Development of ultrafast PCR assays for the event-specific detection of eleven approved genetically modified canola events in South Korea

•Ultrafast PCR assays for eleven GM canola events were developed.•The specificities and the detectability of the developed assays were validated.•The developed assays provide rapid and event-specific detection of GM canola events.•The potential quantitative analyses for GM canola events were evaluat...

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Veröffentlicht in:Food chemistry 2022-03, Vol.373 (Pt A), p.131419-131419, Article 131419
Hauptverfasser: Park, Ji-Eun, Lee, Do-Geun, Kim, Hong-Rae, Kim, Mi-Ju, Kim, Hae-Yeong, Kim, Hyun-Joong
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container_end_page 131419
container_issue Pt A
container_start_page 131419
container_title Food chemistry
container_volume 373
creator Park, Ji-Eun
Lee, Do-Geun
Kim, Hong-Rae
Kim, Mi-Ju
Kim, Hae-Yeong
Kim, Hyun-Joong
description •Ultrafast PCR assays for eleven GM canola events were developed.•The specificities and the detectability of the developed assays were validated.•The developed assays provide rapid and event-specific detection of GM canola events.•The potential quantitative analyses for GM canola events were evaluated. In Korea, genetically modified (GM) canola events derived from eleven single events have been authorized for food and feed, but not for cultivation. Therefore, the development of a rapid and accurate on-site detection method is crucial for the management of these approved GM canola events. In this study, ultrafast polymerase chain reaction (PCR) assays for the event-specific detection of eleven GM canola events were developed. The limit of detection (LOD) on DNA-based and powder-based GM canola samples of each primer set using the ultrafast PCR ranged from 0.1% to 0.01%, while the quantitative analysis of these ultrafast PCR assays, indicated that the correlation coefficient (R2) ranged from 0.98 to 0.9903. These results indicate that the developed assays may have sufficient specificity and LOD capacity to detect the eleven specific GM canola events for the attendant management and monitoring, thus preventing GM canola from contaminating the natural environment.
doi_str_mv 10.1016/j.foodchem.2021.131419
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In Korea, genetically modified (GM) canola events derived from eleven single events have been authorized for food and feed, but not for cultivation. Therefore, the development of a rapid and accurate on-site detection method is crucial for the management of these approved GM canola events. In this study, ultrafast polymerase chain reaction (PCR) assays for the event-specific detection of eleven GM canola events were developed. The limit of detection (LOD) on DNA-based and powder-based GM canola samples of each primer set using the ultrafast PCR ranged from 0.1% to 0.01%, while the quantitative analysis of these ultrafast PCR assays, indicated that the correlation coefficient (R2) ranged from 0.98 to 0.9903. 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In Korea, genetically modified (GM) canola events derived from eleven single events have been authorized for food and feed, but not for cultivation. Therefore, the development of a rapid and accurate on-site detection method is crucial for the management of these approved GM canola events. In this study, ultrafast polymerase chain reaction (PCR) assays for the event-specific detection of eleven GM canola events were developed. The limit of detection (LOD) on DNA-based and powder-based GM canola samples of each primer set using the ultrafast PCR ranged from 0.1% to 0.01%, while the quantitative analysis of these ultrafast PCR assays, indicated that the correlation coefficient (R2) ranged from 0.98 to 0.9903. 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source MEDLINE; Elsevier ScienceDirect Journals
subjects Biological Assay
Brassica napus - genetics
DNA, Plant - genetics
Event-specific detection
Genetically modified canola
Limit of Detection
Oilseed rape
Plants, Genetically Modified - genetics
Polymerase Chain Reaction
Ultrafast polymerase chain reaction (PCR)
title Development of ultrafast PCR assays for the event-specific detection of eleven approved genetically modified canola events in South Korea
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