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Quantification of relative flying fish paste content in the processed seafood ago-noyaki using real-time PCR

机译:使用实时PCR定量加工的海鲜即食烧饼中的相对飞鱼酱含量

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Real-time polymerase chain reaction (PCR) analysis of the 3′-portion of the mitochondrial 16S RNA gene (rDNA) coding sequence was used to determine flying fish paste in ago-noyaki. We quantified the amount of flying fish paste in ago-noyaki samples using flying fish-specific primers (Tobi16SF3/Tobi16SR) and universal primers (Univ16SF2/Univ16SR2). Using real-time PCR of standard ago-noyaki, a standard equation was obtained (y = 1.08x − 3.20; R 2 = 0.977). This equation was then used to estimate the relative flying fish paste contents of eight commercially available ago-noyaki and two similar products. These results verified that the ago-noyaki products that had already been labeled with the E-mark deserved this status.
机译:实时聚合酶链反应(PCR)分析线粒体16S RNA基因(rDNA)编码序列的3'部分被用来确定飞鱼酱。我们使用飞鱼特有的引物(Tobi16SF3 / Tobi16SR)和通用引物(Univ16SF2 / Univ16SR2)定量了早午餐样品中的飞鱼糊含量。使用标准no-noyaki的实时PCR,获得标准方程式(y = 1.08x-3.20; R 2 = 0.977)。然后使用该方程式估算八种市售的早午餐和两种类似产品的相对飞鱼酱含量。这些结果证明,已经贴有E-mark的以前的noakiaki产品应有此地位。

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