The fate of the fusarium mycotoxin zearalenone in maize cell suspension cultures
The fusarium mycotoxin zearalenone was transformed in cell suspension cultures of Zea mays giving α- and β-zearalenol and the β-D-glu cos ides of zearalenone and α- and β-zearalenol. The structure of zearalenone-4-β-D-glucopyranoside was determined by liquid - chromatography-mass spectrometry and sp...
Gespeichert in:
Veröffentlicht in: | Mycotoxin research 1990-03, Vol.6 (1), p.31-40 |
---|---|
Hauptverfasser: | , , , |
Format: | Artikel |
Sprache: | eng |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 40 |
---|---|
container_issue | 1 |
container_start_page | 31 |
container_title | Mycotoxin research |
container_volume | 6 |
creator | Zill, G Engelhardt, G Wohner, B Wallnöfer, P |
description | The fusarium mycotoxin zearalenone was transformed in cell suspension cultures of Zea mays giving α- and β-zearalenol and the β-D-glu cos ides of zearalenone and α- and β-zearalenol. The structure of zearalenone-4-β-D-glucopyranoside was determined by liquid - chromatography-mass spectrometry and specific hydrolysis with β-glucosidase. α- and β-zearalenol and their glucosides were identified by co chromatography using tic and HPLC and glucosidase - treatment Up to 50% of the mycotoxin added was bound to a non extractable or "bound" residue fraction. After treating this residue by a sequential cell wall fractionation procedure, zearalenone was found to be bound mainly to starch, hemicellulose, and lignin fractions. |
doi_str_mv | 10.1007/BF03192136 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1338396625</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1338396625</sourcerecordid><originalsourceid>FETCH-LOGICAL-c200t-d646abcf23c2eada108c6e5a4cdcc234e499efbf2cbe60d10427b0119fdc55273</originalsourceid><addsrcrecordid>eNpFkEFLwzAUx3NQ3Jxe_ACSowjVl6RN06MOp8JAD_Nc0vQFK20zkwbcPv06NvXweO8PP_48foRcMbhjAPn94wIEKzgT8oRMgeUqyZVSE3IewheAFKlUZ2TChYRsnCl5X30itXpA6iwd9ncM2jexo93GuMH9ND3dova6xd71SMfY6WaL1GDb0hDDGvvQuJ6a2A7RY7ggp1a3AS-Pe0Y-Fk-r-UuyfHt-nT8sE8MBhqSWqdSVsVwYjrrWDJSRmOnU1MZwkWJaFGgry02FEmoGKc8rYKywtckynosZuTn0rr37jhiGsmvC_indo4uhZEIoUUjJsxG9PaDGuxA82nLtm077Tcmg3Fsr_62N8PWxN1Yd1n_orzKxA3m0alQ</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1338396625</pqid></control><display><type>article</type><title>The fate of the fusarium mycotoxin zearalenone in maize cell suspension cultures</title><source>Springer Nature - Complete Springer Journals</source><creator>Zill, G ; Engelhardt, G ; Wohner, B ; Wallnöfer, P</creator><creatorcontrib>Zill, G ; Engelhardt, G ; Wohner, B ; Wallnöfer, P</creatorcontrib><description>The fusarium mycotoxin zearalenone was transformed in cell suspension cultures of Zea mays giving α- and β-zearalenol and the β-D-glu cos ides of zearalenone and α- and β-zearalenol. The structure of zearalenone-4-β-D-glucopyranoside was determined by liquid - chromatography-mass spectrometry and specific hydrolysis with β-glucosidase. α- and β-zearalenol and their glucosides were identified by co chromatography using tic and HPLC and glucosidase - treatment Up to 50% of the mycotoxin added was bound to a non extractable or "bound" residue fraction. After treating this residue by a sequential cell wall fractionation procedure, zearalenone was found to be bound mainly to starch, hemicellulose, and lignin fractions.</description><identifier>ISSN: 0178-7888</identifier><identifier>DOI: 10.1007/BF03192136</identifier><identifier>PMID: 23605360</identifier><language>eng</language><publisher>Germany</publisher><ispartof>Mycotoxin research, 1990-03, Vol.6 (1), p.31-40</ispartof><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c200t-d646abcf23c2eada108c6e5a4cdcc234e499efbf2cbe60d10427b0119fdc55273</citedby><cites>FETCH-LOGICAL-c200t-d646abcf23c2eada108c6e5a4cdcc234e499efbf2cbe60d10427b0119fdc55273</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23605360$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zill, G</creatorcontrib><creatorcontrib>Engelhardt, G</creatorcontrib><creatorcontrib>Wohner, B</creatorcontrib><creatorcontrib>Wallnöfer, P</creatorcontrib><title>The fate of the fusarium mycotoxin zearalenone in maize cell suspension cultures</title><title>Mycotoxin research</title><addtitle>Mycotoxin Res</addtitle><description>The fusarium mycotoxin zearalenone was transformed in cell suspension cultures of Zea mays giving α- and β-zearalenol and the β-D-glu cos ides of zearalenone and α- and β-zearalenol. The structure of zearalenone-4-β-D-glucopyranoside was determined by liquid - chromatography-mass spectrometry and specific hydrolysis with β-glucosidase. α- and β-zearalenol and their glucosides were identified by co chromatography using tic and HPLC and glucosidase - treatment Up to 50% of the mycotoxin added was bound to a non extractable or "bound" residue fraction. After treating this residue by a sequential cell wall fractionation procedure, zearalenone was found to be bound mainly to starch, hemicellulose, and lignin fractions.</description><issn>0178-7888</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1990</creationdate><recordtype>article</recordtype><recordid>eNpFkEFLwzAUx3NQ3Jxe_ACSowjVl6RN06MOp8JAD_Nc0vQFK20zkwbcPv06NvXweO8PP_48foRcMbhjAPn94wIEKzgT8oRMgeUqyZVSE3IewheAFKlUZ2TChYRsnCl5X30itXpA6iwd9ncM2jexo93GuMH9ND3dova6xd71SMfY6WaL1GDb0hDDGvvQuJ6a2A7RY7ggp1a3AS-Pe0Y-Fk-r-UuyfHt-nT8sE8MBhqSWqdSVsVwYjrrWDJSRmOnU1MZwkWJaFGgry02FEmoGKc8rYKywtckynosZuTn0rr37jhiGsmvC_indo4uhZEIoUUjJsxG9PaDGuxA82nLtm077Tcmg3Fsr_62N8PWxN1Yd1n_orzKxA3m0alQ</recordid><startdate>199003</startdate><enddate>199003</enddate><creator>Zill, G</creator><creator>Engelhardt, G</creator><creator>Wohner, B</creator><creator>Wallnöfer, P</creator><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>199003</creationdate><title>The fate of the fusarium mycotoxin zearalenone in maize cell suspension cultures</title><author>Zill, G ; Engelhardt, G ; Wohner, B ; Wallnöfer, P</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c200t-d646abcf23c2eada108c6e5a4cdcc234e499efbf2cbe60d10427b0119fdc55273</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1990</creationdate><toplevel>online_resources</toplevel><creatorcontrib>Zill, G</creatorcontrib><creatorcontrib>Engelhardt, G</creatorcontrib><creatorcontrib>Wohner, B</creatorcontrib><creatorcontrib>Wallnöfer, P</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Mycotoxin research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zill, G</au><au>Engelhardt, G</au><au>Wohner, B</au><au>Wallnöfer, P</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The fate of the fusarium mycotoxin zearalenone in maize cell suspension cultures</atitle><jtitle>Mycotoxin research</jtitle><addtitle>Mycotoxin Res</addtitle><date>1990-03</date><risdate>1990</risdate><volume>6</volume><issue>1</issue><spage>31</spage><epage>40</epage><pages>31-40</pages><issn>0178-7888</issn><abstract>The fusarium mycotoxin zearalenone was transformed in cell suspension cultures of Zea mays giving α- and β-zearalenol and the β-D-glu cos ides of zearalenone and α- and β-zearalenol. The structure of zearalenone-4-β-D-glucopyranoside was determined by liquid - chromatography-mass spectrometry and specific hydrolysis with β-glucosidase. α- and β-zearalenol and their glucosides were identified by co chromatography using tic and HPLC and glucosidase - treatment Up to 50% of the mycotoxin added was bound to a non extractable or "bound" residue fraction. After treating this residue by a sequential cell wall fractionation procedure, zearalenone was found to be bound mainly to starch, hemicellulose, and lignin fractions.</abstract><cop>Germany</cop><pmid>23605360</pmid><doi>10.1007/BF03192136</doi><tpages>10</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0178-7888 |
ispartof | Mycotoxin research, 1990-03, Vol.6 (1), p.31-40 |
issn | 0178-7888 |
language | eng |
recordid | cdi_proquest_miscellaneous_1338396625 |
source | Springer Nature - Complete Springer Journals |
title | The fate of the fusarium mycotoxin zearalenone in maize cell suspension cultures |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-21T21%3A36%3A34IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=The%20fate%20of%20the%20fusarium%20mycotoxin%20zearalenone%20in%20maize%20cell%20suspension%20cultures&rft.jtitle=Mycotoxin%20research&rft.au=Zill,%20G&rft.date=1990-03&rft.volume=6&rft.issue=1&rft.spage=31&rft.epage=40&rft.pages=31-40&rft.issn=0178-7888&rft_id=info:doi/10.1007/BF03192136&rft_dat=%3Cproquest_cross%3E1338396625%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1338396625&rft_id=info:pmid/23605360&rfr_iscdi=true |