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Development and validation of multiplex PCR assay for differentiating tunas and billfishes
Commercially available tunas and billfishes are generally processed as steaks, making it difficult to visually distinguish between the two. We developed and validated species-specific primers to prevent the adulteration of tunas by billfishes. Tunas and billfishes primers were designed on the cytoch...
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Published in: | Food science and biotechnology 2021, 30(4), , pp.497-503 |
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creator | Kim, Na-Ye-Seul Park, Eun-Ji Lee, Seo-Hyun Mun, Kwang-Ho Yang, Ji-Young Kim, Jung-Beom |
description | Commercially available tunas and billfishes are generally processed as steaks, making it difficult to visually distinguish between the two. We developed and validated species-specific primers to prevent the adulteration of tunas by billfishes. Tunas and billfishes primers were designed on the cytochrome oxidase subunit I. Multiplex PCR bands obtained were 579 bp, 291 bp and 114 bp for tunas, billfishes and internal control. Sensitivity was determined to be 5 ng for tunas and billfishes. A total of 50 samples were monitored: 49 for tunas and 1 for billfish. As a result of the monitoring, the fake tunas did not show due to the agreement between product name and the raw material of the wrapping paper. Our results indicate that the species-specific primers developed in this study are suitable for differentiating tunas and billfishes. The newly developed multiplex PCR assay is a time and cost effective technique for determining the authenticity of tunas and billfishes. |
doi_str_mv | 10.1007/s10068-021-00893-0 |
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We developed and validated species-specific primers to prevent the adulteration of tunas by billfishes. Tunas and billfishes primers were designed on the cytochrome oxidase subunit I. Multiplex PCR bands obtained were 579 bp, 291 bp and 114 bp for tunas, billfishes and internal control. Sensitivity was determined to be 5 ng for tunas and billfishes. A total of 50 samples were monitored: 49 for tunas and 1 for billfish. As a result of the monitoring, the fake tunas did not show due to the agreement between product name and the raw material of the wrapping paper. Our results indicate that the species-specific primers developed in this study are suitable for differentiating tunas and billfishes. The newly developed multiplex PCR assay is a time and cost effective technique for determining the authenticity of tunas and billfishes.</description><identifier>ISSN: 1226-7708</identifier><identifier>EISSN: 2092-6456</identifier><identifier>DOI: 10.1007/s10068-021-00893-0</identifier><identifier>PMID: 33936840</identifier><language>eng</language><publisher>Singapore: Springer Singapore</publisher><subject>Chemistry ; Chemistry and Materials Science ; Cytochrome ; Cytochromes ; Food Science ; Multiplexing ; Nutrition ; Primers ; Product names ; Research Article ; 식품과학</subject><ispartof>Food Science and Biotechnology, 2021, 30(4), , pp.497-503</ispartof><rights>The Korean Society of Food Science and Technology 2021</rights><rights>The Korean Society of Food Science and Technology 2021.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c508t-5300f42f7a5d25470dfcff7f9d8a5824665765a378cd4741d571c4a6c7b19b83</citedby><cites>FETCH-LOGICAL-c508t-5300f42f7a5d25470dfcff7f9d8a5824665765a378cd4741d571c4a6c7b19b83</cites><orcidid>0000-0002-0290-2687</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8050170/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8050170/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33936840$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://www.kci.go.kr/kciportal/ci/sereArticleSearch/ciSereArtiView.kci?sereArticleSearchBean.artiId=ART002706518$$DAccess content in National Research Foundation of Korea (NRF)$$Hfree_for_read</backlink></links><search><creatorcontrib>Kim, Na-Ye-Seul</creatorcontrib><creatorcontrib>Park, Eun-Ji</creatorcontrib><creatorcontrib>Lee, Seo-Hyun</creatorcontrib><creatorcontrib>Mun, Kwang-Ho</creatorcontrib><creatorcontrib>Yang, Ji-Young</creatorcontrib><creatorcontrib>Kim, Jung-Beom</creatorcontrib><title>Development and validation of multiplex PCR assay for differentiating tunas and billfishes</title><title>Food science and biotechnology</title><addtitle>Food Sci Biotechnol</addtitle><addtitle>Food Sci Biotechnol</addtitle><description>Commercially available tunas and billfishes are generally processed as steaks, making it difficult to visually distinguish between the two. We developed and validated species-specific primers to prevent the adulteration of tunas by billfishes. Tunas and billfishes primers were designed on the cytochrome oxidase subunit I. Multiplex PCR bands obtained were 579 bp, 291 bp and 114 bp for tunas, billfishes and internal control. Sensitivity was determined to be 5 ng for tunas and billfishes. A total of 50 samples were monitored: 49 for tunas and 1 for billfish. As a result of the monitoring, the fake tunas did not show due to the agreement between product name and the raw material of the wrapping paper. Our results indicate that the species-specific primers developed in this study are suitable for differentiating tunas and billfishes. The newly developed multiplex PCR assay is a time and cost effective technique for determining the authenticity of tunas and billfishes.</description><subject>Chemistry</subject><subject>Chemistry and Materials Science</subject><subject>Cytochrome</subject><subject>Cytochromes</subject><subject>Food Science</subject><subject>Multiplexing</subject><subject>Nutrition</subject><subject>Primers</subject><subject>Product names</subject><subject>Research Article</subject><subject>식품과학</subject><issn>1226-7708</issn><issn>2092-6456</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNp9kU1v1DAQhi0EokvhD3BAkbjAIe34K3YuSNXyValSUbUnLpY3sbduHXuxkxX993g3pQUOXDyHed7XM_Mi9BrDCQYQp7m8jayB4BpAtrSGJ2hBoCV1w3jzFC0wIU0tBMgj9CLnm0JjIthzdERpSxvJYIG-fzQ74-N2MGGsdOirnfau16OLoYq2GiY_uq03P6tvy6tK56zvKhtT1TtrTSoaV9CwqcYp6HzQr5331uVrk1-iZ1b7bF7d12O0-vxptfxaX1x-OV-eXdQdBznWnAJYRqzQvCecCehtZ62wbS81l4Q1DRcN11TIrmeC4Z4L3DHddGKN27Wkx-j9bBuSVbedU1G7Q91EdZvU2dXqXLVCMI5FYT_M7HZaD6bvygJJe7VNbtDp7qD8uxPcdfHZKQkcsIBi8O7eIMUfk8mjGlzujPc6mDhlRTjBrOUSSEHf_oPexCmFcolCYUpaytr99GSmuhRzTsY-DINB7VNWc8qqpKwOKav9FG_-XONB8jvWAtAZyKUVNiY9_v0f21_A5rKi</recordid><startdate>20210401</startdate><enddate>20210401</enddate><creator>Kim, Na-Ye-Seul</creator><creator>Park, Eun-Ji</creator><creator>Lee, Seo-Hyun</creator><creator>Mun, Kwang-Ho</creator><creator>Yang, Ji-Young</creator><creator>Kim, Jung-Beom</creator><general>Springer Singapore</general><general>Springer Nature B.V</general><general>한국식품과학회</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope><scope>ACYCR</scope><orcidid>https://orcid.org/0000-0002-0290-2687</orcidid></search><sort><creationdate>20210401</creationdate><title>Development and validation of multiplex PCR assay for differentiating tunas and billfishes</title><author>Kim, Na-Ye-Seul ; Park, Eun-Ji ; Lee, Seo-Hyun ; Mun, Kwang-Ho ; Yang, Ji-Young ; Kim, Jung-Beom</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c508t-5300f42f7a5d25470dfcff7f9d8a5824665765a378cd4741d571c4a6c7b19b83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Chemistry</topic><topic>Chemistry and Materials Science</topic><topic>Cytochrome</topic><topic>Cytochromes</topic><topic>Food Science</topic><topic>Multiplexing</topic><topic>Nutrition</topic><topic>Primers</topic><topic>Product names</topic><topic>Research Article</topic><topic>식품과학</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kim, Na-Ye-Seul</creatorcontrib><creatorcontrib>Park, Eun-Ji</creatorcontrib><creatorcontrib>Lee, Seo-Hyun</creatorcontrib><creatorcontrib>Mun, Kwang-Ho</creatorcontrib><creatorcontrib>Yang, Ji-Young</creatorcontrib><creatorcontrib>Kim, Jung-Beom</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>Korean Citation Index</collection><jtitle>Food science and biotechnology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kim, Na-Ye-Seul</au><au>Park, Eun-Ji</au><au>Lee, Seo-Hyun</au><au>Mun, Kwang-Ho</au><au>Yang, Ji-Young</au><au>Kim, Jung-Beom</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Development and validation of multiplex PCR assay for differentiating tunas and billfishes</atitle><jtitle>Food science and biotechnology</jtitle><stitle>Food Sci Biotechnol</stitle><addtitle>Food Sci Biotechnol</addtitle><date>2021-04-01</date><risdate>2021</risdate><volume>30</volume><issue>4</issue><spage>497</spage><epage>503</epage><pages>497-503</pages><issn>1226-7708</issn><eissn>2092-6456</eissn><abstract>Commercially available tunas and billfishes are generally processed as steaks, making it difficult to visually distinguish between the two. We developed and validated species-specific primers to prevent the adulteration of tunas by billfishes. Tunas and billfishes primers were designed on the cytochrome oxidase subunit I. Multiplex PCR bands obtained were 579 bp, 291 bp and 114 bp for tunas, billfishes and internal control. Sensitivity was determined to be 5 ng for tunas and billfishes. A total of 50 samples were monitored: 49 for tunas and 1 for billfish. As a result of the monitoring, the fake tunas did not show due to the agreement between product name and the raw material of the wrapping paper. Our results indicate that the species-specific primers developed in this study are suitable for differentiating tunas and billfishes. The newly developed multiplex PCR assay is a time and cost effective technique for determining the authenticity of tunas and billfishes.</abstract><cop>Singapore</cop><pub>Springer Singapore</pub><pmid>33936840</pmid><doi>10.1007/s10068-021-00893-0</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0002-0290-2687</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Chemistry Chemistry and Materials Science Cytochrome Cytochromes Food Science Multiplexing Nutrition Primers Product names Research Article 식품과학 |
title | Development and validation of multiplex PCR assay for differentiating tunas and billfishes |
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