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Sulfate is transported at significant rates through the symbiosome membrane and is crucial for nitrogenase biosynthesis
Legume–rhizobia symbioses play a major role in food production for an ever growing human population. In this symbiosis, dinitrogen is reduced (“fixed”) to ammonia by the rhizobial nitrogenase enzyme complex and is secreted to the plant host cells, whereas dicarboxylic acids derived from photosynthet...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6446814/ https://www.ncbi.nlm.nih.gov/pubmed/30443991 http://dx.doi.org/10.1111/pce.13481 |
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author | Schneider, Sebastian Schintlmeister, Arno Becana, Manuel Wagner, Michael Woebken, Dagmar Wienkoop, Stefanie |
author_facet | Schneider, Sebastian Schintlmeister, Arno Becana, Manuel Wagner, Michael Woebken, Dagmar Wienkoop, Stefanie |
author_sort | Schneider, Sebastian |
collection | PubMed |
description | Legume–rhizobia symbioses play a major role in food production for an ever growing human population. In this symbiosis, dinitrogen is reduced (“fixed”) to ammonia by the rhizobial nitrogenase enzyme complex and is secreted to the plant host cells, whereas dicarboxylic acids derived from photosynthetically produced sucrose are transported into the symbiosomes and serve as respiratory substrates for the bacteroids. The symbiosome membrane contains high levels of SST1 protein, a sulfate transporter. Sulfate is an essential nutrient for all living organisms, but its importance for symbiotic nitrogen fixation and nodule metabolism has long been underestimated. Using chemical imaging, we demonstrate that the bacteroids take up 20‐fold more sulfate than the nodule host cells. Furthermore, we show that nitrogenase biosynthesis relies on high levels of imported sulfate, making sulfur as essential as carbon for the regulation and functioning of symbiotic nitrogen fixation. Our findings thus establish the importance of sulfate and its active transport for the plant–microbe interaction that is most relevant for agriculture and soil fertility. |
format | Online Article Text |
id | pubmed-6446814 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-64468142019-04-10 Sulfate is transported at significant rates through the symbiosome membrane and is crucial for nitrogenase biosynthesis Schneider, Sebastian Schintlmeister, Arno Becana, Manuel Wagner, Michael Woebken, Dagmar Wienkoop, Stefanie Plant Cell Environ Original Articles Legume–rhizobia symbioses play a major role in food production for an ever growing human population. In this symbiosis, dinitrogen is reduced (“fixed”) to ammonia by the rhizobial nitrogenase enzyme complex and is secreted to the plant host cells, whereas dicarboxylic acids derived from photosynthetically produced sucrose are transported into the symbiosomes and serve as respiratory substrates for the bacteroids. The symbiosome membrane contains high levels of SST1 protein, a sulfate transporter. Sulfate is an essential nutrient for all living organisms, but its importance for symbiotic nitrogen fixation and nodule metabolism has long been underestimated. Using chemical imaging, we demonstrate that the bacteroids take up 20‐fold more sulfate than the nodule host cells. Furthermore, we show that nitrogenase biosynthesis relies on high levels of imported sulfate, making sulfur as essential as carbon for the regulation and functioning of symbiotic nitrogen fixation. Our findings thus establish the importance of sulfate and its active transport for the plant–microbe interaction that is most relevant for agriculture and soil fertility. John Wiley and Sons Inc. 2019-01-28 2019-04 /pmc/articles/PMC6446814/ /pubmed/30443991 http://dx.doi.org/10.1111/pce.13481 Text en © 2018 The Authors Plant, Cell & Environment Published by John Wiley & Sons Ltd 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 | Original Articles Schneider, Sebastian Schintlmeister, Arno Becana, Manuel Wagner, Michael Woebken, Dagmar Wienkoop, Stefanie Sulfate is transported at significant rates through the symbiosome membrane and is crucial for nitrogenase biosynthesis |
title | Sulfate is transported at significant rates through the symbiosome membrane and is crucial for nitrogenase biosynthesis |
title_full | Sulfate is transported at significant rates through the symbiosome membrane and is crucial for nitrogenase biosynthesis |
title_fullStr | Sulfate is transported at significant rates through the symbiosome membrane and is crucial for nitrogenase biosynthesis |
title_full_unstemmed | Sulfate is transported at significant rates through the symbiosome membrane and is crucial for nitrogenase biosynthesis |
title_short | Sulfate is transported at significant rates through the symbiosome membrane and is crucial for nitrogenase biosynthesis |
title_sort | sulfate is transported at significant rates through the symbiosome membrane and is crucial for nitrogenase biosynthesis |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6446814/ https://www.ncbi.nlm.nih.gov/pubmed/30443991 http://dx.doi.org/10.1111/pce.13481 |
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