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1.
BMC Genomics ; 14: 54, 2013 Jan 25.
Article in English | MEDLINE | ID: mdl-23350846

ABSTRACT

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.


Subject(s)
Genome, Bacterial/genetics , Host-Pathogen Interactions/genetics , Pseudomonas fluorescens/genetics , Pseudomonas fluorescens/physiology , Rhizosphere , Adaptation, Physiological/genetics , Animals , Bacterial Proteins/metabolism , Chemotaxis/genetics , Genomics , Phylogeny , Plant Development , Plants/microbiology , Prophages/genetics , Pseudomonas fluorescens/cytology , Pseudomonas fluorescens/virology
2.
J Bacteriol ; 194(5): 1273-4, 2012 Mar.
Article in English | MEDLINE | ID: mdl-22328765

ABSTRACT

Pseudomonas fluorescens F113 is a plant growth-promoting rhizobacterium (PGPR) that has biocontrol activity against fungal plant pathogens and is a model for rhizosphere colonization. Here, we present its complete genome sequence, which shows that besides a core genome very similar to those of other strains sequenced within this species, F113 possesses a wide array of genes encoding specialized functions for thriving in the rhizosphere and interacting with eukaryotic organisms.


Subject(s)
DNA, Bacterial/chemistry , DNA, Bacterial/genetics , Genome, Bacterial , Pseudomonas fluorescens/genetics , Pseudomonas fluorescens/isolation & purification , Rhizosphere , Molecular Sequence Data , Plants/microbiology , Sequence Analysis, DNA
3.
Appl Environ Microbiol ; 75(7): 2122-31, 2009 Apr.
Article in English | MEDLINE | ID: mdl-19181839

ABSTRACT

Pseudomonas fluorescens is of agricultural and economic importance as a biological control agent largely because of its plant association and production of secondary metabolites, in particular 2,4-diacetylphloroglucinol (2,4-DAPG). This polyketide, which is encoded by the eight-gene phl cluster, has antimicrobial effects on phytopathogens, promotes amino acid exudation from plant roots, and induces systemic resistance in plants. Despite its importance, 2,4-DAPG production is limited to a subset of P. fluorescens strains. Determination of the evolution of the phl cluster and understanding the selective pressures promoting its retention or loss in lineages of P. fluorescens will help in the development of P. fluorescens as a viable and effective inoculant for application in agriculture. In this study, genomic and sequence-based approaches were integrated to reconstruct the phylogeny of P. fluorescens and the phl cluster. It was determined that 2,4-DAPG production is an ancestral trait in the species P. fluorescens but that most lineages have lost this capacity through evolution. Furthermore, intragenomic recombination has relocated the phl cluster within the P. fluorescens genome at least three times, but the integrity of the cluster has always been maintained. The possible evolutionary and functional implications for retention of the phl cluster and 2,4-DAPG production in some lineages of P. fluorescens are discussed.


Subject(s)
Evolution, Molecular , Metabolic Networks and Pathways/genetics , Multigene Family , Pseudomonas fluorescens/genetics , Pseudomonas fluorescens/metabolism , Amino Acid Sequence , Cluster Analysis , DNA, Bacterial/chemistry , DNA, Bacterial/genetics , Gene Order , Genes, Bacterial , Genome, Bacterial , Molecular Sequence Data , Phloroglucinol/analogs & derivatives , Phloroglucinol/metabolism , Phylogeny , Plants/microbiology , Recombination, Genetic , Sequence Alignment , Sequence Analysis, DNA , Sequence Deletion , Sequence Homology , Synteny
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