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Reductions in mesophyll and guard cell photosynthesis impact on the control of stomatal responses to light and CO(2)

Transgenic antisense tobacco plants with a range of reductions in sedoheptulose-1,7-bisphosphatase (SBPase) activity were used to investigate the role of photosynthesis in stomatal opening responses. High resolution chlorophyll a fluorescence imaging showed that the quantum efficiency of photosystem...

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Autores principales: Lawson, Tracy, Lefebvre, Stephane, Baker, Neil R., Morison, James I. L., Raines, Christine A.
Formato: Texto
Lenguaje:English
Publicado: Oxford University Press 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2561148/
https://www.ncbi.nlm.nih.gov/pubmed/18836187
http://dx.doi.org/10.1093/jxb/ern211
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author Lawson, Tracy
Lefebvre, Stephane
Baker, Neil R.
Morison, James I. L.
Raines, Christine A.
author_facet Lawson, Tracy
Lefebvre, Stephane
Baker, Neil R.
Morison, James I. L.
Raines, Christine A.
author_sort Lawson, Tracy
collection PubMed
description Transgenic antisense tobacco plants with a range of reductions in sedoheptulose-1,7-bisphosphatase (SBPase) activity were used to investigate the role of photosynthesis in stomatal opening responses. High resolution chlorophyll a fluorescence imaging showed that the quantum efficiency of photosystem II electron transport (F(q)(′)/F(m)(′)) was decreased similarly in both guard and mesophyll cells of the SBPase antisense plants compared to the wild-type plants. This demonstrated for the first time that photosynthetic operating efficiency in the guard cells responds to changes in the regeneration capacity of the Calvin cycle. The rate of stomatal opening in response to a 30 min, 10-fold step increase in red photon flux density in the leaves from the SBPase antisense plants was significantly greater than wild-type plants. Final stomatal conductance under red and mixed blue/red irradiance was greater in the antisense plants than in the wild-type control plants despite lower CO(2) assimilation rates and higher internal CO(2) concentrations. Increasing CO(2) concentration resulted in a similar stomatal closing response in wild-type and antisense plants when measured in red light. However, in the antisense plants with small reductions in SBPase activity greater stomatal conductances were observed at all C(i) levels. Together, these data suggest that the primary light-induced opening or CO(2)-dependent closing response of stomata is not dependent upon guard or mesophyll cell photosynthetic capacity, but that photosynthetic electron transport, or its end-products, regulate the control of stomatal responses to light and CO(2).
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spelling pubmed-25611482009-02-25 Reductions in mesophyll and guard cell photosynthesis impact on the control of stomatal responses to light and CO(2) Lawson, Tracy Lefebvre, Stephane Baker, Neil R. Morison, James I. L. Raines, Christine A. J Exp Bot Research Papers Transgenic antisense tobacco plants with a range of reductions in sedoheptulose-1,7-bisphosphatase (SBPase) activity were used to investigate the role of photosynthesis in stomatal opening responses. High resolution chlorophyll a fluorescence imaging showed that the quantum efficiency of photosystem II electron transport (F(q)(′)/F(m)(′)) was decreased similarly in both guard and mesophyll cells of the SBPase antisense plants compared to the wild-type plants. This demonstrated for the first time that photosynthetic operating efficiency in the guard cells responds to changes in the regeneration capacity of the Calvin cycle. The rate of stomatal opening in response to a 30 min, 10-fold step increase in red photon flux density in the leaves from the SBPase antisense plants was significantly greater than wild-type plants. Final stomatal conductance under red and mixed blue/red irradiance was greater in the antisense plants than in the wild-type control plants despite lower CO(2) assimilation rates and higher internal CO(2) concentrations. Increasing CO(2) concentration resulted in a similar stomatal closing response in wild-type and antisense plants when measured in red light. However, in the antisense plants with small reductions in SBPase activity greater stomatal conductances were observed at all C(i) levels. Together, these data suggest that the primary light-induced opening or CO(2)-dependent closing response of stomata is not dependent upon guard or mesophyll cell photosynthetic capacity, but that photosynthetic electron transport, or its end-products, regulate the control of stomatal responses to light and CO(2). Oxford University Press 2008-10 /pmc/articles/PMC2561148/ /pubmed/18836187 http://dx.doi.org/10.1093/jxb/ern211 Text en © 2008 The Author(s). This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.0/uk/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. This paper is available online free of all access charges (see http://jxb.oxfordjournals.org/open_access.html for further details)
spellingShingle Research Papers
Lawson, Tracy
Lefebvre, Stephane
Baker, Neil R.
Morison, James I. L.
Raines, Christine A.
Reductions in mesophyll and guard cell photosynthesis impact on the control of stomatal responses to light and CO(2)
title Reductions in mesophyll and guard cell photosynthesis impact on the control of stomatal responses to light and CO(2)
title_full Reductions in mesophyll and guard cell photosynthesis impact on the control of stomatal responses to light and CO(2)
title_fullStr Reductions in mesophyll and guard cell photosynthesis impact on the control of stomatal responses to light and CO(2)
title_full_unstemmed Reductions in mesophyll and guard cell photosynthesis impact on the control of stomatal responses to light and CO(2)
title_short Reductions in mesophyll and guard cell photosynthesis impact on the control of stomatal responses to light and CO(2)
title_sort reductions in mesophyll and guard cell photosynthesis impact on the control of stomatal responses to light and co(2)
topic Research Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2561148/
https://www.ncbi.nlm.nih.gov/pubmed/18836187
http://dx.doi.org/10.1093/jxb/ern211
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