Cargando…
Co‐catabolism of arginine and succinate drives symbiotic nitrogen fixation
Biological nitrogen fixation emerging from the symbiosis between bacteria and crop plants holds promise to increase the sustainability of agriculture. One of the biggest hurdles for the engineering of nitrogen‐fixing organisms is an incomplete knowledge of metabolic interactions between microbe and...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7268258/ https://www.ncbi.nlm.nih.gov/pubmed/32490601 http://dx.doi.org/10.15252/msb.20199419 |
_version_ | 1783541577479618560 |
---|---|
author | Flores‐Tinoco, Carlos Eduardo Tschan, Flavia Fuhrer, Tobias Margot, Céline Sauer, Uwe Christen, Matthias Christen, Beat |
author_facet | Flores‐Tinoco, Carlos Eduardo Tschan, Flavia Fuhrer, Tobias Margot, Céline Sauer, Uwe Christen, Matthias Christen, Beat |
author_sort | Flores‐Tinoco, Carlos Eduardo |
collection | PubMed |
description | Biological nitrogen fixation emerging from the symbiosis between bacteria and crop plants holds promise to increase the sustainability of agriculture. One of the biggest hurdles for the engineering of nitrogen‐fixing organisms is an incomplete knowledge of metabolic interactions between microbe and plant. In contrast to the previously assumed supply of only succinate, we describe here the CATCH‐N cycle as a novel metabolic pathway that co‐catabolizes plant‐provided arginine and succinate to drive the energy‐demanding process of symbiotic nitrogen fixation in endosymbiotic rhizobia. Using systems biology, isotope labeling studies and transposon sequencing in conjunction with biochemical characterization, we uncovered highly redundant network components of the CATCH‐N cycle including transaminases that interlink the co‐catabolism of arginine and succinate. The CATCH‐N cycle uses N(2) as an additional sink for reductant and therefore delivers up to 25% higher yields of nitrogen than classical arginine catabolism—two alanines and three ammonium ions are secreted for each input of arginine and succinate. We argue that the CATCH‐N cycle has evolved as part of a synergistic interaction to sustain bacterial metabolism in the microoxic and highly acid environment of symbiosomes. Thus, the CATCH‐N cycle entangles the metabolism of both partners to promote symbiosis. Our results provide a theoretical framework and metabolic blueprint for the rational design of plants and plant‐associated organisms with new properties to improve nitrogen fixation. |
format | Online Article Text |
id | pubmed-7268258 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-72682582020-06-04 Co‐catabolism of arginine and succinate drives symbiotic nitrogen fixation Flores‐Tinoco, Carlos Eduardo Tschan, Flavia Fuhrer, Tobias Margot, Céline Sauer, Uwe Christen, Matthias Christen, Beat Mol Syst Biol Articles Biological nitrogen fixation emerging from the symbiosis between bacteria and crop plants holds promise to increase the sustainability of agriculture. One of the biggest hurdles for the engineering of nitrogen‐fixing organisms is an incomplete knowledge of metabolic interactions between microbe and plant. In contrast to the previously assumed supply of only succinate, we describe here the CATCH‐N cycle as a novel metabolic pathway that co‐catabolizes plant‐provided arginine and succinate to drive the energy‐demanding process of symbiotic nitrogen fixation in endosymbiotic rhizobia. Using systems biology, isotope labeling studies and transposon sequencing in conjunction with biochemical characterization, we uncovered highly redundant network components of the CATCH‐N cycle including transaminases that interlink the co‐catabolism of arginine and succinate. The CATCH‐N cycle uses N(2) as an additional sink for reductant and therefore delivers up to 25% higher yields of nitrogen than classical arginine catabolism—two alanines and three ammonium ions are secreted for each input of arginine and succinate. We argue that the CATCH‐N cycle has evolved as part of a synergistic interaction to sustain bacterial metabolism in the microoxic and highly acid environment of symbiosomes. Thus, the CATCH‐N cycle entangles the metabolism of both partners to promote symbiosis. Our results provide a theoretical framework and metabolic blueprint for the rational design of plants and plant‐associated organisms with new properties to improve nitrogen fixation. John Wiley and Sons Inc. 2020-06-03 /pmc/articles/PMC7268258/ /pubmed/32490601 http://dx.doi.org/10.15252/msb.20199419 Text en © 2020 The Authors. Published under the terms of the CC BY 4.0 license This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Articles Flores‐Tinoco, Carlos Eduardo Tschan, Flavia Fuhrer, Tobias Margot, Céline Sauer, Uwe Christen, Matthias Christen, Beat Co‐catabolism of arginine and succinate drives symbiotic nitrogen fixation |
title | Co‐catabolism of arginine and succinate drives symbiotic nitrogen fixation |
title_full | Co‐catabolism of arginine and succinate drives symbiotic nitrogen fixation |
title_fullStr | Co‐catabolism of arginine and succinate drives symbiotic nitrogen fixation |
title_full_unstemmed | Co‐catabolism of arginine and succinate drives symbiotic nitrogen fixation |
title_short | Co‐catabolism of arginine and succinate drives symbiotic nitrogen fixation |
title_sort | co‐catabolism of arginine and succinate drives symbiotic nitrogen fixation |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7268258/ https://www.ncbi.nlm.nih.gov/pubmed/32490601 http://dx.doi.org/10.15252/msb.20199419 |
work_keys_str_mv | AT florestinococarloseduardo cocatabolismofarginineandsuccinatedrivessymbioticnitrogenfixation AT tschanflavia cocatabolismofarginineandsuccinatedrivessymbioticnitrogenfixation AT fuhrertobias cocatabolismofarginineandsuccinatedrivessymbioticnitrogenfixation AT margotceline cocatabolismofarginineandsuccinatedrivessymbioticnitrogenfixation AT saueruwe cocatabolismofarginineandsuccinatedrivessymbioticnitrogenfixation AT christenmatthias cocatabolismofarginineandsuccinatedrivessymbioticnitrogenfixation AT christenbeat cocatabolismofarginineandsuccinatedrivessymbioticnitrogenfixation |