Abstract

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.

Highlights

  • Data in support of the detection of genetically modified organisms (GMOs) in food and feed samples

  • GMO detection was conducted by Polymerase Chain Reaction (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)

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Summary

Data accessibility

Biotechnology Genetics and molecular biology, plant biotechnology, Genetically Modified Organisms (GMOs) Table, text file, primer sequences and characteristics, figures Polymerase Chain Reaction (PCR) Thermocycler System, (Mastercycler Eppendrof) Germany. The 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. Foodstuff, feed and agricultural samples were randomly collected from different sources, including local and imported materials from the Syrian local market to screen them for detecting the presence of GMOs using PCR, nested PCR- and multiplex PCR-based techniques using specific primers for the most commonly used foreign DNA commonly used in genetic transformation procedures, i.e., 35S promoter, T-nos, epsps, cryIA(b) gene and nptII gene [1,2,3,4,5,6,7,8,9,10,11,12,13,14,15,16,17]

Sample collection
DNA extraction and quantification
PCR amplification
Agarose gel electrophoresis and documentation
DNA extraction and amplification
Screening method
Confirmation of results
Full Text
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