Nikolić Zorica, Petrović Gordana, Panković Dejana, Ignjatov Maja, Marinković Dragana, Stojanović Milan, Đorđević Vuk
Institute of Field and Vegetable Crops, Maksima Gorkog 30, RS-21000 Novi Sad, Serbia.
Educons University, Vojvode putnika 85-87, RS-21208 Sremska Kamenica, Serbia.
Food Technol Biotechnol. 2017 Dec;55(4):439-444. doi: 10.17113/ftb.55.04.17.5192.
The aim of this study is to assess DNA degradation, DNA amplification, and GMO quantity during tofu production. Soybean seeds were spiked with Roundup Ready soybeans (RRS) at 0.9, 2, 3 and 5% (by mass), to assess the level of RSS that would be of practical interest for threshold labelling. Real-time polymerase chain reaction (PCR) was more effective than conventional PCR in the analysis of raw soymilk, okara, boiled soymilk and tofu. The negative effect of grinding and mechanical manipulation was obvious in the okara sample prepared with 3 and 5% RRS, where GMO content was reduced to (2.28±0.23) and (2.74±0.26) %, respectively. However, heating at 100 °C for 10 min did not cause significant degradation of DNA in all samples. The content of RRS in the final product, tofu, was reduced tenfold during processing, ranging from 0.07 to 0.46%, which was below the labelling threshold level. The results are discussed in terms of global harmonization of GMO standards, which could have the positive effect on the trade of lightly processed foodstuffs such as tofu, especially regarding the labelling policies.
本研究的目的是评估豆腐生产过程中的DNA降解、DNA扩增及转基因生物(GMO)含量。将抗草甘膦转基因大豆(RRS)以0.9%、2%、3%和5%(质量比)的比例添加到大豆种子中,以评估对于阈值标签具有实际意义的RRS水平。在对生豆浆、豆渣、煮豆浆和豆腐的分析中,实时聚合酶链反应(PCR)比传统PCR更有效。在以3%和5% RRS制备的豆渣样品中,研磨和机械操作的负面影响明显,其中转基因生物含量分别降至(2.28±0.23)%和(2.74±0.26)%。然而,在100℃加热10分钟并未导致所有样品中的DNA显著降解。最终产品豆腐中的RRS含量在加工过程中降低了十倍,范围为0.07%至0.46%,低于标签阈值水平。从转基因生物标准的全球协调角度对结果进行了讨论,这可能对豆腐等轻度加工食品的贸易产生积极影响,特别是在标签政策方面。