Vahdani Melika, Sahari Mohammad Ali, Tanavar Mehrnaz
Department of Food Science and Technology, College of Agriculture, Tarbiat Modares University, P. O. Box, 14115-336 Tehran, Iran.
Department of Plant Genetics and Breeding, College of Agriculture, Tarbiat Modares University, Tehran, Iran.
Food Chem (Oxf). 2024 Mar 21;8:100201. doi: 10.1016/j.fochms.2024.100201. eCollection 2024 Jul 30.
The objective of this study was to develop a DNA-based method for the identification and tracking of edible oils, which is important for health management. Three different DNA extraction methods (CTAB, MBST kit, and manual hexane-based method) were used to obtain high-purity DNA from crude and refined soybean, maize, and canola oils. PCR was then conducted using specific primers to identify the presence of genes related to each oil type and to assess transgenicity. The results showed that DNA was present in crude and refined oils, but in very low amounts. However, using method 3 for DNA extraction provided sufficient quantity and quality of DNA for successful PCR amplification. The study concluded that the main challenge in DNA extraction from oils is the presence of PCR inhibitors, which can be overcome using the manual hexanebased method. Also, the examination of protein presence in the oils using SDS-PAGE did not indicate any protein bands.
本研究的目的是开发一种基于DNA的食用油鉴定和追踪方法,这对健康管理很重要。使用三种不同的DNA提取方法(CTAB法、MBST试剂盒法和基于己烷的手工法)从粗制和精制大豆油、玉米油和菜籽油中获取高纯度DNA。然后使用特异性引物进行PCR,以鉴定与每种油类型相关的基因的存在并评估转基因情况。结果表明,粗制油和精制油中存在DNA,但含量非常低。然而,使用方法3进行DNA提取可提供足够数量和质量的DNA用于成功的PCR扩增。该研究得出结论,从油中提取DNA的主要挑战是存在PCR抑制剂,使用基于己烷的手工法可以克服这一问题。此外,使用SDS-PAGE检测油中蛋白质的存在未显示任何蛋白条带。