4.7 Article

Genome sequence reveals that Pseudomonas fluorescens F113 possesses a large and diverse array of systems for rhizosphere function and host interaction

Journal

BMC GENOMICS
Volume 14, Issue -, Pages -

Publisher

BMC
DOI: 10.1186/1471-2164-14-54

Keywords

-

Funding

  1. MICROAMBIENTE-CM
  2. Marie Curie MIGENOF113
  3. Science Foundation of Ireland [07IN.1/B948, 08/RFP/GEN1295, 08/RFP/GEN1319, SFI09/RFP/BMT2350]
  4. Department of Agriculture, Fisheries and Food [06-321, 06-377, 06RDC459 06RDC506, 08RDC629]
  5. European Commission [MTKD-CT-2006-042062, EU256596, MicroB3-287589-OCEAN2012, MACUMBA-CP-TP 311975, PharmaSea-CP-TP 312184]
  6. IRCSET [05/EDIV/FP107/INTERPAM]
  7. Marine Institute [CCRA 2007/082]
  8. Environmental Protection Agency [EPA 2006-PhD-S-21, EPA 2008-PhD-S-2]
  9. HRB [RP/2006/271, RP/2007/290, HRA/2009/146]
  10. SFI
  11. Department of Education TSR III Agribiotics project
  12. [BIO2009-08254]
  13. Health Research Board (HRB) [HRA-2009-146] Funding Source: Health Research Board (HRB)

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Background: Pseudomonas fluorescens F113 is a plant growth-promoting rhizobacterium (PGPR) isolated from the sugar-beet rhizosphere. This bacterium has been extensively studied as a model strain for genetic regulation of secondary metabolite production in P. fluorescens, as a candidate biocontrol agent against phytopathogens, and as a heterologous host for expression of genes with biotechnological application. The F113 genome sequence and annotation has been recently reported. Results: Comparative analysis of 50 genome sequences of strains belonging to the P. fluorescens group has revealed the existence of five distinct subgroups. F113 belongs to subgroup I, which is mostly composed of strains classified as P. brassicacearum. The core genome of these five strains is highly conserved and represents approximately 76% of the protein-coding genes in any given genome. Despite this strong conservation, F113 also contains a large number of unique protein-coding genes that encode traits potentially involved in the rhizocompetence of this strain. These features include protein coding genes required for denitrification, diterpenoids catabolism, motility and chemotaxis, protein secretion and production of antimicrobial compounds and insect toxins. Conclusions: The genome of P. fluorescens F113 is composed of numerous protein-coding genes, not usually found together in previously sequenced genomes, which are potentially decisive during the colonisation of the rhizosphere and/or interaction with other soil organisms. This includes genes encoding proteins involved in the production of a second flagellar apparatus, the use of abietic acid as a growth substrate, the complete denitrification pathway, the possible production of a macrolide antibiotic and the assembly of multiple protein secretion systems.

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