A QUANTITATIVE COMPETITOR PCR ASSAY TO DETECT GENETICALLY MODIFIED ROUNDUP-READY SOYBEANS IN COMMERCIALLY SOLD FOODS IN IRAN

E. Ghazizadeh, A. Mousavi, Faranak Hadi
{"title":"A QUANTITATIVE COMPETITOR PCR ASSAY TO DETECT GENETICALLY MODIFIED ROUNDUP-READY SOYBEANS IN COMMERCIALLY SOLD FOODS IN IRAN","authors":"E. Ghazizadeh, A. Mousavi, Faranak Hadi","doi":"10.22059/PBS.2014.52302","DOIUrl":null,"url":null,"abstract":"Due to ever-increasing global diffusion and related socio-economic implications, the detection of genetically modified organisms (GMOs) is very important. In this study, we design a plasmid containing two genes in mutated form as construct-specific (cp4 epsps) and event-specific (pd35S). It is applied for quantitative-competitor (QC) PCR as a simple and reliable method for the detection of GM food. This plasmid is calibrated with the external standard of the IRMM (The Institute for Reference Materials and Measurements), and then used to detect the presence of cp4 epsps and pd35S sequences in five foods derived from GM round-ready (RR) soya sold commercially in Iran. The results indicate the presence of GM RR soya in these products, quantitatively. In order to detect whether they contain more or less than 1% RR soya DNA, QCPCR with various amounts of DNA plasmids as a standard was performed. The results show that this plasmid can be used as a calibrator for 1% cp4 epsps and pd35S, and that it can also be applied instead of 1% IRMM genomics.","PeriodicalId":20726,"journal":{"name":"Progress in Biological Sciences","volume":"5 1","pages":"235-243"},"PeriodicalIF":0.0000,"publicationDate":"2014-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Progress in Biological Sciences","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.22059/PBS.2014.52302","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 1

Abstract

Due to ever-increasing global diffusion and related socio-economic implications, the detection of genetically modified organisms (GMOs) is very important. In this study, we design a plasmid containing two genes in mutated form as construct-specific (cp4 epsps) and event-specific (pd35S). It is applied for quantitative-competitor (QC) PCR as a simple and reliable method for the detection of GM food. This plasmid is calibrated with the external standard of the IRMM (The Institute for Reference Materials and Measurements), and then used to detect the presence of cp4 epsps and pd35S sequences in five foods derived from GM round-ready (RR) soya sold commercially in Iran. The results indicate the presence of GM RR soya in these products, quantitatively. In order to detect whether they contain more or less than 1% RR soya DNA, QCPCR with various amounts of DNA plasmids as a standard was performed. The results show that this plasmid can be used as a calibrator for 1% cp4 epsps and pd35S, and that it can also be applied instead of 1% IRMM genomics.
在伊朗商业销售的食品中检测转基因抗草甘膦大豆的定量竞争者PCR测定
由于不断增加的全球传播和相关的社会经济影响,转基因生物(GMOs)的检测是非常重要的。在这项研究中,我们设计了一个含有两个突变形式的质粒,分别是结构特异性(cp4 epsps)和事件特异性(pd35S)。作为一种简便、可靠的转基因食品检测方法,应用于定量竞争PCR (QC)中。该质粒使用IRMM(标准物质和测量研究所)的外部标准进行校准,然后用于检测在伊朗商业销售的五种转基因大豆衍生食品中cp4 epsps和pd35S序列的存在。结果定量地表明这些产品中存在转基因抗草甘膦大豆。为了检测它们是否含有多于或少于1%的RR大豆DNA,以不同数量的DNA质粒作为标准进行QCPCR。结果表明,该质粒可作为1% cp4 epsps和pd35S的校定剂,也可替代1% IRMM基因组学。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信