Determination of dihydroergosine in sorghum ergot using an immunoassayExport / Share PlumX View Altmetrics View AltmetricsMolloy, J. B., Moore, C.J., Bruyeres, A. G., Murray, S.A. and Blaney, B.J. (2003) Determination of dihydroergosine in sorghum ergot using an immunoassay. Journal of Agricultural and Food Chemistry, 51 (14). pp. 3916-3919. ISSN 0021-8561 Full text not currently attached. Access may be available via the Publisher's website or OpenAccess link. Article Link: https://doi.org/10.1021/jf0212284 AbstractDihydroergosine (DHES) is the principal toxic alkaloid produced by sorghum ergot (Claviceps africana). It has recently been shown that DHES levels as low as 1 mg/kg in animal feed can cause significant production losses. Quantitative immunoassays for detecting the related rye ergot alkaloid, ergotamine, are described in the literature, but those assays are relatively insensitive for DHES. This paper describes competitive enzyme-linked immunosorbent assays (ELISA) for measuring the DHES concentration in grains and mixed animal feed. The assays were developed using a DHES specific mouse monoclonal antibody and rabbit polyclonal antibodies raised against DHES conjugated to bovine serum albumin. Recoveries of between 77 and 103% were obtained from spiked grain using a simple, one step extraction with 70% methanol. Both the monoclonal and the polyclonal assays are capable of detecting DHES concentrations above 0.01 mg/kg, but quantification is most reliable at concentrations of 0.1 mg/kg or higher.
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