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Visualization of plant cell wall lignification using fluorescence-tagged monolignols
Lignin is an abundant phenylpropanoid polymer produced by the oxidative polymerization of p-hydroxycinnamyl alcohols (monolignols). Lignification, i.e., deposition of lignin, is a defining feature of secondary cell wall formation in vascular plants, and provides an important mechanism for their dise...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BlackWell Publishing Ltd
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4238399/ https://www.ncbi.nlm.nih.gov/pubmed/23889038 http://dx.doi.org/10.1111/tpj.12299 |
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author | Tobimatsu, Yuki Wagner, Armin Donaldson, Lloyd Mitra, Prajakta Niculaes, Claudiu Dima, Oana Kim, Jeong Im Anderson, Nickolas Loque, Dominique Boerjan, Wout Chapple, Clint Ralph, John |
author_facet | Tobimatsu, Yuki Wagner, Armin Donaldson, Lloyd Mitra, Prajakta Niculaes, Claudiu Dima, Oana Kim, Jeong Im Anderson, Nickolas Loque, Dominique Boerjan, Wout Chapple, Clint Ralph, John |
author_sort | Tobimatsu, Yuki |
collection | PubMed |
description | Lignin is an abundant phenylpropanoid polymer produced by the oxidative polymerization of p-hydroxycinnamyl alcohols (monolignols). Lignification, i.e., deposition of lignin, is a defining feature of secondary cell wall formation in vascular plants, and provides an important mechanism for their disease resistance; however, many aspects of the cell wall lignification process remain unclear partly because of a lack of suitable imaging methods to monitor the process in vivo. In this study, a set of monolignol analogs γ-linked to fluorogenic aminocoumarin and nitrobenzofuran dyes were synthesized and tested as imaging probes to visualize the cell wall lignification process in Arabidopsis thaliana and Pinus radiata under various feeding regimens. In particular, we demonstrate that the fluorescence-tagged monolignol analogs can penetrate into live plant tissues and cells, and appear to be metabolically incorporated into lignifying cell walls in a highly specific manner. The localization of the fluorogenic lignins synthesized during the feeding period can be readily visualized by fluorescence microscopy and is distinguishable from the other wall components such as polysaccharides as well as the pre-existing lignin that was deposited earlier in development. |
format | Online Article Text |
id | pubmed-4238399 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | BlackWell Publishing Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-42383992014-11-28 Visualization of plant cell wall lignification using fluorescence-tagged monolignols Tobimatsu, Yuki Wagner, Armin Donaldson, Lloyd Mitra, Prajakta Niculaes, Claudiu Dima, Oana Kim, Jeong Im Anderson, Nickolas Loque, Dominique Boerjan, Wout Chapple, Clint Ralph, John Plant J Featured Article Lignin is an abundant phenylpropanoid polymer produced by the oxidative polymerization of p-hydroxycinnamyl alcohols (monolignols). Lignification, i.e., deposition of lignin, is a defining feature of secondary cell wall formation in vascular plants, and provides an important mechanism for their disease resistance; however, many aspects of the cell wall lignification process remain unclear partly because of a lack of suitable imaging methods to monitor the process in vivo. In this study, a set of monolignol analogs γ-linked to fluorogenic aminocoumarin and nitrobenzofuran dyes were synthesized and tested as imaging probes to visualize the cell wall lignification process in Arabidopsis thaliana and Pinus radiata under various feeding regimens. In particular, we demonstrate that the fluorescence-tagged monolignol analogs can penetrate into live plant tissues and cells, and appear to be metabolically incorporated into lignifying cell walls in a highly specific manner. The localization of the fluorogenic lignins synthesized during the feeding period can be readily visualized by fluorescence microscopy and is distinguishable from the other wall components such as polysaccharides as well as the pre-existing lignin that was deposited earlier in development. BlackWell Publishing Ltd 2013-11 2013-08-23 /pmc/articles/PMC4238399/ /pubmed/23889038 http://dx.doi.org/10.1111/tpj.12299 Text en © 2013 The Authors The Plant Journal © 2013 John Wiley & Sons Ltd http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open access article under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made. |
spellingShingle | Featured Article Tobimatsu, Yuki Wagner, Armin Donaldson, Lloyd Mitra, Prajakta Niculaes, Claudiu Dima, Oana Kim, Jeong Im Anderson, Nickolas Loque, Dominique Boerjan, Wout Chapple, Clint Ralph, John Visualization of plant cell wall lignification using fluorescence-tagged monolignols |
title | Visualization of plant cell wall lignification using fluorescence-tagged monolignols |
title_full | Visualization of plant cell wall lignification using fluorescence-tagged monolignols |
title_fullStr | Visualization of plant cell wall lignification using fluorescence-tagged monolignols |
title_full_unstemmed | Visualization of plant cell wall lignification using fluorescence-tagged monolignols |
title_short | Visualization of plant cell wall lignification using fluorescence-tagged monolignols |
title_sort | visualization of plant cell wall lignification using fluorescence-tagged monolignols |
topic | Featured Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4238399/ https://www.ncbi.nlm.nih.gov/pubmed/23889038 http://dx.doi.org/10.1111/tpj.12299 |
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