Please use this identifier to cite or link to this item: http://hdl.handle.net/11189/6780
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dc.contributor.authorShephard, Gordon Seymouren_US
dc.contributor.authorBurger, HMen_US
dc.contributor.authorGambacorta, Len_US
dc.contributor.authorKrska, Ren_US
dc.contributor.authorPowers, SPen_US
dc.contributor.authorRheeder, JPen_US
dc.contributor.authorSolfrizzo, Men_US
dc.contributor.authorSulyok, Men_US
dc.contributor.authorVisconti, Aen_US
dc.contributor.authorWarth, Ben_US
dc.contributor.authorVan der Westhuizen, Lianaen_US
dc.date.accessioned2019-01-29T06:58:12Z-
dc.date.available2019-01-29T06:58:12Z-
dc.date.issued2013-
dc.identifier.citationJ. Agric. Food Chem. 2013, 61, 34:8232-8240en_US
dc.identifier.urihttp://hdl.handle.net/11189/6780-
dc.descriptionArticleen_US
dc.description.abstractMaize harvested in the Centane region of the former Transkei, Eastern Cape Province, South Africa, by subsistence farmers has been shown over many seasons to be contaminated with fumonisin mycotoxins. However, there are limited data on the presence of other mycotoxins. Two multimycotoxin LC-MS/MS methods were applied to good and moldy maize samples, as separated by the farmers themselves from the 2011 harvest. One method involved extract cleanup on multitoxin immunoaffinity columns before LC-MS/MS analysis for aflatoxins, fumonisins, deoxynivalenol (DON), zearalenone (ZEN), and T-2 and HT-2 toxins. The other method was based on a "dilute-and-shoot" approach for the above mycotoxins and a wide range of other fungal secondary metabolites. Both methods showed high incidences of fumonisins B1 and B2 (FB1 and FB2) in good maize (100% for both by the first method, means were 2083 and 927 μg/kg for the two analogues; 93% for both by the second method, positive means of 2764 and 1050 μg/kg, respectively). All samples of moldy maize were contaminated (mean FB1 of 27.64 and 35.98 mg/kg, respectively; mean FB2 of 10.58 and 14.14 mg/kg, respectively). Comparison of the two methods for FB1 and FB2 over the entire range of samples gave R(2) values 0.9144 and 0.8859, respectively. Low levels of DON were found by both methods (positive means of 12 and 4.7 μg/kg in good maize, respectively, and of 14 and 5.8 μg/kg in moldy maize, respectively). ZEN was determined with positive means of 108 and 25 μg/kg in good maize, respectively, and of 111 and 135 μg/kg in moldy maize, respectively. No aflatoxins, OTA, or T-2 or HT-2 toxins were detected. A wide range of other Fusarium , Aspergillus , Alternaria , and Penicillium mycotoxins and secondary metabolites were determined.en_US
dc.language.isoenen_US
dc.publisherAmerican Chemical Societyen_US
dc.relation.ispartofJournal of Agricultural and Food Chemistry 2013, 61(34):8232-8240en_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/3.0/za/-
dc.subjectdeoxynivalenolen_US
dc.subjectfumonisinen_US
dc.subjectmaizeen_US
dc.subjectmultimycotoxinen_US
dc.subjectmycotoxinen_US
dc.subjectochratoxinen_US
dc.subjectsecondary metabolitesen_US
dc.subjectzearalenoneen_US
dc.titleMycological analysis and multimycotoxins in maize from rural subsistence farmers in the former Transkei, South Africaen_US
dc.type.patentArticleen_US
dc.identifier.doi10.1021/jf4021762-
Appears in Collections:HWSci - Journal Articles (DHET subsidised)
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