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Characterisation of three fungal glucuronoyl esterases on glucuronic acid ester model compounds

The glucuronoyl esterases (GEs) that have been identified so far belong to family 15 of the carbohydrate esterases in the CAZy classification system and are presumed to target ester bonds between lignin alcohols and (4-O-methyl-)d-glucuronic acid residues of xylan. Few GEs have been cloned, expresse...

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Autores principales: Hüttner, Silvia, Klaubauf, Sylvia, de Vries, Ronald P., Olsson, Lisbeth
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5486812/
https://www.ncbi.nlm.nih.gov/pubmed/28429057
http://dx.doi.org/10.1007/s00253-017-8266-9
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author Hüttner, Silvia
Klaubauf, Sylvia
de Vries, Ronald P.
Olsson, Lisbeth
author_facet Hüttner, Silvia
Klaubauf, Sylvia
de Vries, Ronald P.
Olsson, Lisbeth
author_sort Hüttner, Silvia
collection PubMed
description The glucuronoyl esterases (GEs) that have been identified so far belong to family 15 of the carbohydrate esterases in the CAZy classification system and are presumed to target ester bonds between lignin alcohols and (4-O-methyl-)d-glucuronic acid residues of xylan. Few GEs have been cloned, expressed and characterised to date. Characterisation has been done on a variety of synthetic substrates; however, the number of commercially available substrates is very limited. We identified novel putative GEs from a wide taxonomic range of fungi and expressed the enzymes originating from Acremonium alcalophilum and Wolfiporia cocos as well as the previously described PcGE1 from Phanerochaete chrysosporium. All three fungal GEs were active on the commercially available compounds benzyl glucuronic acid (BnGlcA), allyl glucuronic acid (allylGlcA) and to a lower degree on methyl glucuronic acid (MeGlcA). The enzymes showed pH stability over a wide pH range and tolerated 6-h incubations of up to 50 °C. Kinetic parameters were determined for BnGlcA. This study shows the suitability of the commercially available model compounds BnGlcA, MeGlcA and allylGlcA in GE activity screening and characterisation experiments. We enriched the spectrum of characterised GEs with two new members of a relatively young enzyme family. Due to its biotechnological significance, this family deserves to be more extensively studied. The presented enzymes are promising candidates as auxiliary enzymes to improve saccharification of plant biomass. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00253-017-8266-9) contains supplementary material, which is available to authorized users.
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spelling pubmed-54868122017-07-11 Characterisation of three fungal glucuronoyl esterases on glucuronic acid ester model compounds Hüttner, Silvia Klaubauf, Sylvia de Vries, Ronald P. Olsson, Lisbeth Appl Microbiol Biotechnol Biotechnologically Relevant Enzymes and Proteins The glucuronoyl esterases (GEs) that have been identified so far belong to family 15 of the carbohydrate esterases in the CAZy classification system and are presumed to target ester bonds between lignin alcohols and (4-O-methyl-)d-glucuronic acid residues of xylan. Few GEs have been cloned, expressed and characterised to date. Characterisation has been done on a variety of synthetic substrates; however, the number of commercially available substrates is very limited. We identified novel putative GEs from a wide taxonomic range of fungi and expressed the enzymes originating from Acremonium alcalophilum and Wolfiporia cocos as well as the previously described PcGE1 from Phanerochaete chrysosporium. All three fungal GEs were active on the commercially available compounds benzyl glucuronic acid (BnGlcA), allyl glucuronic acid (allylGlcA) and to a lower degree on methyl glucuronic acid (MeGlcA). The enzymes showed pH stability over a wide pH range and tolerated 6-h incubations of up to 50 °C. Kinetic parameters were determined for BnGlcA. This study shows the suitability of the commercially available model compounds BnGlcA, MeGlcA and allylGlcA in GE activity screening and characterisation experiments. We enriched the spectrum of characterised GEs with two new members of a relatively young enzyme family. Due to its biotechnological significance, this family deserves to be more extensively studied. The presented enzymes are promising candidates as auxiliary enzymes to improve saccharification of plant biomass. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00253-017-8266-9) contains supplementary material, which is available to authorized users. Springer Berlin Heidelberg 2017-04-20 2017 /pmc/articles/PMC5486812/ /pubmed/28429057 http://dx.doi.org/10.1007/s00253-017-8266-9 Text en © The Author(s) 2017 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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.
spellingShingle Biotechnologically Relevant Enzymes and Proteins
Hüttner, Silvia
Klaubauf, Sylvia
de Vries, Ronald P.
Olsson, Lisbeth
Characterisation of three fungal glucuronoyl esterases on glucuronic acid ester model compounds
title Characterisation of three fungal glucuronoyl esterases on glucuronic acid ester model compounds
title_full Characterisation of three fungal glucuronoyl esterases on glucuronic acid ester model compounds
title_fullStr Characterisation of three fungal glucuronoyl esterases on glucuronic acid ester model compounds
title_full_unstemmed Characterisation of three fungal glucuronoyl esterases on glucuronic acid ester model compounds
title_short Characterisation of three fungal glucuronoyl esterases on glucuronic acid ester model compounds
title_sort characterisation of three fungal glucuronoyl esterases on glucuronic acid ester model compounds
topic Biotechnologically Relevant Enzymes and Proteins
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5486812/
https://www.ncbi.nlm.nih.gov/pubmed/28429057
http://dx.doi.org/10.1007/s00253-017-8266-9
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