The Forl strain was cultured on PDA supplied with 0.8 mL/L linalool for 6 days at 25°C. The fungal strain on PDA supplied with only 0.1% Tween80 was cultured as the control. Three biological replicates were established for each treatment. An appropriate amount of mycelia (100 mg) was taken and ground in liquid nitrogen. Protein were extracted using buffer and subjected to HPLC-MS.