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Design and Synthesis of a Chitodisaccharide-Based Affinity Resin for Chitosanases Purification
Chitooligosaccharides (CHOS) have gained increasing attention because of their important biological activities. Enhancing the efficiency of CHOS production essentially requires screening of novel chitosanase with unique characteristics. Therefore, a rapid and efficient one-step affinity purification...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6356299/ https://www.ncbi.nlm.nih.gov/pubmed/30669556 http://dx.doi.org/10.3390/md17010068 |
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author | Li, Shangyong Wang, Linna Chen, Xuehong Sun, Mi Han, Yantao |
author_facet | Li, Shangyong Wang, Linna Chen, Xuehong Sun, Mi Han, Yantao |
author_sort | Li, Shangyong |
collection | PubMed |
description | Chitooligosaccharides (CHOS) have gained increasing attention because of their important biological activities. Enhancing the efficiency of CHOS production essentially requires screening of novel chitosanase with unique characteristics. Therefore, a rapid and efficient one-step affinity purification procedure plays important roles in screening native chitosanases. In this study, we report the design and synthesis of affinity resin for efficient purification of native chitosanases without any tags, using chitodisaccharides (CHDS) as an affinity ligand, to couple with Sepharose 6B via a spacer, cyanuric chloride. Based on the CHDS-modified affinity resin, a one-step affinity purification method was developed and optimized, and then applied to purify three typical glycoside hydrolase (GH) families: 46, 75, and 80 chitosanase. The three purified chitosanases were homogeneous with purities of greater than 95% and bioactivity recovery of more than 40%. Moreover, we also developed a rapid and efficient affinity purification procedure, in which tag-free chitosanase could be directly purified from supernatant of bacterial culture. The purified chitosanases samples using such a procedure had apparent homogeneity, with more than 90% purity and 10–50% yield. The novel purification methods established in this work can be applied to purify native chitosanases in various scales, such as laboratory and industrial scales. |
format | Online Article Text |
id | pubmed-6356299 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-63562992019-02-05 Design and Synthesis of a Chitodisaccharide-Based Affinity Resin for Chitosanases Purification Li, Shangyong Wang, Linna Chen, Xuehong Sun, Mi Han, Yantao Mar Drugs Article Chitooligosaccharides (CHOS) have gained increasing attention because of their important biological activities. Enhancing the efficiency of CHOS production essentially requires screening of novel chitosanase with unique characteristics. Therefore, a rapid and efficient one-step affinity purification procedure plays important roles in screening native chitosanases. In this study, we report the design and synthesis of affinity resin for efficient purification of native chitosanases without any tags, using chitodisaccharides (CHDS) as an affinity ligand, to couple with Sepharose 6B via a spacer, cyanuric chloride. Based on the CHDS-modified affinity resin, a one-step affinity purification method was developed and optimized, and then applied to purify three typical glycoside hydrolase (GH) families: 46, 75, and 80 chitosanase. The three purified chitosanases were homogeneous with purities of greater than 95% and bioactivity recovery of more than 40%. Moreover, we also developed a rapid and efficient affinity purification procedure, in which tag-free chitosanase could be directly purified from supernatant of bacterial culture. The purified chitosanases samples using such a procedure had apparent homogeneity, with more than 90% purity and 10–50% yield. The novel purification methods established in this work can be applied to purify native chitosanases in various scales, such as laboratory and industrial scales. MDPI 2019-01-21 /pmc/articles/PMC6356299/ /pubmed/30669556 http://dx.doi.org/10.3390/md17010068 Text en © 2019 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Li, Shangyong Wang, Linna Chen, Xuehong Sun, Mi Han, Yantao Design and Synthesis of a Chitodisaccharide-Based Affinity Resin for Chitosanases Purification |
title | Design and Synthesis of a Chitodisaccharide-Based Affinity Resin for Chitosanases Purification |
title_full | Design and Synthesis of a Chitodisaccharide-Based Affinity Resin for Chitosanases Purification |
title_fullStr | Design and Synthesis of a Chitodisaccharide-Based Affinity Resin for Chitosanases Purification |
title_full_unstemmed | Design and Synthesis of a Chitodisaccharide-Based Affinity Resin for Chitosanases Purification |
title_short | Design and Synthesis of a Chitodisaccharide-Based Affinity Resin for Chitosanases Purification |
title_sort | design and synthesis of a chitodisaccharide-based affinity resin for chitosanases purification |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6356299/ https://www.ncbi.nlm.nih.gov/pubmed/30669556 http://dx.doi.org/10.3390/md17010068 |
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