Identification of Ingredient in Mullet Roe Products by the Real-Time PCR Method
Autor: | Hsiu-Wei Tsuei, Hwei-Fang Cheng, Bo-Lin Chen, Je-Hung Kuo, Jung Kuan, Chang Yuan-Hsin, Zih-Ling Jia, Che-Yang Lin, Lih-Ching Chiueh, Hsu-Yang Lin, Daniel Yang-Chih Shih |
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Rok vydání: | 2017 |
Předmět: |
Serial dilution
biology business.industry 010401 analytical chemistry 04 agricultural and veterinary sciences Amplicon biology.organism_classification 16S ribosomal RNA 040401 food science 01 natural sciences Applied Microbiology and Biotechnology 18S ribosomal RNA Mullet 0104 chemical sciences Analytical Chemistry Biotechnology Ingredient 0404 agricultural biotechnology Real-time polymerase chain reaction TaqMan Food science Safety Risk Reliability and Quality business Safety Research Food Science |
Zdroj: | Food Analytical Methods. 11:992-1000 |
ISSN: | 1936-976X 1936-9751 |
DOI: | 10.1007/s12161-017-1043-7 |
Popis: | Mullet roe is a product of high economic value in a number of Asian countries, particularly Taiwan. However, actual mullet roe is commonly adulterated by the addition of other species, such as escolar and oilfish. The purpose of this study was to develop a method to detect the ingredient of mullet roe products. Based on the TaqMan real-time PCR assay, we designed the specific primers-probe set (mullet) that targets the mitochondrial 16S ribosomal RNA gene. Meanwhile, the positive amplification control is designed based on the eukaryotic 18S rRNA gene. The PCR amplicon used to identify fish species in processed roe products is smaller than 200 bp. Method specificity was evaluated by analyzing tissue samples of 29 food fish and 9 puffer fish species. No indications of cross-reactivity toward non-target species were observed. Sensitivity and linearity tests were conducted using five-fold serial dilutions of target DNA from processed mullet roe, and we determined that our proposed method has a sensitivity of 1.2 ng. Further tests on a random survey of commercial fish roe products demonstrated the efficacy of the technique in the detection of mullet DNA. The real-time PCR methods developed in this study could be used to verify the labeling of actual mullet roe products. |
Databáze: | OpenAIRE |
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