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dc.creatorTorrado Maya, Alejandroes
dc.creatorIniesta Pallarés, Macarenaes
dc.creatorVelázquez Campoy, Adriánes
dc.creatorÁlvarez Núñez, Consolaciónes
dc.creatorMariscal, Vicentees
dc.creatorMolina Heredia, Fernando Publioes
dc.date.accessioned2023-09-11T14:31:26Z
dc.date.available2023-09-11T14:31:26Z
dc.date.issued2023
dc.identifier.citationTorrado Maya, A., Iniesta Pallarés, M., Velázquez Campoy, A., Álvarez Núñez, C., Mariscal, V. y Molina Heredia, F.P. (2023). Phylogenetic and functional analysis of cyanobacterial Cytochrome c6-like proteins. Frontiers in Plant Science, 14, 1227492. https://doi.org/10.3389/fpls.2023.1227492.
dc.identifier.issn1664-462Xes
dc.identifier.urihttps://hdl.handle.net/11441/148865
dc.description.abstractAll known photosynthetic cyanobacteria carry a cytochrome c6 protein that acts transferring electrons from cytochrome b6f complex to photosystem I, in photosynthesis, or cytochrome c oxidase, in respiration. In most of the cyanobacteria, at least one homologue to cytochrome c6 is found, the so-called cytochrome c6B or cytochrome c6C. However, the function of these cytochrome c6-like proteins is still unknown. Recently, it has been proposed a common origin of these proteins as well as the reclassification of the cytochrome c6C group as c6B, renaming the new joint group as cytochrome c6BC. Another homologue to cytochrome c6 has not been classified yet, the formerly called cytochrome c6-3, which is present in the heterocyst-forming filamentous cyanobacteria Nostoc sp. PCC 7119. In this work, we propose the inclusion of this group as an independent group in the genealogy of cytochrome c6-like proteins with significant differences from cytochrome c6 and cytochrome c6BC, with the proposed name cytochrome c6D. To support this proposal, new data about phylogeny, genome localisation and functional properties of cytochrome c6-like proteins is provided. Also, we have analysed the interaction of cytochrome c6-like proteins with cytochrome f by isothermal titration calorimetry and by molecular docking, concluding that c6-like proteins could interact with cytochrome b6f complex in a similar fashion as cytochrome c6. Finally, we have analysed the reactivity of cytochrome c6-like proteins with membranes enriched in terminal oxidases of cyanobacteria by oxygen uptake experiments, concluding that cytochrome c6D is able to react with the specific copper-oxidase of the heterocysts, the cytochrome c oxidase 2.es
dc.description.sponsorshipFundación de Investigación de la Universidad de Sevilla FIUS05710000es
dc.description.sponsorshipJunta de Andalucía PAIDI AGR-288es
dc.description.sponsorshipConsejo Superior de Investigaciones Científicas 20225278es
dc.formatapplication/pdfes
dc.format.extent10 p.es
dc.language.isoenges
dc.publisherFrontiers Media S.A.es
dc.relation.ispartofFrontiers in Plant Science, 14, 1227492.
dc.rightsAtribución 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.subjectCytochrome c6es
dc.subjectCytochrome c6-like proteinses
dc.subjectCytochrome c oxidasees
dc.subjectCyanobacteriaes
dc.subjectCytochrome b6f complexes
dc.subjectPhotosynthesises
dc.subjectRespirationes
dc.subjectElectron transferes
dc.titlePhylogenetic and functional analysis of cyanobacterial Cytochrome c6-like proteinses
dc.typeinfo:eu-repo/semantics/articlees
dcterms.identifierhttps://ror.org/03yxnpp24
dc.type.versioninfo:eu-repo/semantics/publishedVersiones
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses
dc.contributor.affiliationUniversidad de Sevilla. Departamento de Bioquímica Vegetal y Biología Moleculares
dc.relation.projectIDFIUS05710000es
dc.relation.projectIDPAIDI AGR-288es
dc.relation.projectID20225278es
dc.relation.publisherversionhttps://doi.org/10.3389/fpls.2023.1227492es
dc.identifier.doi10.3389/fpls.2023.1227492es
dc.journaltitleFrontiers in Plant Sciencees
dc.publication.volumen14es
dc.publication.initialPage1227492es
dc.contributor.funderFundación de Investigación de la Universidad de Sevillaes
dc.contributor.funderJunta de Andalucíaes
dc.contributor.funderConsejo Superior de Investigaciones Científicas (CSIC)es

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