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The contribution of PIP2-type aquaporins to photosynthetic response to increased vapour pressure deficit
The roles of different plasma membrane aquaporins (PIPs) in leaf-level gas exchange of Arabidopsis thaliana were examined using knockout mutants. Since multiple Arabidopsis PIPs are implicated in CO(2) transport across cell membranes, we focused on identifying the effects of the knockout mutations o...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8219038/ https://www.ncbi.nlm.nih.gov/pubmed/33928350 http://dx.doi.org/10.1093/jxb/erab187 |
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author | Israel, David Khan, Shanjida Warren, Charles R Zwiazek, Janusz J Robson, T Matthew |
author_facet | Israel, David Khan, Shanjida Warren, Charles R Zwiazek, Janusz J Robson, T Matthew |
author_sort | Israel, David |
collection | PubMed |
description | The roles of different plasma membrane aquaporins (PIPs) in leaf-level gas exchange of Arabidopsis thaliana were examined using knockout mutants. Since multiple Arabidopsis PIPs are implicated in CO(2) transport across cell membranes, we focused on identifying the effects of the knockout mutations on photosynthesis, and whether they are mediated through the control of stomatal conductance of water vapour (g(s)), mesophyll conductance of CO(2) (g(m)), or both. We grew Arabidopsis plants in low and high humidity environments and found that the contribution of PIPs to g(s) was larger under low air humidity when the evaporative demand was high, whereas any effect of a lack of PIP function was minimal under higher humidity. The pip2;4 knockout mutant had 44% higher g(s) than wild-type plants under low humidity, which in turn resulted in an increased net photosynthetic rate (A(net)). We also observed a 23% increase in whole-plant transpiration (E) for this knockout mutant. The lack of functional plasma membrane aquaporin AtPIP2;5 did not affect g(s) or E, but resulted in homeostasis of g(m) despite changes in humidity, indicating a possible role in regulating CO(2) membrane permeability. CO(2) transport measurements in yeast expressing AtPIP2;5 confirmed that this aquaporin is indeed permeable to CO(2). |
format | Online Article Text |
id | pubmed-8219038 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-82190382021-06-23 The contribution of PIP2-type aquaporins to photosynthetic response to increased vapour pressure deficit Israel, David Khan, Shanjida Warren, Charles R Zwiazek, Janusz J Robson, T Matthew J Exp Bot Research Papers The roles of different plasma membrane aquaporins (PIPs) in leaf-level gas exchange of Arabidopsis thaliana were examined using knockout mutants. Since multiple Arabidopsis PIPs are implicated in CO(2) transport across cell membranes, we focused on identifying the effects of the knockout mutations on photosynthesis, and whether they are mediated through the control of stomatal conductance of water vapour (g(s)), mesophyll conductance of CO(2) (g(m)), or both. We grew Arabidopsis plants in low and high humidity environments and found that the contribution of PIPs to g(s) was larger under low air humidity when the evaporative demand was high, whereas any effect of a lack of PIP function was minimal under higher humidity. The pip2;4 knockout mutant had 44% higher g(s) than wild-type plants under low humidity, which in turn resulted in an increased net photosynthetic rate (A(net)). We also observed a 23% increase in whole-plant transpiration (E) for this knockout mutant. The lack of functional plasma membrane aquaporin AtPIP2;5 did not affect g(s) or E, but resulted in homeostasis of g(m) despite changes in humidity, indicating a possible role in regulating CO(2) membrane permeability. CO(2) transport measurements in yeast expressing AtPIP2;5 confirmed that this aquaporin is indeed permeable to CO(2). Oxford University Press 2021-04-30 /pmc/articles/PMC8219038/ /pubmed/33928350 http://dx.doi.org/10.1093/jxb/erab187 Text en © The Author(s) 2021. Published by Oxford University Press on behalf of the Society for Experimental Biology. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Papers Israel, David Khan, Shanjida Warren, Charles R Zwiazek, Janusz J Robson, T Matthew The contribution of PIP2-type aquaporins to photosynthetic response to increased vapour pressure deficit |
title | The contribution of PIP2-type aquaporins to photosynthetic response to increased vapour pressure deficit |
title_full | The contribution of PIP2-type aquaporins to photosynthetic response to increased vapour pressure deficit |
title_fullStr | The contribution of PIP2-type aquaporins to photosynthetic response to increased vapour pressure deficit |
title_full_unstemmed | The contribution of PIP2-type aquaporins to photosynthetic response to increased vapour pressure deficit |
title_short | The contribution of PIP2-type aquaporins to photosynthetic response to increased vapour pressure deficit |
title_sort | contribution of pip2-type aquaporins to photosynthetic response to increased vapour pressure deficit |
topic | Research Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8219038/ https://www.ncbi.nlm.nih.gov/pubmed/33928350 http://dx.doi.org/10.1093/jxb/erab187 |
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