Cargando…

The role of Cytochrome b(6)f in the control of steady-state photosynthesis: a conceptual and quantitative model

Here, we present a conceptual and quantitative model to describe the role of the Cytochrome [Formula: see text] complex in controlling steady-state electron transport in [Formula: see text] leaves. The model is based on new experimental methods to diagnose the maximum activity of Cyt [Formula: see t...

Descripción completa

Detalles Bibliográficos
Autores principales: Johnson, J. E., Berry, J. A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Netherlands 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8292351/
https://www.ncbi.nlm.nih.gov/pubmed/33999328
http://dx.doi.org/10.1007/s11120-021-00840-4
_version_ 1783724814653980672
author Johnson, J. E.
Berry, J. A.
author_facet Johnson, J. E.
Berry, J. A.
author_sort Johnson, J. E.
collection PubMed
description Here, we present a conceptual and quantitative model to describe the role of the Cytochrome [Formula: see text] complex in controlling steady-state electron transport in [Formula: see text] leaves. The model is based on new experimental methods to diagnose the maximum activity of Cyt [Formula: see text] in vivo, and to identify conditions under which photosynthetic control of Cyt [Formula: see text] is active or relaxed. With these approaches, we demonstrate that Cyt [Formula: see text] controls the trade-off between the speed and efficiency of electron transport under limiting light, and functions as a metabolic switch that transfers control to carbon metabolism under saturating light. We also present evidence that the onset of photosynthetic control of Cyt [Formula: see text] occurs within milliseconds of exposure to saturating light, much more quickly than the induction of non-photochemical quenching. We propose that photosynthetic control is the primary means of photoprotection and functions to manage excitation pressure, whereas non-photochemical quenching functions to manage excitation balance. We use these findings to extend the Farquhar et al. (Planta 149:78–90, 1980) model of [Formula: see text] photosynthesis to include a mechanistic description of the electron transport system. This framework relates the light captured by PS I and PS II to the energy and mass fluxes linking the photoacts with Cyt [Formula: see text] , the ATP synthase, and Rubisco. It enables quantitative interpretation of pulse-amplitude modulated fluorometry and gas-exchange measurements, providing a new basis for analyzing how the electron transport system coordinates the supply of Fd, NADPH, and ATP with the dynamic demands of carbon metabolism, how efficient use of light is achieved under limiting light, and how photoprotection is achieved under saturating light. The model is designed to support forward as well as inverse applications. It can either be used in a stand-alone mode at the leaf-level or coupled to other models that resolve finer-scale or coarser-scale phenomena.
format Online
Article
Text
id pubmed-8292351
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Springer Netherlands
record_format MEDLINE/PubMed
spelling pubmed-82923512021-07-23 The role of Cytochrome b(6)f in the control of steady-state photosynthesis: a conceptual and quantitative model Johnson, J. E. Berry, J. A. Photosynth Res Original Article Here, we present a conceptual and quantitative model to describe the role of the Cytochrome [Formula: see text] complex in controlling steady-state electron transport in [Formula: see text] leaves. The model is based on new experimental methods to diagnose the maximum activity of Cyt [Formula: see text] in vivo, and to identify conditions under which photosynthetic control of Cyt [Formula: see text] is active or relaxed. With these approaches, we demonstrate that Cyt [Formula: see text] controls the trade-off between the speed and efficiency of electron transport under limiting light, and functions as a metabolic switch that transfers control to carbon metabolism under saturating light. We also present evidence that the onset of photosynthetic control of Cyt [Formula: see text] occurs within milliseconds of exposure to saturating light, much more quickly than the induction of non-photochemical quenching. We propose that photosynthetic control is the primary means of photoprotection and functions to manage excitation pressure, whereas non-photochemical quenching functions to manage excitation balance. We use these findings to extend the Farquhar et al. (Planta 149:78–90, 1980) model of [Formula: see text] photosynthesis to include a mechanistic description of the electron transport system. This framework relates the light captured by PS I and PS II to the energy and mass fluxes linking the photoacts with Cyt [Formula: see text] , the ATP synthase, and Rubisco. It enables quantitative interpretation of pulse-amplitude modulated fluorometry and gas-exchange measurements, providing a new basis for analyzing how the electron transport system coordinates the supply of Fd, NADPH, and ATP with the dynamic demands of carbon metabolism, how efficient use of light is achieved under limiting light, and how photoprotection is achieved under saturating light. The model is designed to support forward as well as inverse applications. It can either be used in a stand-alone mode at the leaf-level or coupled to other models that resolve finer-scale or coarser-scale phenomena. Springer Netherlands 2021-05-17 2021 /pmc/articles/PMC8292351/ /pubmed/33999328 http://dx.doi.org/10.1007/s11120-021-00840-4 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Original Article
Johnson, J. E.
Berry, J. A.
The role of Cytochrome b(6)f in the control of steady-state photosynthesis: a conceptual and quantitative model
title The role of Cytochrome b(6)f in the control of steady-state photosynthesis: a conceptual and quantitative model
title_full The role of Cytochrome b(6)f in the control of steady-state photosynthesis: a conceptual and quantitative model
title_fullStr The role of Cytochrome b(6)f in the control of steady-state photosynthesis: a conceptual and quantitative model
title_full_unstemmed The role of Cytochrome b(6)f in the control of steady-state photosynthesis: a conceptual and quantitative model
title_short The role of Cytochrome b(6)f in the control of steady-state photosynthesis: a conceptual and quantitative model
title_sort role of cytochrome b(6)f in the control of steady-state photosynthesis: a conceptual and quantitative model
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8292351/
https://www.ncbi.nlm.nih.gov/pubmed/33999328
http://dx.doi.org/10.1007/s11120-021-00840-4
work_keys_str_mv AT johnsonje theroleofcytochromeb6finthecontrolofsteadystatephotosynthesisaconceptualandquantitativemodel
AT berryja theroleofcytochromeb6finthecontrolofsteadystatephotosynthesisaconceptualandquantitativemodel
AT johnsonje roleofcytochromeb6finthecontrolofsteadystatephotosynthesisaconceptualandquantitativemodel
AT berryja roleofcytochromeb6finthecontrolofsteadystatephotosynthesisaconceptualandquantitativemodel