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logo citeas Torrado, A., Iniesta-Pallarés, M., Velázquez-Campoy, A., Álvarez, C., Mariscal, V., & Molina-Heredia, F. P. (2023, September 6). Phylogenetic and functional analysis of cyanobacterial Cytochrome c6-like proteins. Frontiers in Plant Science. Frontiers Media SA. http://doi.org/10.3389/fpls.2023.1227492
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Título

Phylogenetic and functional analysis of cyanobacterial Cytochrome c6-like proteins

AutorTorrado, Alejandro CSIC ORCID; Iniesta-Pallarés, Macarena; Velázquez-Campoy, Adrián; Álvarez, Consolación CSIC ORCID; Mariscal, Vicente CSIC ORCID ; Molina-Heredia, Fernando P. CSIC ORCID
FinanciadoresFundación de Investigación de la Universidad de Sevilla
Universidad de Sevilla
Junta de Andalucía
Agencia Estatal de Investigación (España)
Palabras claveCyanobacteria
Cytochrome b6f complex
Cytochrome c oxidase
Cytochrome c6
Cytochrome c6-like proteins
Electron transfer
Photosynthesis
Respiration
Fecha de publicación6-sep-2023
EditorFrontiers Media
CitaciónFrontiers in Plant Science 14: 1-10 (2023)
ResumenAll known photosynthetic cyanobacteria carry a cytochrome c 6 protein that acts transferring electrons from cytochrome b 6 f complex to photosystem I, in photosynthesis, or cytochrome c oxidase, in respiration. In most of the cyanobacteria, at least one homologue to cytochrome c 6 is found, the so-called cytochrome c 6B or cytochrome c 6C. However, the function of these cytochrome c 6-like proteins is still unknown. Recently, it has been proposed a common origin of these proteins as well as the reclassification of the cytochrome c 6C group as c 6B, renaming the new joint group as cytochrome c 6BC. Another homologue to cytochrome c 6 has not been classified yet, the formerly called cytochrome c 6-3, 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 c 6-like proteins with significant differences from cytochrome c 6 and cytochrome c 6BC, with the proposed name cytochrome c 6D. To support this proposal, new data about phylogeny, genome localisation and functional properties of cytochrome c 6-like proteins is provided. Also, we have analysed the interaction of cytochrome c 6-like proteins with cytochrome f by isothermal titration calorimetry and by molecular docking, concluding that c 6-like proteins could interact with cytochrome b 6 f complex in a similar fashion as cytochrome c 6. Finally, we have analysed the reactivity of cytochrome c 6-like proteins with membranes enriched in terminal oxidases of cyanobacteria by oxygen uptake experiments, concluding that cytochrome c 6D is able to react with the specific copper-oxidase of the heterocysts, the cytochrome c oxidase 2.
Versión del editorhttps://doi.org/10.3389/fpls.2023.1227492
URIhttp://hdl.handle.net/10261/354819
DOI10.3389/fpls.2023.1227492
ISSN1664-462X
Licencia de usohttps://creativecommons.org/licenses/by/4.0/
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