Du Yan, Chen Fusheng, Chen Chen, Liu Kunlun
College of Food Science and Technology, Henan University of Technology, 100, Lianhua Street, High-tech, Zhengzhou 450001, Henan, People's Republic of China.
R Soc Open Sci. 2020 Oct 7;7(10):201147. doi: 10.1098/rsos.201147. eCollection 2020 Oct.
To evaluate DNA fragmentation and GMO quantification during soya bean protein concentrate and isolate preparation, genetically modified soya bean event GTS 40-3-2 (Roundup Ready soya bean, RRS) was blended with conventional soya beans at mass percentages of 0.9%, 2%, 3%, 5% and 10%. Qualitative PCR and real-time PCR were used to monitor the taxon-specific and exogenous target levels in all of the main products and by-products, which has practical significance for RRS labelling threshold and traceability. Along the preparation chain, the majority of DNA was distributed in main products, and the DNA degradation was noticed. From a holistic perspective, the target degraded more than target during both of the two soya bean proteins preparations. Therefore, the transgenic contents in the final protein products were higher than the actual mass percentages of RRS in raw materials. Our results are beneficial to the improvement of GMO labelling legislation and the protection of consumer rights.
为评估大豆浓缩蛋白和分离蛋白制备过程中的DNA片段化和转基因生物(GMO)定量情况,将转基因大豆事件GTS 40-3-2(抗草甘膦转基因大豆,RRS)与常规大豆按质量百分比0.9%、2%、3%、5%和10%进行混合。采用定性PCR和实时PCR监测所有主要产品和副产品中的分类群特异性和外源目标水平,这对RRS标签阈值和可追溯性具有实际意义。在制备链中,大部分DNA分布在主要产品中,且观察到了DNA降解。从整体角度来看,在两种大豆蛋白制备过程中,目标降解程度均高于目标。因此,最终蛋白产品中的转基因含量高于原料中RRS的实际质量百分比。我们的结果有助于改进转基因生物标签立法和保护消费者权益。