Qualitative and quantitative evaluation of the genomic DNA extracted from GMO and Non-GMO foodstuffs with four different extraction methods

被引:98
作者
Peano, C [1 ]
Samson, MC [1 ]
Palmieri, L [1 ]
Gulli, M [1 ]
Marmiroli, N [1 ]
机构
[1] Univ Parma, Dept Environm Sci, I-43100 Parma, Italy
关键词
food traceability; GMO; DNA extraction; DNA degradation; real-time PCR;
D O I
10.1021/jf040008i
中图分类号
S [农业科学];
学科分类号
09 ;
摘要
The presence of DNA in foodstuffs derived from or containing genetically modified organisms (GMO) is the basic requirement for labeling of GMO foods in Council Directive 2001/18/CE (Off. J. Eur. Communities 2001, L1 06/2). In this work, four different methods for DNA extraction were evaluated and compared. To rank the different methods, the quality and quantity of DNA extracted from standards, containing known percentages of GMO material and from different food products, were considered. The food products analyzed derived from both soybean and maize and were chosen on the basis of the mechanical, technological, and chemical treatment they had been subjected to during processing. Degree of DNA degradation at various stages of food production was evaluated through the amplification of different DNA fragments belonging to the endogenous genes of both maize and soybean. Genomic DNA was extracted from Roundup Ready soybean and maize MON810 standard flours, according to four different methods, and quantified by real-time Polymerase Chain Reaction (PCR), with the aim of determining the influence of the extraction methods on the DNA quantification through real-time PCR.
引用
收藏
页码:6962 / 6968
页数:7
相关论文
共 21 条
[1]   POLYMERASE CHAIN-REACTION (PCR) - A POSSIBLE ALTERNATIVE TO IMMUNOCHEMICAL METHODS ASSURING SAFETY AND QUALITY OF FOOD - DETECTION OF WHEAT CONTAMINATION IN NON-WHEAT FOOD-PRODUCTS [J].
ALLMANN, M ;
CANDRIAN, U ;
HOFELEIN, C ;
LUTHY, J .
ZEITSCHRIFT FUR LEBENSMITTEL-UNTERSUCHUNG UND-FORSCHUNG, 1993, 196 (03) :248-251
[2]   Analytical methods for detection and determination of genetically modified organisms in agricultural crops and plant-derived food products [J].
Anklam, E ;
Gadani, F ;
Heinze, P ;
Pijnenburg, H ;
Van Den Eede, G .
EUROPEAN FOOD RESEARCH AND TECHNOLOGY, 2002, 214 (01) :3-26
[3]   Automated DNA preparation from maize tissues and food samples suitable for real-time PCR detection of native genes [J].
Hahnen, S ;
Offermann, S ;
Miedl, B ;
Rüger, B ;
Peterhänsel, C .
EUROPEAN FOOD RESEARCH AND TECHNOLOGY, 2002, 215 (05) :443-446
[4]  
Hemmer W., 1997, 297 BATS
[5]   Detection of genetically modified insect-resistant Bt maize by means of polymerase chain reaction [J].
Hupfer, C ;
Hotzel, H ;
Sachse, K ;
Engel, KH .
ZEITSCHRIFT FUR LEBENSMITTEL-UNTERSUCHUNG UND-FORSCHUNG A-FOOD RESEARCH AND TECHNOLOGY, 1997, 205 (06) :442-445
[6]   Detection of the genetic modification in heat-treated products of Bt maize by polymerase chain reaction [J].
Hupfer, C ;
Hotzel, H ;
Sachse, K ;
Engel, KH .
ZEITSCHRIFT FUR LEBENSMITTEL-UNTERSUCHUNG UND-FORSCHUNG A-FOOD RESEARCH AND TECHNOLOGY, 1998, 206 (03) :203-207
[7]  
HURST DC, 1999, MOL BREEDING, V6, P579
[8]  
LIVIERO L, 1998, THESIS U STUDI VERON
[9]  
LOCATELLI G, 1999, PE BIOSYSTEMS
[10]   Detection of genetically engineered plants by polymerase chain reaction (PCR) using the FLAVR SAVR(TM) tomato as an example [J].
Meyer, R .
ZEITSCHRIFT FUR LEBENSMITTEL-UNTERSUCHUNG UND-FORSCHUNG, 1995, 201 (06) :583-586