首页> 外文学位 >The plant growth-promoting rhizobacterium Pseudomonas sp. GR12-2 is closely related to the Pseudomonas syringae group of plant pathogens: phylogenetics, ecology, and plasmid biology.
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The plant growth-promoting rhizobacterium Pseudomonas sp. GR12-2 is closely related to the Pseudomonas syringae group of plant pathogens: phylogenetics, ecology, and plasmid biology.

机译:促进植物生长的根瘤菌假单胞菌sp。 GR12-2与丁香假单胞菌属植物病原体密切相关:系统发生学,生态学和质粒生物学。

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摘要

Pseudomonas putida GR12-2 is a well known plant growth-promoting rhizobacterium (PGPR); however, 16S rRNA gene sequence analysis showed that this strain shared 99% sequence identity with the Pseudomonas syringae complex, which is composed of plant pathogens. A phylogenetic analysis of the Pseudomonas group using a multi-locus sequence typing (MLST) protocol of four housekeeping genes showed that the GR12-2 strain and the P. syringae complex form a monophyletic group. A fine scale phylogenetic analysis using the gyrB gene confirmed this result. On the basis of these sequence analyses we suggest that P. putida GR12-2 be re-designated Pseudomonas sp. GR12-2. To compare the ecological roles of Pseudomonas sp. GR12-2 with its close relatives, P. syringae pathovar (pv.) tomato DC3000 and P. syringae pv. syringae B728a, we investigated their ability to cause disease and promote plant growth. When introduced on tobacco or tomato leaves, Pseudomonas sp. GR12-2 was unable to elicit a hypersensitive response or cause disease, which are characteristic responses of P. syringae DC3000 and B728a, nor were type III secretion system genes required for virulence detected in Pseudomonas sp. GR12-2 by PCR or DNA hybridization. In contrast to Pseudomonas sp. GR12-2, neither of the phytopathogens was able to promote root growth when inoculated onto canola seeds. Finally, to compare the role of the native plasmid of Pseudomonas sp. GR12-2 with the native plasmids of P. syringae , we attempted to cure the strain of its plasmid.
机译:恶臭假单胞菌GR12-2是一种众所周知的促进植物生长的根瘤菌(PGPR)。然而,16S rRNA基因序列分析表明,该菌株与由植物病原体组成的丁香假单胞菌复合物具有99%的序列同一性。使用四个管家基因的多位点序列分型(MLST)方案对假单胞菌群进行系统发育分析,结果表明GR12-2菌株和丁香假单胞菌复合体形成一个单系统群。使用gyrB基因的精细系统发育分析证实了这一结果。在这些序列分析的基础上,我们建议将恶臭假单胞菌GR12-2重新命名为假单胞菌。 GR12-2。比较假单胞菌的生态作用。 GR12-2及其近亲,丁香假单胞菌番茄(pv。)番茄DC3000和丁香假单胞菌pv。丁香B728a,我们调查了它们引起疾病和促进植物生长的能力。当引入烟草或番茄叶上时,假单胞菌属种。 GR12-2不能引起过敏反应或引起疾病,这是丁香假单胞菌DC3000和B728a的特征性反应,在假单胞菌sp。中也未检测到毒性所需的III型分泌系统基因。 GR12-2通过PCR或DNA杂交。与假单胞菌sp。 GR12-2,接种到双低油菜籽中后,两种植物病原体均不能促进根系生长。最后,比较假单胞菌sp。天然质粒的作用。 GR12-2与丁香假单胞菌的天然质粒,我们试图治愈其质粒菌株。

著录项

  • 作者

    Blakney, Andrew J. C.;

  • 作者单位

    University of New Brunswick (Canada).;

  • 授予单位 University of New Brunswick (Canada).;
  • 学科 Biology Microbiology.;Agriculture Soil Science.;Agriculture Plant Pathology.
  • 学位 M.Sc.
  • 年度 2011
  • 页码 122 p.
  • 总页数 122
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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