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A novel and efficient fungal delignification strategy based on versatile peroxidase for lignocellulose bioconversion

BACKGROUND: The selective lignin-degrading white-rot fungi are regarded to be the best lignin degraders and have been widely used for reducing the saccharification recalcitrance of lignocellulose. However, the biological delignification and conversion of lignocellulose in biorefinery is still limite...

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Autores principales: Kong, Wen, Fu, Xiao, Wang, Lei, Alhujaily, Ahmad, Zhang, Jingli, Ma, Fuying, Zhang, Xiaoyu, Yu, Hongbo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5598073/
https://www.ncbi.nlm.nih.gov/pubmed/28924453
http://dx.doi.org/10.1186/s13068-017-0906-x
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author Kong, Wen
Fu, Xiao
Wang, Lei
Alhujaily, Ahmad
Zhang, Jingli
Ma, Fuying
Zhang, Xiaoyu
Yu, Hongbo
author_facet Kong, Wen
Fu, Xiao
Wang, Lei
Alhujaily, Ahmad
Zhang, Jingli
Ma, Fuying
Zhang, Xiaoyu
Yu, Hongbo
author_sort Kong, Wen
collection PubMed
description BACKGROUND: The selective lignin-degrading white-rot fungi are regarded to be the best lignin degraders and have been widely used for reducing the saccharification recalcitrance of lignocellulose. However, the biological delignification and conversion of lignocellulose in biorefinery is still limited. It is necessary to develop novel and more efficient bio-delignification systems. RESULTS: Physisporinus vitreus relies on a new versatile peroxidase (VP)-based delignification strategy to remove enzymatic recalcitrance of corn stover efficiently, so that saccharification of corn stover was significantly enhanced to 349.1 mg/g biomass (yield of glucose) and 91.5% (hydrolysis yield of cellulose) at 28 days, as high as levels reached by thermochemical treatment. Analysis of the lignin structure using pyrolysis–gas chromatography–mass spectrometry (Py–GC/MS) showed that the total abundance of lignin-derived compounds decreased by 54.0% and revealed a notable demethylation during lignin degradation by P. vitreus. Monomeric and dimeric lignin model compounds were used to confirm the ligninolytic capabilities of extracellular ligninases secreted by P. vitreus. The laccase (Lac) from P. vitreus could not oxidize nonphenolic lignin compounds and polymerized β-O-4 and 5-5′ dimers to precipitate which had a negative effect on the enzymatic hydrolysis of corn stover in vitro. However, the VP from P. vitreus could oxidize both phenolic and nonphenolic lignin model compounds as well as break the β-O-4 and 5-5′ dimers into monomeric compounds, which were measured by high-performance liquid chromatography–electrospray ionization–mass spectrometry (LC–ESI–MS). Moreover, we showed that addition of purified VP in vitro improved the enzymatic hydrolysis of corn stover by 14.1%. CONCLUSIONS: From the highly efficient system of enzymatic recalcitrance removal by new white-rot fungus, we identified a new delignification strategy based on VP which could oxidize both phenolic and nonphenolic lignin units and break different linkages in lignin. In addition, this is the first evidence that VP could break 5-5′ linkage efficiently in vitro. Moreover, VP improved the enzymatic hydrolysis of corn stover in vitro. The remarkable lignin-degradative potential makes VP attractive for biotechnological applications. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13068-017-0906-x) contains supplementary material, which is available to authorized users.
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spelling pubmed-55980732017-09-18 A novel and efficient fungal delignification strategy based on versatile peroxidase for lignocellulose bioconversion Kong, Wen Fu, Xiao Wang, Lei Alhujaily, Ahmad Zhang, Jingli Ma, Fuying Zhang, Xiaoyu Yu, Hongbo Biotechnol Biofuels Research BACKGROUND: The selective lignin-degrading white-rot fungi are regarded to be the best lignin degraders and have been widely used for reducing the saccharification recalcitrance of lignocellulose. However, the biological delignification and conversion of lignocellulose in biorefinery is still limited. It is necessary to develop novel and more efficient bio-delignification systems. RESULTS: Physisporinus vitreus relies on a new versatile peroxidase (VP)-based delignification strategy to remove enzymatic recalcitrance of corn stover efficiently, so that saccharification of corn stover was significantly enhanced to 349.1 mg/g biomass (yield of glucose) and 91.5% (hydrolysis yield of cellulose) at 28 days, as high as levels reached by thermochemical treatment. Analysis of the lignin structure using pyrolysis–gas chromatography–mass spectrometry (Py–GC/MS) showed that the total abundance of lignin-derived compounds decreased by 54.0% and revealed a notable demethylation during lignin degradation by P. vitreus. Monomeric and dimeric lignin model compounds were used to confirm the ligninolytic capabilities of extracellular ligninases secreted by P. vitreus. The laccase (Lac) from P. vitreus could not oxidize nonphenolic lignin compounds and polymerized β-O-4 and 5-5′ dimers to precipitate which had a negative effect on the enzymatic hydrolysis of corn stover in vitro. However, the VP from P. vitreus could oxidize both phenolic and nonphenolic lignin model compounds as well as break the β-O-4 and 5-5′ dimers into monomeric compounds, which were measured by high-performance liquid chromatography–electrospray ionization–mass spectrometry (LC–ESI–MS). Moreover, we showed that addition of purified VP in vitro improved the enzymatic hydrolysis of corn stover by 14.1%. CONCLUSIONS: From the highly efficient system of enzymatic recalcitrance removal by new white-rot fungus, we identified a new delignification strategy based on VP which could oxidize both phenolic and nonphenolic lignin units and break different linkages in lignin. In addition, this is the first evidence that VP could break 5-5′ linkage efficiently in vitro. Moreover, VP improved the enzymatic hydrolysis of corn stover in vitro. The remarkable lignin-degradative potential makes VP attractive for biotechnological applications. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13068-017-0906-x) contains supplementary material, which is available to authorized users. BioMed Central 2017-09-13 /pmc/articles/PMC5598073/ /pubmed/28924453 http://dx.doi.org/10.1186/s13068-017-0906-x Text en © The Author(s) 2017 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
Kong, Wen
Fu, Xiao
Wang, Lei
Alhujaily, Ahmad
Zhang, Jingli
Ma, Fuying
Zhang, Xiaoyu
Yu, Hongbo
A novel and efficient fungal delignification strategy based on versatile peroxidase for lignocellulose bioconversion
title A novel and efficient fungal delignification strategy based on versatile peroxidase for lignocellulose bioconversion
title_full A novel and efficient fungal delignification strategy based on versatile peroxidase for lignocellulose bioconversion
title_fullStr A novel and efficient fungal delignification strategy based on versatile peroxidase for lignocellulose bioconversion
title_full_unstemmed A novel and efficient fungal delignification strategy based on versatile peroxidase for lignocellulose bioconversion
title_short A novel and efficient fungal delignification strategy based on versatile peroxidase for lignocellulose bioconversion
title_sort novel and efficient fungal delignification strategy based on versatile peroxidase for lignocellulose bioconversion
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5598073/
https://www.ncbi.nlm.nih.gov/pubmed/28924453
http://dx.doi.org/10.1186/s13068-017-0906-x
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