Cargando…
Real-time imaging reveals that lytic polysaccharide monooxygenase promotes cellulase activity by increasing cellulose accessibility
BACKGROUND: The high cost of enzymes is one of the key technical barriers that must be overcome to realize the economical production of biofuels and biomaterials from biomass. Supplementation of enzyme cocktails with lytic polysaccharide monooxygenase (LPMO) can increase the efficiency of these cell...
Autores principales: | , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5815216/ https://www.ncbi.nlm.nih.gov/pubmed/29467819 http://dx.doi.org/10.1186/s13068-018-1023-1 |
_version_ | 1783300463160983552 |
---|---|
author | Song, Bo Li, Bingyao Wang, Xiaoyan Shen, Wei Park, Sungjin Collings, Cynthia Feng, Anran Smith, Steve J. Walton, Jonathan D. Ding, Shi-You |
author_facet | Song, Bo Li, Bingyao Wang, Xiaoyan Shen, Wei Park, Sungjin Collings, Cynthia Feng, Anran Smith, Steve J. Walton, Jonathan D. Ding, Shi-You |
author_sort | Song, Bo |
collection | PubMed |
description | BACKGROUND: The high cost of enzymes is one of the key technical barriers that must be overcome to realize the economical production of biofuels and biomaterials from biomass. Supplementation of enzyme cocktails with lytic polysaccharide monooxygenase (LPMO) can increase the efficiency of these cellulase mixtures for biomass conversion. The previous studies have revealed that LPMOs cleave polysaccharide chains by oxidization of the C1 and/or C4 carbons of the monomeric units. However, how LPMOs enhance enzymatic degradation of lignocellulose is still poorly understood. RESULTS: In this study, we combined enzymatic assays and real-time imaging using atomic force microscopy (AFM) to study the molecular interactions of an LPMO [TrAA9A, formerly known as TrCel61A) from Trichoderma reesei] and a cellobiohydrolase I (TlCel7A from T. longibrachiatum) with bacterial microcrystalline cellulose (BMCC) as a substrate. Cellulose conversion by TlCel7A alone was enhanced from 46 to 54% by the addition of TrAA9A. Conversion by a mixture of TlCel7A, endoglucanase, and β-glucosidase was increased from 79 to 87% using pretreated BMCC with TrAA9A for 72 h. AFM imaging demonstrated that individual TrAA9A molecules exhibited intermittent random movement along, across, and penetrating into the ribbon-like microfibril structure of BMCC, which was concomitant with the release of a small amount of oxidized sugars and the splitting of large cellulose ribbons into fibrils with smaller diameters. The dividing effect of the cellulose microfibril occurred more rapidly when TrAA9A and TlCel7A were added together compared to TrAA9A alone; TlCel7A alone caused no separation. CONCLUSIONS: TrAA9A increases the accessible surface area of BMCC by separating large cellulose ribbons, and thereby enhances cellulose hydrolysis yield. By providing the first direct observation of LPMO action on a cellulosic substrate, this study sheds new light on the mechanisms by which LPMO enhances biomass conversion. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13068-018-1023-1) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5815216 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-58152162018-02-21 Real-time imaging reveals that lytic polysaccharide monooxygenase promotes cellulase activity by increasing cellulose accessibility Song, Bo Li, Bingyao Wang, Xiaoyan Shen, Wei Park, Sungjin Collings, Cynthia Feng, Anran Smith, Steve J. Walton, Jonathan D. Ding, Shi-You Biotechnol Biofuels Research BACKGROUND: The high cost of enzymes is one of the key technical barriers that must be overcome to realize the economical production of biofuels and biomaterials from biomass. Supplementation of enzyme cocktails with lytic polysaccharide monooxygenase (LPMO) can increase the efficiency of these cellulase mixtures for biomass conversion. The previous studies have revealed that LPMOs cleave polysaccharide chains by oxidization of the C1 and/or C4 carbons of the monomeric units. However, how LPMOs enhance enzymatic degradation of lignocellulose is still poorly understood. RESULTS: In this study, we combined enzymatic assays and real-time imaging using atomic force microscopy (AFM) to study the molecular interactions of an LPMO [TrAA9A, formerly known as TrCel61A) from Trichoderma reesei] and a cellobiohydrolase I (TlCel7A from T. longibrachiatum) with bacterial microcrystalline cellulose (BMCC) as a substrate. Cellulose conversion by TlCel7A alone was enhanced from 46 to 54% by the addition of TrAA9A. Conversion by a mixture of TlCel7A, endoglucanase, and β-glucosidase was increased from 79 to 87% using pretreated BMCC with TrAA9A for 72 h. AFM imaging demonstrated that individual TrAA9A molecules exhibited intermittent random movement along, across, and penetrating into the ribbon-like microfibril structure of BMCC, which was concomitant with the release of a small amount of oxidized sugars and the splitting of large cellulose ribbons into fibrils with smaller diameters. The dividing effect of the cellulose microfibril occurred more rapidly when TrAA9A and TlCel7A were added together compared to TrAA9A alone; TlCel7A alone caused no separation. CONCLUSIONS: TrAA9A increases the accessible surface area of BMCC by separating large cellulose ribbons, and thereby enhances cellulose hydrolysis yield. By providing the first direct observation of LPMO action on a cellulosic substrate, this study sheds new light on the mechanisms by which LPMO enhances biomass conversion. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13068-018-1023-1) contains supplementary material, which is available to authorized users. BioMed Central 2018-02-15 /pmc/articles/PMC5815216/ /pubmed/29467819 http://dx.doi.org/10.1186/s13068-018-1023-1 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 Song, Bo Li, Bingyao Wang, Xiaoyan Shen, Wei Park, Sungjin Collings, Cynthia Feng, Anran Smith, Steve J. Walton, Jonathan D. Ding, Shi-You Real-time imaging reveals that lytic polysaccharide monooxygenase promotes cellulase activity by increasing cellulose accessibility |
title | Real-time imaging reveals that lytic polysaccharide monooxygenase promotes cellulase activity by increasing cellulose accessibility |
title_full | Real-time imaging reveals that lytic polysaccharide monooxygenase promotes cellulase activity by increasing cellulose accessibility |
title_fullStr | Real-time imaging reveals that lytic polysaccharide monooxygenase promotes cellulase activity by increasing cellulose accessibility |
title_full_unstemmed | Real-time imaging reveals that lytic polysaccharide monooxygenase promotes cellulase activity by increasing cellulose accessibility |
title_short | Real-time imaging reveals that lytic polysaccharide monooxygenase promotes cellulase activity by increasing cellulose accessibility |
title_sort | real-time imaging reveals that lytic polysaccharide monooxygenase promotes cellulase activity by increasing cellulose accessibility |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5815216/ https://www.ncbi.nlm.nih.gov/pubmed/29467819 http://dx.doi.org/10.1186/s13068-018-1023-1 |
work_keys_str_mv | AT songbo realtimeimagingrevealsthatlyticpolysaccharidemonooxygenasepromotescellulaseactivitybyincreasingcelluloseaccessibility AT libingyao realtimeimagingrevealsthatlyticpolysaccharidemonooxygenasepromotescellulaseactivitybyincreasingcelluloseaccessibility AT wangxiaoyan realtimeimagingrevealsthatlyticpolysaccharidemonooxygenasepromotescellulaseactivitybyincreasingcelluloseaccessibility AT shenwei realtimeimagingrevealsthatlyticpolysaccharidemonooxygenasepromotescellulaseactivitybyincreasingcelluloseaccessibility AT parksungjin realtimeimagingrevealsthatlyticpolysaccharidemonooxygenasepromotescellulaseactivitybyincreasingcelluloseaccessibility AT collingscynthia realtimeimagingrevealsthatlyticpolysaccharidemonooxygenasepromotescellulaseactivitybyincreasingcelluloseaccessibility AT fenganran realtimeimagingrevealsthatlyticpolysaccharidemonooxygenasepromotescellulaseactivitybyincreasingcelluloseaccessibility AT smithstevej realtimeimagingrevealsthatlyticpolysaccharidemonooxygenasepromotescellulaseactivitybyincreasingcelluloseaccessibility AT waltonjonathand realtimeimagingrevealsthatlyticpolysaccharidemonooxygenasepromotescellulaseactivitybyincreasingcelluloseaccessibility AT dingshiyou realtimeimagingrevealsthatlyticpolysaccharidemonooxygenasepromotescellulaseactivitybyincreasingcelluloseaccessibility |