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Oxidation of P700 Induces Alternative Electron Flow in Photosystem I in Wheat Leaves
Oxygen (O(2))-evolving photosynthetic organisms oxidize the reaction center chlorophyll, P700, in photosystem I (PSI) to suppress the production of reactive oxygen species. The oxidation of P700 is accompanied by alternative electron flow in PSI (AEF-I), which is not required for photosynthetic line...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6631986/ https://www.ncbi.nlm.nih.gov/pubmed/31195693 http://dx.doi.org/10.3390/plants8060152 |
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author | Kadota, Kanae Furutani, Riu Makino, Amane Suzuki, Yuji Wada, Shinya Miyake, Chikahiro |
author_facet | Kadota, Kanae Furutani, Riu Makino, Amane Suzuki, Yuji Wada, Shinya Miyake, Chikahiro |
author_sort | Kadota, Kanae |
collection | PubMed |
description | Oxygen (O(2))-evolving photosynthetic organisms oxidize the reaction center chlorophyll, P700, in photosystem I (PSI) to suppress the production of reactive oxygen species. The oxidation of P700 is accompanied by alternative electron flow in PSI (AEF-I), which is not required for photosynthetic linear electron flow (LEF). To characterize AEF-I, we compared the redox reactions of P700 and ferredoxin (Fd) during the induction of carbon dioxide (CO(2)) assimilation in wheat leaves, using dark-interval relaxation kinetics analysis. Switching on an actinic light (1000 μmol photons m(−2) s(−1)) at ambient CO(2) partial pressure of 40 Pa and ambient O(2) partial pressure of 21 kPa gradually oxidized P700 (P700(+)) and enhanced the reduction rate of P700(+) (vP700) and oxidation rate of reduced Fd (vFd). The vFd showed a positive linear relationship with an apparent photosynthetic quantum yield of PSII (Y[II]) originating at point zero; the redox turnover of Fd is regulated by LEF via CO(2) assimilation and photorespiration. The vP700 also showed a positive linear relationship with Y(II), but the intercept was positive, not zero. That is, the electron flux in PSI included the electron flux in AEF-I in addition to that in LEF. This indicates that the oxidation of P700 induces AEF-I. We propose a possible mechanism underlying AEF-I and its physiological role in the mitigation of oxidative damage. |
format | Online Article Text |
id | pubmed-6631986 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-66319862019-08-19 Oxidation of P700 Induces Alternative Electron Flow in Photosystem I in Wheat Leaves Kadota, Kanae Furutani, Riu Makino, Amane Suzuki, Yuji Wada, Shinya Miyake, Chikahiro Plants (Basel) Article Oxygen (O(2))-evolving photosynthetic organisms oxidize the reaction center chlorophyll, P700, in photosystem I (PSI) to suppress the production of reactive oxygen species. The oxidation of P700 is accompanied by alternative electron flow in PSI (AEF-I), which is not required for photosynthetic linear electron flow (LEF). To characterize AEF-I, we compared the redox reactions of P700 and ferredoxin (Fd) during the induction of carbon dioxide (CO(2)) assimilation in wheat leaves, using dark-interval relaxation kinetics analysis. Switching on an actinic light (1000 μmol photons m(−2) s(−1)) at ambient CO(2) partial pressure of 40 Pa and ambient O(2) partial pressure of 21 kPa gradually oxidized P700 (P700(+)) and enhanced the reduction rate of P700(+) (vP700) and oxidation rate of reduced Fd (vFd). The vFd showed a positive linear relationship with an apparent photosynthetic quantum yield of PSII (Y[II]) originating at point zero; the redox turnover of Fd is regulated by LEF via CO(2) assimilation and photorespiration. The vP700 also showed a positive linear relationship with Y(II), but the intercept was positive, not zero. That is, the electron flux in PSI included the electron flux in AEF-I in addition to that in LEF. This indicates that the oxidation of P700 induces AEF-I. We propose a possible mechanism underlying AEF-I and its physiological role in the mitigation of oxidative damage. MDPI 2019-06-05 /pmc/articles/PMC6631986/ /pubmed/31195693 http://dx.doi.org/10.3390/plants8060152 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Kadota, Kanae Furutani, Riu Makino, Amane Suzuki, Yuji Wada, Shinya Miyake, Chikahiro Oxidation of P700 Induces Alternative Electron Flow in Photosystem I in Wheat Leaves |
title | Oxidation of P700 Induces Alternative Electron Flow in Photosystem I in Wheat Leaves |
title_full | Oxidation of P700 Induces Alternative Electron Flow in Photosystem I in Wheat Leaves |
title_fullStr | Oxidation of P700 Induces Alternative Electron Flow in Photosystem I in Wheat Leaves |
title_full_unstemmed | Oxidation of P700 Induces Alternative Electron Flow in Photosystem I in Wheat Leaves |
title_short | Oxidation of P700 Induces Alternative Electron Flow in Photosystem I in Wheat Leaves |
title_sort | oxidation of p700 induces alternative electron flow in photosystem i in wheat leaves |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6631986/ https://www.ncbi.nlm.nih.gov/pubmed/31195693 http://dx.doi.org/10.3390/plants8060152 |
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