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Application of PCR‐SSCP to Species Identification of Fishery Products

Identifieur interne : 000696 ( Istex/Corpus ); précédent : 000695; suivant : 000697

Application of PCR‐SSCP to Species Identification of Fishery Products

Auteurs : Hartmut Rehbein ; Gabriele Kress ; Thomas Schmidt

Source :

RBID : ISTEX:65F6116D23BA359901B093A0E758F6E5B3613F51

English descriptors

Abstract

A method of DNA analysis has been developed to verify authenticity of labelled raw material of canned fish or in products made from closely related fish species (tuna, eel, salmon, trout and sturgeon). Short segments (123–358 bp) of the mitochondrial cytochrome b gene were amplified by the polymerase chain reaction (PCR) and analysed by single strand conformation polymorphism (SSCP) to get species‐specific patterns of single‐stranded DNA (ssDNA). DNA strands were separated by polyacrylamide gel electrophoresis and visualised by silver staining. Differentiation between four eel species was possible. Each of three types of sturgeon caviar gave a characteristic pattern of ssDNA. Canned sardine, herring, tuna and other species expressed specific bands of ssDNA. © 1997 SCI.

Url:
DOI: 10.1002/(SICI)1097-0010(199705)74:1<35::AID-JSFA765>3.0.CO;2-2

Links to Exploration step

ISTEX:65F6116D23BA359901B093A0E758F6E5B3613F51

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<affiliation>Institute of Biochemistry and Technology, Federal Research Centre for Fisheries, Palmaille 9, D‐22767 Hamburg, Germany</affiliation>
<role>
<roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal">
<namePart type="given">Gabriele</namePart>
<namePart type="family">Kress</namePart>
<affiliation>Institute of Biochemistry and Technology, Federal Research Centre for Fisheries, Palmaille 9, D‐22767 Hamburg, Germany</affiliation>
<role>
<roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal">
<namePart type="given">Thomas</namePart>
<namePart type="family">Schmidt</namePart>
<affiliation>Institute of Biochemistry and Technology, Federal Research Centre for Fisheries, Palmaille 9, D‐22767 Hamburg, Germany</affiliation>
<role>
<roleTerm type="text">author</roleTerm>
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<typeOfResource>text</typeOfResource>
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<publisher>John Wiley & Sons, Ltd</publisher>
<place>
<placeTerm type="text">London</placeTerm>
</place>
<dateIssued encoding="w3cdtf">1997-05</dateIssued>
<dateCaptured encoding="w3cdtf">1996-03-08</dateCaptured>
<dateValid encoding="w3cdtf">1996-10-14</dateValid>
<copyrightDate encoding="w3cdtf">1997</copyrightDate>
</originInfo>
<language>
<languageTerm type="code" authority="rfc3066">en</languageTerm>
<languageTerm type="code" authority="iso639-2b">eng</languageTerm>
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<extent unit="figures">5</extent>
<extent unit="tables">1</extent>
<extent unit="references">22</extent>
</physicalDescription>
<abstract lang="en">A method of DNA analysis has been developed to verify authenticity of labelled raw material of canned fish or in products made from closely related fish species (tuna, eel, salmon, trout and sturgeon). Short segments (123–358 bp) of the mitochondrial cytochrome b gene were amplified by the polymerase chain reaction (PCR) and analysed by single strand conformation polymorphism (SSCP) to get species‐specific patterns of single‐stranded DNA (ssDNA). DNA strands were separated by polyacrylamide gel electrophoresis and visualised by silver staining. Differentiation between four eel species was possible. Each of three types of sturgeon caviar gave a characteristic pattern of ssDNA. Canned sardine, herring, tuna and other species expressed specific bands of ssDNA. © 1997 SCI.</abstract>
<subject lang="en">
<genre>keywords</genre>
<topic>PCR</topic>
<topic>SSCP</topic>
<topic>eel</topic>
<topic>caviar</topic>
<topic>salmon</topic>
<topic>trout</topic>
<topic>canned fish</topic>
<topic>fish</topic>
<topic>food</topic>
<topic>species identification</topic>
</subject>
<relatedItem type="host">
<titleInfo>
<title>Journal of the Science of Food and Agriculture</title>
</titleInfo>
<titleInfo type="abbreviated">
<title>J. Sci. Food Agric.</title>
</titleInfo>
<genre type="journal">journal</genre>
<subject>
<genre>article-category</genre>
<topic>Research Article</topic>
</subject>
<identifier type="ISSN">0022-5142</identifier>
<identifier type="eISSN">1097-0010</identifier>
<identifier type="DOI">10.1002/(ISSN)1097-0010</identifier>
<identifier type="PublisherID">JSFA</identifier>
<part>
<date>1997</date>
<detail type="volume">
<caption>vol.</caption>
<number>74</number>
</detail>
<detail type="issue">
<caption>no.</caption>
<number>1</number>
</detail>
<extent unit="pages">
<start>35</start>
<end>41</end>
<total>7</total>
</extent>
</part>
</relatedItem>
<identifier type="istex">65F6116D23BA359901B093A0E758F6E5B3613F51</identifier>
<identifier type="DOI">10.1002/(SICI)1097-0010(199705)74:1<35::AID-JSFA765>3.0.CO;2-2</identifier>
<identifier type="ArticleID">JSFA765</identifier>
<accessCondition type="use and reproduction" contentType="copyright">Copyright © 1997 SCI</accessCondition>
<recordInfo>
<recordContentSource>WILEY</recordContentSource>
<recordOrigin>John Wiley & Sons, Ltd</recordOrigin>
</recordInfo>
</mods>
</metadata>
<serie></serie>
</istex>
</record>

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