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The structural characterization of a polysaccharide exhibiting antitumor effect from Pholiota adiposa mycelia
PAP80-2a, purified from Pholiota adiposa mycelia, is a polysaccharide exhibiting prominent antitumor effects. However, the yield of PAP80-2a was low and its structure has not been characterized, impeding the exploration of its structure-function relationship, thus influencing the development of oral...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6370848/ https://www.ncbi.nlm.nih.gov/pubmed/30741980 http://dx.doi.org/10.1038/s41598-018-38251-6 |
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author | Zou, Yajie Du, Fang Hu, Qingxiu Wang, Hexiang |
author_facet | Zou, Yajie Du, Fang Hu, Qingxiu Wang, Hexiang |
author_sort | Zou, Yajie |
collection | PubMed |
description | PAP80-2a, purified from Pholiota adiposa mycelia, is a polysaccharide exhibiting prominent antitumor effects. However, the yield of PAP80-2a was low and its structure has not been characterized, impeding the exploration of its structure-function relationship, thus influencing the development of oral drugs for antitumor therapy and immunomodulation. In order to improve the yield of PAP80-2a, response surface methodology along with Box-Behnken design was applied to optimize the ultrasonic-assisted extraction conditions for polysaccharides. Then, the structure of PAP80-2a exhibiting antitumor activity was determined from different angles. The results showed that the extraction yield of P. adiposa polysaccharides increased by 11.5% under optimized ultrasonic extraction conditions. Structural analysis showed that PAP80-2a was mainly composed of glucose, rhamnose, xylose, and galactose in a ratio of 10.00: 2.09: 4.09: 1.13. The total amino acid content in the sugar chain was 69.92 μg/mL. The sugar chain structure was [α-Rha (1 → 3)-]n, and rhamnose was located at the non-reducing end of the sugar chain, while glucose was located at the non-reducing end or in the sugar chain in 1,2,6- and 1,3,6-linked forms. Our study clearly illuminates the primary structure of PAP80-2a, but 3D structure of PAP80-2a and its structure–function relationship is a future challenge. |
format | Online Article Text |
id | pubmed-6370848 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-63708482019-02-15 The structural characterization of a polysaccharide exhibiting antitumor effect from Pholiota adiposa mycelia Zou, Yajie Du, Fang Hu, Qingxiu Wang, Hexiang Sci Rep Article PAP80-2a, purified from Pholiota adiposa mycelia, is a polysaccharide exhibiting prominent antitumor effects. However, the yield of PAP80-2a was low and its structure has not been characterized, impeding the exploration of its structure-function relationship, thus influencing the development of oral drugs for antitumor therapy and immunomodulation. In order to improve the yield of PAP80-2a, response surface methodology along with Box-Behnken design was applied to optimize the ultrasonic-assisted extraction conditions for polysaccharides. Then, the structure of PAP80-2a exhibiting antitumor activity was determined from different angles. The results showed that the extraction yield of P. adiposa polysaccharides increased by 11.5% under optimized ultrasonic extraction conditions. Structural analysis showed that PAP80-2a was mainly composed of glucose, rhamnose, xylose, and galactose in a ratio of 10.00: 2.09: 4.09: 1.13. The total amino acid content in the sugar chain was 69.92 μg/mL. The sugar chain structure was [α-Rha (1 → 3)-]n, and rhamnose was located at the non-reducing end of the sugar chain, while glucose was located at the non-reducing end or in the sugar chain in 1,2,6- and 1,3,6-linked forms. Our study clearly illuminates the primary structure of PAP80-2a, but 3D structure of PAP80-2a and its structure–function relationship is a future challenge. Nature Publishing Group UK 2019-02-11 /pmc/articles/PMC6370848/ /pubmed/30741980 http://dx.doi.org/10.1038/s41598-018-38251-6 Text en © The Author(s) 2019 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 Zou, Yajie Du, Fang Hu, Qingxiu Wang, Hexiang The structural characterization of a polysaccharide exhibiting antitumor effect from Pholiota adiposa mycelia |
title | The structural characterization of a polysaccharide exhibiting antitumor effect from Pholiota adiposa mycelia |
title_full | The structural characterization of a polysaccharide exhibiting antitumor effect from Pholiota adiposa mycelia |
title_fullStr | The structural characterization of a polysaccharide exhibiting antitumor effect from Pholiota adiposa mycelia |
title_full_unstemmed | The structural characterization of a polysaccharide exhibiting antitumor effect from Pholiota adiposa mycelia |
title_short | The structural characterization of a polysaccharide exhibiting antitumor effect from Pholiota adiposa mycelia |
title_sort | structural characterization of a polysaccharide exhibiting antitumor effect from pholiota adiposa mycelia |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6370848/ https://www.ncbi.nlm.nih.gov/pubmed/30741980 http://dx.doi.org/10.1038/s41598-018-38251-6 |
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