018年06期
页码:
1392-1400
栏目:
加工贮藏·质量安全
出版日期:
2018-12-25

文章信息/Info

Title:
Construction of standard plasmid molecules of regulatory elements to detect genetically modified crop
作者:
邢宇俊陆丹丹吴季荣徐剑宏王园园梁杰史建荣
(江苏省农业科学院农产品质量安全与营养研究所/江苏省食品质量安全重点实验室-省部共建国家重点实验室培育基地/农业部农产品质量安全控制技术与标准重点实验室/农业部农产品质量安全风险评估实验室/江苏省转基因安全评价公共服务中心/江苏省现代粮食流通与安全协同创新中心/中德农产品质量安全评估技术研发中心,江苏南京210014)
Author(s):
XING Yu-junLU Dan-danWU Ji-rongXU Jian-hongWANG Yuan-yuanLIANG JieSHI Jian-rong
(Institute of Food Safety and Nutrition, Jiangsu Academy of Agricultural Sciences/Laboratory for Food Quality and Safety-State Key Laboratory Cultivation Base of Ministry of Science and Technology/Key Laboratory of Control Technology and Standard for Agro-product Safety and Quality, Ministry of Agriculture/Key Laboratory of Agro-product Safety Risk Evaluation, Ministry of Agriculture/Jiangsu Center for GMO Evaluation and Detection/Collaborative Innovation Center for Modern Grain Circulation and Safety/The Sino-German R&D Center for Agro-product Safety and Quality Control, Nanjing 210014, China)
关键词:
转基因作物质粒标准分子调控元件
Keywords:
genetically modified cropstandard plasmid moleculesregulatory element
分类号:
TS207.3
DOI:
doi:10.3969/j.issn.1000-4440.2018.06.027
文献标志码:
A
摘要:
为解决转基因农产品检测中阳性标准物质匮乏的问题,利用重叠PCR技术将检测过程中常用的调控元件CaMV35S启动子、FMV35S启动子、PAT29启动子、Ubiquitin启动子、NOS启动子、35S终止子、NOS终止子和E9终止子依次连接获得融合片段,再利用分子克隆技术将融合片段转化到载体pMD-19T中,获得含有调控元件的标准质粒pMD-RG。PCR和测序结果验证了标准分子构建的正确性,并且标准质粒的均匀性和稳定性比较好,符合标准物质候选物的要求,可代替阳性标准物质用于转基因成分的检测和研究。该质粒可用于大多数已经批准的转基因作物的检测和监管工作中。
Abstract:
In order to solve the problem of the lack of positive standard material for PCR detection of genetically modified(GM) crops, common regulatory elements during the detection process, such as CaMV35S promoter, FMV35S promoter, PAT29 promoter, Ubiquitin promoter, NOS promoter, 35S terminator, NOS terminator and E9 terminator, were selected and connected successively by overlapping PCR technology to obtain the fusion gene fragments. The fragments were fused to pMD-19T vector to get the standard plasmid pMD-RG by the molecular cloning technology. The accuracy of standard molecular construction was verified by PCR and sequencing. The uniformity and stability of reference molecules were very well, and the reference molecule could be used as the candidate of reference material. The constructed plasmids can be used in the detection and supervision of most approved GM crops.

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备注/Memo

备注/Memo:
收稿日期:2018-01-11 基金项目:国家转基因生物新品种培育重大专项(2016ZX08011-003);国家自然科学基金项目(31301488);江苏省农业科技自主创新基金项目[CX(14)5065] 作者简介:邢宇俊(1977-),女,山东莱芜人,博士,副研究员,主要从事转基因产品检测技术研究;(E-mail)xingyujun106@126.com 通讯作者:史建荣,(E-mail) shiji@jaas.ac.cn
更新日期/Last Update: 2018-12-28