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Regulation of cyclic electron flow by chloroplast NADPH‐dependent thioredoxin system
Linear electron transport in the thylakoid membrane drives photosynthetic NADPH and ATP production, while cyclic electron flow (CEF) around photosystem I only promotes the translocation of protons from stroma to thylakoid lumen. The chloroplast NADH dehydrogenase‐like complex (NDH) participates in o...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6508795/ https://www.ncbi.nlm.nih.gov/pubmed/31245694 http://dx.doi.org/10.1002/pld3.93 |
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author | Nikkanen, Lauri Toivola, Jouni Trotta, Andrea Diaz, Manuel Guinea Tikkanen, Mikko Aro, Eva‐Mari Rintamäki, Eevi |
author_facet | Nikkanen, Lauri Toivola, Jouni Trotta, Andrea Diaz, Manuel Guinea Tikkanen, Mikko Aro, Eva‐Mari Rintamäki, Eevi |
author_sort | Nikkanen, Lauri |
collection | PubMed |
description | Linear electron transport in the thylakoid membrane drives photosynthetic NADPH and ATP production, while cyclic electron flow (CEF) around photosystem I only promotes the translocation of protons from stroma to thylakoid lumen. The chloroplast NADH dehydrogenase‐like complex (NDH) participates in one CEF route transferring electrons from ferredoxin back to the plastoquinone pool with concomitant proton pumping to the lumen. CEF has been proposed to balance the ratio of ATP/NADPH production and to control the redox poise particularly in fluctuating light conditions, but the mechanisms regulating the NDH complex remain unknown. We have investigated potential regulation of the CEF pathways by the chloroplast NADPH‐thioredoxin reductase (NTRC) in vivo by using an Arabidopsis knockout line of NTRC as well as lines overexpressing NTRC. Here, we present biochemical and biophysical evidence showing that NTRC stimulates the activity of NDH‐dependent CEF and is involved in the regulation of generation of proton motive force, thylakoid conductivity to protons, and redox balance between the thylakoid electron transfer chain and the stroma during changes in light conditions. Furthermore, protein–protein interaction assays suggest a putative thioredoxin‐target site in close proximity to the ferredoxin‐binding domain of NDH, thus providing a plausible mechanism for redox regulation of the NDH ferredoxin:plastoquinone oxidoreductase activity. |
format | Online Article Text |
id | pubmed-6508795 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-65087952019-06-26 Regulation of cyclic electron flow by chloroplast NADPH‐dependent thioredoxin system Nikkanen, Lauri Toivola, Jouni Trotta, Andrea Diaz, Manuel Guinea Tikkanen, Mikko Aro, Eva‐Mari Rintamäki, Eevi Plant Direct Original Research Linear electron transport in the thylakoid membrane drives photosynthetic NADPH and ATP production, while cyclic electron flow (CEF) around photosystem I only promotes the translocation of protons from stroma to thylakoid lumen. The chloroplast NADH dehydrogenase‐like complex (NDH) participates in one CEF route transferring electrons from ferredoxin back to the plastoquinone pool with concomitant proton pumping to the lumen. CEF has been proposed to balance the ratio of ATP/NADPH production and to control the redox poise particularly in fluctuating light conditions, but the mechanisms regulating the NDH complex remain unknown. We have investigated potential regulation of the CEF pathways by the chloroplast NADPH‐thioredoxin reductase (NTRC) in vivo by using an Arabidopsis knockout line of NTRC as well as lines overexpressing NTRC. Here, we present biochemical and biophysical evidence showing that NTRC stimulates the activity of NDH‐dependent CEF and is involved in the regulation of generation of proton motive force, thylakoid conductivity to protons, and redox balance between the thylakoid electron transfer chain and the stroma during changes in light conditions. Furthermore, protein–protein interaction assays suggest a putative thioredoxin‐target site in close proximity to the ferredoxin‐binding domain of NDH, thus providing a plausible mechanism for redox regulation of the NDH ferredoxin:plastoquinone oxidoreductase activity. John Wiley and Sons Inc. 2018-11-07 /pmc/articles/PMC6508795/ /pubmed/31245694 http://dx.doi.org/10.1002/pld3.93 Text en © 2018 The Authors. Plant Direct published by American Society of Plant Biologists, Society for Experimental Biology and John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Research Nikkanen, Lauri Toivola, Jouni Trotta, Andrea Diaz, Manuel Guinea Tikkanen, Mikko Aro, Eva‐Mari Rintamäki, Eevi Regulation of cyclic electron flow by chloroplast NADPH‐dependent thioredoxin system |
title | Regulation of cyclic electron flow by chloroplast NADPH‐dependent thioredoxin system |
title_full | Regulation of cyclic electron flow by chloroplast NADPH‐dependent thioredoxin system |
title_fullStr | Regulation of cyclic electron flow by chloroplast NADPH‐dependent thioredoxin system |
title_full_unstemmed | Regulation of cyclic electron flow by chloroplast NADPH‐dependent thioredoxin system |
title_short | Regulation of cyclic electron flow by chloroplast NADPH‐dependent thioredoxin system |
title_sort | regulation of cyclic electron flow by chloroplast nadph‐dependent thioredoxin system |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6508795/ https://www.ncbi.nlm.nih.gov/pubmed/31245694 http://dx.doi.org/10.1002/pld3.93 |
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