The hyphal fragments were placed on plant leaves. Photographs were taken 36 h after inoculation. The plants transformed into pLGNL were used as controls. Malondialdehyde (MDA) content and catalase (CAT) activity were determined using a Malondialdehyde Assay Kit (Solarbio, Beijing, China) and a Catalase Assay Kit (Solarbio, Beijing, China) according to the manufacturer’s instructions. All treatments were repeated three times. The content of superoxide radical (O2) and hydrogen peroxide (H2O2) in leaves was determined by nitroblue tetrazole (NBT) and 3,3′-diaminobenzidine (DAB) staining as described previously [37 (link),38 (link)].
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