Genome sequence reveals that Pseudomonas fluorescens F113 possesses a large and diverse array of systems for rhizosphere function and host interaction
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Date
2013Author
Redondo-Nieto, Miguel
Barret, Matthieu
Morrissey, John
Germaine, Kieran J.
Martinez-Granero, Francisco
Barahona, Emma
Navazo, Ana
Sánchez-Contrerasa, María
Moynihan, Jennifer A.
Candela, Muriel
Dowling, David N.
O'Gara, Fergal
Martín, Marta
Rivilla, Rafael
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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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