Centre for Research of Innovation and Sustainable Development (CRISD)

Paper of the Month:

Developing high-accuracy food authentication technologies to prevent food adulteration activities.

Ts Nurhayatie and Mr Koh from the Bioresources Research Cluster, CRISD with their collaborators from University Putra Malaysia have demonstrated the high-accuracy DNA-based technique called the TaqMan probe real-time PCR in food authentication. The work has been published in the Food Research Journal.

Meatballs are a common meat-based product that is so vulnerable to food adulteration activities in the food industries. (Photo credit: RitaE | pixabay )

Summary

Food adulteration is a growing concern amongst the consumers. Moreover, food adulteration might affect various consumer groups who have strict diet requirements, whether due to religious belief or health reasons. Food adulteration also contributes to an unfair trade competition that might indirectly affect the economy.

Adulteration of meat-based products involving replacing high-priced meat with lower-priced meat accounts for 19.25% of all food fraud activities, according to the European Commission’s studies in 2018. DNA-based techniques are often used for fraud detection in raw meat species and heat-processed meat products. The reason is that DNA has better resilience towards high heat, especially during food processing such as cooking. In the case of Ts. Nurhayatie et al., they are using the TaqMan-based real-time PCR assay technique. The real advantage of this technique compared to the other DNA-based techniques is that it is more sensitive, and able to provide quantitative output without the need of post-PCR processing.

Ts. Nurhayatie et al. have demonstrated the technique on the detection of pork DNA on the spiked chicken and beef meatball models. Initially, these 35 g per piece chicken and beef meatball models were spiked with 10% (weight for weight) pork meat. The technique has demonstrated that it can detect as low as 0.01 nanogram per microlitre and 0.1 nanogram per microlitre of pork DNA in uncooked spiked beef and chicken meatball models, respectively. For cooked spiked beef and chicken meatball models, the pork DNA was detected at a concentration of 0.1 nanogram per microlitre. The ability to detect the pork DNA even for cooked meatball models shows the workability of the technique proposed by the Ts Nurhayatie et al.

Details of the paper:

N. Sajali, S.M.L. Ting, C.C. Koh, M.N.M. Desa, S.C. Wong, S. Abu Bakar, Meatball model of porcine DNA detection by TaqMan probe real-time PCR, Food Research 6 (2022) 136–144. https://doi.org/10.26656/fr.2017.6(3).384.