Alasaad Noor, Alzubi Hussein, Kader Ahmad Abdul
General Commission for Scientific Agricultural Research (GCSAR), Biotechnology Department, Damascus, P.O. Box 12573, Syria.
Data Brief. 2016 Feb 20;7:243-52. doi: 10.1016/j.dib.2016.02.035. eCollection 2016 Jun.
Food and feed samples were randomly collected from different sources, including local and imported materials from the Syrian local market. These included maize, barley, soybean, fresh food samples and raw material. GMO detection was conducted by PCR and nested PCR-based techniques using specific primers for the most used foreign DNA commonly used in genetic transformation procedures, i.e., 35S promoter, T-nos, epsps, cryIA(b) gene and nptII gene. The results revealed for the first time in Syria the presence of GM foods and feeds with glyphosate-resistant trait of P35S promoter and NOS terminator in the imported soybean samples with high frequency (5 out of the 6 imported soybean samples). While, tests showed negative results for the local samples. Also, tests revealed existence of GMOs in two imported maize samples detecting the presence of 35S promoter and nos terminator. Nested PCR results using two sets of primers confirmed our data. The methods applied in the brief data are based on DNA analysis by Polymerase Chain Reaction (PCR). This technique is specific, practical, reproducible and sensitive enough to detect up to 0.1% GMO in food and/or feedstuffs. Furthermore, all of the techniques mentioned are economic and can be applied in Syria and other developing countries. For all these reasons, the DNA-based analysis methods were chosen and preferred over protein-based analysis.
食品和饲料样本从不同来源随机采集,包括叙利亚当地市场的本地和进口材料。这些材料包括玉米、大麦、大豆、新鲜食品样本和原材料。采用聚合酶链式反应(PCR)和基于巢式PCR的技术,使用针对遗传转化过程中最常用的外源DNA(即35S启动子、T - 诺思终止子、5 - 烯醇丙酮酰莽草酸 - 3 - 磷酸合酶基因(epsps)、苏云金芽孢杆菌晶体蛋白基因cryIA(b)和新霉素磷酸转移酶基因nptII)的特异性引物进行转基因检测。结果首次在叙利亚发现,进口大豆样本中存在具有P35S启动子和NOS终止子抗草甘膦特性的转基因食品和饲料,且出现频率较高(6个进口大豆样本中有5个)。而本地样本检测结果为阴性。此外,检测还发现两个进口玉米样本中存在转基因生物,检测到35S启动子和诺思终止子的存在。使用两组引物的巢式PCR结果证实了我们的数据。简要数据中应用的方法基于聚合酶链式反应(PCR)的DNA分析。该技术具有特异性、实用性、可重复性,且灵敏度足以检测食品和/或饲料中低至0.1%的转基因生物。此外,上述所有技术都经济实惠,可在叙利亚和其他发展中国家应用。基于所有这些原因,选择了基于DNA的分析方法,且相较于基于蛋白质的分析方法更受青睐。