A. Saienko, M. Peka, Viktor Balatsky, S. Korinnyi, O. Tsereniuk
{"title":"GMO analysis technique based on PCR and real-time PCR methods","authors":"A. Saienko, M. Peka, Viktor Balatsky, S. Korinnyi, O. Tsereniuk","doi":"10.37143/0371-4365-2021-75-76-06","DOIUrl":null,"url":null,"abstract":"The use of genetically modified organisms (GMOs) is promising for overcoming the\nshortage of food products in the world and solving the problem of hunger arising in\nvarious 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\nassociated with GMOs cause public concern, which has led to the restriction of the use\nof GMOs and their products in many countries and the need for constant control of their\ncontent in food products. This study describes methods based on the polymerase chain\nreaction (PCR), such as Real-time PCR and PCR with electrophoretic separation of\namplificates, which are generally accepted in GMO analysis. In order to control the\npresence of GMOs in food raw materials, feed and finished products of plant and animal\norigin, 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.\nBoth Real-time PCR and PCR with electrophoretic separation of amplificates allow to\nestablish the presence of GMOs with high accuracy, and Real-time PCR is also used to\ndetermine the concentration of GMOs in the studied samples. The work presents a typical electrophoresis with visualization of the obtained PCR fragments that required\nelectrophoretic separation and fragments that were synthesized in the Real-time PCR\nreaction, and determined the approximate sizes of the obtained fragments relative to the pBR322 DNA-MspI molecular weight marker. The approach described in this study,\nbased on the use of PCR techniques, can be successfully used for GMO analysis of all\ngroups of raw materials and finished products of animal and plant origin, and is also\nwell 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\nefficiency of such analysis and continue its application in relation to new genetic\nengineering structures used during the creation of GMOs.\nKeywords: genetically modified organisms (GMOs), PCR methods, GMO analysis,\nraw materials and finished products of plant and animal origin","PeriodicalId":178711,"journal":{"name":"Pig breeding the interdepartmental subject scientific digest","volume":"119 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2021-12-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Pig breeding the interdepartmental subject scientific digest","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.37143/0371-4365-2021-75-76-06","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
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