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dc.contributor.authorRedondo-Nieto, Miguel
dc.contributor.authorBarret, Matthieu
dc.contributor.authorMorrissey, John
dc.contributor.authorGermaine, Kieran J.
dc.contributor.authorMartinez-Granero, Francisco
dc.contributor.authorBarahona, Emma
dc.contributor.authorNavazo, Ana
dc.contributor.authorSánchez-Contrerasa, María
dc.contributor.authorMoynihan, Jennifer A.
dc.contributor.authorCandela, Muriel
dc.contributor.authorDowling, David N.
dc.contributor.authorO'Gara, Fergal
dc.contributor.authorMartín, Marta
dc.contributor.authorRivilla, Rafael
dc.date.accessioned2018-08-17T13:11:56Z
dc.date.available2018-08-17T13:11:56Z
dc.date.copyright2013-01-23
dc.date.issued2013
dc.identifier.citationRedondo-Nieto, M., Barret, M., Morrissey, J., Germaine, K., Martinez-Granero, F., Barahona, E., . . . Rivilla, R. (2013). Genome sequence reveals that Pseudomonas fluorescens F113 possesses a large and diverse array of systems for rhizosphere function and host interaction. BMC Genomics, 14. doi:10.1186/1471-2164-14-54en_US
dc.identifier.issn1471-2164
dc.identifier.urihttps://research.thea.ie/handle/20.500.12065/2328
dc.description.abstractBackground: 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.en_US
dc.formatPDFen_US
dc.language.isoenen_US
dc.publisherBioMed Centralen_US
dc.relation.ispartofBMC Genomicsen_US
dc.rightsAttribution-NonCommercial-NoDerivs 3.0 Ireland*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/ie/*
dc.subjectcore genomeen_US
dc.subjectabietic aciden_US
dc.subjectpolar flagellumen_US
dc.subjectflagellar geneen_US
dc.subjectfluorescens groupen_US
dc.titleGenome sequence reveals that Pseudomonas fluorescens F113 possesses a large and diverse array of systems for rhizosphere function and host interactionen_US
dc.typeArticleen_US
dc.contributor.sponsorResearch at UAM was funded by grants MICROAMBIENTE-CM (to R.R.), BIO2009-08254 (to M.M.), and Marie Curie MIGENOF113 (to M.S.-C. and R.R.). This research was supported in parts by grants awarded to FOG by the Science Foundation of Ireland (07IN.1/B948, 08/RFP/GEN1295, 08/RFP/ GEN1319, SFI09/RFP/BMT2350); the Department of Agriculture, Fisheries and Food (RSF grants 06–321 and 06–377; FIRM grants 06RDC459 06RDC506 and 08RDC629); the European Commission (MTKD-CT-2006-042062, Marie Curie TOK:TRAMWAYS, EU256596, MicroB3-287589-OCEAN2012, MACUMBA-CP-TP 311975; PharmaSea-CP-TP 312184); IRCSET (05/EDIV/FP107/INTERPAM, EMBARK), the Marine Institute Beaufort award (C&CRA 2007/082), the Environmental Protection Agency (EPA 2006-PhD-S-21, EPA 2008-PhD-S-2) and the HRB (RP/2006/271, RP/2007/290, HRA/2009/146). The Lab of KG & DD was in part funded by an SFI Tida award and the Department of Education TSR III Agribiotics project. The authors would like to acknowledge the Centro de Computación Científica at Universidad Autónoma de Madrid and the Boole Centre for Research in Informatics at University College Cork for providing access to computational facilities.en_US
dc.description.peerreviewyesen_US
dc.identifier.urlhttp://dx.doi.org/10.1186/1471-2164-14-54en_US
dc.rights.accessinfo:eu-repo/semantics/openAccessen_US
dc.subject.departmentenviroCORE - IT Carlowen_US


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