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β-1,4-Xylan backbone synthesis in higher plants: How complex can it be?
Xylan is a hemicellulose present in the cell walls of all land plants. Glycosyltransferases of the GT43 (IRX9/IRX9L and IRX14/IRX14L) and GT47 (IRX10/IRX10L) families are involved in the biosynthesis of its β-1,4-linked xylose backbone, which can be further modified by acetylation and sugar side cha...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9874913/ https://www.ncbi.nlm.nih.gov/pubmed/36714768 http://dx.doi.org/10.3389/fpls.2022.1076298 |
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author | Anders, Nadine Wilson, Louis Frederick Lundy Sorieul, Mathias Nikolovski, Nino Dupree, Paul |
author_facet | Anders, Nadine Wilson, Louis Frederick Lundy Sorieul, Mathias Nikolovski, Nino Dupree, Paul |
author_sort | Anders, Nadine |
collection | PubMed |
description | Xylan is a hemicellulose present in the cell walls of all land plants. Glycosyltransferases of the GT43 (IRX9/IRX9L and IRX14/IRX14L) and GT47 (IRX10/IRX10L) families are involved in the biosynthesis of its β-1,4-linked xylose backbone, which can be further modified by acetylation and sugar side chains. However, it remains unclear how the different enzymes work together to synthesize the xylan backbone. A xylan synthesis complex (XSC) has been described in the monocots wheat and asparagus, and co-expression of asparagus AoIRX9, AoIRX10 and AoIRX14A is required to form a catalytically active complex for secondary cell wall xylan biosynthesis. Here, we argue that an equivalent XSC exists for the synthesis of the primary cell wall of the eudicot Arabidopsis thaliana, consisting of IRX9L, IRX10L and IRX14. This would suggest the existence of distinct XSCs for primary and secondary cell wall xylan synthesis, reminiscent of the distinct cellulose synthesis complexes (CSCs) of the primary and secondary cell wall. In contrast to the CSC, in which each CESA protein has catalytic activity, the XSC seems to contain proteins with non-catalytic function with each component bearing potentially unique but crucial roles. Moreover, the core XSC formed by a combination of IRX9/IRX9L, IRX10/IRX10L and IRX14/IRX14L might not be stable in its composition during transit from the endoplasmic reticulum to the Golgi apparatus. Instead, potential dynamic changes of the XSC might be a means of regulating xylan biosynthesis to facilitate coordinated deposition of tailored polysaccharides in the plant cell wall. |
format | Online Article Text |
id | pubmed-9874913 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-98749132023-01-26 β-1,4-Xylan backbone synthesis in higher plants: How complex can it be? Anders, Nadine Wilson, Louis Frederick Lundy Sorieul, Mathias Nikolovski, Nino Dupree, Paul Front Plant Sci Plant Science Xylan is a hemicellulose present in the cell walls of all land plants. Glycosyltransferases of the GT43 (IRX9/IRX9L and IRX14/IRX14L) and GT47 (IRX10/IRX10L) families are involved in the biosynthesis of its β-1,4-linked xylose backbone, which can be further modified by acetylation and sugar side chains. However, it remains unclear how the different enzymes work together to synthesize the xylan backbone. A xylan synthesis complex (XSC) has been described in the monocots wheat and asparagus, and co-expression of asparagus AoIRX9, AoIRX10 and AoIRX14A is required to form a catalytically active complex for secondary cell wall xylan biosynthesis. Here, we argue that an equivalent XSC exists for the synthesis of the primary cell wall of the eudicot Arabidopsis thaliana, consisting of IRX9L, IRX10L and IRX14. This would suggest the existence of distinct XSCs for primary and secondary cell wall xylan synthesis, reminiscent of the distinct cellulose synthesis complexes (CSCs) of the primary and secondary cell wall. In contrast to the CSC, in which each CESA protein has catalytic activity, the XSC seems to contain proteins with non-catalytic function with each component bearing potentially unique but crucial roles. Moreover, the core XSC formed by a combination of IRX9/IRX9L, IRX10/IRX10L and IRX14/IRX14L might not be stable in its composition during transit from the endoplasmic reticulum to the Golgi apparatus. Instead, potential dynamic changes of the XSC might be a means of regulating xylan biosynthesis to facilitate coordinated deposition of tailored polysaccharides in the plant cell wall. Frontiers Media S.A. 2023-01-11 /pmc/articles/PMC9874913/ /pubmed/36714768 http://dx.doi.org/10.3389/fpls.2022.1076298 Text en Copyright © 2023 Anders, Wilson, Sorieul, Nikolovski and Dupree https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Plant Science Anders, Nadine Wilson, Louis Frederick Lundy Sorieul, Mathias Nikolovski, Nino Dupree, Paul β-1,4-Xylan backbone synthesis in higher plants: How complex can it be? |
title | β-1,4-Xylan backbone synthesis in higher plants: How complex can it be? |
title_full | β-1,4-Xylan backbone synthesis in higher plants: How complex can it be? |
title_fullStr | β-1,4-Xylan backbone synthesis in higher plants: How complex can it be? |
title_full_unstemmed | β-1,4-Xylan backbone synthesis in higher plants: How complex can it be? |
title_short | β-1,4-Xylan backbone synthesis in higher plants: How complex can it be? |
title_sort | β-1,4-xylan backbone synthesis in higher plants: how complex can it be? |
topic | Plant Science |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9874913/ https://www.ncbi.nlm.nih.gov/pubmed/36714768 http://dx.doi.org/10.3389/fpls.2022.1076298 |
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