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Detection of celery (Apium graveolens), mustard (Sinapis alba, Brassica juncea, Brassica nigra) and sesame (Sesamum indicum) in food by real-time PCR

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Kjetil Aune

Bibliotekleder
kjetil.aune@nofima.no

European Food Research and Technology ; Volume 226. p. 771–778. 2008

Mustorp, Stina L.; Engdahl-Axelsson, C.; Svensson, U.; Holck, Askild Lorentz

Legislation requires labelling of foods containing allergic ingredients, amongst them celery, mustard and sesame. Here we present robust quantitative and sensitive methods for real-time PCR detection of celery, mustard (Sinapis alba and Brassica sp.) and sesame in food. The development of the DNA-based assays was part of an eVort to generate alternative detection methods for allergens for which eVective protein- based assays are lacking. The celery and sesame methods were speciWc for the celery mannitol dehydrogenase gene and the sesame allergen encoding 2S albumin gene, respectively, when tested against a range of plant materials. The mustard method was speciWc for the allergen encoding sinA gene and its homologues present in diVerent Brassica sp. All primer probe pairs gave high ampliWcation eYciency and sensitivities below approximately ten molecules of puriWed template DNA. These DNA-based detection methods will constitute supplementary and complementary methods to the traditional protein-based methods. Laboratories may choose diVerent analysis formats depending on the food matrix, the availability of speciWc tests and the performance characteristics of the tests.

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