Discovery of okadaic acid esters in the toxic dinoflagellate Dinophysis acuta from New Zealand using liquid chromatography/tandem mass spectrometry

The dinoflagellate Dinophysis acuta has been associated with various incidents of diarrhetic shellfish poisoning. A sample of Dinophysis acuta collected from New Zealand waters in 2002 was previously found to contain high levels of pectenotoxins, but only a very low level of the diarrhea‐inducing ok...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Rapid communications in mass spectrometry 2004-01, Vol.18 (10), p.1131-1138
Hauptverfasser: Suzuki, T., Beuzenberg, V., Mackenzie, L., Quilliam, M. A.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 1138
container_issue 10
container_start_page 1131
container_title Rapid communications in mass spectrometry
container_volume 18
creator Suzuki, T.
Beuzenberg, V.
Mackenzie, L.
Quilliam, M. A.
description The dinoflagellate Dinophysis acuta has been associated with various incidents of diarrhetic shellfish poisoning. A sample of Dinophysis acuta collected from New Zealand waters in 2002 was previously found to contain high levels of pectenotoxins, but only a very low level of the diarrhea‐inducing okadaic acid (OA). After hydrolysis under basic conditions, however, the concentration of OA increased substantially, indicating the presence of conjugated forms of OA. Using various liquid chromatography/electrospray ionization tandem mass spectrometry (LC/ESI‐MS/MS) techniques, a number of OA esters were detected in the original extract. The principal compound was identified as a C8 diol‐ester of OA (OA‐D8), which had been identified previously in another dinoflagellate, Prorocentrum lima. The retention time, as well as positive and negative ion MS, MS/MS and UV spectra of the D. acuta compound, matched exactly those of OA‐D8 isolated from P. lima. In addition to OA‐D8, several other novel OA esters were detected in the D. acuta but these have not yet been identified. This is the first report identifying the presence of OA esters in Dinophysis species. Copyright © 2004 Crown in the right of Canada. Published by John Wiley & Sons, Ltd.
doi_str_mv 10.1002/rcm.1455
format Article
fullrecord <record><control><sourceid>istex_cross</sourceid><recordid>TN_cdi_crossref_primary_10_1002_rcm_1455</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>ark_67375_WNG_QS5C2111_Q</sourcerecordid><originalsourceid>FETCH-LOGICAL-c4855-3417f55bfb3d797b4f4e6d7174837a739ebd65c9a3a35bc05b4be3287d26311a3</originalsourceid><addsrcrecordid>eNp1kM1u1DAUhS0EokOLxBMgL9mk9Y3jcbJEUyhIpag_CImNdWPfzJgmk6ntoc1z9IXrakawYnV1db5zFh9j70AcgxDlSbDDMVRKvWAzEI0uRCnhJZuJRkFRQVMfsDcx_hYCQJXiNTsABUrUsp6xx1Mf7fiHwsTHjo-36NBbjtY7TjFRiNyveVoRT-NDDpxfj12PS-p7TMRP87tZTdHHXNkm5F0YB35B9_wXYY9rx7fRr5e893fbvGhXOcY0LgPm1knKAA18wBh53JBNOaUUpiP2qsM-0tv9PWQ_Pn-6WXwpzr-ffV18PC9sVStVyAp0p1TbtdLpRrdVV9HcadBVLTVq2VDr5so2KFGq1grVVi3JstaunEsAlIfsw27XhjHGQJ3ZBD9gmAwI8-zVZK_m2WtG3-_QzbYdyP0D9yIzUOyAe9_T9N8hc7X4th_c8z5bfvjLY7g1cy21Mj8vzszltVqUAGAu5RPycZPw</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Discovery of okadaic acid esters in the toxic dinoflagellate Dinophysis acuta from New Zealand using liquid chromatography/tandem mass spectrometry</title><source>MEDLINE</source><source>Access via Wiley Online Library</source><creator>Suzuki, T. ; Beuzenberg, V. ; Mackenzie, L. ; Quilliam, M. A.</creator><creatorcontrib>Suzuki, T. ; Beuzenberg, V. ; Mackenzie, L. ; Quilliam, M. A.</creatorcontrib><description>The dinoflagellate Dinophysis acuta has been associated with various incidents of diarrhetic shellfish poisoning. A sample of Dinophysis acuta collected from New Zealand waters in 2002 was previously found to contain high levels of pectenotoxins, but only a very low level of the diarrhea‐inducing okadaic acid (OA). After hydrolysis under basic conditions, however, the concentration of OA increased substantially, indicating the presence of conjugated forms of OA. Using various liquid chromatography/electrospray ionization tandem mass spectrometry (LC/ESI‐MS/MS) techniques, a number of OA esters were detected in the original extract. The principal compound was identified as a C8 diol‐ester of OA (OA‐D8), which had been identified previously in another dinoflagellate, Prorocentrum lima. The retention time, as well as positive and negative ion MS, MS/MS and UV spectra of the D. acuta compound, matched exactly those of OA‐D8 isolated from P. lima. In addition to OA‐D8, several other novel OA esters were detected in the D. acuta but these have not yet been identified. This is the first report identifying the presence of OA esters in Dinophysis species. Copyright © 2004 Crown in the right of Canada. Published by John Wiley &amp; Sons, Ltd.</description><identifier>ISSN: 0951-4198</identifier><identifier>EISSN: 1097-0231</identifier><identifier>DOI: 10.1002/rcm.1455</identifier><identifier>PMID: 15150838</identifier><language>eng</language><publisher>Chichester, UK: John Wiley &amp; Sons, Ltd</publisher><subject>Animals ; Chromatography, Liquid - methods ; Dinoflagellida - chemistry ; Esterification ; Molecular Structure ; New Zealand ; Okadaic Acid - analogs &amp; derivatives ; Okadaic Acid - analysis ; Okadaic Acid - chemistry ; Spectrometry, Mass, Electrospray Ionization - methods</subject><ispartof>Rapid communications in mass spectrometry, 2004-01, Vol.18 (10), p.1131-1138</ispartof><rights>Copyright © 2004 Crown in the right of Canada. Published by John Wiley &amp; Sons, Ltd.</rights><rights>Copyright 2004 Crown in the right of Canada. Published by John Wiley &amp; Sons, Ltd.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4855-3417f55bfb3d797b4f4e6d7174837a739ebd65c9a3a35bc05b4be3287d26311a3</citedby><cites>FETCH-LOGICAL-c4855-3417f55bfb3d797b4f4e6d7174837a739ebd65c9a3a35bc05b4be3287d26311a3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Frcm.1455$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Frcm.1455$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15150838$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Suzuki, T.</creatorcontrib><creatorcontrib>Beuzenberg, V.</creatorcontrib><creatorcontrib>Mackenzie, L.</creatorcontrib><creatorcontrib>Quilliam, M. A.</creatorcontrib><title>Discovery of okadaic acid esters in the toxic dinoflagellate Dinophysis acuta from New Zealand using liquid chromatography/tandem mass spectrometry</title><title>Rapid communications in mass spectrometry</title><addtitle>Rapid Commun. Mass Spectrom</addtitle><description>The dinoflagellate Dinophysis acuta has been associated with various incidents of diarrhetic shellfish poisoning. A sample of Dinophysis acuta collected from New Zealand waters in 2002 was previously found to contain high levels of pectenotoxins, but only a very low level of the diarrhea‐inducing okadaic acid (OA). After hydrolysis under basic conditions, however, the concentration of OA increased substantially, indicating the presence of conjugated forms of OA. Using various liquid chromatography/electrospray ionization tandem mass spectrometry (LC/ESI‐MS/MS) techniques, a number of OA esters were detected in the original extract. The principal compound was identified as a C8 diol‐ester of OA (OA‐D8), which had been identified previously in another dinoflagellate, Prorocentrum lima. The retention time, as well as positive and negative ion MS, MS/MS and UV spectra of the D. acuta compound, matched exactly those of OA‐D8 isolated from P. lima. In addition to OA‐D8, several other novel OA esters were detected in the D. acuta but these have not yet been identified. This is the first report identifying the presence of OA esters in Dinophysis species. Copyright © 2004 Crown in the right of Canada. Published by John Wiley &amp; Sons, Ltd.</description><subject>Animals</subject><subject>Chromatography, Liquid - methods</subject><subject>Dinoflagellida - chemistry</subject><subject>Esterification</subject><subject>Molecular Structure</subject><subject>New Zealand</subject><subject>Okadaic Acid - analogs &amp; derivatives</subject><subject>Okadaic Acid - analysis</subject><subject>Okadaic Acid - chemistry</subject><subject>Spectrometry, Mass, Electrospray Ionization - methods</subject><issn>0951-4198</issn><issn>1097-0231</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kM1u1DAUhS0EokOLxBMgL9mk9Y3jcbJEUyhIpag_CImNdWPfzJgmk6ntoc1z9IXrakawYnV1db5zFh9j70AcgxDlSbDDMVRKvWAzEI0uRCnhJZuJRkFRQVMfsDcx_hYCQJXiNTsABUrUsp6xx1Mf7fiHwsTHjo-36NBbjtY7TjFRiNyveVoRT-NDDpxfj12PS-p7TMRP87tZTdHHXNkm5F0YB35B9_wXYY9rx7fRr5e893fbvGhXOcY0LgPm1knKAA18wBh53JBNOaUUpiP2qsM-0tv9PWQ_Pn-6WXwpzr-ffV18PC9sVStVyAp0p1TbtdLpRrdVV9HcadBVLTVq2VDr5so2KFGq1grVVi3JstaunEsAlIfsw27XhjHGQJ3ZBD9gmAwI8-zVZK_m2WtG3-_QzbYdyP0D9yIzUOyAe9_T9N8hc7X4th_c8z5bfvjLY7g1cy21Mj8vzszltVqUAGAu5RPycZPw</recordid><startdate>20040101</startdate><enddate>20040101</enddate><creator>Suzuki, T.</creator><creator>Beuzenberg, V.</creator><creator>Mackenzie, L.</creator><creator>Quilliam, M. A.</creator><general>John Wiley &amp; Sons, Ltd</general><scope>BSCLL</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20040101</creationdate><title>Discovery of okadaic acid esters in the toxic dinoflagellate Dinophysis acuta from New Zealand using liquid chromatography/tandem mass spectrometry</title><author>Suzuki, T. ; Beuzenberg, V. ; Mackenzie, L. ; Quilliam, M. A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4855-3417f55bfb3d797b4f4e6d7174837a739ebd65c9a3a35bc05b4be3287d26311a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>Animals</topic><topic>Chromatography, Liquid - methods</topic><topic>Dinoflagellida - chemistry</topic><topic>Esterification</topic><topic>Molecular Structure</topic><topic>New Zealand</topic><topic>Okadaic Acid - analogs &amp; derivatives</topic><topic>Okadaic Acid - analysis</topic><topic>Okadaic Acid - chemistry</topic><topic>Spectrometry, Mass, Electrospray Ionization - methods</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Suzuki, T.</creatorcontrib><creatorcontrib>Beuzenberg, V.</creatorcontrib><creatorcontrib>Mackenzie, L.</creatorcontrib><creatorcontrib>Quilliam, M. A.</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><jtitle>Rapid communications in mass spectrometry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Suzuki, T.</au><au>Beuzenberg, V.</au><au>Mackenzie, L.</au><au>Quilliam, M. A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Discovery of okadaic acid esters in the toxic dinoflagellate Dinophysis acuta from New Zealand using liquid chromatography/tandem mass spectrometry</atitle><jtitle>Rapid communications in mass spectrometry</jtitle><addtitle>Rapid Commun. Mass Spectrom</addtitle><date>2004-01-01</date><risdate>2004</risdate><volume>18</volume><issue>10</issue><spage>1131</spage><epage>1138</epage><pages>1131-1138</pages><issn>0951-4198</issn><eissn>1097-0231</eissn><abstract>The dinoflagellate Dinophysis acuta has been associated with various incidents of diarrhetic shellfish poisoning. A sample of Dinophysis acuta collected from New Zealand waters in 2002 was previously found to contain high levels of pectenotoxins, but only a very low level of the diarrhea‐inducing okadaic acid (OA). After hydrolysis under basic conditions, however, the concentration of OA increased substantially, indicating the presence of conjugated forms of OA. Using various liquid chromatography/electrospray ionization tandem mass spectrometry (LC/ESI‐MS/MS) techniques, a number of OA esters were detected in the original extract. The principal compound was identified as a C8 diol‐ester of OA (OA‐D8), which had been identified previously in another dinoflagellate, Prorocentrum lima. The retention time, as well as positive and negative ion MS, MS/MS and UV spectra of the D. acuta compound, matched exactly those of OA‐D8 isolated from P. lima. In addition to OA‐D8, several other novel OA esters were detected in the D. acuta but these have not yet been identified. This is the first report identifying the presence of OA esters in Dinophysis species. Copyright © 2004 Crown in the right of Canada. Published by John Wiley &amp; Sons, Ltd.</abstract><cop>Chichester, UK</cop><pub>John Wiley &amp; Sons, Ltd</pub><pmid>15150838</pmid><doi>10.1002/rcm.1455</doi><tpages>8</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0951-4198
ispartof Rapid communications in mass spectrometry, 2004-01, Vol.18 (10), p.1131-1138
issn 0951-4198
1097-0231
language eng
recordid cdi_crossref_primary_10_1002_rcm_1455
source MEDLINE; Access via Wiley Online Library
subjects Animals
Chromatography, Liquid - methods
Dinoflagellida - chemistry
Esterification
Molecular Structure
New Zealand
Okadaic Acid - analogs & derivatives
Okadaic Acid - analysis
Okadaic Acid - chemistry
Spectrometry, Mass, Electrospray Ionization - methods
title Discovery of okadaic acid esters in the toxic dinoflagellate Dinophysis acuta from New Zealand using liquid chromatography/tandem mass spectrometry
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-20T19%3A37%3A14IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-istex_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Discovery%20of%20okadaic%20acid%20esters%20in%20the%20toxic%20dinoflagellate%20Dinophysis%20acuta%20from%20New%20Zealand%20using%20liquid%20chromatography/tandem%20mass%20spectrometry&rft.jtitle=Rapid%20communications%20in%20mass%20spectrometry&rft.au=Suzuki,%20T.&rft.date=2004-01-01&rft.volume=18&rft.issue=10&rft.spage=1131&rft.epage=1138&rft.pages=1131-1138&rft.issn=0951-4198&rft.eissn=1097-0231&rft_id=info:doi/10.1002/rcm.1455&rft_dat=%3Cistex_cross%3Eark_67375_WNG_QS5C2111_Q%3C/istex_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/15150838&rfr_iscdi=true