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Physiological performance of transplastomic tobacco plants overexpressing aquaporin AQP1 in chloroplast membranes

The leaf mesophyll CO(2) conductance and the concentration of CO(2) within the chloroplast are major factors affecting photosynthetic performance. Previous studies have shown that the aquaporin NtAQP1 (which localizes to the plasma membrane and chloroplast inner envelope membrane) is involved in CO(...

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Autores principales: Fernández-San Millán, Alicia, Aranjuelo, Iker, Douthe, Cyril, Nadal, Miquel, Ancín, María, Larraya, Luis, Farran, Inmaculada, Flexas, Jaume, Veramendi, Jon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6022695/
https://www.ncbi.nlm.nih.gov/pubmed/29912355
http://dx.doi.org/10.1093/jxb/ery148
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author Fernández-San Millán, Alicia
Aranjuelo, Iker
Douthe, Cyril
Nadal, Miquel
Ancín, María
Larraya, Luis
Farran, Inmaculada
Flexas, Jaume
Veramendi, Jon
author_facet Fernández-San Millán, Alicia
Aranjuelo, Iker
Douthe, Cyril
Nadal, Miquel
Ancín, María
Larraya, Luis
Farran, Inmaculada
Flexas, Jaume
Veramendi, Jon
author_sort Fernández-San Millán, Alicia
collection PubMed
description The leaf mesophyll CO(2) conductance and the concentration of CO(2) within the chloroplast are major factors affecting photosynthetic performance. Previous studies have shown that the aquaporin NtAQP1 (which localizes to the plasma membrane and chloroplast inner envelope membrane) is involved in CO(2) permeability in the chloroplast. Levels of NtAQP1 in plants genetically engineered to overexpress the protein correlated positively with leaf mesophyll CO(2) conductance and photosynthetic rate. In these studies, the nuclear transformation method used led to changes in NtAQP1 levels in the plasma membrane and the chloroplast inner envelope membrane. In the present work, NtAQP1 levels were increased up to 16-fold in the chloroplast membranes alone by the overexpression of NtAQP1 from the plastid genome. Despite the high NtAQP1 levels achieved, transplastomic plants showed lower photosynthetic rates than wild-type plants. This result was associated with lower Rubisco maximum carboxylation rate and ribulose 1,5-bisphosphate regeneration. Transplastomic plants showed reduced mesophyll CO(2) conductance but no changes in chloroplast CO(2) concentration. The absence of differences in chloroplast CO(2) concentration was associated with the lower CO(2) fixation activity of the transplastomic plants. These findings suggest that non-functional pores of recombinant NtAQP1 may be produced in the chloroplast inner envelope membrane.
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spelling pubmed-60226952018-07-05 Physiological performance of transplastomic tobacco plants overexpressing aquaporin AQP1 in chloroplast membranes Fernández-San Millán, Alicia Aranjuelo, Iker Douthe, Cyril Nadal, Miquel Ancín, María Larraya, Luis Farran, Inmaculada Flexas, Jaume Veramendi, Jon J Exp Bot Research Papers The leaf mesophyll CO(2) conductance and the concentration of CO(2) within the chloroplast are major factors affecting photosynthetic performance. Previous studies have shown that the aquaporin NtAQP1 (which localizes to the plasma membrane and chloroplast inner envelope membrane) is involved in CO(2) permeability in the chloroplast. Levels of NtAQP1 in plants genetically engineered to overexpress the protein correlated positively with leaf mesophyll CO(2) conductance and photosynthetic rate. In these studies, the nuclear transformation method used led to changes in NtAQP1 levels in the plasma membrane and the chloroplast inner envelope membrane. In the present work, NtAQP1 levels were increased up to 16-fold in the chloroplast membranes alone by the overexpression of NtAQP1 from the plastid genome. Despite the high NtAQP1 levels achieved, transplastomic plants showed lower photosynthetic rates than wild-type plants. This result was associated with lower Rubisco maximum carboxylation rate and ribulose 1,5-bisphosphate regeneration. Transplastomic plants showed reduced mesophyll CO(2) conductance but no changes in chloroplast CO(2) concentration. The absence of differences in chloroplast CO(2) concentration was associated with the lower CO(2) fixation activity of the transplastomic plants. These findings suggest that non-functional pores of recombinant NtAQP1 may be produced in the chloroplast inner envelope membrane. Oxford University Press 2018-07-10 2018-04-18 /pmc/articles/PMC6022695/ /pubmed/29912355 http://dx.doi.org/10.1093/jxb/ery148 Text en © The Author(s) 2018. Published by Oxford University Press on behalf of the Society for Experimental Biology. http://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/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Papers
Fernández-San Millán, Alicia
Aranjuelo, Iker
Douthe, Cyril
Nadal, Miquel
Ancín, María
Larraya, Luis
Farran, Inmaculada
Flexas, Jaume
Veramendi, Jon
Physiological performance of transplastomic tobacco plants overexpressing aquaporin AQP1 in chloroplast membranes
title Physiological performance of transplastomic tobacco plants overexpressing aquaporin AQP1 in chloroplast membranes
title_full Physiological performance of transplastomic tobacco plants overexpressing aquaporin AQP1 in chloroplast membranes
title_fullStr Physiological performance of transplastomic tobacco plants overexpressing aquaporin AQP1 in chloroplast membranes
title_full_unstemmed Physiological performance of transplastomic tobacco plants overexpressing aquaporin AQP1 in chloroplast membranes
title_short Physiological performance of transplastomic tobacco plants overexpressing aquaporin AQP1 in chloroplast membranes
title_sort physiological performance of transplastomic tobacco plants overexpressing aquaporin aqp1 in chloroplast membranes
topic Research Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6022695/
https://www.ncbi.nlm.nih.gov/pubmed/29912355
http://dx.doi.org/10.1093/jxb/ery148
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