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Appl. Environ. Microbiol., Oct 1997, 3825-3830, Vol 63, No. 10
J Shima, S Takase, Y Takahashi, Y Iwai, H Fujimoto, M Yamazaki and K Ochi
A mixed microbial culture capable of metabolizing deoxynivalenol was
obtained from soil samples by an enrichment culture procedure. A bacterium
(strain E3-39) isolated from the enrichment culture completely removed
exogenously supplied deoxynivalenol from culture medium after incubation
for 1 day. On the basis of morphological, physiological, and phylogenetic
studies, strain E3-39 was classified as a bacterium belonging to the
Agrobacterium-Rhizobium group. Thin-layer chromatographic analysis
indicated the presence of one major and two minor metabolites of
deoxynivalenol in ethyl acetate extracts of the E3- 39 culture filtrates.
The main metabolite was identified as 3-keto-4- deoxynivalenol by mass
spectroscopy and 1H and 13C nuclear magnetic resonance analysis. The
immunosuppressive toxicity of 3-keto-4- deoxynivalenol was evaluated by
means of a bioassay based on the mitogen-induced and mitogen-free
proliferations of mouse spleen lymphocytes. This compound exhibited a
remarkably decreased (to less than one tenth) immunosuppressive toxicity
relative to deoxynivalenol, indicating that the 3-OH group in
deoxynivalenol is likely to be involved in exerting its immunosuppressive
toxicity. Strain E3-39 was also capable of transforming
3-acetyldeoxynivalenol but not nivalenol and fusarenon-X.
Copyright © 1997, American Society for Microbiology
Novel detoxification of the trichothecene mycotoxin deoxynivalenol by a soil bacterium isolated by enrichment culture
National Food Research Institute, Ibaraki, Japan.
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