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Development of multiplex and construct specific PCR assay for detection of cry2Ab transgene in genetically modified crops and product

机译:开发用于检测转基因作物和产品中cry2Ab转基因的多重和特异性PCR检测方法

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摘要

An efficient detection system for trait validation and screening of GMOs is a much sought after procedure, which could also help in regulatory compliance. Currently, in India, a number of cry2Ab transgene carrying GM crops are undergoing field trial i.e., MON15985 cotton, Bt rice, Bt okra, Bt corn, Bt brinjal, Bt potato and Bt tomato. In this study, we report a qualitative assay for detection for cry2Ab (326 bp). Further, the amplification compatibility with promoter, p35S (195 bp), terminator, t-nos(180 bp) and marker gene, npt // (275 bp) was also confirmed using Bt cotton event MON15985 as reference material. The detection sensitivity was 0.1% that is far below the requirement of the stringent European Union (EU) regulations of 0.9%. The targetDNA when spiked with either MECH-12 (crylAc), RR-soya (epsps) or MON-810 (crylAb) showed no inhibitory effect on cry2Ab detection. Moreover, the cry2Ab specific transgene construct (1.9 kb) was amplified and its identity confirmed by a nested PCR. Hence,a comprehensive multiplex PCR method for detection of cry2Ab gene in a GM crop/products was established. This is possibly a first report showing concurrent amplification of cry2Ab transgene, promoter, terminator and marker gene.
机译:一个非常有效的检测系统,用于特征验证和转基因生物筛选,这是一个非常受追捧的程序,它也可能有助于法规遵从。目前,在印度,许多携带转基因作物的cry2Ab转基因正在接受田间试验,即MON15985棉花,Bt水稻,Bt秋葵,Bt玉米,Bt茄子,Bt马铃薯和Bt番茄。在这项研究中,我们报告了检测cry2Ab(326 bp)的定性分析。此外,还使用Bt棉花事件MON15985作为参考材料,证实了与启动子p35S(195 bp),终止子,t-nos(180 bp)和标记基因npt //(275 bp)的扩增相容性。检测灵敏度为0.1%,远低于严格的欧盟(EU)法规0.9%的要求。掺入MECH-12(crylAc),RR-大豆(epsps)或MON-810(crylAb)的目标DNA对cry2Ab检测没有抑制作用。此外,扩增了cry2Ab特异性转基因构建体(1.9kb),并通过巢式PCR证实了其身份。因此,建立了一种用于检测转基因作物/产品中cry2Ab基因的综合多重PCR方法。这可能是第一个报告,显示了cry2Ab转基因,启动子,终止子和标记基因的同时扩增。

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