Development and Validation of a Real-Time PCR Based Assay to Detect Adulteration with Corn in Commercial Turmeric Powder Products

被引:25
|
作者
Oh, Su Hong [1 ]
Jang, Cheol Seong [1 ]
机构
[1] Kangwon Natl Univ, Dept Bioresource Sci, Plant Genom Lab, Chunchon 24341, South Korea
关键词
anti food fraud; Curcuma longa; DNA markers; species identification; SYBR-GREEN; real-time PCR; Zea mays; CURCUMIN; FOOD; BARCODE; SAFETY;
D O I
10.3390/foods9070882
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
Turmeric, or Curcuma longa, is commonly consumed in the South East Asian countries as a medical product and as food due to its therapeutic properties. However, with increasing demand for turmeric powder, adulterated turmeric powders mixed with other cheap starch powders, such as from corn or cassava, are being distributed by food suppliers for economic benefit. Here, we developed molecular markers using quantitative real-time PCR to identify adulteration in commercial turmeric powder products. Chloroplast genes, such as matK, atpF, and ycf2, were used to design species-specific primers for C. longa and Zea mays. Of the six primer pairs designed and tested, the correlation coefficients (R-2 ) were higher than 0.99 and slopes were -3.136 to -3.498. The efficiency of the primers was between 93.14 and 108.4%. The specificity of the primers was confirmed with ten other species, which could be intentionally added to C. longa powders or used as ingredients in complex turmeric foods. In total, 20 blind samples and 10 commercial C. longa food products were tested with the designed primer sets to demonstrate the effectiveness of this approach to detect the addition of Z. mays products in turmeric powders. Taken together, the real-time PCR assay developed here has the potential to contribute to food safety and the protection of consumer's rights.
引用
收藏
页数:12
相关论文
共 50 条
  • [41] Development and validation of real-time PCR for the detection of Yersinia ruckeri
    Keeling, S. E.
    Johnston, C.
    Wallis, R.
    Brosnahan, C. L.
    Gudkovs, N.
    McDonald, W. L.
    JOURNAL OF FISH DISEASES, 2012, 35 (02) : 119 - 125
  • [42] Development of a HOG-based real-time PCR method to detect stress response changes in mycotoxigenic moulds
    Rodriguez, Alicia
    Medina, Angel
    Cordoba, Juan J.
    Magan, Naresh
    FOOD MICROBIOLOGY, 2016, 57 : 109 - 115
  • [43] Development of a TaqMan-based real-time PCR assay for the detection of Novel GPV
    Niu, Xiaoyu
    Chen, Hao
    Yang, Jing
    Yu, Xianglong
    Ti, Jinfeng
    Wang, Aihua
    Diao, Youxiang
    JOURNAL OF VIROLOGICAL METHODS, 2016, 237 : 32 - 37
  • [44] Development of a real-time PCR assay targeting the sporulation gene, spo0A, for the enumeration of thermophilic bacilli in milk powder
    Rueckert, A
    Ronimus, RS
    Morgan, HW
    FOOD MICROBIOLOGY, 2006, 23 (03) : 220 - 230
  • [45] Development and validation of a real-time PCR assay for the detection of Toxoplasma gondii DNA in animal and meat samples
    Marino, Anna Maria Fausta
    Percipalle, Maurizio
    Giunta, Renato Paolo
    Salvaggio, Antonio
    Caracappa, Giulia
    Alfonzetti, Tiziana
    Aparo, Alessandra
    Reale, Stefano
    JOURNAL OF VETERINARY DIAGNOSTIC INVESTIGATION, 2017, 29 (02) : 203 - 207
  • [46] Development and validation of a fast quantitative real-time PCR assay for the detection of African swine fever virus
    Hwang, Hyun Jin
    Choi, Yun Seong
    Song, Kyungyoung
    Frant, Maciej
    Kim, Jeong Hee
    FRONTIERS IN VETERINARY SCIENCE, 2023, 9
  • [47] Development and validation of a TaqMan™ fluorescent quantitative real-time PCR assay for the rapid detection of Edwardsiella tarda
    Guosi Xie
    Jie Huang
    Qingli Zhang
    Nana Han
    Chengyin Shi
    Xiuhua Wang
    Acta Oceanologica Sinica, 2012, 31 : 140 - 148
  • [49] Development and validation of a TaqMan™ fluorescent quantitative real-time PCR assay for the rapid detection of Edwardsiella tarda
    Xie Guosi
    Huang Jie
    Zhang Qingli
    Han Nana
    Shi Chengyin
    Wang Xiuhua
    ACTA OCEANOLOGICA SINICA, 2012, 31 (04) : 140 - 148
  • [50] Development and validation of a real-time Taqman® PCR assay for the detection and quantitation of infectious laryngotracheitis virus in poultry
    Callison, S. A.
    Riblet, S. M.
    Oldoni, I.
    Sun, S.
    Zavala, G.
    Williams, S.
    Resurreccion, R. S.
    Spackman, E.
    Garcia, M.
    JOURNAL OF VIROLOGICAL METHODS, 2007, 139 (01) : 31 - 38