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基于ITS1-rDNA的方法来鉴定全球范围内无须鳕属的无须鳕种类。

ITS1-rDNA-based methodology to identify world-wide hake species of the Genus Merluccius.

作者信息

Pérez Montse, Vieites Juan M, Presa Pablo

机构信息

Department of Biochemistry, Genetics, and Immunology, Faculty of Biology, University of Vigo, Spain.

出版信息

J Agric Food Chem. 2005 Jun 29;53(13):5239-47. doi: 10.1021/jf048012h.

Abstract

Species-specific DNA-based tags are valuable tools for the management of both fisheries and commercial fish products. In this study, we have developed a two-step molecular tool to detect the presence of hake DNA (Merluccius spp.) and to identify the exact hake species present in an blind sample. The first test involves PCR amplification of an ITS1-rDNA fragment of 193 bp using nested primers that are interspecifically conserved in Merluccius spp. and Atlantic cod, Gadus morhua. The second test consists of the PCR amplification of a 602-659 bp DNA fragment spanning part of the ribosomal cluster 18S-ITS1-5.8S and digesting it with four restriction enzymes whose targets map at interspecifically nonconserved sites of the ITS1. Alternatively, the identification of hake species can be achieved by FINS or BLAST, using the nucleotide sequence of either the whole ITS1 sequence or its nested fragment of 193 bp. Because of their high reproducibility and ease of execution, these procedures allow for routine analysis and constitute high reliable tools for the rapid identification of 12 species of hake.

摘要

基于物种特异性DNA的标签是渔业和商业鱼类产品管理的宝贵工具。在本研究中,我们开发了一种两步分子工具,用于检测无须鳕DNA(无须鳕属)的存在,并识别盲样中存在的具体无须鳕物种。第一步测试涉及使用在无须鳕属和大西洋鳕鱼( Gadus morhua)中种间保守的巢式引物对193 bp的ITS1-rDNA片段进行PCR扩增。第二步测试包括对跨越核糖体簇18S-ITS1-5.8S部分的602-659 bp DNA片段进行PCR扩增,并用四种限制性内切酶进行消化,这些酶的靶点位于ITS1的种间非保守位点。或者,使用整个ITS1序列或其193 bp的巢式片段的核苷酸序列,通过FINS或BLAST可以实现无须鳕物种的鉴定。由于这些程序具有高重现性且易于执行,它们可用于常规分析,并构成了用于快速鉴定12种无须鳕的高度可靠工具。

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