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N(2) Fixation in Trichodesmium Does Not Require Spatial Segregation from Photosynthesis
The dominant marine filamentous N(2) fixer, Trichodesmium, conducts photosynthesis and N(2) fixation during the daytime. Because N(2) fixation is sensitive to O(2), some previous studies suggested that spatial segregation of N(2) fixation and photosynthesis is essential in Trichodesmium. However, th...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society for Microbiology
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9426587/ https://www.ncbi.nlm.nih.gov/pubmed/35862813 http://dx.doi.org/10.1128/msystems.00538-22 |
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author | Luo, Weicheng Inomura, Keisuke Zhang, Han Luo, Ya-Wei |
author_facet | Luo, Weicheng Inomura, Keisuke Zhang, Han Luo, Ya-Wei |
author_sort | Luo, Weicheng |
collection | PubMed |
description | The dominant marine filamentous N(2) fixer, Trichodesmium, conducts photosynthesis and N(2) fixation during the daytime. Because N(2) fixation is sensitive to O(2), some previous studies suggested that spatial segregation of N(2) fixation and photosynthesis is essential in Trichodesmium. However, this hypothesis conflicts with some observations where all the cells contain both photosystems and the N(2)-fixing enzyme nitrogenase. Here, we construct a systematic model simulating Trichodesmium metabolism, showing that the hypothetical spatial segregation is probably useless in increasing the Trichodesmium growth and N(2) fixation, unless substances can efficiently transfer among cells with low loss to the environment. The model suggests that Trichodesmium accumulates fixed carbon in the morning and uses that in respiratory protection to reduce intracellular O(2) during the mid-daytime, when photosynthesis is downregulated, allowing the occurrence of N(2) fixation. A cell membrane barrier against O(2) and alternative non-O(2) evolving electron transfer also contribute to maintaining low intracellular O(2). Our study provides a mechanism enabling N(2) fixation despite the presence of photosynthesis across Trichodesmium. IMPORTANCE The filamentous Trichodesmium is a globally prominent marine nitrogen fixer. A long-standing paradox is that the nitrogen-fixing enzyme nitrogenase is sensitive to oxygen, but Trichodesmium conducts both nitrogen fixation and oxygen-evolving photosynthesis during the daytime. Previous studies using immunoassays reported that nitrogenase was limited in some specialized Trichodesmium cells (termed diazocytes), suggesting the necessity of spatial segregation of nitrogen fixation and photosynthesis. However, attempts using other methods failed to find diazocytes in Trichodesmium, causing controversy on the existence of the spatial segregation. Here, our physiological model shows that Trichodesmium can maintain low intracellular O(2) in mid-daytime and achieve feasible nitrogen fixation and growth rates even without the spatial segregation, while the hypothetical spatial segregation might not be useful if substantial loss of substances to the environment occurs when they transfer among the Trichodesmium cells. Our study then suggests a possible mechanism by which Trichodesmium can survive without the spatial segregation. |
format | Online Article Text |
id | pubmed-9426587 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Society for Microbiology |
record_format | MEDLINE/PubMed |
spelling | pubmed-94265872022-08-31 N(2) Fixation in Trichodesmium Does Not Require Spatial Segregation from Photosynthesis Luo, Weicheng Inomura, Keisuke Zhang, Han Luo, Ya-Wei mSystems Research Article The dominant marine filamentous N(2) fixer, Trichodesmium, conducts photosynthesis and N(2) fixation during the daytime. Because N(2) fixation is sensitive to O(2), some previous studies suggested that spatial segregation of N(2) fixation and photosynthesis is essential in Trichodesmium. However, this hypothesis conflicts with some observations where all the cells contain both photosystems and the N(2)-fixing enzyme nitrogenase. Here, we construct a systematic model simulating Trichodesmium metabolism, showing that the hypothetical spatial segregation is probably useless in increasing the Trichodesmium growth and N(2) fixation, unless substances can efficiently transfer among cells with low loss to the environment. The model suggests that Trichodesmium accumulates fixed carbon in the morning and uses that in respiratory protection to reduce intracellular O(2) during the mid-daytime, when photosynthesis is downregulated, allowing the occurrence of N(2) fixation. A cell membrane barrier against O(2) and alternative non-O(2) evolving electron transfer also contribute to maintaining low intracellular O(2). Our study provides a mechanism enabling N(2) fixation despite the presence of photosynthesis across Trichodesmium. IMPORTANCE The filamentous Trichodesmium is a globally prominent marine nitrogen fixer. A long-standing paradox is that the nitrogen-fixing enzyme nitrogenase is sensitive to oxygen, but Trichodesmium conducts both nitrogen fixation and oxygen-evolving photosynthesis during the daytime. Previous studies using immunoassays reported that nitrogenase was limited in some specialized Trichodesmium cells (termed diazocytes), suggesting the necessity of spatial segregation of nitrogen fixation and photosynthesis. However, attempts using other methods failed to find diazocytes in Trichodesmium, causing controversy on the existence of the spatial segregation. Here, our physiological model shows that Trichodesmium can maintain low intracellular O(2) in mid-daytime and achieve feasible nitrogen fixation and growth rates even without the spatial segregation, while the hypothetical spatial segregation might not be useful if substantial loss of substances to the environment occurs when they transfer among the Trichodesmium cells. Our study then suggests a possible mechanism by which Trichodesmium can survive without the spatial segregation. American Society for Microbiology 2022-07-11 /pmc/articles/PMC9426587/ /pubmed/35862813 http://dx.doi.org/10.1128/msystems.00538-22 Text en Copyright © 2022 Luo et al. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Research Article Luo, Weicheng Inomura, Keisuke Zhang, Han Luo, Ya-Wei N(2) Fixation in Trichodesmium Does Not Require Spatial Segregation from Photosynthesis |
title | N(2) Fixation in Trichodesmium Does Not Require Spatial Segregation from Photosynthesis |
title_full | N(2) Fixation in Trichodesmium Does Not Require Spatial Segregation from Photosynthesis |
title_fullStr | N(2) Fixation in Trichodesmium Does Not Require Spatial Segregation from Photosynthesis |
title_full_unstemmed | N(2) Fixation in Trichodesmium Does Not Require Spatial Segregation from Photosynthesis |
title_short | N(2) Fixation in Trichodesmium Does Not Require Spatial Segregation from Photosynthesis |
title_sort | n(2) fixation in trichodesmium does not require spatial segregation from photosynthesis |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9426587/ https://www.ncbi.nlm.nih.gov/pubmed/35862813 http://dx.doi.org/10.1128/msystems.00538-22 |
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