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Chinese Journal of Biological Control ›› 2023, Vol. 39 ›› Issue (4): 875-884.DOI: 10.16409/j.cnki.2095-039x.2023.02.036

• RESEARCH REPORTS • Previous Articles     Next Articles

Identification of Streptomyces and Its Metabolites Antagonizing Fusarium oxysporum and Phytophthora parasitica in Tobacco Based on Non-Target Metabolomics

LIU He1, SHAN Yuhang1, QIU Rui2, LI Shujun2, ZHANG Chong1, WU Yuanhua1, AN Mengnan1   

  1. 1. College of Plant Protection, Shenyang Agricultural University, Shenyang 110866, China;
    2. Key Laboratory for Green Preservation & Control of Tobacco Diseases and Pests in Huanghuai Growing Area/Tobacco Research Institute, Henan Academy of Agricultural Sciences, Xuchang 461000, China
  • Received:2022-11-08 Online:2023-08-25 Published:2023-08-25

Abstract: To develop effective biocontrol products against two soil-borne diseases, root rot (Fusarium oxysporum) and black shank (Phytophthora parasitica), a Streptomyces strain with good control effect was screened by our laboratory from tobacco rhizosphere soil. It was identified as Streptomyces diastatochromogenes by morphological, physiological, biochemical characteristics and molecular biological analysis. The main active metabolite of the biocontrol Streptomyces was identified as anisomycin by LC/MS non-target metabolomics analysis. The product was verified and content determined by high performance liquid chromatography, and it was found that anisamycin contained 423.98 µg per gram of crude extract. The inhibition results on mycelial morphology and mycelial growth showed that anisomycin could cause the mycelia of F. oxysporum and P. parasitica to expand and distort. The EC50 values for F. oxysporum and P. parasitica were 1556.36 mg/mL and 40.74 mg/mL, respectively. This study provides a new source of biocontrol agents for tobacco root rot and black shank diseases, and provided valuable insights into the further use of anisomycin.

Key words: Fusarium oxysporum, Phytophthora parasitica, Streptomyces diastatochromogenes, LC/MS non-target metabolomics, anisomycin

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