Detection and identification of genetically modified EE-1 brinjal (Solanum melongena) by single, multiplex and SYBR® real-time PCR

被引:10
作者
Ballari, Rajashekhar V. [1 ]
Martin, Asha [1 ]
Gowda, Lalitha R. [1 ]
机构
[1] CSIR Cent Food Technol Res Inst, Dept Food Safety & Analyt, Qual Control Lab, Mysore 570020, Karnataka, India
关键词
genetically modified organisms; cry1Ac gene; event-specific PCR; Bt brinjal; POLYMERASE-CHAIN-REACTION; EVENT-SPECIFIC DETECTION; MODIFIED ORGANISMS; QUANTITATIVE PCR; MAIZE; QUANTIFICATION; PRODUCTS; COTTON; BT11; SEQUENCE;
D O I
10.1002/jsfa.5764
中图分类号
S [农业科学];
学科分类号
09 ;
摘要
BACKGROUND: Brinjal is an important vegetable crop. Major crop loss of brinjal is due to insect attack. Insect-resistant EE-1 brinjal has been developed and is awaiting approval for commercial release. Consumer health concerns and implementation of international labelling legislation demand reliable analytical detection methods for genetically modified (GM) varieties. RESULTS: End-point and real-time polymerase chain reaction (PCR) methods were used to detect EE-1 brinjal. In end-point PCR, primer pairs specific to 35S CaMV promoter, NOS terminator and nptII gene common to other GM crops were used. Based on the revealed 3' transgene integration sequence, primers specific for the event EE-1 brinjal were designed. These primers were used for end-point single, multiplex and SYBR-based real-time PCR. End-point single PCR showed that the designed primers were highly specific to event EE-1 with a sensitivity of 20 pg of genomic DNA, corresponding to 20 copies of haploid EE-1 brinjal genomic DNA. The limits of detection and quantification for SYBR-based real-time PCR assay were 10 and 100 copies respectively. CONCLUSION: The prior development of detection methods for this important vegetable crop will facilitate compliance with any forthcoming labelling regulations. (C) 2012 Society of Chemical Industry
引用
收藏
页码:340 / 347
页数:8
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