Rapid Fluorescence Polarization Immunoassay for the Mycotoxin Deoxynivalenol in Wheat
The fungus Fusarium graminearum, a pathogen of both wheat and maize, produces a toxin, deoxynivalenol (DON), that causes disease in livestock. A rapid test for DON in wheat was developed using the principle of fluorescence polarization (FP) immunoassay. The assay was based on the competition between...
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Veröffentlicht in: | Journal of agricultural and food chemistry 2002-03, Vol.50 (7), p.1827-1832 |
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creator | Maragos, Chris M Plattner, Ronald D |
description | The fungus Fusarium graminearum, a pathogen of both wheat and maize, produces a toxin, deoxynivalenol (DON), that causes disease in livestock. A rapid test for DON in wheat was developed using the principle of fluorescence polarization (FP) immunoassay. The assay was based on the competition between DON and a novel DON-fluorescein tracer (DON-FL2) for a DON-specific monoclonal antibody in solution. The method, which is a substantial improvement over our previous DON FP immunoassay, combined a rapid (3 min) extraction step with a rapid (2 min) detection step. A series of naturally contaminated wheat and maize samples were analyzed by both FP immunoassay and liquid chromatography (HPLC−UV). For wheat the HPLC−UV and FP methods agreed well (linear regression r 2 = 0.936), but for maize the two methods did not (r 2 = 0.849). We conclude that the FP method is useful for screening wheat, but not maize, for DON. Keywords: Deoxynivalenol; vomitoxin; fluorescence polarization; immunoassay |
doi_str_mv | 10.1021/jf011487d |
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A rapid test for DON in wheat was developed using the principle of fluorescence polarization (FP) immunoassay. The assay was based on the competition between DON and a novel DON-fluorescein tracer (DON-FL2) for a DON-specific monoclonal antibody in solution. The method, which is a substantial improvement over our previous DON FP immunoassay, combined a rapid (3 min) extraction step with a rapid (2 min) detection step. A series of naturally contaminated wheat and maize samples were analyzed by both FP immunoassay and liquid chromatography (HPLC−UV). For wheat the HPLC−UV and FP methods agreed well (linear regression r 2 = 0.936), but for maize the two methods did not (r 2 = 0.849). We conclude that the FP method is useful for screening wheat, but not maize, for DON. 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Agric. Food Chem</addtitle><description>The fungus Fusarium graminearum, a pathogen of both wheat and maize, produces a toxin, deoxynivalenol (DON), that causes disease in livestock. A rapid test for DON in wheat was developed using the principle of fluorescence polarization (FP) immunoassay. The assay was based on the competition between DON and a novel DON-fluorescein tracer (DON-FL2) for a DON-specific monoclonal antibody in solution. The method, which is a substantial improvement over our previous DON FP immunoassay, combined a rapid (3 min) extraction step with a rapid (2 min) detection step. A series of naturally contaminated wheat and maize samples were analyzed by both FP immunoassay and liquid chromatography (HPLC−UV). For wheat the HPLC−UV and FP methods agreed well (linear regression r 2 = 0.936), but for maize the two methods did not (r 2 = 0.849). We conclude that the FP method is useful for screening wheat, but not maize, for DON. Keywords: Deoxynivalenol; vomitoxin; fluorescence polarization; immunoassay</description><subject>Biological and medical sciences</subject><subject>Chromatography, High Pressure Liquid</subject><subject>Fluorescence Polarization Immunoassay - methods</subject><subject>Food Contamination</subject><subject>Food industries</subject><subject>Food toxicology</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Sensitivity and Specificity</subject><subject>Trichothecenes - analysis</subject><subject>Triticum - chemistry</subject><subject>Zea mays - chemistry</subject><issn>0021-8561</issn><issn>1520-5118</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2002</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpt0E9v0zAYBnALMbEyOPAFUC4gcQjzG__NEQ0KE5s2lU0crTeJo7kkdrET1PLpMWq1Xnay5OenR_ZDyBugH4FWcL7uKQDXqntGFiAqWgoA_ZwsaA5LLSSckpcprSmlWij6gpwC1LSqoV6Q-xVuXFcshzlEm1rrW1vchgGj-4uTC764HMfZB0wJd0UfYjE92OJ614YpbJ0vPtuw3Xn3Bwfrw1Dkm58PFqdX5KTHIdnXh_OM3C-_3F18K69uvl5efLoqkSs5lVID1ZLyGjSg7GvNWM15RxuruOyankvNkLKK9qxrKpCct1pQllPRNXVVszPyft-7ieH3bNNkRpc_MQzobZiTAS214Epk-GEP2xhSirY3m-hGjDsD1Pzf0DxumO3bQ-ncjLY7ysNoGbw7AEwtDn1E37p0dEwoxlmVXbl3Lk12-5hj_GWkYkqYu9sfRi1X1_B9pQw79mKbzDrM0eftnnjgP1tJkx0</recordid><startdate>20020327</startdate><enddate>20020327</enddate><creator>Maragos, Chris M</creator><creator>Plattner, Ronald D</creator><general>American Chemical Society</general><scope>BSCLL</scope><scope>IQODW</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><scope>7QO</scope><scope>7T7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>P64</scope></search><sort><creationdate>20020327</creationdate><title>Rapid Fluorescence Polarization Immunoassay for the Mycotoxin Deoxynivalenol in Wheat</title><author>Maragos, Chris M ; Plattner, Ronald D</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a476t-681086049181a6f9833944d0be746dbf4683a0320f3db21644c8503e745db9293</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2002</creationdate><topic>Biological and medical sciences</topic><topic>Chromatography, High Pressure Liquid</topic><topic>Fluorescence Polarization Immunoassay - methods</topic><topic>Food Contamination</topic><topic>Food industries</topic><topic>Food toxicology</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Sensitivity and Specificity</topic><topic>Trichothecenes - analysis</topic><topic>Triticum - chemistry</topic><topic>Zea mays - chemistry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Maragos, Chris M</creatorcontrib><creatorcontrib>Plattner, Ronald D</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><jtitle>Journal of agricultural and food chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Maragos, Chris M</au><au>Plattner, Ronald D</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Rapid Fluorescence Polarization Immunoassay for the Mycotoxin Deoxynivalenol in Wheat</atitle><jtitle>Journal of agricultural and food chemistry</jtitle><addtitle>J. Agric. Food Chem</addtitle><date>2002-03-27</date><risdate>2002</risdate><volume>50</volume><issue>7</issue><spage>1827</spage><epage>1832</epage><pages>1827-1832</pages><issn>0021-8561</issn><eissn>1520-5118</eissn><coden>JAFCAU</coden><abstract>The fungus Fusarium graminearum, a pathogen of both wheat and maize, produces a toxin, deoxynivalenol (DON), that causes disease in livestock. A rapid test for DON in wheat was developed using the principle of fluorescence polarization (FP) immunoassay. The assay was based on the competition between DON and a novel DON-fluorescein tracer (DON-FL2) for a DON-specific monoclonal antibody in solution. The method, which is a substantial improvement over our previous DON FP immunoassay, combined a rapid (3 min) extraction step with a rapid (2 min) detection step. A series of naturally contaminated wheat and maize samples were analyzed by both FP immunoassay and liquid chromatography (HPLC−UV). For wheat the HPLC−UV and FP methods agreed well (linear regression r 2 = 0.936), but for maize the two methods did not (r 2 = 0.849). We conclude that the FP method is useful for screening wheat, but not maize, for DON. Keywords: Deoxynivalenol; vomitoxin; fluorescence polarization; immunoassay</abstract><cop>Washington, DC</cop><pub>American Chemical Society</pub><pmid>11902919</pmid><doi>10.1021/jf011487d</doi><tpages>6</tpages></addata></record> |
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subjects | Biological and medical sciences Chromatography, High Pressure Liquid Fluorescence Polarization Immunoassay - methods Food Contamination Food industries Food toxicology Fundamental and applied biological sciences. Psychology Sensitivity and Specificity Trichothecenes - analysis Triticum - chemistry Zea mays - chemistry |
title | Rapid Fluorescence Polarization Immunoassay for the Mycotoxin Deoxynivalenol in Wheat |
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