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Detection and Monitoring of Food and Food Products 467<br />

modifi ed plant material in food and food products (Table 16.1). Detection methods can be<br />

based on detection of DNA, RNA, or the transgene product associated with the genetic<br />

modifi cation. The majority of the methods developed for detection of genetically modifi ed<br />

products are based on DNA, while a few are based on RNA. The DNA can be purifi ed in<br />

billions of copies while the multiplication of RNA or the protein is more complicated and<br />

a slow process. The RNA and the protein molecules are also less stable. The relationship<br />

between quantity of genetically modifi ed foods and DNA is linear if genetically modifi ed<br />

DNA is nuclear, but there is no such correlation between the quantity of genetically modifi<br />

ed food and the RNA or protein (Holst-Jensen, 2006). The most commonly used methods<br />

are gel electrophoresis and hybridization techniques that allow the size and amount of<br />

DNA to be estimated. This can be coupled with digestion of DNA with restriction enzymes<br />

that are known to cut a PCR fragment into segments of specifi ed sizes. Determination of<br />

melting point profi les, which is characteristic of a specifi c DNA sequence, can also be used<br />

for detection of food derived from genetically modifi ed crops. Another alternative is to use<br />

short synthetic molecules called probes (similar to, but smaller than primers) and allow<br />

TABLE 16.1<br />

Methods for Detection of Genetically Modifi ed Food and Food Products<br />

Method Target Sequence References<br />

Plant-derived DNA Chloroplast tRNALeu gene (trnL) intron Taberlet et al. (1991)<br />

Specifi c plant species Maize single copy invertase (Ivr) gene Ehlers et al. (1997)<br />

Soybean single copy lectin gene Meyer et al. (1996)<br />

Tomato single copy polygalacturonase gene Busch et al. (1999)<br />

Gene-specifi c methods Caulifl ower mosaic virus promoter (P-35S) Pietsch et al. (1997)<br />

Nopaline synthase terminator (T-Nos) Pietsch et al. (1997)<br />

Bar (phosphoinothricin acetyltransferase) gene Ehlers et al. (1997)<br />

Synthetic cry1Ab gene Ehlers et al. (1997),<br />

Vaitilingom et al. (1999)<br />

Construct-specifi c Bt11 maize: junction alcohol dehydrogenase 1S Matsuoka et al. (2001)<br />

methods<br />

intron IVS6 (enhancer)—cry1Ab gene<br />

Bt176 maize: junction CDPK (calcium dependent<br />

protein-kinase) promoter—synthetic cry1Ab gene<br />

Hupfer et al. (1998)<br />

GA21 maize: OTP (enhancer)—epsps gene<br />

(RoundupReady tolerance)<br />

Matsuoka et al. (2001)<br />

Mon810 maize: junction P-35S—heat shock protein<br />

(hsp) 70 intron I (enhancer)<br />

Zimmermann et al. (1998)<br />

Mon810 maize: junction hsp 70 intron—cry1Ab gene Matsuoka et al. (2001)<br />

RoundupReady ® : junction P-35S—Petunia hybrida<br />

CTP (chloroplast transit peptide)<br />

Wurz and Willmund (1997)<br />

T25 maize: junction pat (phosphoinothricin<br />

acetyltransferase) gene—T-35S<br />

Matsuoka et al. (2001)<br />

Zeneca tomato: junction T-Nos-truncated tomato<br />

polygalacturonase gene<br />

Busch et al. (1999)<br />

Event-specifi c methods Bt11 maize: junction host plant genome—<br />

Zimmermann, Luthy, and<br />

integrated recombinant DNA<br />

Pauli (2000)<br />

Roundup Ready ® soybean: junction host plant Berdal and Holst-Jensen (2006),<br />

genome—integrated recombinant DNA<br />

Taverniers et al. (2001),<br />

Terry and Harris (2001)

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