4.7 Article

DNA-based qualitative and quantitative identification of bovine whey powder in goat dairy products

期刊

JOURNAL OF DAIRY SCIENCE
卷 105, 期 6, 页码 4749-4759

出版社

ELSEVIER SCIENCE INC
DOI: 10.3168/jds.2021-21618

关键词

bovine whey powder; DNA quality; PCR; adulteration detection

资金

  1. Shaanxi Province Key Research and Development Projects (Xi'an, China) [2019ZDLNY06-05]
  2. Fundamental Research Funds of the Central Universities in China (Beijing, China) [GK202001002]
  3. Science and Technology Plan Projects in Xianyang City of Shaanxi Province (Xianyang, China) [2021ZDZX-NY-0014]
  4. Shaanxi Province Forestry Science and Technology Plan Projects of China (Xi'an, China) [SXLK2021-0221]
  5. Youth Innovation Team of Shaanxi University (Xi'an, China)

向作者/读者索取更多资源

This study explores qualitative and quantitative methods based on DNA to identify adulteration of bovine whey powder in goat dairy products. The results show that real-time PCR is more sensitive than conventional PCR in detecting bovine whey powder. This research provides a realistic and effective method for qualitative and quantitative identification of bovine whey powder in goat dairy products.
As one of the main ingredients in some milk powders, whey powder is sometimes added to pure goat milk products, which can cause health risks, economic fraud, and unfair competition of food industries. This study is the first to explore qualitative and quantitative methods to identify adulteration of bovine whey powder in goat dairy products based on DNA. We extracted DNA from whey powder using a modified DNA extraction method; this exhibited good quality and integrity, with purity of 1.53 to 1.75 and concentration of 122 to 179 ng/mu L. Conventional PCR and real-time PCR were compared for qualitative detection of bovine whey powder; real-time PCR demonstrated sensitivity of 0.01 ng/mu L, which was higher than the 0.05 ng/mu L detected by the conventional PCR method. Furthermore, real-time PCR was conducted for DNA quantitative detection, with good linearity (R-2 = 0.9858) obtained for bovine whey powder contents from 0.1% to 30%. Relative error decreased with increase of the mixing proportion of whey powder; the coefficient of variation above 0.1% of the mixing ratio was close to or less than 5%; and the relative standard deviation of repeatability results was less than 5%. Considering the economic costs of testing, conventional PCR could be performed first, and samples with obvious intentional adulteration detected can be further accurately quantified by real-time PCR. Overall, this research provides a realistic and effective method for qualitative and quantitative identification of bovine whey powder in goat dairy products, thus laying a good foundation for verification of goat dairy product label claims and industrial control.

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