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Fenton reaction facilitates organic nitrogen acquisition by an ectomycorrhizal fungus

Boreal trees rely on their ectomycorrhizal fungal symbionts to acquire growth‐limiting nutrients, such as nitrogen (N), which mainly occurs as proteins complexed in soil organic matter (SOM). The mechanisms for liberating this N are unclear as ectomycorrhizal fungi have lost many genes encoding lign...

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Autores principales: Op De Beeck, Michiel, Troein, Carl, Peterson, Carsten, Persson, Per, Tunlid, Anders
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5873446/
https://www.ncbi.nlm.nih.gov/pubmed/29297591
http://dx.doi.org/10.1111/nph.14971
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author Op De Beeck, Michiel
Troein, Carl
Peterson, Carsten
Persson, Per
Tunlid, Anders
author_facet Op De Beeck, Michiel
Troein, Carl
Peterson, Carsten
Persson, Per
Tunlid, Anders
author_sort Op De Beeck, Michiel
collection PubMed
description Boreal trees rely on their ectomycorrhizal fungal symbionts to acquire growth‐limiting nutrients, such as nitrogen (N), which mainly occurs as proteins complexed in soil organic matter (SOM). The mechanisms for liberating this N are unclear as ectomycorrhizal fungi have lost many genes encoding lignocellulose‐degrading enzymes present in their saprotrophic ancestors. We hypothesized that hydroxyl radicals ((˙) OH), produced by the ectomycorrhizal fungus Paxillus involutus during growth on SOM, are involved in liberating organic N. Paxillus involutus was grown for 7 d on N‐containing or N‐free substrates that represent major organic compounds of SOM. (˙) OH production, ammonium assimilation, and proteolytic activity were measured daily. (˙) OH production was strongly induced when P. involutus switched from ammonium to protein as the main N source. Extracellular proteolytic activity was initiated shortly after the oxidation. Oxidized protein substrates induced higher proteolytic activity than unmodified proteins. Dynamic modeling predicted that (˙) OH production occurs in a burst, regulated mainly by ammonium and ferric iron concentrations. We propose that the production of (˙) OH and extracellular proteolytic enzymes are regulated by similar nutritional signals. Oxidation works in concert with proteolysis, improving N liberation from proteins in SOM. Organic N mining by ectomycorrhizal fungi has, until now, only been attributed to proteolysis.
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spelling pubmed-58734462018-03-31 Fenton reaction facilitates organic nitrogen acquisition by an ectomycorrhizal fungus Op De Beeck, Michiel Troein, Carl Peterson, Carsten Persson, Per Tunlid, Anders New Phytol Research Boreal trees rely on their ectomycorrhizal fungal symbionts to acquire growth‐limiting nutrients, such as nitrogen (N), which mainly occurs as proteins complexed in soil organic matter (SOM). The mechanisms for liberating this N are unclear as ectomycorrhizal fungi have lost many genes encoding lignocellulose‐degrading enzymes present in their saprotrophic ancestors. We hypothesized that hydroxyl radicals ((˙) OH), produced by the ectomycorrhizal fungus Paxillus involutus during growth on SOM, are involved in liberating organic N. Paxillus involutus was grown for 7 d on N‐containing or N‐free substrates that represent major organic compounds of SOM. (˙) OH production, ammonium assimilation, and proteolytic activity were measured daily. (˙) OH production was strongly induced when P. involutus switched from ammonium to protein as the main N source. Extracellular proteolytic activity was initiated shortly after the oxidation. Oxidized protein substrates induced higher proteolytic activity than unmodified proteins. Dynamic modeling predicted that (˙) OH production occurs in a burst, regulated mainly by ammonium and ferric iron concentrations. We propose that the production of (˙) OH and extracellular proteolytic enzymes are regulated by similar nutritional signals. Oxidation works in concert with proteolysis, improving N liberation from proteins in SOM. Organic N mining by ectomycorrhizal fungi has, until now, only been attributed to proteolysis. John Wiley and Sons Inc. 2018-01-03 2018-04 /pmc/articles/PMC5873446/ /pubmed/29297591 http://dx.doi.org/10.1111/nph.14971 Text en © 2018 The Authors. New Phytologist © 2018 New Phytologist Trust This is an open access article under the terms of the Creative Commons Attribution (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 Research
Op De Beeck, Michiel
Troein, Carl
Peterson, Carsten
Persson, Per
Tunlid, Anders
Fenton reaction facilitates organic nitrogen acquisition by an ectomycorrhizal fungus
title Fenton reaction facilitates organic nitrogen acquisition by an ectomycorrhizal fungus
title_full Fenton reaction facilitates organic nitrogen acquisition by an ectomycorrhizal fungus
title_fullStr Fenton reaction facilitates organic nitrogen acquisition by an ectomycorrhizal fungus
title_full_unstemmed Fenton reaction facilitates organic nitrogen acquisition by an ectomycorrhizal fungus
title_short Fenton reaction facilitates organic nitrogen acquisition by an ectomycorrhizal fungus
title_sort fenton reaction facilitates organic nitrogen acquisition by an ectomycorrhizal fungus
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5873446/
https://www.ncbi.nlm.nih.gov/pubmed/29297591
http://dx.doi.org/10.1111/nph.14971
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