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Competition between plant and bacterial cells at the microscale regulates the dynamics of nitrogen acquisition in wheat (Triticum aestivum)

The ability of plants to compete effectively for nitrogen (N) resources is critical to plant survival. However, controversy surrounds the importance of organic and inorganic sources of N in plant nutrition because of our poor ability to visualize and understand processes happening at the root–microb...

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Autores principales: Jones, David L, Clode, Peta L, Kilburn, Matt R, Stockdale, Elizabeth A, Murphy, Daniel V
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3916831/
https://www.ncbi.nlm.nih.gov/pubmed/23845035
http://dx.doi.org/10.1111/nph.12405
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author Jones, David L
Clode, Peta L
Kilburn, Matt R
Stockdale, Elizabeth A
Murphy, Daniel V
author_facet Jones, David L
Clode, Peta L
Kilburn, Matt R
Stockdale, Elizabeth A
Murphy, Daniel V
author_sort Jones, David L
collection PubMed
description The ability of plants to compete effectively for nitrogen (N) resources is critical to plant survival. However, controversy surrounds the importance of organic and inorganic sources of N in plant nutrition because of our poor ability to visualize and understand processes happening at the root–microbial–soil interface. Using high-resolution nano-scale secondary ion mass spectrometry stable isotope imaging (NanoSIMS-SII), we quantified the fate of (15)N over both space and time within the rhizosphere. We pulse-labelled the soil surrounding wheat (Triticum aestivum) roots with either [Image: see text] or (15)N-glutamate and traced the movement of (15)N over 24 h. Imaging revealed that glutamate was rapidly depleted from the rhizosphere and that most (15)N was captured by rhizobacteria, leading to very high (15)N microbial enrichment. After microbial capture, approximately half of the (15)N-glutamate was rapidly mineralized, leading to the excretion of [Image: see text], which became available for plant capture. Roots proved to be poor competitors for (15)N-glutamate and took up N mainly as [Image: see text]. Spatial mapping of (15)N revealed differential patterns of (15)N uptake within bacteria and the rapid uptake and redistribution of (15)N within roots. In conclusion, we demonstrate the rapid cycling and transformation of N at the soil–root interface and that wheat capture of organic N is low in comparison to inorganic N under the conditions tested.
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spelling pubmed-39168312014-02-13 Competition between plant and bacterial cells at the microscale regulates the dynamics of nitrogen acquisition in wheat (Triticum aestivum) Jones, David L Clode, Peta L Kilburn, Matt R Stockdale, Elizabeth A Murphy, Daniel V New Phytol Research The ability of plants to compete effectively for nitrogen (N) resources is critical to plant survival. However, controversy surrounds the importance of organic and inorganic sources of N in plant nutrition because of our poor ability to visualize and understand processes happening at the root–microbial–soil interface. Using high-resolution nano-scale secondary ion mass spectrometry stable isotope imaging (NanoSIMS-SII), we quantified the fate of (15)N over both space and time within the rhizosphere. We pulse-labelled the soil surrounding wheat (Triticum aestivum) roots with either [Image: see text] or (15)N-glutamate and traced the movement of (15)N over 24 h. Imaging revealed that glutamate was rapidly depleted from the rhizosphere and that most (15)N was captured by rhizobacteria, leading to very high (15)N microbial enrichment. After microbial capture, approximately half of the (15)N-glutamate was rapidly mineralized, leading to the excretion of [Image: see text], which became available for plant capture. Roots proved to be poor competitors for (15)N-glutamate and took up N mainly as [Image: see text]. Spatial mapping of (15)N revealed differential patterns of (15)N uptake within bacteria and the rapid uptake and redistribution of (15)N within roots. In conclusion, we demonstrate the rapid cycling and transformation of N at the soil–root interface and that wheat capture of organic N is low in comparison to inorganic N under the conditions tested. Blackwell Publishing Ltd 2013-11 2013-07-12 /pmc/articles/PMC3916831/ /pubmed/23845035 http://dx.doi.org/10.1111/nph.12405 Text en © 2013 The Authors New Phytologist © 2013 New Phytologist Trust http://creativecommons.org/licenses/by/3.0/ This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Jones, David L
Clode, Peta L
Kilburn, Matt R
Stockdale, Elizabeth A
Murphy, Daniel V
Competition between plant and bacterial cells at the microscale regulates the dynamics of nitrogen acquisition in wheat (Triticum aestivum)
title Competition between plant and bacterial cells at the microscale regulates the dynamics of nitrogen acquisition in wheat (Triticum aestivum)
title_full Competition between plant and bacterial cells at the microscale regulates the dynamics of nitrogen acquisition in wheat (Triticum aestivum)
title_fullStr Competition between plant and bacterial cells at the microscale regulates the dynamics of nitrogen acquisition in wheat (Triticum aestivum)
title_full_unstemmed Competition between plant and bacterial cells at the microscale regulates the dynamics of nitrogen acquisition in wheat (Triticum aestivum)
title_short Competition between plant and bacterial cells at the microscale regulates the dynamics of nitrogen acquisition in wheat (Triticum aestivum)
title_sort competition between plant and bacterial cells at the microscale regulates the dynamics of nitrogen acquisition in wheat (triticum aestivum)
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3916831/
https://www.ncbi.nlm.nih.gov/pubmed/23845035
http://dx.doi.org/10.1111/nph.12405
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