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Volume 38 Issue 1
Jan.  2023
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Article Contents
WANG X W, YU C, PAN H X. Process Optimization and Antimicrobial Effect of Cytobacillus kochii H Protease [J]. Fujian Journal of Agricultural Sciences,2023,38(1):47−57 doi: 10.19303/j.issn.1008-0384.2023.01.007
Citation: WANG X W, YU C, PAN H X. Process Optimization and Antimicrobial Effect of Cytobacillus kochii H Protease [J]. Fujian Journal of Agricultural Sciences,2023,38(1):47−57 doi: 10.19303/j.issn.1008-0384.2023.01.007

Process Optimization and Antimicrobial Effect of Cytobacillus kochii H Protease

doi: 10.19303/j.issn.1008-0384.2023.01.007
  • Received Date: 2022-08-29
  • Rev Recd Date: 2022-11-21
  • Available Online: 2023-02-08
  • Publish Date: 2023-01-28
  •   Objective  Taxonomy of antimicrobial protease-producing Cytobacillus kochii H was studied for the development of a natural disease control agent on plants.   Method   Taxonomy of C. kochii H was determined by physiological, biochemical, electron microscopy scanning, and 16sRNA sequencing methods. A process of producing the antimicrobial protease secreted by the bacterium was optimized in single-factor and orthogonal experiments. The efficacy of the culture broth on 4 selected pathogenic fungi was applied in an in vitro test as the evaluation criterium.   Result   The optimized C. kochii H protease-producing process was conducted in a 250 mL triangular flask using 50 mL of pH 8.0 medium, which contained 20.0 g·L−1 of glucose, 8.0 g·L−1 of peptone, 1.0 g·L−1 of MgSO4, and 0.1g·L−1 of CaSO4-2H2O, inoculated with 2.5 mL of 108 CFU·mL−1 C. kochii H fermentation liquid. After 24 h of incubation, the protease activity reached 402.2 U·mL−1, which was 13.92 times greater than it was prior to the optimization. The antimicrobial rates of the broth against Fusarium oxysporum and Phytophthora capsici were 67.32% and 44.87%, respectively, i.e., 9.15% and 12.82%, respectively, increases over those before the optimization.   Conclusion  The antimicrobial protease-producing C. kochii H was identified taxonomically. The culture process of the enzyme production was optimized to deliver significant in vitro inhibition rates on F. oxysporum and P. capsici.
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