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中国生物防治学报 ›› 2021, Vol. 37 ›› Issue (1): 130-138.DOI: 10.16409/j.cnki.2095-039x.2021.01.003

• 研究论文 • 上一篇    

产酶溶杆菌OH11中LysR和GntR家族基因的功能分析

林龙1, 葛程程1, 蒋建东2, 钱国良1   

  1. 1. 南京农业大学植物保护学院, 南京 210095;
    2. 南京农业大学生命科学学院, 南京 210095
  • 收稿日期:2020-05-30 发布日期:2021-02-23
  • 通讯作者: 钱国良,博士,教授,E-mail:glqian@njau.edu.cn。
  • 作者简介:林龙,博士,E-mail:linlong@njau.edu.cn
  • 基金资助:
    江苏省自然科学基金(BK20190026,BK20181325);国家自然科学基金(31872016,32001955);中央高校基本科研业务费专项资金(KJJQ202001,KYT201805,KYTZ201403,KYT202001,KYXK202012);江苏省农业科技自主创新资金(CX(18)1003)

Function Analysis of LysR and GntR Family Genes in Lysobacter enzymogenes OH11

LIN Long1, GE Chengcheng1, JIANG Jiandong2, QIAN Guoliang1   

  1. 1. College of Plant Protection, Nanjing Agricultural University, Nanjing 210095, China;
    2. College of Life Science, Nanjing Agricultural University, Nanjing 210095, China
  • Received:2020-05-30 Published:2021-02-23

摘要: 产酶溶杆菌Lysobacter enzymogenes OH11可以通过蹭行运动(Twitching motility)接近并附着在病原真菌和卵菌上,进而分泌各种胞外酶和次级代谢产物抑制病原菌的生长,其中热稳定抗真菌因子(heat-stable antifungal factor,HSAF)是一种新型的抗真菌代谢物,具有研发为新型生防杀真菌剂的潜力。转录因子在基因的转录调控中起到关键的作用,鉴于LysR和GntR家族的转录因子在病原细菌中对运动性和致病性具有重要调控作用,本研究在OH11基因组中选取了3个LysR家族蛋白(Le1404、Le2114和Le3293)以及2个GntR蛋白(Le1155和Le1310)的编码基因进行敲除,构建相应的突变体,以明确它们是否可以调控OH11的蹭行运动和HSAF的合成。结果表明,在OH11中分别敲除Le2114Le1155均导致该菌株丧失蹭行运动;而敲除Le1155能显著降低HSAF的产量,说明Le2114可以特异地调控蹭行运动,而Le1155可以调控蹭行运动和HSAF合成两个生理过程。

关键词: 产酶溶杆菌, 蹭行运动, HSAF, LysR, GntR

Abstract: Lysobacter enzymogenes OH11 can approach and adhere to the hypha of pathogenic fungi and oomycetes through twitching motility. Then OH11 secretes enzymes and secondary metabolites including HSAF (heat-stable antifungal factor), which is a new type of anti-fungal secondary metabolite and a potential resource for new bio-control fungicide, to inhibit pathogen growth. Transcription factor (TF) plays a key role in regulation of gene expression. LysR and GntR TF family regulate motility and pathogenicity in pathogenic bacteria. In this paper, we knocked out encoding genes of 3 LysR TFs (Le1404, Le2114 and Le3293) and 2 GntR TFs (Le1155 and Le1310) to investigate whether they regulate twitching motility and HSAF biosynthesis. ΔLe2114 and ΔLe1155 showed defect in twitching motility; ΔLe1155 produced lower amount of HSAF compared with wild-type. These results indicated Le2114 specifically regulated twitching motility and Le1155 regulated both twitching motility and HSAF biosynthesis.

Key words: Lysobacter enzymogenes, twitching motility, HSAF, LysR, GntR

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