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Fast preparation of RG-I enriched ultra-low molecular weight pectin by an ultrasound accelerated Fenton process
Pectin, a natural polysaccharide found in the cell wall of most higher plant such as citrus, has drawn much attention due to its potential beneficial role in facilitating the treatment of many diseases like cancer, hyper cholesterol and diabetes. However, the broad application of pectin faces great...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5428719/ https://www.ncbi.nlm.nih.gov/pubmed/28373642 http://dx.doi.org/10.1038/s41598-017-00572-3 |
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author | Zhi, Zijian Chen, Jianle Li, Shan Wang, Wenjun Huang, Rui Liu, Donghong Ding, Tian Linhardt, Robert John Chen, Shiguo Ye, Xingqian |
author_facet | Zhi, Zijian Chen, Jianle Li, Shan Wang, Wenjun Huang, Rui Liu, Donghong Ding, Tian Linhardt, Robert John Chen, Shiguo Ye, Xingqian |
author_sort | Zhi, Zijian |
collection | PubMed |
description | Pectin, a natural polysaccharide found in the cell wall of most higher plant such as citrus, has drawn much attention due to its potential beneficial role in facilitating the treatment of many diseases like cancer, hyper cholesterol and diabetes. However, the broad application of pectin faces great limitations as the large molecular size of pectin severely prevents its bioavailability in vivo. In this study, we report an effective and highly convenient approach to degrade natural pectin into lower molecular pectin. By combining ultrasound with Fenton system (US-Fenton), we show that ultrasound synergistically enhances the efficiency of Fenton reaction to degrade pectin into 5.5 kDa within only 35 minutes. Importantly, RG-I domain, the most effective portion of natural pectin, was well preserved and highly enriched. In addition, the antioxidant activities of US-Fenton-treated pectin was significantly elevated. The mechanism of this novel observation was further investigated through the multiple structural analyses including HPLC, IR and NMR. Taken together, we present a novel and convenient approach to generate ultra-low molecular weight pectin with high efficiency and higher bioactivity. We expect our approach will have broader applications in improving the bioavailability and bioactivity of other polysaccharide-based natural compounds. |
format | Online Article Text |
id | pubmed-5428719 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-54287192017-05-15 Fast preparation of RG-I enriched ultra-low molecular weight pectin by an ultrasound accelerated Fenton process Zhi, Zijian Chen, Jianle Li, Shan Wang, Wenjun Huang, Rui Liu, Donghong Ding, Tian Linhardt, Robert John Chen, Shiguo Ye, Xingqian Sci Rep Article Pectin, a natural polysaccharide found in the cell wall of most higher plant such as citrus, has drawn much attention due to its potential beneficial role in facilitating the treatment of many diseases like cancer, hyper cholesterol and diabetes. However, the broad application of pectin faces great limitations as the large molecular size of pectin severely prevents its bioavailability in vivo. In this study, we report an effective and highly convenient approach to degrade natural pectin into lower molecular pectin. By combining ultrasound with Fenton system (US-Fenton), we show that ultrasound synergistically enhances the efficiency of Fenton reaction to degrade pectin into 5.5 kDa within only 35 minutes. Importantly, RG-I domain, the most effective portion of natural pectin, was well preserved and highly enriched. In addition, the antioxidant activities of US-Fenton-treated pectin was significantly elevated. The mechanism of this novel observation was further investigated through the multiple structural analyses including HPLC, IR and NMR. Taken together, we present a novel and convenient approach to generate ultra-low molecular weight pectin with high efficiency and higher bioactivity. We expect our approach will have broader applications in improving the bioavailability and bioactivity of other polysaccharide-based natural compounds. Nature Publishing Group UK 2017-04-03 /pmc/articles/PMC5428719/ /pubmed/28373642 http://dx.doi.org/10.1038/s41598-017-00572-3 Text en © The Author(s) 2017 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 Zhi, Zijian Chen, Jianle Li, Shan Wang, Wenjun Huang, Rui Liu, Donghong Ding, Tian Linhardt, Robert John Chen, Shiguo Ye, Xingqian Fast preparation of RG-I enriched ultra-low molecular weight pectin by an ultrasound accelerated Fenton process |
title | Fast preparation of RG-I enriched ultra-low molecular weight pectin by an ultrasound accelerated Fenton process |
title_full | Fast preparation of RG-I enriched ultra-low molecular weight pectin by an ultrasound accelerated Fenton process |
title_fullStr | Fast preparation of RG-I enriched ultra-low molecular weight pectin by an ultrasound accelerated Fenton process |
title_full_unstemmed | Fast preparation of RG-I enriched ultra-low molecular weight pectin by an ultrasound accelerated Fenton process |
title_short | Fast preparation of RG-I enriched ultra-low molecular weight pectin by an ultrasound accelerated Fenton process |
title_sort | fast preparation of rg-i enriched ultra-low molecular weight pectin by an ultrasound accelerated fenton process |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5428719/ https://www.ncbi.nlm.nih.gov/pubmed/28373642 http://dx.doi.org/10.1038/s41598-017-00572-3 |
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