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Investigating the role of AA9 LPMOs in enzymatic hydrolysis of differentially steam-pretreated spruce
BACKGROUND: To realize the full potential of softwood-based forest biorefineries, the bottlenecks of enzymatic saccharification of softwood need to be better understood. Here, we investigated the potential of lytic polysaccharide monooxygenases (LPMO9s) in softwood saccharification. Norway spruce wa...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10114483/ https://www.ncbi.nlm.nih.gov/pubmed/37076886 http://dx.doi.org/10.1186/s13068-023-02316-0 |
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author | Caputo, Fabio Tõlgo, Monika Naidjonoka, Polina Krogh, Kristian B. R. M. Novy, Vera Olsson, Lisbeth |
author_facet | Caputo, Fabio Tõlgo, Monika Naidjonoka, Polina Krogh, Kristian B. R. M. Novy, Vera Olsson, Lisbeth |
author_sort | Caputo, Fabio |
collection | PubMed |
description | BACKGROUND: To realize the full potential of softwood-based forest biorefineries, the bottlenecks of enzymatic saccharification of softwood need to be better understood. Here, we investigated the potential of lytic polysaccharide monooxygenases (LPMO9s) in softwood saccharification. Norway spruce was steam-pretreated at three different severities, leading to varying hemicellulose retention, lignin condensation, and cellulose ultrastructure. Hydrolyzability of the three substrates was assessed after pretreatment and after an additional knife-milling step, comparing the efficiency of cellulolytic Celluclast + Novozym 188 and LPMO-containing Cellic CTec2 cocktails. The role of Thermoascus aurantiacus TaLPMO9 in saccharification was assessed through time-course analysis of sugar release and accumulation of oxidized sugars, as well as wide-angle X-ray scattering analysis of cellulose ultrastructural changes. RESULTS: Glucose yield was 6% (w/w) with the mildest pretreatment (steam pretreatment at 210 °C without catalyst) and 66% (w/w) with the harshest (steam pretreatment at 210 °C with 3%(w/w) SO(2)) when using Celluclast + Novozym 188. Surprisingly, the yield was lower with all substrates when Cellic CTec2 was used. Therefore, the conditions for optimal LPMO activity were tested and it was found that enough O(2) was present over the headspace and that the reducing power of the lignin of all three substrates was sufficient for the LPMOs in Cellic CTec2 to be active. Supplementation of Celluclast + Novozym 188 with TaLPMO9 increased the conversion of glucan by 1.6-fold and xylan by 1.5-fold, which was evident primarily in the later stages of saccharification (24–72 h). Improved glucan conversion could be explained by drastically reduced cellulose crystallinity of spruce substrates upon TaLPMO9 supplementation. CONCLUSION: Our study demonstrated that LPMO addition to hydrolytic enzymes improves the release of glucose and xylose from steam-pretreated softwood substrates. Furthermore, softwood lignin provides enough reducing power for LPMOs, irrespective of pretreatment severity. These results provided new insights into the potential role of LPMOs in saccharification of industrially relevant softwood substrates. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13068-023-02316-0. |
format | Online Article Text |
id | pubmed-10114483 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-101144832023-04-20 Investigating the role of AA9 LPMOs in enzymatic hydrolysis of differentially steam-pretreated spruce Caputo, Fabio Tõlgo, Monika Naidjonoka, Polina Krogh, Kristian B. R. M. Novy, Vera Olsson, Lisbeth Biotechnol Biofuels Bioprod Research BACKGROUND: To realize the full potential of softwood-based forest biorefineries, the bottlenecks of enzymatic saccharification of softwood need to be better understood. Here, we investigated the potential of lytic polysaccharide monooxygenases (LPMO9s) in softwood saccharification. Norway spruce was steam-pretreated at three different severities, leading to varying hemicellulose retention, lignin condensation, and cellulose ultrastructure. Hydrolyzability of the three substrates was assessed after pretreatment and after an additional knife-milling step, comparing the efficiency of cellulolytic Celluclast + Novozym 188 and LPMO-containing Cellic CTec2 cocktails. The role of Thermoascus aurantiacus TaLPMO9 in saccharification was assessed through time-course analysis of sugar release and accumulation of oxidized sugars, as well as wide-angle X-ray scattering analysis of cellulose ultrastructural changes. RESULTS: Glucose yield was 6% (w/w) with the mildest pretreatment (steam pretreatment at 210 °C without catalyst) and 66% (w/w) with the harshest (steam pretreatment at 210 °C with 3%(w/w) SO(2)) when using Celluclast + Novozym 188. Surprisingly, the yield was lower with all substrates when Cellic CTec2 was used. Therefore, the conditions for optimal LPMO activity were tested and it was found that enough O(2) was present over the headspace and that the reducing power of the lignin of all three substrates was sufficient for the LPMOs in Cellic CTec2 to be active. Supplementation of Celluclast + Novozym 188 with TaLPMO9 increased the conversion of glucan by 1.6-fold and xylan by 1.5-fold, which was evident primarily in the later stages of saccharification (24–72 h). Improved glucan conversion could be explained by drastically reduced cellulose crystallinity of spruce substrates upon TaLPMO9 supplementation. CONCLUSION: Our study demonstrated that LPMO addition to hydrolytic enzymes improves the release of glucose and xylose from steam-pretreated softwood substrates. Furthermore, softwood lignin provides enough reducing power for LPMOs, irrespective of pretreatment severity. These results provided new insights into the potential role of LPMOs in saccharification of industrially relevant softwood substrates. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13068-023-02316-0. BioMed Central 2023-04-19 /pmc/articles/PMC10114483/ /pubmed/37076886 http://dx.doi.org/10.1186/s13068-023-02316-0 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Caputo, Fabio Tõlgo, Monika Naidjonoka, Polina Krogh, Kristian B. R. M. Novy, Vera Olsson, Lisbeth Investigating the role of AA9 LPMOs in enzymatic hydrolysis of differentially steam-pretreated spruce |
title | Investigating the role of AA9 LPMOs in enzymatic hydrolysis of differentially steam-pretreated spruce |
title_full | Investigating the role of AA9 LPMOs in enzymatic hydrolysis of differentially steam-pretreated spruce |
title_fullStr | Investigating the role of AA9 LPMOs in enzymatic hydrolysis of differentially steam-pretreated spruce |
title_full_unstemmed | Investigating the role of AA9 LPMOs in enzymatic hydrolysis of differentially steam-pretreated spruce |
title_short | Investigating the role of AA9 LPMOs in enzymatic hydrolysis of differentially steam-pretreated spruce |
title_sort | investigating the role of aa9 lpmos in enzymatic hydrolysis of differentially steam-pretreated spruce |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10114483/ https://www.ncbi.nlm.nih.gov/pubmed/37076886 http://dx.doi.org/10.1186/s13068-023-02316-0 |
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