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Nativity of lignin carbohydrate bonds substantiated by biomimetic synthesis

The question of whether lignin is covalently linked to carbohydrates in native wood, forming what is referred to as lignin–carbohydrate complexes (LCCs), still lacks unequivocal proof. This is mainly due to the need to isolate lignin from woody materials prior to analysis, under conditions leading t...

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Autores principales: Giummarella, Nicola, Balakshin, Mikhail, Koutaniemi, Sanna, Kärkönen, Anna, Lawoko, Martin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6812735/
https://www.ncbi.nlm.nih.gov/pubmed/31294799
http://dx.doi.org/10.1093/jxb/erz324
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author Giummarella, Nicola
Balakshin, Mikhail
Koutaniemi, Sanna
Kärkönen, Anna
Lawoko, Martin
author_facet Giummarella, Nicola
Balakshin, Mikhail
Koutaniemi, Sanna
Kärkönen, Anna
Lawoko, Martin
author_sort Giummarella, Nicola
collection PubMed
description The question of whether lignin is covalently linked to carbohydrates in native wood, forming what is referred to as lignin–carbohydrate complexes (LCCs), still lacks unequivocal proof. This is mainly due to the need to isolate lignin from woody materials prior to analysis, under conditions leading to partial chemical modification of the native wood polymers. Thus, the correlation between the structure of the isolated LCCs and LCCs in situ remains open. As a way to circumvent the problematic isolation, biomimicking lignin polymerization in vivo and in vitro is an interesting option. Herein, we report the detection of lignin–carbohydrate bonds in the extracellular lignin formed by tissue-cultured Norway spruce cells, and in modified biomimetic lignin synthesis (dehydrogenation polymers). Semi-quantitative 2D heteronuclear singular quantum coherence (HSQC)-, (31)P -, and (13)C-NMR spectroscopy were applied as analytical tools. Combining results from these systems, four types of lignin–carbohydrate bonds were detected; benzyl ether, benzyl ester, γ-ester, and phenyl glycoside linkages, providing direct evidence of lignin–carbohydrate bond formation in biomimicked lignin polymerization. Based on our findings, we propose a sequence for lignin–carbohydrate bond formation in plant cell walls.
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spelling pubmed-68127352019-10-28 Nativity of lignin carbohydrate bonds substantiated by biomimetic synthesis Giummarella, Nicola Balakshin, Mikhail Koutaniemi, Sanna Kärkönen, Anna Lawoko, Martin J Exp Bot Research Papers The question of whether lignin is covalently linked to carbohydrates in native wood, forming what is referred to as lignin–carbohydrate complexes (LCCs), still lacks unequivocal proof. This is mainly due to the need to isolate lignin from woody materials prior to analysis, under conditions leading to partial chemical modification of the native wood polymers. Thus, the correlation between the structure of the isolated LCCs and LCCs in situ remains open. As a way to circumvent the problematic isolation, biomimicking lignin polymerization in vivo and in vitro is an interesting option. Herein, we report the detection of lignin–carbohydrate bonds in the extracellular lignin formed by tissue-cultured Norway spruce cells, and in modified biomimetic lignin synthesis (dehydrogenation polymers). Semi-quantitative 2D heteronuclear singular quantum coherence (HSQC)-, (31)P -, and (13)C-NMR spectroscopy were applied as analytical tools. Combining results from these systems, four types of lignin–carbohydrate bonds were detected; benzyl ether, benzyl ester, γ-ester, and phenyl glycoside linkages, providing direct evidence of lignin–carbohydrate bond formation in biomimicked lignin polymerization. Based on our findings, we propose a sequence for lignin–carbohydrate bond formation in plant cell walls. Oxford University Press 2019-10-15 2019-07-10 /pmc/articles/PMC6812735/ /pubmed/31294799 http://dx.doi.org/10.1093/jxb/erz324 Text en © The Author(s) 2019. Published by Oxford University Press on behalf of the Society for Experimental Biology. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Research Papers
Giummarella, Nicola
Balakshin, Mikhail
Koutaniemi, Sanna
Kärkönen, Anna
Lawoko, Martin
Nativity of lignin carbohydrate bonds substantiated by biomimetic synthesis
title Nativity of lignin carbohydrate bonds substantiated by biomimetic synthesis
title_full Nativity of lignin carbohydrate bonds substantiated by biomimetic synthesis
title_fullStr Nativity of lignin carbohydrate bonds substantiated by biomimetic synthesis
title_full_unstemmed Nativity of lignin carbohydrate bonds substantiated by biomimetic synthesis
title_short Nativity of lignin carbohydrate bonds substantiated by biomimetic synthesis
title_sort nativity of lignin carbohydrate bonds substantiated by biomimetic synthesis
topic Research Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6812735/
https://www.ncbi.nlm.nih.gov/pubmed/31294799
http://dx.doi.org/10.1093/jxb/erz324
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