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Carbohydrate esterases involved in deacetylation of food components by the human gut microbiota

Non-carbohydrate modifications such as acetylations are widespread in food stuffs as well as they play important roles in diverse biological processes. These modifications meet the gut environment and are removed from their carbohydrate substrates by the resident microbiota. Among the most abundant...

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Autores principales: La Rosa, Sabina Leanti, Lindstad, Lars J., Westereng, Bjørge
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Portland Press Ltd. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10154613/
https://www.ncbi.nlm.nih.gov/pubmed/36912209
http://dx.doi.org/10.1042/EBC20220161
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author La Rosa, Sabina Leanti
Lindstad, Lars J.
Westereng, Bjørge
author_facet La Rosa, Sabina Leanti
Lindstad, Lars J.
Westereng, Bjørge
author_sort La Rosa, Sabina Leanti
collection PubMed
description Non-carbohydrate modifications such as acetylations are widespread in food stuffs as well as they play important roles in diverse biological processes. These modifications meet the gut environment and are removed from their carbohydrate substrates by the resident microbiota. Among the most abundant modifications are O-acetylations, contributing to polysaccharides physico-chemical properties such as viscosity and gelling ability, as well as reducing accessibility for glycosyl hydrolases, and thus hindering polysaccharide degradation. Of particular note, O-acetylations increase the overall complexity of a polymer, thus requiring a more advanced degrading machinery for microbes to utilize it. This minireview describes acetylesterases from the gut microbiota that deacetylate various food polysaccharides, either as natural components of food, ingredients, stabilizers of microbial origin, or as part of microbes for food and beverage preparations. These enzymes include members belonging to at least 8 families in the CAZy database, as well as a large number of biochemically characterized esterases that have not been classified yet. Despite different structural folds, most of these acetylesterases have a common acid–base mechanism and belong to the SGNH hydrolase superfamily. We highlight examples of acetylesterases that are highly specific to one substrate and to the position of the acetyl group on the glycosyl residue of the carbohydrate, while other members that have more broad substrate specificity. Current research aimed at unveiling the functions and regioselectivity of acetylesterases will help providing fundamental mechanistic understanding on how dietary components are utilized in the human gut and will aid developing applications of these enzymes to manufacture novel industrial products.
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spelling pubmed-101546132023-05-04 Carbohydrate esterases involved in deacetylation of food components by the human gut microbiota La Rosa, Sabina Leanti Lindstad, Lars J. Westereng, Bjørge Essays Biochem Biotechnology Non-carbohydrate modifications such as acetylations are widespread in food stuffs as well as they play important roles in diverse biological processes. These modifications meet the gut environment and are removed from their carbohydrate substrates by the resident microbiota. Among the most abundant modifications are O-acetylations, contributing to polysaccharides physico-chemical properties such as viscosity and gelling ability, as well as reducing accessibility for glycosyl hydrolases, and thus hindering polysaccharide degradation. Of particular note, O-acetylations increase the overall complexity of a polymer, thus requiring a more advanced degrading machinery for microbes to utilize it. This minireview describes acetylesterases from the gut microbiota that deacetylate various food polysaccharides, either as natural components of food, ingredients, stabilizers of microbial origin, or as part of microbes for food and beverage preparations. These enzymes include members belonging to at least 8 families in the CAZy database, as well as a large number of biochemically characterized esterases that have not been classified yet. Despite different structural folds, most of these acetylesterases have a common acid–base mechanism and belong to the SGNH hydrolase superfamily. We highlight examples of acetylesterases that are highly specific to one substrate and to the position of the acetyl group on the glycosyl residue of the carbohydrate, while other members that have more broad substrate specificity. Current research aimed at unveiling the functions and regioselectivity of acetylesterases will help providing fundamental mechanistic understanding on how dietary components are utilized in the human gut and will aid developing applications of these enzymes to manufacture novel industrial products. Portland Press Ltd. 2023-04 2023-04-18 /pmc/articles/PMC10154613/ /pubmed/36912209 http://dx.doi.org/10.1042/EBC20220161 Text en © 2023 The Author(s). https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article published by Portland Press Limited on behalf of the Biochemical Society and distributed under the Creative Commons Attribution License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Biotechnology
La Rosa, Sabina Leanti
Lindstad, Lars J.
Westereng, Bjørge
Carbohydrate esterases involved in deacetylation of food components by the human gut microbiota
title Carbohydrate esterases involved in deacetylation of food components by the human gut microbiota
title_full Carbohydrate esterases involved in deacetylation of food components by the human gut microbiota
title_fullStr Carbohydrate esterases involved in deacetylation of food components by the human gut microbiota
title_full_unstemmed Carbohydrate esterases involved in deacetylation of food components by the human gut microbiota
title_short Carbohydrate esterases involved in deacetylation of food components by the human gut microbiota
title_sort carbohydrate esterases involved in deacetylation of food components by the human gut microbiota
topic Biotechnology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10154613/
https://www.ncbi.nlm.nih.gov/pubmed/36912209
http://dx.doi.org/10.1042/EBC20220161
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