食品科学 ›› 2024, Vol. 45 ›› Issue (6): 72-79.doi: 10.7506/spkx1002-6630-20230512-108

• 生物工程 • 上一篇    下一篇

芳樟醇对生姜枯萎病菌的抑制作用

周丽荣,张玲玲,熊诗洁,马佳伟,朱永兴,孙冲,朱学栋,刘奕清   

  1. (1.长江大学园艺园林学院,湖北 荆州 434025;2.重庆文理学院园林与生命科学学院(特色植物研究院),重庆 402160;3.重庆市渝东南农业科学院,重庆 408000)
  • 出版日期:2024-03-25 发布日期:2024-04-03
  • 基金资助:
    湖北省重点研发计划项目(2022BBA0061;2021BBA096);重庆市农委创新团队重大专项(2021-2023-07); 荆州市2022年度科技计划项目(2022BB36);重庆英才优秀科学项目(2022CQYC0101514)

Inhibitory Effect of Linalool against the Ginger Fusarium Wilt Pathogen

ZHOU Lirong, ZHANG Lingling, XIONG Shijie, MA Jiawei, ZHU Yongxing, SUN Chong, ZHU Xuedong, LIU Yiqing   

  1. (1. College of Horticulture and Gardening, Yangtze University, Jingzhou 434025, China; 2. College of Landscape Architecture and Life Science/Institute of Special Plants, Chongqing University of Arts and Sciences, Chongqing 402160, China; 3. Yudongnan Academy of Agricultural Sciences, Chongqing 408000, China)
  • Online:2024-03-25 Published:2024-04-03

摘要: 为明确芳樟醇对生姜枯萎病菌尖孢镰刀菌(Fusarium oxysporum)的抑菌效果与作用机制,以不同质量浓度的芳樟醇处理尖孢镰刀菌,对尖孢镰刀菌菌丝体生长、孢子萌发和细胞膜的损伤以及防治效果进行系统研究。结果表明:芳樟醇可显著抑制尖孢镰刀菌的菌丝生长,其半数有效浓度为1.183 g/L,最小抑菌浓度(minimal inhibitory concentration,MIC)为2.0 g/L,抑制效果与芳樟醇质量浓度呈剂量效应关系;以芳樟醇MIC处理尖孢镰刀菌6 h,其孢子浓度为(1.43±0.12)×104 spores/mL,显著低于对照组((5.79±0.19)×104 spores/mL)(P<0.05);MIC芳樟醇处理枯萎病菌尖孢镰刀菌12 h,其孢子萌发率仅为(5.83±2.16)%,显著低于对照组((95.12±3.78)%)(P<0.05)。1/2 MIC与MIC芳樟醇处理破坏了细胞膜的完整性,导致菌丝悬液中相对电导率、核酸渗漏量显著增加,菌丝中丙二醛浓度也显著增加,麦角固醇含量显著降低,减弱了尖孢镰刀菌的致病力;MIC芳樟醇处理3 d后姜块上没有病斑产生,有良好的防治效果。综上所述,芳樟醇通过抑制生姜枯萎病菌尖孢镰刀菌菌丝生长与孢子萌发、破坏细胞结构从而影响其正常的生理功能,本研究可为防治生姜枯萎病提供新思路。

关键词: 芳樟醇;尖孢镰刀菌;抑菌作用;膜通透性

Abstract: To study the antifungal effect and mechanism of linalool against Fusarium oxysporum FOX-1, the causative agent of ginger Fusarium wilt, the damaging effects of different concentrations of linalool on the mycelial growth, spore germination and cell membrane of F. oxysporum FOX-1, and its control effect on ginger Fusarium wilt were systemically investigated. The results showed that linalool could significantly inhibit the mycelial growth of F. oxysporum FOX-1 in a concentration-dependent manner, and the half maximal effective concentration (EC50) and the minimum inhibitory concentration (MICs) were 1.183 and 2 g/L, respectively. The spore concentration of F. oxysporum FOX-1 treated with linalool at MIC for 6 h was (1.43 ± 0.12) × 104 spores/mL, which was significantly lower than that of the control group ((5.79 ± 0.19) × 104 spores/mL) (P < 0.05), and the spore germination rate of F. oxysporum FOX-1 treated with linalool at MIC for 12 h was (5.83 ± 2.16)%, which was significantly lower than that of the control group ((95.12 ± 3.78)%) (P < 0.05). Treatment with linalool at 1/2 MIC and MIC damaged the integrity of the cell membrane, resulting in a significant increase in relative electrical conductivity and nucleic acid leakage in the mycelial suspension and malondialdehyde (MDA) content in the mycelium, and a significant decrease in ergosterol content, finally weakening the pathogenicity of the fungus. No lesions appeared on ginger pieces after treatment with linalool at MIC for 3 days. In conclusion, linalool affects the normal physiological function of F. oxysporum FOX-1 by inhibiting its spore germination and mycelial growth and destroying its cellular structure. This study provides a new direction for the effective control of Fusarium wilt.

Key words: linalool; Fusarium oxysporum; antifungal activity; membrane permeability

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