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Regioselectivity of oxidation by a polysaccharide monooxygenase from Chaetomium thermophilum
BACKGROUND: Polysaccharide monooxygenases (PMOs) of the auxiliary activity 9 (AA9) family have been reported to oxidize C1, C4, and C6 positions in cellulose. However, currently no direct evidence exists that PMOs oxidize C6 positions in cellulose, and molecular mechanism of C1, C4 and C6 oxidation...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5987470/ https://www.ncbi.nlm.nih.gov/pubmed/29991963 http://dx.doi.org/10.1186/s13068-018-1156-2 |
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author | Chen, Chen Chen, Jinyin Geng, Zhigang Wang, Meixia Liu, Ning Li, Duochuan |
author_facet | Chen, Chen Chen, Jinyin Geng, Zhigang Wang, Meixia Liu, Ning Li, Duochuan |
author_sort | Chen, Chen |
collection | PubMed |
description | BACKGROUND: Polysaccharide monooxygenases (PMOs) of the auxiliary activity 9 (AA9) family have been reported to oxidize C1, C4, and C6 positions in cellulose. However, currently no direct evidence exists that PMOs oxidize C6 positions in cellulose, and molecular mechanism of C1, C4 and C6 oxidation is unclear. RESULTS: In this study, a PMO gene (Ctpmo1) belonging to AA9 was isolated from Chaetomium thermophilum and successfully expressed and correctly processed in Pichia pastoris. A simple and effective chemical method of using Br(2) to oxidize CtPMO1 reaction products was developed to directly identify C4- and C6-oxidized products by matrix-assisted laser desorption/ionization-time-of-flight tandem mass spectrometry (MALDI-TOF–MS). The PMO (CtPMO1) cleaves phosphoric acid-swollen cellulose (PASC) and celloheptaose, resulting in the formation of oxidized and nonoxidized oligosaccharides. Product identification shows that the enzyme can oxidize C1, C4, and C6 in PASC and cello-oligosaccharides. Mutagenesis of the aromatic residues Tyr27, His64, His157 and residue Tyr206 on the flat surface of CtPMO1 was carried out using site-directed mutagenesis to form the mutated enzymes Y27A, H64A, H157A, and Y206A. It was demonstrated that Y27A retained complete activity of C1, C4, and C6 oxidation on cellulose; Y206A retained partial activity of C1 and C4 oxidation but completely lost activity of C6 oxidation on cellulose; H64A almost completely lost activity of C1, C4, and C6 oxidation on cellulose; and H157A completely lost activity of C1, C4, and C6 oxidation on cellulose. CONCLUSIONS: This finding provides direct and molecular evidence for C1, C4, especially C6 oxidation by lytic polysaccharide monooxygenase. CtPMO1 oxidizes not only C1 and C4 but also C6 positions in cellulose. The aromatic acid residues His64, His157 and residue Tyr206 on CtPMO1 flat surface are involved in activity of C1, C4, C6 oxidation. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13068-018-1156-2) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5987470 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-59874702018-07-10 Regioselectivity of oxidation by a polysaccharide monooxygenase from Chaetomium thermophilum Chen, Chen Chen, Jinyin Geng, Zhigang Wang, Meixia Liu, Ning Li, Duochuan Biotechnol Biofuels Research BACKGROUND: Polysaccharide monooxygenases (PMOs) of the auxiliary activity 9 (AA9) family have been reported to oxidize C1, C4, and C6 positions in cellulose. However, currently no direct evidence exists that PMOs oxidize C6 positions in cellulose, and molecular mechanism of C1, C4 and C6 oxidation is unclear. RESULTS: In this study, a PMO gene (Ctpmo1) belonging to AA9 was isolated from Chaetomium thermophilum and successfully expressed and correctly processed in Pichia pastoris. A simple and effective chemical method of using Br(2) to oxidize CtPMO1 reaction products was developed to directly identify C4- and C6-oxidized products by matrix-assisted laser desorption/ionization-time-of-flight tandem mass spectrometry (MALDI-TOF–MS). The PMO (CtPMO1) cleaves phosphoric acid-swollen cellulose (PASC) and celloheptaose, resulting in the formation of oxidized and nonoxidized oligosaccharides. Product identification shows that the enzyme can oxidize C1, C4, and C6 in PASC and cello-oligosaccharides. Mutagenesis of the aromatic residues Tyr27, His64, His157 and residue Tyr206 on the flat surface of CtPMO1 was carried out using site-directed mutagenesis to form the mutated enzymes Y27A, H64A, H157A, and Y206A. It was demonstrated that Y27A retained complete activity of C1, C4, and C6 oxidation on cellulose; Y206A retained partial activity of C1 and C4 oxidation but completely lost activity of C6 oxidation on cellulose; H64A almost completely lost activity of C1, C4, and C6 oxidation on cellulose; and H157A completely lost activity of C1, C4, and C6 oxidation on cellulose. CONCLUSIONS: This finding provides direct and molecular evidence for C1, C4, especially C6 oxidation by lytic polysaccharide monooxygenase. CtPMO1 oxidizes not only C1 and C4 but also C6 positions in cellulose. The aromatic acid residues His64, His157 and residue Tyr206 on CtPMO1 flat surface are involved in activity of C1, C4, C6 oxidation. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13068-018-1156-2) contains supplementary material, which is available to authorized users. BioMed Central 2018-06-05 /pmc/articles/PMC5987470/ /pubmed/29991963 http://dx.doi.org/10.1186/s13068-018-1156-2 Text en © The Author(s) 2018 Open AccessThis 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. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Chen, Chen Chen, Jinyin Geng, Zhigang Wang, Meixia Liu, Ning Li, Duochuan Regioselectivity of oxidation by a polysaccharide monooxygenase from Chaetomium thermophilum |
title | Regioselectivity of oxidation by a polysaccharide monooxygenase from Chaetomium thermophilum |
title_full | Regioselectivity of oxidation by a polysaccharide monooxygenase from Chaetomium thermophilum |
title_fullStr | Regioselectivity of oxidation by a polysaccharide monooxygenase from Chaetomium thermophilum |
title_full_unstemmed | Regioselectivity of oxidation by a polysaccharide monooxygenase from Chaetomium thermophilum |
title_short | Regioselectivity of oxidation by a polysaccharide monooxygenase from Chaetomium thermophilum |
title_sort | regioselectivity of oxidation by a polysaccharide monooxygenase from chaetomium thermophilum |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5987470/ https://www.ncbi.nlm.nih.gov/pubmed/29991963 http://dx.doi.org/10.1186/s13068-018-1156-2 |
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