High-throughput multiplex microsatellite marker assay for detection and quantification of adulteration in Basmati rice (Oryza sativa)

被引:46
作者
Archak, Sunil [1 ]
Lakshminarayanareddy, V. [1 ]
Nagaraju, Javaregowda [1 ]
机构
[1] Ctr DNA Fingerprinting & Diagnost, Mol Genet Lab, Hyderabad 500076, Andhra Pradesh, India
关键词
adulteration; Basmati rice; CE; microsatellite markers; multiplex assay; PCR;
D O I
10.1002/elps.200600646
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Basmati rice is a very special type of aromatic rice known world-wide for its extra long grains and pleasant and distinct aroma. Traditional Basmati rice cultivars, confined to Indo-Gangetic regions of the Indian subcontinent, are often reported to be adulterated with crossbred Basmati varieties and long-grain non-Basmati varieties in the export market. At present, there is no commercial scale technology to reliably detect adulteration. We report here a CE-based multiplex microsatellite marker assay for detection as well as quantification of adulteration in Basmati rice samples. The single-tube assay multiplexes eight microsatellite loci to generate variety-specific allele profiles that can detect adulteration from 1% upwards. The protocol also incorporates a quantitative-competitive PCR-based analysis for quantification of adulteration. Accuracy of quantification has been shown to be +/- 1.5%. The experiments used to develop and validate the methodology are described.
引用
收藏
页码:2396 / 2405
页数:10
相关论文
共 32 条
[1]   A real-time quantitative PCR detection method specific to widestrike transgenic cotton (event 281-24-236/3006-210-23) [J].
Baeumler, Stefan ;
Wulff, Doerte ;
Tagliani, Laura ;
Song, Ping .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 2006, 54 (18) :6527-6534
[2]   Polymerase chain reaction-based analysis to detect terrestrial animal protein in fish meal [J].
Bellagamba, F ;
Valfrè, F ;
Panseri, S ;
Moretti, VM .
JOURNAL OF FOOD PROTECTION, 2003, 66 (04) :682-685
[3]   Application of quantitative real-time PCR in the detection of prion-protein gene species-specific DNA sequences in animal meals and feedstuffs [J].
Bellagamba, F ;
Comincini, S ;
Ferretti, L ;
Valfrè, F ;
Moretti, VM .
JOURNAL OF FOOD PROTECTION, 2006, 69 (04) :891-896
[4]   Fluorescent-labeled microsatellite panels useful for detecting allelic diversity in cultivated rice (Oryza sativa L.) [J].
Blair, MW ;
Hedetale, V ;
McCouch, SR .
THEORETICAL AND APPLIED GENETICS, 2002, 105 (2-3) :449-457
[6]   The gene for fragrance in rice [J].
Bradbury, LMT ;
Fitzgerald, TL ;
Henry, RJ ;
Jin, QS ;
Waters, DLE .
PLANT BIOTECHNOLOGY JOURNAL, 2005, 3 (03) :363-370
[7]   Use of real-time PCR for determining copy number and zygosity in transgenic plants [J].
Bubner, B ;
Baldwin, IT .
PLANT CELL REPORTS, 2004, 23 (05) :263-271
[8]   Quantitative PCR detection of pork in raw and heated ground beef and pate [J].
Calvo, JH ;
Osta, R ;
Zaragoza, P .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 2002, 50 (19) :5265-5267
[9]   Critical points of DNA quantification by real-time PCR - effects of DNA extraction method and sample matrix on quantification of genetically modified organisms [J].
Cankar, Katarina ;
Stebih, Dejan ;
Dreo, Tanja ;
Zel, Jana ;
Gruden, Kristina .
BMC BIOTECHNOLOGY, 2006, 6 (1)
[10]   Design and application of microsatellite marker panels for semiautomated genotyping of rice (Oryza sativa L.) [J].
Coburn, JR ;
Temnykh, SV ;
Paul, EM ;
McCouch, SR .
CROP SCIENCE, 2002, 42 (06) :2092-2099