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Disaccharide phosphorylases: Structure, catalytic mechanisms and directed evolution

Disaccharide phosphorylases (DSPs) are carbohydrate-active enzymes with outstanding potential for the biocatalytic conversion of common table sugar into products with attractive properties. They are modular enzymes that form active homo-oligomers. From a mechanistic as well as a structural point of...

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Autores principales: Sun, Shangshang, You, Chun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: KeAi Publishing 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7896129/
https://www.ncbi.nlm.nih.gov/pubmed/33665389
http://dx.doi.org/10.1016/j.synbio.2021.01.004
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author Sun, Shangshang
You, Chun
author_facet Sun, Shangshang
You, Chun
author_sort Sun, Shangshang
collection PubMed
description Disaccharide phosphorylases (DSPs) are carbohydrate-active enzymes with outstanding potential for the biocatalytic conversion of common table sugar into products with attractive properties. They are modular enzymes that form active homo-oligomers. From a mechanistic as well as a structural point of view, they are similar to glycoside hydrolases or glycosyltransferases. As the majority of DSPs show strict stereo- and regiospecificities, these enzymes were used to synthesize specific disaccharides. Currently, protein engineering of DSPs is pursued in different laboratories to broaden the donor and acceptor substrate specificities or improve the industrial particularity of naturally existing enzymes, to eventually generate a toolbox of new catalysts for glycoside synthesis. Herein we review the characteristics and classifications of reported DSPs and the glycoside products that they have been used to synthesize.
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spelling pubmed-78961292021-03-03 Disaccharide phosphorylases: Structure, catalytic mechanisms and directed evolution Sun, Shangshang You, Chun Synth Syst Biotechnol Original Research Article Disaccharide phosphorylases (DSPs) are carbohydrate-active enzymes with outstanding potential for the biocatalytic conversion of common table sugar into products with attractive properties. They are modular enzymes that form active homo-oligomers. From a mechanistic as well as a structural point of view, they are similar to glycoside hydrolases or glycosyltransferases. As the majority of DSPs show strict stereo- and regiospecificities, these enzymes were used to synthesize specific disaccharides. Currently, protein engineering of DSPs is pursued in different laboratories to broaden the donor and acceptor substrate specificities or improve the industrial particularity of naturally existing enzymes, to eventually generate a toolbox of new catalysts for glycoside synthesis. Herein we review the characteristics and classifications of reported DSPs and the glycoside products that they have been used to synthesize. KeAi Publishing 2021-02-13 /pmc/articles/PMC7896129/ /pubmed/33665389 http://dx.doi.org/10.1016/j.synbio.2021.01.004 Text en © 2021 Production and hosting by Elsevier B.V. on behalf of KeAi Communications Co. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Research Article
Sun, Shangshang
You, Chun
Disaccharide phosphorylases: Structure, catalytic mechanisms and directed evolution
title Disaccharide phosphorylases: Structure, catalytic mechanisms and directed evolution
title_full Disaccharide phosphorylases: Structure, catalytic mechanisms and directed evolution
title_fullStr Disaccharide phosphorylases: Structure, catalytic mechanisms and directed evolution
title_full_unstemmed Disaccharide phosphorylases: Structure, catalytic mechanisms and directed evolution
title_short Disaccharide phosphorylases: Structure, catalytic mechanisms and directed evolution
title_sort disaccharide phosphorylases: structure, catalytic mechanisms and directed evolution
topic Original Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7896129/
https://www.ncbi.nlm.nih.gov/pubmed/33665389
http://dx.doi.org/10.1016/j.synbio.2021.01.004
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