Transgenic Food

Electronic Journal of Biotechnology ISSN: 0717-3458 Vol. 9 No. 3, Special Issue, 2006
© 2006 by Pontificia Universidad Católica de Valparaíso -- Chile  
DOI: 10.2225/vol9-issue3-fulltext-3  
RESEARCH ARTICLE

Semiquantitative analysis of genetically modified maize and soybean in food

María Laura Cazzola
Centro de Investigación y Desarrollo en Criotecnología de Alimentos
Facultad de Ciencias Exactas
 Universidad Nacional de La Plata
Calle 47 y 116 (1900) La Plata, Argentina
Tel/Fax: 54 221 4249287/4254853
E-mail: lauracazzola@yahoo.com.ar

Silvana Petruccelli*
Centro de Investigación y Desarrollo en Criotecnología de Alimentos
Facultad de Ciencias Exactas
 Universidad Nacional de La Plata
Calle 47 y 116 (1900) La Plata, Argentina
Tel/Fax: 54 221 4249287/4254853
E-mail: silvana@biol.unlp.edu.ar

*Corresponding author

Financial support: MTHA-UNLP (Maestría de Tecnología e Higiene de Alimentos de la Universidad Nacional de La Plata) and Federación Bioquímica-Pcia. Buenos Aires. SP is member of the research career of CONICET (Argentina).

Keywords: Bt maize, genetically modified organisms, semi-quantitative PCR, RR-soybean, transgenic food.

Abbreviations:

CONABIA: Argentinean National Advisory Committee on Agricultural Biosafety
CRY: Bacillus thuringensis d endotoxine
EPSPS: 5-enolpyruvylshikimate-3 phosphate synthase
EU: European Union
GM: genetically modified
GMO: genetically modified organisms
IC: inhibitors' control
ISO: International Organisation for Standardisation
IVR, maize invertase
JRC: Joint Research Centre
LE: soybean lectine
PCR Polymerase Chain Reaction
Ta: temperature of annealing
RR soybean: Round Ready Soybean
Bt maize: Bacillus thuringiensis maize

Abstract
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The aim of this study was to analyze quantitatively the presence of genetically modified organism in food with different composition and degree of processing. Total DNA was extracted by Dellaporta's method and GMO analysis was performed using two consecutives PCR reactions with specie specific primers (IVR and LE), screening primers (35S) and transgen specific primers (CRY and EPSPS). The quantification within the sensitivity establish by the EU was possible only in some foods (ice-cream, flours, soybean isolates and concentrates, starch). Samples with high lipid content or subjected to intense thermal treatments (such as some snacks, mayonnaise, creamy soup) could not be amplified mainly due to the presence of PCR inhibitors. Therefore the method was adequate for identification of food as GM, within the limits establish by EU, only for some Argentinean commercial food products. These findings showed that the develop method was satisfactory only for simple food that were not subject to intense thermal treatments and that do not have high lipid content and that the main limitation of the method is DNA purity.

 
Supported by UNESCO / MIRCEN network 
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