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Reassessment of chitosanase substrate specificities and classification
Chitosanases can be used to produce partially acetylated chitosan oligosaccharides (paCOS) for different applications, provided they are thoroughly characterized. However, recent studies indicate that the established classification system for chitosanases is too simplistic. Here, we apply a highly s...
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/PMC5700058/ https://www.ncbi.nlm.nih.gov/pubmed/29167423 http://dx.doi.org/10.1038/s41467-017-01667-1 |
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author | Weikert, Tobias Niehues, Anna Cord-Landwehr, Stefan Hellmann, Margareta J. Moerschbacher, Bruno M. |
author_facet | Weikert, Tobias Niehues, Anna Cord-Landwehr, Stefan Hellmann, Margareta J. Moerschbacher, Bruno M. |
author_sort | Weikert, Tobias |
collection | PubMed |
description | Chitosanases can be used to produce partially acetylated chitosan oligosaccharides (paCOS) for different applications, provided they are thoroughly characterized. However, recent studies indicate that the established classification system for chitosanases is too simplistic. Here, we apply a highly sensitive method for quantitatively sequencing paCOS to reassess the substrate specificities of the best-characterized class I–III chitosanases. The enzymes’ abilities to cleave bonds at GlcNAc residues positioned at subsite (−1) or (+1), on which the classification system is based, vary especially when the substrates have different fractions of acetylation (F(A)). Conflicts with the recent classification are observed at higher F(A), which were not investigated in prior specificity determinations. Initial analyses of pectin-degrading enzymes reveal that classifications of other polysaccharide-degrading enzymes should also be critically reassessed. Based on our results, we tentatively suggest a chitosanase classification system which is based on specificities and preferences of subsites (−2) to (+2). |
format | Online Article Text |
id | pubmed-5700058 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-57000582017-11-24 Reassessment of chitosanase substrate specificities and classification Weikert, Tobias Niehues, Anna Cord-Landwehr, Stefan Hellmann, Margareta J. Moerschbacher, Bruno M. Nat Commun Article Chitosanases can be used to produce partially acetylated chitosan oligosaccharides (paCOS) for different applications, provided they are thoroughly characterized. However, recent studies indicate that the established classification system for chitosanases is too simplistic. Here, we apply a highly sensitive method for quantitatively sequencing paCOS to reassess the substrate specificities of the best-characterized class I–III chitosanases. The enzymes’ abilities to cleave bonds at GlcNAc residues positioned at subsite (−1) or (+1), on which the classification system is based, vary especially when the substrates have different fractions of acetylation (F(A)). Conflicts with the recent classification are observed at higher F(A), which were not investigated in prior specificity determinations. Initial analyses of pectin-degrading enzymes reveal that classifications of other polysaccharide-degrading enzymes should also be critically reassessed. Based on our results, we tentatively suggest a chitosanase classification system which is based on specificities and preferences of subsites (−2) to (+2). Nature Publishing Group UK 2017-11-22 /pmc/articles/PMC5700058/ /pubmed/29167423 http://dx.doi.org/10.1038/s41467-017-01667-1 Text en © The Author(s) 2017 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 Weikert, Tobias Niehues, Anna Cord-Landwehr, Stefan Hellmann, Margareta J. Moerschbacher, Bruno M. Reassessment of chitosanase substrate specificities and classification |
title | Reassessment of chitosanase substrate specificities and classification |
title_full | Reassessment of chitosanase substrate specificities and classification |
title_fullStr | Reassessment of chitosanase substrate specificities and classification |
title_full_unstemmed | Reassessment of chitosanase substrate specificities and classification |
title_short | Reassessment of chitosanase substrate specificities and classification |
title_sort | reassessment of chitosanase substrate specificities and classification |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5700058/ https://www.ncbi.nlm.nih.gov/pubmed/29167423 http://dx.doi.org/10.1038/s41467-017-01667-1 |
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