scholarly journals Simplex and Duplex Polymerase Chain Reaction Analysis of Herculex® RW (59122) Maize Based on One Reference Molecule Including Separated Fragments of 5 Integration Site and Endogenous Gene

2009 ◽  
Vol 92 (5) ◽  
pp. 1472-1483 ◽  
Author(s):  
Xiang Li ◽  
Litao Yang ◽  
Jianzhong Zhang ◽  
Shu Wang ◽  
Kailin Shen ◽  
...  

Abstract Reference molecules, as positive controls and calibrators, have been recently developed in genetically modified organism analysis as a potential substitute for reference materials derived from plant raw materials. In this study, a novel reference molecule p59122, including the revealed 5 integration sequence of maize Herculex® RW (59122), was constructed that was suitable for simplex and duplex event-specific qualitative and quantitative PCR detections. The LOD values were 10 copies both for simplex and duplex qualitative PCR when p59122 was used as the calibrator. These values were comparable to those of using genomic DNA samples with 0.01 and 0.05, approximately 5 and 25 hyploid genomic DNA copies, respectively. The absolute LOD and LOQ values were confirmed to be as low as 10 and 25 copies of p59122 DNA both in simplex and duplex quantitative systems. Furthermore, ideal quantification data with low bias, SD and RSD values were obtained from the practical samples analyses in simplex and duplex real-time PCR systems using the reference molecule p59122 as a calibrator. All these results suggested that the developed reference molecule p59122 and the qualitative and quantitative PCR detection methods are suitable for identification and quantification of GM maize 59122 and its derived products.

Molecules ◽  
2019 ◽  
Vol 24 (3) ◽  
pp. 455
Author(s):  
Luying Shan ◽  
Dazhou Wang ◽  
Yinjiao Li ◽  
Shi Zheng ◽  
Wentao Xu ◽  
...  

Tricholoma matsutake is a rare, precious, and wild edible fungus that could not be cultivated artificially until now. This situation has given way to the introduction of fake T. matsutake commodities to the mushroom market. Among the methods used to detect food adulteration, amplification of species-specific diagnostic marker is particularly important and accurate. In this study, the Pol gene is reported as a species-specific diagnostic marker to identify three T. matsutake varieties and 10 other types of edible mushrooms through qualitative and quantitative PCR. The PCR results did not reveal variations in the amplified region, and the detection limits of qualitative and quantitative PCR were found to be 8 ng and 32 pg, respectively. Southern blot showed that the Pol gene exists as a single copy in the T. matsutake genome. The method that produced the purest DNA of T. matsutake in this study was also determined, and the high-concentration salt precipitation method was confirmed to be the most suitable among the methods tested. The assay proposed in this work is applicable not only to the detection of raw materials but also to the examination of processed products containing T. matsutake.


2010 ◽  
Vol 93 (2) ◽  
pp. 663-675
Author(s):  
Kailin Shen ◽  
Xiang Li ◽  
Shu Wang ◽  
Yingjie Pan ◽  
Zhiyi Shi ◽  
...  

Abstract Despite rapid developments in the detection techniques for genetically modified organisms (GMOs), the event-specific PCR method with high specificity is still the most used technique. In this study, event-specific simplex and duplex qualitative and quantitative detection systems were developed targeting the 3 insertion site of GM maize SYN-E3272-5 (3272) construct. A reference molecule p3272 was constructed to act as positive control and as calibrator for quantitative analysis. The LOD for simplex and duplex qualitative PCR assays was 10 copies of p3272 control DNA. LOD and the LOQ for simplex and duplex quantitative PCR assays were 10 and 25 copies of p3272 DNA, respectively. Furthermore, four practical GM maize samples were quantified using the established simplex and duplex quantitative PCR systems by in-house validation. Results from five operators showed that the bias ranged from 3.44 to 17.24 in the simplex system and from 0.42 to 16.06 in the duplex system, respectively. These results demonstrated that the established event-specific simplex and duplex qualitative and quantitative PCR systems combined with the reference molecule p3272 are suitable for the detection of GM maize 3272 and its derived products.


2016 ◽  
Vol 192 ◽  
pp. 336-342 ◽  
Author(s):  
Jai-Hong Cheng ◽  
Hsiao-Ting Chou ◽  
Meng-Shiou Lee ◽  
Shyang-Chwen Sheu

Sign in / Sign up

Export Citation Format

Share Document