Fusarium culmorum, a fungal pathogen
of small grain cereals, produces 4-deoxynivalenol and its acetylated
derivatives that may cause toxicoses on humans or animals consuming
contaminated food or feed. Natural and natural-like compounds belonging
to phenol and hydroxylated biphenyl structural classes were tested in vitro to determine their activity on vegetative growth
and trichothecene biosynthesis by F. culmorum. Most of the compounds tested at 1.5 or 1.0 mM reduced 3-acetyl-4-deoxynivalenol
production by over 70% compared to the control, without affecting
fungal growth significantly. Furthermore, several compounds retained
their ability to inhibit toxin in vitro production
at the lowest concentrations of 0.5 and 0.25 mM. Magnolol 27 showed fungicidal activity even at 0.1 mM. No linear correlation
was observed between antioxidant properties of the compounds and their
ability to inhibit fungal growth and mycotoxigenic capacity. A guaiacyl
unit in the structure may play a key role in trichothecene inhibition.