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Nanoscale chemical mapping of exometabolites at fungal–mineral interfaces

Mineral‐associated organic matter is an integral part of soil carbon pool. Biological processes contribute to the formation of such organo‐mineral complexes when soil microbes, and in particular soil fungi, deposit a suite of extracellular metabolic compounds and their necromass on the mineral surfa...

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Autores principales: Pucetaite, Milda, Hitchcock, Adam, Obst, Martin, Persson, Per, Hammer, Edith C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9546123/
https://www.ncbi.nlm.nih.gov/pubmed/35686583
http://dx.doi.org/10.1111/gbi.12504
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author Pucetaite, Milda
Hitchcock, Adam
Obst, Martin
Persson, Per
Hammer, Edith C.
author_facet Pucetaite, Milda
Hitchcock, Adam
Obst, Martin
Persson, Per
Hammer, Edith C.
author_sort Pucetaite, Milda
collection PubMed
description Mineral‐associated organic matter is an integral part of soil carbon pool. Biological processes contribute to the formation of such organo‐mineral complexes when soil microbes, and in particular soil fungi, deposit a suite of extracellular metabolic compounds and their necromass on the mineral surfaces. While studied in bulk, micro‐ to nanoscale fungal–mineral interactions remain elusive. Of particular interest are the mutual effects at the interface between the fungal exometabolites and proximal mineral particles. In this work, we have grown saprotrophic and symbiotic fungi in contact with two soil minerals with contrasting properties: quartz and goethite, on top of X‐ray transparent silicon nitride membrane windows and analyzed fungal hyphae by synchrotron‐based scanning transmission X‐ray microscopy in combination with near edge X‐ray fine structure spectroscopy at C(K) and Fe(L) absorption edges. In the resultant chemical maps, we were able to visualize and differentiate organic compounds constituting the fungal cells, their extracellular metabolites, and the exometabolites adsorbing on the minerals. We found that the composition of the exometabolites differed between the fungal functional guilds, particularly, in their sugar to protein ratio and potassium concentration. In samples with quartz and goethite, we observed adsorption of the exometabolic compounds on the mineral surfaces with variations in their chemical composition around the particles. Although we did not observe clear alteration in the exometabolite chemistry upon mineral encounters, we show that fungal–mineral interaction result in reduction of Fe(III) in goethite. This process has been demonstrated for bulk systems, but, to our knowledge, this is the first observation on a single hypha scale offering insight into its underlying biological mechanisms. This demonstrates the link between processes initiated at the single‐cell level to macroscale phenomena. Thus, spatially resolved chemical characterization of the microbial–mineral interfaces is crucial for an increased understanding of overall carbon cycling in soil.
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spelling pubmed-95461232022-10-14 Nanoscale chemical mapping of exometabolites at fungal–mineral interfaces Pucetaite, Milda Hitchcock, Adam Obst, Martin Persson, Per Hammer, Edith C. Geobiology Original Articles Mineral‐associated organic matter is an integral part of soil carbon pool. Biological processes contribute to the formation of such organo‐mineral complexes when soil microbes, and in particular soil fungi, deposit a suite of extracellular metabolic compounds and their necromass on the mineral surfaces. While studied in bulk, micro‐ to nanoscale fungal–mineral interactions remain elusive. Of particular interest are the mutual effects at the interface between the fungal exometabolites and proximal mineral particles. In this work, we have grown saprotrophic and symbiotic fungi in contact with two soil minerals with contrasting properties: quartz and goethite, on top of X‐ray transparent silicon nitride membrane windows and analyzed fungal hyphae by synchrotron‐based scanning transmission X‐ray microscopy in combination with near edge X‐ray fine structure spectroscopy at C(K) and Fe(L) absorption edges. In the resultant chemical maps, we were able to visualize and differentiate organic compounds constituting the fungal cells, their extracellular metabolites, and the exometabolites adsorbing on the minerals. We found that the composition of the exometabolites differed between the fungal functional guilds, particularly, in their sugar to protein ratio and potassium concentration. In samples with quartz and goethite, we observed adsorption of the exometabolic compounds on the mineral surfaces with variations in their chemical composition around the particles. Although we did not observe clear alteration in the exometabolite chemistry upon mineral encounters, we show that fungal–mineral interaction result in reduction of Fe(III) in goethite. This process has been demonstrated for bulk systems, but, to our knowledge, this is the first observation on a single hypha scale offering insight into its underlying biological mechanisms. This demonstrates the link between processes initiated at the single‐cell level to macroscale phenomena. Thus, spatially resolved chemical characterization of the microbial–mineral interfaces is crucial for an increased understanding of overall carbon cycling in soil. John Wiley and Sons Inc. 2022-06-10 2022-09 /pmc/articles/PMC9546123/ /pubmed/35686583 http://dx.doi.org/10.1111/gbi.12504 Text en © 2022 The Authors. Geobiology published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://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
Pucetaite, Milda
Hitchcock, Adam
Obst, Martin
Persson, Per
Hammer, Edith C.
Nanoscale chemical mapping of exometabolites at fungal–mineral interfaces
title Nanoscale chemical mapping of exometabolites at fungal–mineral interfaces
title_full Nanoscale chemical mapping of exometabolites at fungal–mineral interfaces
title_fullStr Nanoscale chemical mapping of exometabolites at fungal–mineral interfaces
title_full_unstemmed Nanoscale chemical mapping of exometabolites at fungal–mineral interfaces
title_short Nanoscale chemical mapping of exometabolites at fungal–mineral interfaces
title_sort nanoscale chemical mapping of exometabolites at fungal–mineral interfaces
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9546123/
https://www.ncbi.nlm.nih.gov/pubmed/35686583
http://dx.doi.org/10.1111/gbi.12504
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