Gå til hovedinnhold

Publisert 2008

Les på engelsk

Publikasjonsdetaljer

Tidsskrift : European Food Research and Technology , vol. 226 , p. 771–778 , 2008

Utgiver : Springer

Internasjonale standardnummer :
Trykt : 1438-2377
Elektronisk : 1438-2385

Publikasjonstype : Vitenskapelig artikkel

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

Har du spørsmål om noe vedrørende publikasjonen, kan du kontakte Nofimas bibliotekleder.

Kjetil Aune
Bibliotekleder
kjetil.aune@nofima.no

Sammendrag

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.

Kontaktpersoner: