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中国农学通报 ›› 2016, Vol. 32 ›› Issue (6): 193-197.doi: 10.11924/j.issn.1000-6850.casb15090138

所属专题: 生物技术

• 植物保护 农药 • 上一篇    下一篇

交替氧化酶可增强核盘菌对多菌灵的敏感性

梁五生1,徐 婷1,姚 飞1,李永红2,王政逸1   

  1. (1浙江大学农业与生物技术学院生物技术研究所/水稻生物学国家重点实验室,杭州 310058;2陕西省杂交油菜研究中心,陕西大荔 715105)
  • 收稿日期:2015-09-30 修回日期:2016-01-29 接受日期:2015-11-24 出版日期:2016-03-07 发布日期:2016-03-07
  • 通讯作者: 梁五生
  • 基金资助:
    浙江省教育厅科研计划项目“交替氧化酶在核盘菌对杀菌剂敏感性中的作用”(Y201327327);浙江省自然科学基金资助项目“油菜转录因子BnWRKY40和BnWRKY75的抗病功能研究”(LY13C140001);国家自然科学基金资助项目“线粒体和呼吸作用参与化学杂交剂SX-1杀雄的机理研究”(31370279)。

Enhancing Effect of Alternative Oxidase on Sensitivity of Sclerotinia sclerotiorum to Carbendazim

Liang Wusheng1, Xu Ting1, Yao Fei 1, Li Yonghong2, Wang Zhengyi1   

  1. (1Institute of Biotechnology/State Key Laboratory of Rice Biology, College of Agriculture and Biotechnology,Zhejiang University, Hangzhou 310058;2Hybrid Rapeseed Research Center of Shaanxi Province, Dali Shaanxi 715105)
  • Received:2015-09-30 Revised:2016-01-29 Accepted:2015-11-24 Online:2016-03-07 Published:2016-03-07

摘要: 为了探明交替氧化酶是否参与核盘菌对杀菌剂多菌灵敏感性的调控,研究了交替氧化酶对多菌灵抑制核盘菌生长效力的影响,以及多菌灵对核盘菌呼吸活性和交替氧化酶编码基因aox表达的效应。结果发现:抑制交替氧化酶可削弱多菌灵对核盘菌生长的抑制作用,显示交替氧化酶可提高核盘菌对多菌灵的敏感性;多菌灵对核盘菌的细胞色素途径和交替途径活性都没有即时影响;多菌灵预处理24 h对核盘菌aox基因的转录水平没有影响,但对其交替途径活性仍有显著诱导作用。研究结果有助于全面了解多菌灵的杀菌活性调控机制。而且研究结果表明,生产实践中有望应用交替氧化酶的诱导剂或活化剂来提高多菌灵防治核盘菌的效能。

关键词: 梨, 梨, SSR, SRAP, ISSR, 分子遗传连锁图谱

Abstract: In order to study whether alternative oxidase is involved in sensitivity regulation of Sclerotinia sclerotiorum to carbendazim, the influences of this fungicide on mycelial growth, respiration and alternative oxidase encoding gene (aox) expression of S. sclerotiorum were determined. It was found that the inhibition of alternative oxidase alleviated the inhibitory effect of carbendazim on the fungal mycelial growth, indicating that alternative oxidase could increase the sensitivity of S. sclerotiorum to carbendazim. Carbendazim showed no immediate impact on the activities of both cytochrome respiratory pathway and alternative respiratory pathway of S. sclerotiorum mycelia. Pre-treatment for 24 h with carbendazim did not affect the transcript level of aox gene of S. sclerotiorum. However, such pre-treatment obviously induced the alternative respiratory pathway activity of S. sclerotiorum mycelia. The results are helpful for deep understanding of the regulation mechanism of fungicidal activity of carbendazim. Furthermore, they suggest that inducers or activators of alternative oxidase should be applied to acquiring a better controlling effect of carbendazim on S. sclerotiorum in agricultural activities.

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