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Preparation of uniformly labelled (13)C- and (15)N-plants using customised growth chambers

BACKGROUND: Stable isotopically labelled organisms have found wide application in life science research including plant physiology, plant stress and defense as well as metabolism related sciences. Therefore, the reproducible production of plant material enriched with stable isotopes such as (13)C an...

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Autores principales: Ćeranić, Asja, Doppler, Maria, Büschl, Christoph, Parich, Alexandra, Xu, Kangkang, Koutnik, Andrea, Bürstmayr, Hermann, Lemmens, Marc, Schuhmacher, Rainer
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7137243/
https://www.ncbi.nlm.nih.gov/pubmed/32280362
http://dx.doi.org/10.1186/s13007-020-00590-9
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author Ćeranić, Asja
Doppler, Maria
Büschl, Christoph
Parich, Alexandra
Xu, Kangkang
Koutnik, Andrea
Bürstmayr, Hermann
Lemmens, Marc
Schuhmacher, Rainer
author_facet Ćeranić, Asja
Doppler, Maria
Büschl, Christoph
Parich, Alexandra
Xu, Kangkang
Koutnik, Andrea
Bürstmayr, Hermann
Lemmens, Marc
Schuhmacher, Rainer
author_sort Ćeranić, Asja
collection PubMed
description BACKGROUND: Stable isotopically labelled organisms have found wide application in life science research including plant physiology, plant stress and defense as well as metabolism related sciences. Therefore, the reproducible production of plant material enriched with stable isotopes such as (13)C and (15)N is of considerable interest. A high degree of enrichment (> 96 atom %) with a uniformly distributed isotope (global labelling) is accomplished by a continuous substrate supply during plant growth/cultivation. In the case of plants, (13)C-labelling can be achieved by growth in (13)CO(2(g)) atmosphere while global (15)N-labelling needs (15)N- containing salts in the watering/nutrient solution. Here, we present a method for the preparation of (13)C and (15)N-labelled plants by the use of closed growth chambers and hydroponic nutrient supply. The method is exemplified with durum wheat. RESULTS: In total, 330 g of globally (13)C- and 295 g of (15)N-labelled Triticum durum wheat was produced during 87 cultivation days. For this, a total of 3.88 mol of (13)CO(2(g)) and 58 mmol of (15)N were consumed. The degree of enrichment was determined by LC-HRMS and ranged between 96 and 98 atom % for (13)C and 95–99 atom % for (15)N, respectively. Additionally, the isotopically labelled plant extracts were successfully used for metabolome-wide internal standardisation of native T.durum plants. Application of an isotope-assisted LC-HRMS workflow enabled the detection of 652 truly wheat-derived metabolites out of which 143 contain N. CONCLUSION: A reproducible cultivation which makes use of climate chambers and hydroponics was successfully adapted to produce highly enriched, uniformly (13)C- and (15)N-labelled wheat. The obtained plant material is suitable to be used in all kinds of isotope-assisted research. The described technical equipment and protocol can easily be applied to other plants to produce (13)C-enriched biological samples when the necessary specific adaptations e.g. temperature and light regime, as well as nutrient supply are considered. Additionally, the (15)N-labelling method can also be carried out under regular glasshouse conditions without the need for customised atmosphere.
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spelling pubmed-71372432020-04-11 Preparation of uniformly labelled (13)C- and (15)N-plants using customised growth chambers Ćeranić, Asja Doppler, Maria Büschl, Christoph Parich, Alexandra Xu, Kangkang Koutnik, Andrea Bürstmayr, Hermann Lemmens, Marc Schuhmacher, Rainer Plant Methods Methodology BACKGROUND: Stable isotopically labelled organisms have found wide application in life science research including plant physiology, plant stress and defense as well as metabolism related sciences. Therefore, the reproducible production of plant material enriched with stable isotopes such as (13)C and (15)N is of considerable interest. A high degree of enrichment (> 96 atom %) with a uniformly distributed isotope (global labelling) is accomplished by a continuous substrate supply during plant growth/cultivation. In the case of plants, (13)C-labelling can be achieved by growth in (13)CO(2(g)) atmosphere while global (15)N-labelling needs (15)N- containing salts in the watering/nutrient solution. Here, we present a method for the preparation of (13)C and (15)N-labelled plants by the use of closed growth chambers and hydroponic nutrient supply. The method is exemplified with durum wheat. RESULTS: In total, 330 g of globally (13)C- and 295 g of (15)N-labelled Triticum durum wheat was produced during 87 cultivation days. For this, a total of 3.88 mol of (13)CO(2(g)) and 58 mmol of (15)N were consumed. The degree of enrichment was determined by LC-HRMS and ranged between 96 and 98 atom % for (13)C and 95–99 atom % for (15)N, respectively. Additionally, the isotopically labelled plant extracts were successfully used for metabolome-wide internal standardisation of native T.durum plants. Application of an isotope-assisted LC-HRMS workflow enabled the detection of 652 truly wheat-derived metabolites out of which 143 contain N. CONCLUSION: A reproducible cultivation which makes use of climate chambers and hydroponics was successfully adapted to produce highly enriched, uniformly (13)C- and (15)N-labelled wheat. The obtained plant material is suitable to be used in all kinds of isotope-assisted research. The described technical equipment and protocol can easily be applied to other plants to produce (13)C-enriched biological samples when the necessary specific adaptations e.g. temperature and light regime, as well as nutrient supply are considered. Additionally, the (15)N-labelling method can also be carried out under regular glasshouse conditions without the need for customised atmosphere. BioMed Central 2020-04-06 /pmc/articles/PMC7137243/ /pubmed/32280362 http://dx.doi.org/10.1186/s13007-020-00590-9 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Methodology
Ćeranić, Asja
Doppler, Maria
Büschl, Christoph
Parich, Alexandra
Xu, Kangkang
Koutnik, Andrea
Bürstmayr, Hermann
Lemmens, Marc
Schuhmacher, Rainer
Preparation of uniformly labelled (13)C- and (15)N-plants using customised growth chambers
title Preparation of uniformly labelled (13)C- and (15)N-plants using customised growth chambers
title_full Preparation of uniformly labelled (13)C- and (15)N-plants using customised growth chambers
title_fullStr Preparation of uniformly labelled (13)C- and (15)N-plants using customised growth chambers
title_full_unstemmed Preparation of uniformly labelled (13)C- and (15)N-plants using customised growth chambers
title_short Preparation of uniformly labelled (13)C- and (15)N-plants using customised growth chambers
title_sort preparation of uniformly labelled (13)c- and (15)n-plants using customised growth chambers
topic Methodology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7137243/
https://www.ncbi.nlm.nih.gov/pubmed/32280362
http://dx.doi.org/10.1186/s13007-020-00590-9
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