Abstract
Development of deoxynivalenol (DON) in wheat with a low contamination withFusarium spp. was investigated under suboptimal storage conditions (17% and 20% grain moisture, 20°C). The influence of storage on the relative DNA content of potential DON producers was also determined. The DON contents were quantified using an ELISA. The Tox5 PCR was used for the detection of potential trichothecene producers and for the estimation of their relative DNA content. ThegaoA gene was subsequently amplified by PCR to detect specificallyFusarium graminearum. The concentration ofF. graminearum DNA was semiquantitatively determined using a Light Cycler™. The DON concentrations increased during storage trials but the intensity of PCR signals decreased.
Zusammenfassung
Die Bildung von Deoxynivalenol (DON) in Weizen wurde, ausgehend von einem geringen Besatz mitFusarium spp., unter suboptimalen Lagerbedingungen (17% und 20% Kornfeuchte, 20°C) untersucht. Der Einfluss der Lagerung auf die relative DNA-Masse potentieller DON-Bildner wurde ebenso ermittelt. Die DON-Gehalte wurden mittels ELISA quantifiziert. Die Tox5-PCR wurde zur Detektion potentieller Trichothecen-Bildner und zur Abschätzung ihrer relativen DNA-Masse eingesetzt. DasgaoA-Gen wurde anschließend mit der PCR amplifiziert, um spezifischFusarium graminearum nachzuweisen. Die Konzentration derF. graminearum-DNA wurde im Light Cycler™ semiquantitativ bestimmt. Die DON-Konzentrationen nahmen im Verlauf der Lagerungsversuche zu, während die Intensität der PCR-Signale abnahm.
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Birzele, B., Prange, A., Schönling, J. et al. Development of deoxynivalenol contents in relation to the PCR detection of potentially trichothecene producingFusarium spp. during storage of wheat. Mycotox Res 16 (Suppl 1), 46–49 (2000). https://doi.org/10.1007/BF02942979
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DOI: https://doi.org/10.1007/BF02942979