GMO analysis technique based on PCR and real-time PCR methods

A. Saienko, M. Peka, Viktor Balatsky, S. Korinnyi, O. Tsereniuk
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Abstract

The use of genetically modified organisms (GMOs) is promising for overcoming the shortage of food products in the world and solving the problem of hunger arising in various regions. At the same time, the use of GMOs has become a cause of debate, as the safety of consuming GMO products for human health remains unproven. The risks associated with GMOs cause public concern, which has led to the restriction of the use of GMOs and their products in many countries and the need for constant control of their content in food products. This study describes methods based on the polymerase chain reaction (PCR), such as Real-time PCR and PCR with electrophoretic separation of amplificates, which are generally accepted in GMO analysis. In order to control the presence of GMOs in food raw materials, feed and finished products of plant and animal origin, screening is carried out for the presence of the most common genetic engineering structures used during the creation of GMOs: CaMV 35S promoter and NOS terminator. Both Real-time PCR and PCR with electrophoretic separation of amplificates allow to establish the presence of GMOs with high accuracy, and Real-time PCR is also used to determine the concentration of GMOs in the studied samples. The work presents a typical electrophoresis with visualization of the obtained PCR fragments that required electrophoretic separation and fragments that were synthesized in the Real-time PCR reaction, and determined the approximate sizes of the obtained fragments relative to the pBR322 DNA-MspI molecular weight marker. The approach described in this study, based on the use of PCR techniques, can be successfully used for GMO analysis of all groups of raw materials and finished products of animal and plant origin, and is also well adapted for the detection of various genetic engineering structures, not limited to the CaMV 35S promoter and terminator NOS, which makes it possible to increase the efficiency of such analysis and continue its application in relation to new genetic engineering structures used during the creation of GMOs. Keywords: genetically modified organisms (GMOs), PCR methods, GMO analysis, raw materials and finished products of plant and animal origin
基于PCR和实时PCR方法的转基因生物分析技术
转基因生物的应用有望克服世界粮食产品短缺问题,解决世界各地出现的饥饿问题。与此同时,使用转基因生物已成为争论的一个原因,因为食用转基因产品对人类健康的安全性仍未得到证实。与转基因生物相关的风险引起了公众的关注,这导致许多国家限制使用转基因生物及其产品,并需要不断控制其在食品中的含量。本研究描述了基于聚合酶链反应(PCR)的方法,如Real-time PCR和扩增物电泳分离PCR,这些方法在转基因生物分析中被普遍接受。为了控制转基因生物在食品原料、饲料和动植物源性成品中的存在,对转基因生物产生过程中使用的最常见基因工程结构进行了筛选:CaMV 35S启动子和NOS终止子。Real-time PCR和扩增物电泳分离的PCR都可以高精度地确定转基因生物的存在,Real-time PCR也可用于确定所研究样品中转基因生物的浓度。这项工作展示了一种典型的电泳,显示了所获得的需要电泳分离的PCR片段和在实时PCR反应中合成的片段,并确定了所获得的片段相对于pBR322 DNA-MspI分子量标记的大致大小。本研究中描述的方法基于PCR技术的使用,可以成功地用于所有组动物和植物来源的原料和成品的转基因分析,并且也很好地适用于各种基因工程结构的检测,不限于CaMV 35S启动子和终止子NOS。这就有可能提高这种分析的效率,并继续将其应用于转基因生物创造过程中使用的新基因工程结构。关键词:转基因生物,PCR方法,转基因分析,动植物源性原料和成品
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