期刊文献+

绿针假单胞菌HT66中ompR基因的功能 被引量:1

Function of ompR gene in Pseudomonas chlororaphis HT66
原文传递
导出
摘要 【背景】植物根部存在大量对植物生长有促进或对病原菌有拮抗作用的有益细菌,是当前农业微生物研究的热点之一。其中,绿针假单胞菌HT66是一株可高效合成吩嗪-1-甲酰胺(PCN)的环境友好型生防菌株。【目的】探究在绿针假单胞菌HT66中ompR基因的生理功能,以及其对菌株生防作用的影响。【方法】通过基因无痕敲除的方法构建HT66菌株的ompR基因缺失突变株,对比研究突变株与野生株在生长速率、渗透压感应、生物膜的合成、pH耐受性、群集运动和PCN产量的变化。【结果】与野生株相比,ompR基因缺失突变株的细胞生物量微量减少,生物膜的合成减少31.5%,群集运动以及对渗透压和pH的耐受性明显下降,但是其PCN产量较野生株提高了57.8%。【结论】在HT66菌株中,ompR基因对其运动性、环境耐受性和生理生防功能均有一定程度的调控作用。本研究丰富了绿针假单胞菌的代谢通路,此报道将对后续PCN合成机制的研究和应用提供一定的理论依据。 [Background] Plant rhizosphere growth-promoting bacteria are one of the hotspots in the current research of agricultural microorganisms because they promote plant growth or have antagonistic effects on pathogenic bacteria. Among them, Pseudomonas chlororaphis HT66 is a non-pathogenic biocontrol strain that can efficiently synthesize phenazine-1-carboxamide(PCN) — a promising and environmental friendly agricultural antibiotic. [Objective] To study the physiological function of ompR gene in P. chlororaphis HT66 and its biocontrol efficiency. [Methods] The ompR gene deletion mutant of HT66 strain was constructed by scar-less gene knockout method. We studied the effects of the mutation on the growth rate, biofilm synthesis, tolerance to pH and osmotic pressure, swarming mobility and PCN production. [Results] Compared with the wild-type strain, the ompR gene deletion inactivated mutant showed a slight reduction in cell biomass. The biofilm decreased by 31.5%, whereas the swarming mobility of the strain and the tolerance to osmotic pressure and pH decreased. However, the yield of PCN increased by 57.8% in the mutant strain. In HT66 strain, the ompR gene has a certain degree of regulation of its motility, environmental tolerance and physiological and biological functions. [Conclusion] Our findings enriched the metabolic pathway of P. chlororaphis, and will provide a basis for the research and application of the subsequent PCN synthesis mechanism.
作者 侯博文 郭树奇 彭华松 张雪洪 HOU Bo-Wen;GUO Shu-Qi;PENG Hua-Song;ZHANG Xue-Hong(State Key Laboratory of Microbial Metabolism,School of Life Sciences and Biotechnology,Shanghai Jiao Tong University,Shanghai 200240,Chin)
出处 《微生物学通报》 CAS CSCD 北大核心 2018年第8期1719-1725,共7页 Microbiology China
基金 国家自然科学基金(31270084) 国家高技术研究发展计划(863计划)(2012AA022107) 国家重点基础研究发展规划(973计划)(2012CB721005)~~
关键词 假单胞菌 基因敲除 OMPR 吩嗪-1-甲酰胺 Pseudomonas Gene knockout ompR Phenazine-1-carboxamide
  • 相关文献

参考文献5

二级参考文献91

  • 1陈鸿锐,陈碧瑶,陈玲玲.吩嗪-1-羧酸发酵培养基配方的初步确定[J].生物技术世界,2012,9(3):21-21. 被引量:2
  • 2许煜泉.绿色微生物源抗菌剂申嗪霉素(M18)[J].精细与专用化学品,2004,12(20):8-9. 被引量:40
  • 3ZHOUHongyou,WEIHailei,LIUXili,WANGYe,ZHANGLiqun,TANGWenhua.Improving biocontrol activity of Pseudomonas fluorescens through chromosomal inte-gration of 2,4-diacetylphloro-glucinol biosynthesis genes[J].Chinese Science Bulletin,2005,50(8):775-781. 被引量:4
  • 4Tian T,Wu X G,Duan H M, et al.The resistance-nodulation-division efflux pump EmhABC influences the production of 2,4-diacetylphloroglucinol in Pseudomonas fluorescens 2P24[J].Microbiology-GSM,2010,156(1):39-48.
  • 5Bang I S,Audia J P,Park Y K,et al.Autoinduction of the ompR response regulator by acid shock and control of the Salmonella enterica acid tolerance response[J].Molecular Microbiology,2002,44(5):1 235-1 250.
  • 6Dekkers L C,Bloemendaal C P,De Weger L A,et al.A two-co mponent system plays an important role in the root-colonizing ability o f Pseudomonas fluorescens strain WCS365 [J].Molecular Plant-Microbe Interactions,1998,11(1):45-5 6.
  • 7Jubelin G,Vianney A,Beloin C,et al.CpxR/OmpR interplay regulates curli gene expression in response to osmolarity in Escherichia coli [J]. Journal of Bacteriology,2005,187(6):2038-2049.
  • 8Garmendia J,Beuzon C R,Ruiz-Albert J,et al.The roles of SsrA SsrB and OmpR EnvZ in the regulation of genes encoding the Salmonella typhimurium SPI-2 type III secretion system[J].Microbiology-GSM,2003,149(9):2385-2396.
  • 9McCarthy C N,Woods R G,Beacham I R.Regulation of the aprX-lipA operon of Pseudomonas fluorescens B52:Dierential regulation of the proximal and distal genes,encoding protease and lipase,by ompR-envZ[J].FEMS Microbiology Letters,2004,241:243-248.
  • 10Bangera M G,Thomashow L S.Identification and characterization of a gene cluster fo rsynthesis of the polyketide antibiotic 2,4-diacetylphloroglucinol from Pseudomonas fluorescens Q2¨C87[J].J Bacteriol,1999,181:3155-3163.

共引文献27

同被引文献11

引证文献1

二级引证文献7

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部