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A cellulose synthase-derived enzyme catalyses 3-O-glucuronosylation in saponin biosynthesis
Triterpenoid saponins are specialised metabolites distributed widely in the plant kingdom that consist of one or more sugar moieties attached to triterpenoid aglycones. Despite the widely accepted view that glycosylation is catalysed by UDP-dependent glycosyltransferase (UGT), the UGT which catalyse...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7669905/ https://www.ncbi.nlm.nih.gov/pubmed/33199711 http://dx.doi.org/10.1038/s41467-020-19399-0 |
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author | Chung, Soo Yeon Seki, Hikaru Fujisawa, Yukiko Shimoda, Yoshikazu Hiraga, Susumu Nomura, Yuhta Saito, Kazuki Ishimoto, Masao Muranaka, Toshiya |
author_facet | Chung, Soo Yeon Seki, Hikaru Fujisawa, Yukiko Shimoda, Yoshikazu Hiraga, Susumu Nomura, Yuhta Saito, Kazuki Ishimoto, Masao Muranaka, Toshiya |
author_sort | Chung, Soo Yeon |
collection | PubMed |
description | Triterpenoid saponins are specialised metabolites distributed widely in the plant kingdom that consist of one or more sugar moieties attached to triterpenoid aglycones. Despite the widely accepted view that glycosylation is catalysed by UDP-dependent glycosyltransferase (UGT), the UGT which catalyses the transfer of the conserved glucuronic acid moiety at the C-3 position of glycyrrhizin and various soyasaponins has not been determined. Here, we report that a cellulose synthase superfamily-derived glycosyltransferase (CSyGT) catalyses 3-O-glucuronosylation of triterpenoid aglycones. Gene co-expression analyses of three legume species (Glycyrrhiza uralensis, Glycine max, and Lotus japonicus) reveal the involvement of CSyGTs in saponin biosynthesis, and we characterise CSyGTs in vivo using Saccharomyces cerevisiae. CSyGT mutants of L. japonicus do not accumulate soyasaponin, but the ectopic expression of endoplasmic reticulum membrane–localised CSyGTs in a L. japonicus mutant background successfully complement soyasaponin biosynthesis. Finally, we produced glycyrrhizin de novo in yeast, paving the way for sustainable production of high-value saponins. |
format | Online Article Text |
id | pubmed-7669905 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-76699052020-11-24 A cellulose synthase-derived enzyme catalyses 3-O-glucuronosylation in saponin biosynthesis Chung, Soo Yeon Seki, Hikaru Fujisawa, Yukiko Shimoda, Yoshikazu Hiraga, Susumu Nomura, Yuhta Saito, Kazuki Ishimoto, Masao Muranaka, Toshiya Nat Commun Article Triterpenoid saponins are specialised metabolites distributed widely in the plant kingdom that consist of one or more sugar moieties attached to triterpenoid aglycones. Despite the widely accepted view that glycosylation is catalysed by UDP-dependent glycosyltransferase (UGT), the UGT which catalyses the transfer of the conserved glucuronic acid moiety at the C-3 position of glycyrrhizin and various soyasaponins has not been determined. Here, we report that a cellulose synthase superfamily-derived glycosyltransferase (CSyGT) catalyses 3-O-glucuronosylation of triterpenoid aglycones. Gene co-expression analyses of three legume species (Glycyrrhiza uralensis, Glycine max, and Lotus japonicus) reveal the involvement of CSyGTs in saponin biosynthesis, and we characterise CSyGTs in vivo using Saccharomyces cerevisiae. CSyGT mutants of L. japonicus do not accumulate soyasaponin, but the ectopic expression of endoplasmic reticulum membrane–localised CSyGTs in a L. japonicus mutant background successfully complement soyasaponin biosynthesis. Finally, we produced glycyrrhizin de novo in yeast, paving the way for sustainable production of high-value saponins. Nature Publishing Group UK 2020-11-16 /pmc/articles/PMC7669905/ /pubmed/33199711 http://dx.doi.org/10.1038/s41467-020-19399-0 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Chung, Soo Yeon Seki, Hikaru Fujisawa, Yukiko Shimoda, Yoshikazu Hiraga, Susumu Nomura, Yuhta Saito, Kazuki Ishimoto, Masao Muranaka, Toshiya A cellulose synthase-derived enzyme catalyses 3-O-glucuronosylation in saponin biosynthesis |
title | A cellulose synthase-derived enzyme catalyses 3-O-glucuronosylation in saponin biosynthesis |
title_full | A cellulose synthase-derived enzyme catalyses 3-O-glucuronosylation in saponin biosynthesis |
title_fullStr | A cellulose synthase-derived enzyme catalyses 3-O-glucuronosylation in saponin biosynthesis |
title_full_unstemmed | A cellulose synthase-derived enzyme catalyses 3-O-glucuronosylation in saponin biosynthesis |
title_short | A cellulose synthase-derived enzyme catalyses 3-O-glucuronosylation in saponin biosynthesis |
title_sort | cellulose synthase-derived enzyme catalyses 3-o-glucuronosylation in saponin biosynthesis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7669905/ https://www.ncbi.nlm.nih.gov/pubmed/33199711 http://dx.doi.org/10.1038/s41467-020-19399-0 |
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