Inhibitory effect of N-( 2,4,5-trichlorophenyl)-2-oxocyclohexylsulfonamide against Botrytis cinerea
QI Zhiqi
Abstract
QI Zhiqi
Abstract
The antifungal activity of cycloalkyl sulfonylureas N-( 2,4,5-trichlorophenyl)-2-oxocyclohexylsulfonamide( compound 108 for short) against Botrytis cinerea was investigated in vitro.The results showed that compound 108 could inhibit different stages of B. cinerea including hyphal growth,spore production and germination,with EC50 values of 6. 90,4. 70 and 4. 11 μg /mL,respectively. The sclerotic production and pathogenicity of B. cinerea could also be inhibited by compound 108,and the hyphal could not produce sclerotia under 20 μg /mL of the compound. The pathogenicity of B. cinerea mycelia treated by compound 108 at 40 μg /mL was significantly lower than that of the control. Morphological and ultrastructural studies showed that compound 108 could cause hyphae collapse,deforming,and cell wall shrinkage,thickening and layering of B. cinerea.
OpenAlex reports 6 citations for this work. Citation counts describe recorded attention and do not establish research quality.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
The antifungal activity of cycloalkyl sulfonylureas N-( 2,4,5-trichlorophenyl)-2-oxocyclohexylsulfonamide( compound 108 for short) against Botrytis cinerea was investigated in vitro.The results showed that compound 108 could inhibit different stages of B. cinerea including hyphal growth,spore production and germination,with EC50 values of 6. 90,4. 70 and 4. 11 μg /mL,respectively. The sclerotic production and pathogenicity of B. cinerea could also be inhibited by compound 108,and the hyphal could not produce sclerotia under 20 μg /mL of the compound. The pathogenicity of B. cinerea mycelia treated by compound 108 at 40 μg /mL was significantly lower than that of the control. Morphological and ultrastructural studies showed that compound 108 could cause hyphae collapse,deforming,and cell wall shrinkage,thickening and layering of B. cinerea.
Key concepts: Botrytis cinerea, Hypha, Mycelium, Spore germination, Pathogenicity, Spore, EC50, Microbiology