华北农学报 ›› 2008, Vol. 23 ›› Issue (2): 180-184. doi: 10.7668/hbnxb.2008.02.040

• 论文 • 上一篇    下一篇

芽孢杆菌B96-II对芦笋茎枯病的防治及机制研究

马利平, 郝变青, 秦曙, 乔雄梧   

  1. 山西省农业科学院, 山西省农药重点实验室, 山西, 太原, 030031
  • 收稿日期:2007-12-07 出版日期:2008-04-28
  • 作者简介:马利平(1957-),女,山西应县人,研究员,主要从事微生物农药研究及开发工作.
  • 基金资助:
    山西省科技攻关项目(2006031033);山西省重点实验室开放基金项目(2006年)

Causal Study on Inhibition Effects of Antagonistic Bacillus Strain B96-II to Asparagus Stem Blight

MA Li-ping, HAO Bian-qing, QIN Shu, QIAO Xiong-wu   

  1. Shanxi Key Laboratory of Pesticide Science, Shanxi Academy of Agricultural Sciences, Taiyuan 030031, China
  • Received:2007-12-07 Published:2008-04-28

摘要: 试验表明,芽孢杆菌B96-II对芦笋茎枯病菌(Phomopsis asparagiSacc)菌丝生长的抑制率为89.62%,对孢子产生的抑制率为99.65%;对芦笋茎枯菌的田间防治效果为93.10%。研究表明,B96-II的拮抗蛋白对芦笋茎枯菌有明显的抑制活性;对芦笋的超氧化物歧化酶(SOD)、过氧化氢酶(CAT)、过氧化物酶(POD)、多酚氧化酶(PPO)、苯丙氨酸解氨酶(PAL)均有激活和诱导作用。B96-II处理后30 d,芦笋组织的SOD活力较对照提高254.98%,CAT活力提高81.84%,POD活性提高22.13%,PPO活力提高146.67%,PAL活力提高171.60%。

关键词: 芦笋茎枯病, 芽胞杆菌, 拮抗蛋白, 诱导抗性, 保护酶

Abstract: Antagonistic Bacillus strain B96一II could effectively inhibite mycelia growth and spore germination ofPhomopsis asparagi Sacc,pathogen of asparagus stem blight. The inhibition rates were 89. 62%and 99. 65%respective-1y. Field trials showed a control efficacy of 93. 10%.Contents of 5 resistance related enzymes in asparagus plants werestimulated distinctly 30 d after treatment with B96一II. Cbmpared with untreated control sample,superoxide dismutase ac-tivity had an increase of 254. 98%,such as 81.84%to catalase,22. 13%to peroxidase,146. 67%to polyphenoloxidase,and 171. 60%to phenylalanin ammonialyase.

Key words: Asparagus stem blight, Bacillus sp, Antagonistic protein, Induced resistance, Protective enzyme

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引用本文

马利平, 郝变青, 秦曙, 乔雄梧. 芽孢杆菌B96-II对芦笋茎枯病的防治及机制研究[J]. 华北农学报, 2008, 23(2): 180-184. doi: 10.7668/hbnxb.2008.02.040.

MA Li-ping, HAO Bian-qing, QIN Shu, QIAO Xiong-wu. Causal Study on Inhibition Effects of Antagonistic Bacillus Strain B96-II to Asparagus Stem Blight[J]. ACTA AGRICULTURAE BOREALI-SINICA, 2008, 23(2): 180-184. doi: 10.7668/hbnxb.2008.02.040.