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Keypoints Fermentation medium with high antagonistic activity of HR10 strain was determined. Antagonistic crude protein of HR10 strain purified by Ion-Exchange Chromatography. Composition of the antagonist protein of HR10 strain was analyzed using LC-MS-MS.

A previous study found that a biocontrol bacterium, Bacillus pumilus HR10, inhibited the Sphaeropsis shoot blight disease of pine, and the fermentation broth of HR10 strain contained protein antifungal substances. The optimal formulation of the fermentation medium for the antagonistic substance of B. pumilus HR10 was finally obtained by single-factor test, Packett-Burman test, steepest ascent test and Box-Behnken Design (BBD) response surface test, and the best formulation of the fermentation medium for the antagonistic substance of B. pumilus HR10 was 12 g/L corn meal, 15 g/L beef extract and 13 g/L magnesium sulfate, with a predicted bacterial inhibition rate of 89%. The fermentation filtrate of B. pumilus HR10 cultured with the optimized medium formulation was verified to have an inhibition rate of (87.04 ± 3.2) % on the growth of Sphaeropsis sapinea by three replicate tests. The antagonistic crude protein of B. pumilus HR10 were further isolated and identified using HiTrap Capto Q strong Ion-Exchange Chromatography and LC–MS-MS, and it was speculated that glycoside hydrolase (Ghy), beta-glucanase (Beta), arabinogalactan endonuclease β-1,4-galactanase (Arab), and immunosuppressant A (ImA) are proteins with antagonistic activity against S. sapinea in the B. pumilus HR10. Keypoints: Fermentation medium with high antagonistic activity of HR10 strain was determined. Antagonistic crude protein of HR10 strain purified by Ion-Exchange Chromatography. Composition of the antagonist protein of HR10 strain was analyzed using LC-MS-MS. [ABSTRACT FROM AUTHOR]