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Fish species identification in canned pet food by BLAST and Forensically Informative Nucleotide Sequencing (FINS) analysis of short fragments of the mitochondrial 16s ribosomal RNA gene (16S rRNA)

机译:鱼类在植物型宠物食品中鉴定爆炸,并对线粒体16S核糖体RNA基因短片段(16s rRNA)的短片段分析

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摘要

Nowadays, pet food claiming high-valued fish among ingredients is largely available on the market. Unfortunately, the modifications induced by processing make species identification by visual inspection difficult and hinder the enforcement of the legislation on traceability. In this work, after aligning 819 sequences of Clupeidae, Engraulidae, Salangidae and Scombridae families, we developed new universal primers for the amplification and sequencing of 2 short fragments (+/- 118 and +/- 213) of the mitochondrial 16s ribosomal RNA (16S rRNA) gene. Once tested on 130 DNA reference samples, these primers were used in the analysis of highly degraded DNA extracted from 43 canned cat food containing whole minnows (whitebait) (M) and tuna, or bonito or mackerel fillets (F). Three M and 2 F samples were analyzed for each can. A BLAST and a FINS analysis, the latter performed only on the 118 bp fragment, were performed separately on the sequences obtained from M and F samples. All the M samples were identified at the species or genus level by both BLAST and FINS analysis. This allowed to highlight an impressive rate of mislabeling (100%). F samples, for which FINS was less performing in species identification, resulted mislabeled in 40% of the products. (C) 2014 Elsevier Ltd. All rights reserved.
机译:如今,在市场上索取高价值鱼的宠物食品在市场上很大程度上可用。不幸的是,通过处理诱导的修改使物种识别通过视觉检查困难并阻碍了立法对可追溯性的执行。在这项工作中,在对准Clupeidae,Engrauridae,沙兰瓜和Scombridae家族的819次序列之后,我们开发了新的通用引物,用于2短片段(+/- 118和+/- 213)的线粒体16s核糖体RNA( 16S rRNA)基因。一旦在130个DNA参考样品上测试,这些引物用于分析从含有整个小鱼(WhiteBait)(M)和金枪鱼或鲣鱼或麦克风或鲭鱼片(F)的43罐罐头食品中提取的高度降解的DNA。分析了三个m和2 f样品。爆炸和鳍片分析,后者仅在118bp片段上进行,分别在从M和F样品获得的序列上进行。通过爆炸和鳍分析在物种或属级别鉴定所有M样品。这允许突出令人印象深刻的错误标签率(100%)。 F样品,鳍片在物种鉴定中表现较低,导致40%的产品中标记为误标。 (c)2014年elestvier有限公司保留所有权利。

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