Cargando…
The plant cell-wall enzyme AtXTH3 catalyses covalent cross-linking between cellulose and cello-oligosaccharide
Cellulose is an economically important material, but routes of its industrial processing have not been fully explored. The plant cell wall – the major source of cellulose – harbours enzymes of the xyloglucan endotransglucosylase/hydrolase (XTH) family. This class of enzymes is unique in that it is c...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5405413/ https://www.ncbi.nlm.nih.gov/pubmed/28443615 http://dx.doi.org/10.1038/srep46099 |
_version_ | 1783231762665570304 |
---|---|
author | Shinohara, Naoki Sunagawa, Naoki Tamura, Satoru Yokoyama, Ryusuke Ueda, Minoru Igarashi, Kiyohiko Nishitani, Kazuhiko |
author_facet | Shinohara, Naoki Sunagawa, Naoki Tamura, Satoru Yokoyama, Ryusuke Ueda, Minoru Igarashi, Kiyohiko Nishitani, Kazuhiko |
author_sort | Shinohara, Naoki |
collection | PubMed |
description | Cellulose is an economically important material, but routes of its industrial processing have not been fully explored. The plant cell wall – the major source of cellulose – harbours enzymes of the xyloglucan endotransglucosylase/hydrolase (XTH) family. This class of enzymes is unique in that it is capable of elongating polysaccharide chains without the requirement for activated nucleotide sugars (e.g., UDP-glucose) and in seamlessly splitting and reconnecting chains of xyloglucan, a naturally occurring soluble analogue of cellulose. Here, we show that a recombinant version of AtXTH3, a thus far uncharacterized member of the Arabidopsis XTH family, catalysed the transglycosylation between cellulose and cello-oligosaccharide, between cellulose and xyloglucan-oligosaccharide, and between xyloglucan and xyloglucan-oligosaccharide, with the highest reaction rate observed for the latter reaction. In addition, this enzyme formed cellulose-like insoluble material from a soluble cello-oligosaccharide in the absence of additional substrates. This newly found activity (designated “cellulose endotransglucosylase,” or CET) can potentially be involved in the formation of covalent linkages between cellulose microfibrils in the plant cell wall. It can also comprise a new route of industrial cellulose functionalization. |
format | Online Article Text |
id | pubmed-5405413 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-54054132017-04-27 The plant cell-wall enzyme AtXTH3 catalyses covalent cross-linking between cellulose and cello-oligosaccharide Shinohara, Naoki Sunagawa, Naoki Tamura, Satoru Yokoyama, Ryusuke Ueda, Minoru Igarashi, Kiyohiko Nishitani, Kazuhiko Sci Rep Article Cellulose is an economically important material, but routes of its industrial processing have not been fully explored. The plant cell wall – the major source of cellulose – harbours enzymes of the xyloglucan endotransglucosylase/hydrolase (XTH) family. This class of enzymes is unique in that it is capable of elongating polysaccharide chains without the requirement for activated nucleotide sugars (e.g., UDP-glucose) and in seamlessly splitting and reconnecting chains of xyloglucan, a naturally occurring soluble analogue of cellulose. Here, we show that a recombinant version of AtXTH3, a thus far uncharacterized member of the Arabidopsis XTH family, catalysed the transglycosylation between cellulose and cello-oligosaccharide, between cellulose and xyloglucan-oligosaccharide, and between xyloglucan and xyloglucan-oligosaccharide, with the highest reaction rate observed for the latter reaction. In addition, this enzyme formed cellulose-like insoluble material from a soluble cello-oligosaccharide in the absence of additional substrates. This newly found activity (designated “cellulose endotransglucosylase,” or CET) can potentially be involved in the formation of covalent linkages between cellulose microfibrils in the plant cell wall. It can also comprise a new route of industrial cellulose functionalization. Nature Publishing Group 2017-04-26 /pmc/articles/PMC5405413/ /pubmed/28443615 http://dx.doi.org/10.1038/srep46099 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Shinohara, Naoki Sunagawa, Naoki Tamura, Satoru Yokoyama, Ryusuke Ueda, Minoru Igarashi, Kiyohiko Nishitani, Kazuhiko The plant cell-wall enzyme AtXTH3 catalyses covalent cross-linking between cellulose and cello-oligosaccharide |
title | The plant cell-wall enzyme AtXTH3 catalyses covalent cross-linking between cellulose and cello-oligosaccharide |
title_full | The plant cell-wall enzyme AtXTH3 catalyses covalent cross-linking between cellulose and cello-oligosaccharide |
title_fullStr | The plant cell-wall enzyme AtXTH3 catalyses covalent cross-linking between cellulose and cello-oligosaccharide |
title_full_unstemmed | The plant cell-wall enzyme AtXTH3 catalyses covalent cross-linking between cellulose and cello-oligosaccharide |
title_short | The plant cell-wall enzyme AtXTH3 catalyses covalent cross-linking between cellulose and cello-oligosaccharide |
title_sort | plant cell-wall enzyme atxth3 catalyses covalent cross-linking between cellulose and cello-oligosaccharide |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5405413/ https://www.ncbi.nlm.nih.gov/pubmed/28443615 http://dx.doi.org/10.1038/srep46099 |
work_keys_str_mv | AT shinoharanaoki theplantcellwallenzymeatxth3catalysescovalentcrosslinkingbetweencelluloseandcellooligosaccharide AT sunagawanaoki theplantcellwallenzymeatxth3catalysescovalentcrosslinkingbetweencelluloseandcellooligosaccharide AT tamurasatoru theplantcellwallenzymeatxth3catalysescovalentcrosslinkingbetweencelluloseandcellooligosaccharide AT yokoyamaryusuke theplantcellwallenzymeatxth3catalysescovalentcrosslinkingbetweencelluloseandcellooligosaccharide AT uedaminoru theplantcellwallenzymeatxth3catalysescovalentcrosslinkingbetweencelluloseandcellooligosaccharide AT igarashikiyohiko theplantcellwallenzymeatxth3catalysescovalentcrosslinkingbetweencelluloseandcellooligosaccharide AT nishitanikazuhiko theplantcellwallenzymeatxth3catalysescovalentcrosslinkingbetweencelluloseandcellooligosaccharide AT shinoharanaoki plantcellwallenzymeatxth3catalysescovalentcrosslinkingbetweencelluloseandcellooligosaccharide AT sunagawanaoki plantcellwallenzymeatxth3catalysescovalentcrosslinkingbetweencelluloseandcellooligosaccharide AT tamurasatoru plantcellwallenzymeatxth3catalysescovalentcrosslinkingbetweencelluloseandcellooligosaccharide AT yokoyamaryusuke plantcellwallenzymeatxth3catalysescovalentcrosslinkingbetweencelluloseandcellooligosaccharide AT uedaminoru plantcellwallenzymeatxth3catalysescovalentcrosslinkingbetweencelluloseandcellooligosaccharide AT igarashikiyohiko plantcellwallenzymeatxth3catalysescovalentcrosslinkingbetweencelluloseandcellooligosaccharide AT nishitanikazuhiko plantcellwallenzymeatxth3catalysescovalentcrosslinkingbetweencelluloseandcellooligosaccharide |