Transfer of benomyl-resistance by hyphal fusion of Botrytis cinerea.

resistance of some botrytis cinerea isolates to fungicides benomyl, iprodione and fenhexamid in west azarbaijan province

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Oxidation of alcohols by Botrytis cinerea.

Crude cell-free preparations of Botrytis cinerea were found to oxidize straight-chain primary alcohols (except methanol), aromatic primary alcohols, and unsaturated primary alcohols. The resulting products were the corresponding aldehydes and an equal molar quantity of hydrogen peroxide.

Biotransformation of (-)-a-pinene by Botrytis cinerea.

(-)-alpha-Pinene (1), a major constituent of many aromatic plants was biotransformed by the plant pathogenic fungus, Botrytis cinerea to afford three new metabolites, characterized as 3beta-hydroxy-(-)-beta-pinene (10%) (3), 9-hydroxy-(-)-a-pinene (12%) (4), 4beta-hydroxy-(-)-alpha-pinene-6-one (16%) (5) by physical and spectroscopic methods. A known metabolite verbenone (2) was also obtained.

Detection of Botrytis cinerea field isolates with multiple fungicide resistance

Isolate Dependency of Brassica rapa Resistance QTLs to Botrytis cinerea

Generalist necrotrophic pathogens including Botrytis cinerea cause significant yield and financial losses on Brassica crops. However, there is little knowledge about the mechanisms underlying the complex interactions encoded by both host and pathogen genomes in this interaction. This potentially includes multiple layers of plant defense and pathogen virulence mechanisms that could complicate in...