Enzyme-Linked Immunosorbent-Assay for Deoxynivalenol (DON)
AbstractDeoxynivalenol (DON), one of the trichothecene mycotoxins, is a worldwide contaminant of wheat and barley, especially when infected by Fusarium graminearum, the causative agent of an epidemic wheat disease called Fusarium Head Blight. Because of the high risk of DON ingestion and the possibility of frequent exposure, it is important to develop a rapid and highly sensitive method for easy identification and quantification of DON in grain samples. In this study, we have developed an indirect competitive enzyme-linked immunosorbent assay (ELISA) to detect DON in wheat. We conjugated 3-O-Hemisuccinyl-DON (3HS-DON) to Bovine serum albumin (BSA) and Ovalbumin (OVA), and obtained DON-specific mice antisera. The indirect competitive ELISA revealed that the optimal concentration of mice serum and the coated antigen was 1/1600 and 1/1500, respectively. The antiserum cross-reacted with the trichothecenes 3-acetyl-DON and T-2 toxin, reaching about 55.2% and 6.3%, respectively, as compared with DON. Results showed that the assay could be performed satisfactorily using an extraction buffer containing less than 15% methanol. Recovery from DON was 82–93% in grains. The linear detection range of DON in grains was between 0.01 and 100 μg/mL.
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Ji, F.; Li, H.; Xu, J.; Shi, J. Enzyme-Linked Immunosorbent-Assay for Deoxynivalenol (DON). Toxins 2011, 3, 968-978.
Ji F, Li H, Xu J, Shi J. Enzyme-Linked Immunosorbent-Assay for Deoxynivalenol (DON). Toxins. 2011; 3(8):968-978.Chicago/Turabian Style
Ji, Fang; Li, Hua; Xu, Jianhong; Shi, Jianrong. 2011. "Enzyme-Linked Immunosorbent-Assay for Deoxynivalenol (DON)." Toxins 3, no. 8: 968-978.