Cargando…
Interaction of Nitrate Assimilation and Photorespiration at Elevated CO(2)
It has been shown repeatedly that exposure to elevated atmospheric CO(2) causes an increased C/N ratio of plant biomass that could result from either increased carbon or – in relation to C acquisition - reduced nitrogen assimilation. Possible reasons for diminished nitrogen assimilation are controve...
Autores principales: | , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9284316/ https://www.ncbi.nlm.nih.gov/pubmed/35845694 http://dx.doi.org/10.3389/fpls.2022.897924 |
_version_ | 1784747533956808704 |
---|---|
author | Krämer, Konrad Brock, Judith Heyer, Arnd G. |
author_facet | Krämer, Konrad Brock, Judith Heyer, Arnd G. |
author_sort | Krämer, Konrad |
collection | PubMed |
description | It has been shown repeatedly that exposure to elevated atmospheric CO(2) causes an increased C/N ratio of plant biomass that could result from either increased carbon or – in relation to C acquisition - reduced nitrogen assimilation. Possible reasons for diminished nitrogen assimilation are controversial, but an impact of reduced photorespiration at elevated CO(2) has frequently been implied. Using a mutant defective in peroxisomal hydroxy-pyruvate reductase (hpr1-1) that is hampered in photorespiratory turnover, we show that indeed, photorespiration stimulates the glutamine-synthetase 2 (GS) / glutamine-oxoglutarate-aminotransferase (GOGAT) cycle, which channels ammonia into amino acid synthesis. However, mathematical flux simulations demonstrated that nitrate assimilation was not reduced at elevated CO(2), pointing to a dilution of nitrogen containing compounds by assimilated carbon at elevated CO(2). The massive growth reduction in the hpr1-1 mutant does not appear to result from nitrogen starvation. Model simulations yield evidence for a loss of cellular energy that is consumed in supporting high flux through the GS/GOGAT cycle that results from inefficient removal of photorespiratory intermediates. This causes a futile cycling of glycolate and hydroxy-pyruvate. In addition to that, accumulation of serine and glycine as well as carboxylates in the mutant creates a metabolic imbalance that could contribute to growth reduction. |
format | Online Article Text |
id | pubmed-9284316 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-92843162022-07-16 Interaction of Nitrate Assimilation and Photorespiration at Elevated CO(2) Krämer, Konrad Brock, Judith Heyer, Arnd G. Front Plant Sci Plant Science It has been shown repeatedly that exposure to elevated atmospheric CO(2) causes an increased C/N ratio of plant biomass that could result from either increased carbon or – in relation to C acquisition - reduced nitrogen assimilation. Possible reasons for diminished nitrogen assimilation are controversial, but an impact of reduced photorespiration at elevated CO(2) has frequently been implied. Using a mutant defective in peroxisomal hydroxy-pyruvate reductase (hpr1-1) that is hampered in photorespiratory turnover, we show that indeed, photorespiration stimulates the glutamine-synthetase 2 (GS) / glutamine-oxoglutarate-aminotransferase (GOGAT) cycle, which channels ammonia into amino acid synthesis. However, mathematical flux simulations demonstrated that nitrate assimilation was not reduced at elevated CO(2), pointing to a dilution of nitrogen containing compounds by assimilated carbon at elevated CO(2). The massive growth reduction in the hpr1-1 mutant does not appear to result from nitrogen starvation. Model simulations yield evidence for a loss of cellular energy that is consumed in supporting high flux through the GS/GOGAT cycle that results from inefficient removal of photorespiratory intermediates. This causes a futile cycling of glycolate and hydroxy-pyruvate. In addition to that, accumulation of serine and glycine as well as carboxylates in the mutant creates a metabolic imbalance that could contribute to growth reduction. Frontiers Media S.A. 2022-07-01 /pmc/articles/PMC9284316/ /pubmed/35845694 http://dx.doi.org/10.3389/fpls.2022.897924 Text en Copyright © 2022 Krämer, Brock and Heyer. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Plant Science Krämer, Konrad Brock, Judith Heyer, Arnd G. Interaction of Nitrate Assimilation and Photorespiration at Elevated CO(2) |
title | Interaction of Nitrate Assimilation and Photorespiration at Elevated CO(2) |
title_full | Interaction of Nitrate Assimilation and Photorespiration at Elevated CO(2) |
title_fullStr | Interaction of Nitrate Assimilation and Photorespiration at Elevated CO(2) |
title_full_unstemmed | Interaction of Nitrate Assimilation and Photorespiration at Elevated CO(2) |
title_short | Interaction of Nitrate Assimilation and Photorespiration at Elevated CO(2) |
title_sort | interaction of nitrate assimilation and photorespiration at elevated co(2) |
topic | Plant Science |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9284316/ https://www.ncbi.nlm.nih.gov/pubmed/35845694 http://dx.doi.org/10.3389/fpls.2022.897924 |
work_keys_str_mv | AT kramerkonrad interactionofnitrateassimilationandphotorespirationatelevatedco2 AT brockjudith interactionofnitrateassimilationandphotorespirationatelevatedco2 AT heyerarndg interactionofnitrateassimilationandphotorespirationatelevatedco2 |