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An improved microtiter plate assay to monitor the oxidative burst in monocot and dicot plant cell suspension cultures

BACKGROUND: A screening method for elicitor and priming agents does not only allow detecting new bioactive substances, it can also be used to understand structure–function relationships of known agents by testing different derivatives of them. This can not only provide new lead compounds for the dev...

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Autores principales: Melcher, Rebecca L. J., Moerschbacher, Bruno M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4729151/
https://www.ncbi.nlm.nih.gov/pubmed/26819624
http://dx.doi.org/10.1186/s13007-016-0110-1
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author Melcher, Rebecca L. J.
Moerschbacher, Bruno M.
author_facet Melcher, Rebecca L. J.
Moerschbacher, Bruno M.
author_sort Melcher, Rebecca L. J.
collection PubMed
description BACKGROUND: A screening method for elicitor and priming agents does not only allow detecting new bioactive substances, it can also be used to understand structure–function relationships of known agents by testing different derivatives of them. This can not only provide new lead compounds for the development of novel, more environment-benign, bio-based agro-chemicals, it may eventually also lead to a better understanding of defense mechanisms in plants. Reactive oxygen species (ROS) are sensitive indicators of these mechanisms but current assay formats are not suitable for multiplex screening, in particularly not in the case of monocot systems. RESULTS: Here we describe continuous monitoring of ROS in 96-well microtiter plates using the chemiluminescent probe L012, a luminol derivative producing chemiluminescence when oxidised by ROS like hydrogen peroxide, superoxide, or hydroxyl radical that can thus be used as an indicator for these ROS. We were able to measure ROS in both monocot (Oryza sativa) and dicot (Medicago truncatula) cell suspension cultures and record dose dependencies for the carbohydrate elicitors and priming agents ulvan and chitosan at low substrate concentrations (0.3–2.5 µg/ml). The method was optimized in terms of cell density, L012 concentration, and pre-incubation time. In contrast to the single peak observed using a cuvette luminometer, the improved method revealed a double burst in both cell systems during the 90-min measuring period, probably due to the detection of multiple ROS rather than only H(2)O(2). CONCLUSION: We provide a medium throughput screening method for monocot and dicot suspension-cultured cells that enables direct comparison of monocot and dicot plant systems regarding their reaction to different signaling molecules. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13007-016-0110-1) contains supplementary material, which is available to authorized users.
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spelling pubmed-47291512016-01-28 An improved microtiter plate assay to monitor the oxidative burst in monocot and dicot plant cell suspension cultures Melcher, Rebecca L. J. Moerschbacher, Bruno M. Plant Methods Methodology BACKGROUND: A screening method for elicitor and priming agents does not only allow detecting new bioactive substances, it can also be used to understand structure–function relationships of known agents by testing different derivatives of them. This can not only provide new lead compounds for the development of novel, more environment-benign, bio-based agro-chemicals, it may eventually also lead to a better understanding of defense mechanisms in plants. Reactive oxygen species (ROS) are sensitive indicators of these mechanisms but current assay formats are not suitable for multiplex screening, in particularly not in the case of monocot systems. RESULTS: Here we describe continuous monitoring of ROS in 96-well microtiter plates using the chemiluminescent probe L012, a luminol derivative producing chemiluminescence when oxidised by ROS like hydrogen peroxide, superoxide, or hydroxyl radical that can thus be used as an indicator for these ROS. We were able to measure ROS in both monocot (Oryza sativa) and dicot (Medicago truncatula) cell suspension cultures and record dose dependencies for the carbohydrate elicitors and priming agents ulvan and chitosan at low substrate concentrations (0.3–2.5 µg/ml). The method was optimized in terms of cell density, L012 concentration, and pre-incubation time. In contrast to the single peak observed using a cuvette luminometer, the improved method revealed a double burst in both cell systems during the 90-min measuring period, probably due to the detection of multiple ROS rather than only H(2)O(2). CONCLUSION: We provide a medium throughput screening method for monocot and dicot suspension-cultured cells that enables direct comparison of monocot and dicot plant systems regarding their reaction to different signaling molecules. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13007-016-0110-1) contains supplementary material, which is available to authorized users. BioMed Central 2016-01-26 /pmc/articles/PMC4729151/ /pubmed/26819624 http://dx.doi.org/10.1186/s13007-016-0110-1 Text en © Melcher and Moerschbacher. 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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.
spellingShingle Methodology
Melcher, Rebecca L. J.
Moerschbacher, Bruno M.
An improved microtiter plate assay to monitor the oxidative burst in monocot and dicot plant cell suspension cultures
title An improved microtiter plate assay to monitor the oxidative burst in monocot and dicot plant cell suspension cultures
title_full An improved microtiter plate assay to monitor the oxidative burst in monocot and dicot plant cell suspension cultures
title_fullStr An improved microtiter plate assay to monitor the oxidative burst in monocot and dicot plant cell suspension cultures
title_full_unstemmed An improved microtiter plate assay to monitor the oxidative burst in monocot and dicot plant cell suspension cultures
title_short An improved microtiter plate assay to monitor the oxidative burst in monocot and dicot plant cell suspension cultures
title_sort improved microtiter plate assay to monitor the oxidative burst in monocot and dicot plant cell suspension cultures
topic Methodology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4729151/
https://www.ncbi.nlm.nih.gov/pubmed/26819624
http://dx.doi.org/10.1186/s13007-016-0110-1
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