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Isolation, Purification, and Antioxidant Activities of Polysaccharides from Choerospondias axillaris Leaves

The extraction, characterization and antioxidant activity of polysaccharides from Choerospondias axillaris leaves were investigated in the present study. Two purified polysaccharide fractions, CALP-1 and CALP-2, were isolated from crude Choerospondias axillaris leaf polysaccharides (CALP) by DEAE-52...

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Autores principales: Zhang, Qiang, Lu, Lianxiang, Zheng, Yanfei, Qin, Chengrong, Chen, Yuexin, Zhou, Zhongjie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9783564/
https://www.ncbi.nlm.nih.gov/pubmed/36558014
http://dx.doi.org/10.3390/molecules27248881
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author Zhang, Qiang
Lu, Lianxiang
Zheng, Yanfei
Qin, Chengrong
Chen, Yuexin
Zhou, Zhongjie
author_facet Zhang, Qiang
Lu, Lianxiang
Zheng, Yanfei
Qin, Chengrong
Chen, Yuexin
Zhou, Zhongjie
author_sort Zhang, Qiang
collection PubMed
description The extraction, characterization and antioxidant activity of polysaccharides from Choerospondias axillaris leaves were investigated in the present study. Two purified polysaccharide fractions, CALP-1 and CALP-2, were isolated from crude Choerospondias axillaris leaf polysaccharides (CALP) by DEAE-52 cellulose chromatography and Sephadex G-100 column chromatography. The characteristics of CAL-1 and CALP-2 were determined by using High-performance Gel Permeation Chromatography (HPGPC), High-Performance Anion-Exchange Chromatography, HPAEC (HPAEC-PAD) and Fourier transform infrared spectroscopy (FTIR). CALP-1 with molecular weight of 11.20 KDa was comprised of Rhamnose, Arabinose, Galactose, Glucose, Xylose, Mannose and galacturonic acid in a molar ratio of 5.16:2.31:5.50:27.18:1.00:0.76:1.07. CAL-2 with molecular weight of 8.03 KDa consisted of Rhamnose, Arabinose, Galactose, Glucose, and galacturonic acid at a ratio of 1.38:3.63:18.84:8.28:1.45. FTIR revealed that CALP-1 and CALP-2 were acidic polysaccharides. The antioxidant activity of crude CALP, CALP-1 and CALP-2 was evaluated in vitro. The fraction CALP-2 was demonstrated to be of polysaccharide nature containing a large percentage of Galactose but no Xylose and Mannose. The antioxidant activity assays showed that CALP-1 and CALP-2 exhibited antioxidant and scavenging activities on hydroxyl and DPPH radicals in vitro. Compared with pure polysaccharide, crude CALP exhibited stronger anti-oxidant activities. These results will provide a better understanding of Choerospondias axillaris leaf polysaccharide and promote the potential applications of Choerospondias axillaris leaf polysaccharide in the pharmacological field and as a natural antioxidant.
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spelling pubmed-97835642022-12-24 Isolation, Purification, and Antioxidant Activities of Polysaccharides from Choerospondias axillaris Leaves Zhang, Qiang Lu, Lianxiang Zheng, Yanfei Qin, Chengrong Chen, Yuexin Zhou, Zhongjie Molecules Article The extraction, characterization and antioxidant activity of polysaccharides from Choerospondias axillaris leaves were investigated in the present study. Two purified polysaccharide fractions, CALP-1 and CALP-2, were isolated from crude Choerospondias axillaris leaf polysaccharides (CALP) by DEAE-52 cellulose chromatography and Sephadex G-100 column chromatography. The characteristics of CAL-1 and CALP-2 were determined by using High-performance Gel Permeation Chromatography (HPGPC), High-Performance Anion-Exchange Chromatography, HPAEC (HPAEC-PAD) and Fourier transform infrared spectroscopy (FTIR). CALP-1 with molecular weight of 11.20 KDa was comprised of Rhamnose, Arabinose, Galactose, Glucose, Xylose, Mannose and galacturonic acid in a molar ratio of 5.16:2.31:5.50:27.18:1.00:0.76:1.07. CAL-2 with molecular weight of 8.03 KDa consisted of Rhamnose, Arabinose, Galactose, Glucose, and galacturonic acid at a ratio of 1.38:3.63:18.84:8.28:1.45. FTIR revealed that CALP-1 and CALP-2 were acidic polysaccharides. The antioxidant activity of crude CALP, CALP-1 and CALP-2 was evaluated in vitro. The fraction CALP-2 was demonstrated to be of polysaccharide nature containing a large percentage of Galactose but no Xylose and Mannose. The antioxidant activity assays showed that CALP-1 and CALP-2 exhibited antioxidant and scavenging activities on hydroxyl and DPPH radicals in vitro. Compared with pure polysaccharide, crude CALP exhibited stronger anti-oxidant activities. These results will provide a better understanding of Choerospondias axillaris leaf polysaccharide and promote the potential applications of Choerospondias axillaris leaf polysaccharide in the pharmacological field and as a natural antioxidant. MDPI 2022-12-14 /pmc/articles/PMC9783564/ /pubmed/36558014 http://dx.doi.org/10.3390/molecules27248881 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Zhang, Qiang
Lu, Lianxiang
Zheng, Yanfei
Qin, Chengrong
Chen, Yuexin
Zhou, Zhongjie
Isolation, Purification, and Antioxidant Activities of Polysaccharides from Choerospondias axillaris Leaves
title Isolation, Purification, and Antioxidant Activities of Polysaccharides from Choerospondias axillaris Leaves
title_full Isolation, Purification, and Antioxidant Activities of Polysaccharides from Choerospondias axillaris Leaves
title_fullStr Isolation, Purification, and Antioxidant Activities of Polysaccharides from Choerospondias axillaris Leaves
title_full_unstemmed Isolation, Purification, and Antioxidant Activities of Polysaccharides from Choerospondias axillaris Leaves
title_short Isolation, Purification, and Antioxidant Activities of Polysaccharides from Choerospondias axillaris Leaves
title_sort isolation, purification, and antioxidant activities of polysaccharides from choerospondias axillaris leaves
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9783564/
https://www.ncbi.nlm.nih.gov/pubmed/36558014
http://dx.doi.org/10.3390/molecules27248881
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