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Redox-coupled proton pumping drives carbon concentration in the photosynthetic complex I
Photosynthetic organisms capture light energy to drive their energy metabolism, and employ the chemical reducing power to convert carbon dioxide (CO(2)) into organic molecules. Photorespiration, however, significantly reduces the photosynthetic yields. To survive under low CO(2) concentrations, cyan...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6981117/ https://www.ncbi.nlm.nih.gov/pubmed/31980611 http://dx.doi.org/10.1038/s41467-020-14347-4 |
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author | Schuller, Jan M. Saura, Patricia Thiemann, Jacqueline Schuller, Sandra K. Gamiz-Hernandez, Ana P. Kurisu, Genji Nowaczyk, Marc M. Kaila, Ville R. I. |
author_facet | Schuller, Jan M. Saura, Patricia Thiemann, Jacqueline Schuller, Sandra K. Gamiz-Hernandez, Ana P. Kurisu, Genji Nowaczyk, Marc M. Kaila, Ville R. I. |
author_sort | Schuller, Jan M. |
collection | PubMed |
description | Photosynthetic organisms capture light energy to drive their energy metabolism, and employ the chemical reducing power to convert carbon dioxide (CO(2)) into organic molecules. Photorespiration, however, significantly reduces the photosynthetic yields. To survive under low CO(2) concentrations, cyanobacteria evolved unique carbon-concentration mechanisms that enhance the efficiency of photosynthetic CO(2) fixation, for which the molecular principles have remained unknown. We show here how modular adaptations enabled the cyanobacterial photosynthetic complex I to concentrate CO(2) using a redox-driven proton-pumping machinery. Our cryo-electron microscopy structure at 3.2 Å resolution shows a catalytic carbonic anhydrase module that harbours a Zn(2+) active site, with connectivity to proton-pumping subunits that are activated by electron transfer from photosystem I. Our findings illustrate molecular principles in the photosynthetic complex I machinery that enabled cyanobacteria to survive in drastically changing CO(2) conditions. |
format | Online Article Text |
id | pubmed-6981117 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-69811172020-01-27 Redox-coupled proton pumping drives carbon concentration in the photosynthetic complex I Schuller, Jan M. Saura, Patricia Thiemann, Jacqueline Schuller, Sandra K. Gamiz-Hernandez, Ana P. Kurisu, Genji Nowaczyk, Marc M. Kaila, Ville R. I. Nat Commun Article Photosynthetic organisms capture light energy to drive their energy metabolism, and employ the chemical reducing power to convert carbon dioxide (CO(2)) into organic molecules. Photorespiration, however, significantly reduces the photosynthetic yields. To survive under low CO(2) concentrations, cyanobacteria evolved unique carbon-concentration mechanisms that enhance the efficiency of photosynthetic CO(2) fixation, for which the molecular principles have remained unknown. We show here how modular adaptations enabled the cyanobacterial photosynthetic complex I to concentrate CO(2) using a redox-driven proton-pumping machinery. Our cryo-electron microscopy structure at 3.2 Å resolution shows a catalytic carbonic anhydrase module that harbours a Zn(2+) active site, with connectivity to proton-pumping subunits that are activated by electron transfer from photosystem I. Our findings illustrate molecular principles in the photosynthetic complex I machinery that enabled cyanobacteria to survive in drastically changing CO(2) conditions. Nature Publishing Group UK 2020-01-24 /pmc/articles/PMC6981117/ /pubmed/31980611 http://dx.doi.org/10.1038/s41467-020-14347-4 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Schuller, Jan M. Saura, Patricia Thiemann, Jacqueline Schuller, Sandra K. Gamiz-Hernandez, Ana P. Kurisu, Genji Nowaczyk, Marc M. Kaila, Ville R. I. Redox-coupled proton pumping drives carbon concentration in the photosynthetic complex I |
title | Redox-coupled proton pumping drives carbon concentration in the photosynthetic complex I |
title_full | Redox-coupled proton pumping drives carbon concentration in the photosynthetic complex I |
title_fullStr | Redox-coupled proton pumping drives carbon concentration in the photosynthetic complex I |
title_full_unstemmed | Redox-coupled proton pumping drives carbon concentration in the photosynthetic complex I |
title_short | Redox-coupled proton pumping drives carbon concentration in the photosynthetic complex I |
title_sort | redox-coupled proton pumping drives carbon concentration in the photosynthetic complex i |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6981117/ https://www.ncbi.nlm.nih.gov/pubmed/31980611 http://dx.doi.org/10.1038/s41467-020-14347-4 |
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