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Structure and function of aldopentose catabolism enzymes involved in oxidative non-phosphorylative pathways
Platform chemicals and polymer precursors can be produced via enzymatic pathways starting from lignocellulosic waste materials. The hemicellulose fraction of lignocellulose contains aldopentose sugars, such as d-xylose and l-arabinose, which can be enzymatically converted into various biobased produ...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9795676/ https://www.ncbi.nlm.nih.gov/pubmed/36578086 http://dx.doi.org/10.1186/s13068-022-02252-5 |
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author | Ren, Yaxin Eronen, Veikko Blomster Andberg, Martina Koivula, Anu Hakulinen, Nina |
author_facet | Ren, Yaxin Eronen, Veikko Blomster Andberg, Martina Koivula, Anu Hakulinen, Nina |
author_sort | Ren, Yaxin |
collection | PubMed |
description | Platform chemicals and polymer precursors can be produced via enzymatic pathways starting from lignocellulosic waste materials. The hemicellulose fraction of lignocellulose contains aldopentose sugars, such as d-xylose and l-arabinose, which can be enzymatically converted into various biobased products by microbial non-phosphorylated oxidative pathways. The Weimberg and Dahms pathways convert pentose sugars into α-ketoglutarate, or pyruvate and glycolaldehyde, respectively, which then serve as precursors for further conversion into a wide range of industrial products. In this review, we summarize the known three-dimensional structures of the enzymes involved in oxidative non-phosphorylative pathways of pentose catabolism. Key structural features and reaction mechanisms of a diverse set of enzymes responsible for the catalytic steps in the reactions are analysed and discussed. |
format | Online Article Text |
id | pubmed-9795676 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-97956762022-12-29 Structure and function of aldopentose catabolism enzymes involved in oxidative non-phosphorylative pathways Ren, Yaxin Eronen, Veikko Blomster Andberg, Martina Koivula, Anu Hakulinen, Nina Biotechnol Biofuels Bioprod Review Platform chemicals and polymer precursors can be produced via enzymatic pathways starting from lignocellulosic waste materials. The hemicellulose fraction of lignocellulose contains aldopentose sugars, such as d-xylose and l-arabinose, which can be enzymatically converted into various biobased products by microbial non-phosphorylated oxidative pathways. The Weimberg and Dahms pathways convert pentose sugars into α-ketoglutarate, or pyruvate and glycolaldehyde, respectively, which then serve as precursors for further conversion into a wide range of industrial products. In this review, we summarize the known three-dimensional structures of the enzymes involved in oxidative non-phosphorylative pathways of pentose catabolism. Key structural features and reaction mechanisms of a diverse set of enzymes responsible for the catalytic steps in the reactions are analysed and discussed. BioMed Central 2022-12-28 /pmc/articles/PMC9795676/ /pubmed/36578086 http://dx.doi.org/10.1186/s13068-022-02252-5 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Review Ren, Yaxin Eronen, Veikko Blomster Andberg, Martina Koivula, Anu Hakulinen, Nina Structure and function of aldopentose catabolism enzymes involved in oxidative non-phosphorylative pathways |
title | Structure and function of aldopentose catabolism enzymes involved in oxidative non-phosphorylative pathways |
title_full | Structure and function of aldopentose catabolism enzymes involved in oxidative non-phosphorylative pathways |
title_fullStr | Structure and function of aldopentose catabolism enzymes involved in oxidative non-phosphorylative pathways |
title_full_unstemmed | Structure and function of aldopentose catabolism enzymes involved in oxidative non-phosphorylative pathways |
title_short | Structure and function of aldopentose catabolism enzymes involved in oxidative non-phosphorylative pathways |
title_sort | structure and function of aldopentose catabolism enzymes involved in oxidative non-phosphorylative pathways |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9795676/ https://www.ncbi.nlm.nih.gov/pubmed/36578086 http://dx.doi.org/10.1186/s13068-022-02252-5 |
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