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Development of Plasmid DNA Reference Material for the Quantification of Genetically Modified Common Bean Embrapa 5.1

机译:用于量化转基因蚕豆Embrapa 5.1的质粒DNA参考材料的开发

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The genetically modified (GM) common bean Embrapa 5.1 was recently approved for commercialization. The reliable detection and quantification of GM organisms is strongly dependent on validated methods as well as calibration systems. This work presents the development of a calibrant plasmid for Embrapa 5.1 common bean detection. The reaction parameters were determined and compared for both the plasmid DNA (pDNA) and the genomic DNA (gDNA). PCR efficiencies for pDNA were 81% for the construction-specific assays and 76% for the taxon-specific assay, whereas for gDNA efficiencies were 94 and 93%, respectively. The limits of detection (LOD) in both qPCR assays were 10~2 and 10~3 copies of gDNA and pDNA per PCR reaction, respectively. This is sufficient to detect 0.067 and 0.67% of GM common bean in 100 ng of DNA, respectively, which is in agreement with detecting the 1% GM content required by the Brazilian legislation.
机译:转基因(GM)普通豆Embrapa 5.1最近被批准商业化。转基因生物的可靠检测和定量很大程度上取决于经过验证的方法以及校准系统。这项工作介绍了用于Embrapa 5.1普通豆检测的校准质粒的开发。确定了反应参数,并比较了质粒DNA(pDNA)和基因组DNA(gDNA)。对于pDNA的PCR效率,针对构建特异性的检测效率为81%,针对分类群特异性的检测效率为76%,而针对gDNA的PCR效率分别为94%和93%。两种qPCR分析中的每次检测反应的检出限(LOD)分别为gDNA和pDNA的10〜2和10〜3拷贝。这足以分别检测100 ng DNA中的0.067和0.67%的GM普通豆,这与检测巴西法律要求的1%GM含量是一致的。

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