Fish Species Identification by Means of Restriction Fragment Length Polymorphism and High‐Performance Liquid Chromatography
Identifieur interne : 000980 ( Istex/Curation ); précédent : 000979; suivant : 000981Fish Species Identification by Means of Restriction Fragment Length Polymorphism and High‐Performance Liquid Chromatography
Auteurs : B. Horstkotte [Allemagne] ; H. Rehbein [Allemagne]Source :
- Journal of Food Science [ 0022-1147 ] ; 2003-11.
Abstract
ABSTRACT The usability of fish species identification with restriction fragment length polymorphism (RFLP) using high‐performance liquid chromatography (HPLC) was evaluated for sturgeon, salmon, and tuna samples. Separations of restriction fragments were performed within about 10 min at alkaline pH using an anion‐ex‐change diethylaminoethyl nonporous column. Unequivocal species identification was achieved with HPLC, despite nucleotide sequence‐depending separation. Separation of DNA fragments by HPLC could be demonstrated to be a fast and reliable alternative to electrophoresis. Calculation of restriction fragment lengths using relative peak areas showed better accordance compared with values obtained by means of DNA size standards. Keywords: species identification, HPLC, RFLP, fish
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DOI: 10.1111/j.1365-2621.2003.tb05785.x
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<affiliation wicri:level="1"><mods:affiliation>Authors Horstkotte and Rehbein are with the Federal Research Centre for Fisheries, Inst. for Fishery Technology and Fish Quality, Palmaille 9, 22335 Hamburg, Germany. Direct inquiries to author Horstkotte (E‐mail: Burkhard.Horstkotte@ibt.bfa‐fisch.de) or author Rehbein (E‐mail: Hartmut.Rehbein@ibt.bfa‐fisch.de).</mods:affiliation>
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<front><div type="abstract">ABSTRACT The usability of fish species identification with restriction fragment length polymorphism (RFLP) using high‐performance liquid chromatography (HPLC) was evaluated for sturgeon, salmon, and tuna samples. Separations of restriction fragments were performed within about 10 min at alkaline pH using an anion‐ex‐change diethylaminoethyl nonporous column. Unequivocal species identification was achieved with HPLC, despite nucleotide sequence‐depending separation. Separation of DNA fragments by HPLC could be demonstrated to be a fast and reliable alternative to electrophoresis. Calculation of restriction fragment lengths using relative peak areas showed better accordance compared with values obtained by means of DNA size standards. Keywords: species identification, HPLC, RFLP, fish</div>
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