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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...

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Autores principales: Flores‐Tinoco, Carlos Eduardo, Tschan, Flavia, Fuhrer, Tobias, Margot, Céline, Sauer, Uwe, Christen, Matthias, Christen, Beat
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
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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.
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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
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