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Isothermal titration calorimetric assessment of lignin conversion by laccases
Lignin valorization may offer a sustainable approach to achieve a chemical industry that is not completely dependent on fossil resources for the production of aromatics. However, lignin is a recalcitrant, heterogeneous, and complex polymeric compound for which only very few catalysts can act in a pr...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9299204/ https://www.ncbi.nlm.nih.gov/pubmed/34796477 http://dx.doi.org/10.1002/bit.27991 |
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author | A. Islam, Shams T. Zhang, Jie Tonin, Fabio Hinderks, Renske Deurloo, Yanthi N. Urlacher, Vlada B. Hagedoorn, Peter‐Leon |
author_facet | A. Islam, Shams T. Zhang, Jie Tonin, Fabio Hinderks, Renske Deurloo, Yanthi N. Urlacher, Vlada B. Hagedoorn, Peter‐Leon |
author_sort | A. Islam, Shams T. |
collection | PubMed |
description | Lignin valorization may offer a sustainable approach to achieve a chemical industry that is not completely dependent on fossil resources for the production of aromatics. However, lignin is a recalcitrant, heterogeneous, and complex polymeric compound for which only very few catalysts can act in a predictable and reproducible manner. Laccase is one of those catalysts and has often been referred to as an ideal “green” catalyst, as it is able to oxidize various linkages within lignin to release aromatic products, with the use of molecular oxygen and formation of water as the only side product. The extent and rate of laccase‐catalyzed lignin conversion were measured using the label‐free analytical technique isothermal titration calorimetry (ITC). IITC provides the molar enthalpy of the reaction, which reflects the extent of conversion and the time‐dependent power trace, which reflects the rate of the reaction. Calorimetric assessment of the lignin conversion brought about by various fungal and bacterial laccases in the absence of mediators showed marked differences in the extent and rate of conversion for the different enzymes. Kraft lignin conversion by Trametes versicolor laccase followed Michaelis–Menten kinetics and was characterized by the following thermodynamic and kinetic parameters ΔH (ITC) = −(2.06 ± 0.06)·10(3) kJ mol(−1), K(M) = 6.6 ± 1.2 μM and V(max) = 0.30 ± 0.02 U/mg at 25°C and pH 6.5. We envision calorimetric techniques as important tools for the development of enzymatic lignin valorization strategies. |
format | Online Article Text |
id | pubmed-9299204 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-92992042022-07-21 Isothermal titration calorimetric assessment of lignin conversion by laccases A. Islam, Shams T. Zhang, Jie Tonin, Fabio Hinderks, Renske Deurloo, Yanthi N. Urlacher, Vlada B. Hagedoorn, Peter‐Leon Biotechnol Bioeng ARTICLES Lignin valorization may offer a sustainable approach to achieve a chemical industry that is not completely dependent on fossil resources for the production of aromatics. However, lignin is a recalcitrant, heterogeneous, and complex polymeric compound for which only very few catalysts can act in a predictable and reproducible manner. Laccase is one of those catalysts and has often been referred to as an ideal “green” catalyst, as it is able to oxidize various linkages within lignin to release aromatic products, with the use of molecular oxygen and formation of water as the only side product. The extent and rate of laccase‐catalyzed lignin conversion were measured using the label‐free analytical technique isothermal titration calorimetry (ITC). IITC provides the molar enthalpy of the reaction, which reflects the extent of conversion and the time‐dependent power trace, which reflects the rate of the reaction. Calorimetric assessment of the lignin conversion brought about by various fungal and bacterial laccases in the absence of mediators showed marked differences in the extent and rate of conversion for the different enzymes. Kraft lignin conversion by Trametes versicolor laccase followed Michaelis–Menten kinetics and was characterized by the following thermodynamic and kinetic parameters ΔH (ITC) = −(2.06 ± 0.06)·10(3) kJ mol(−1), K(M) = 6.6 ± 1.2 μM and V(max) = 0.30 ± 0.02 U/mg at 25°C and pH 6.5. We envision calorimetric techniques as important tools for the development of enzymatic lignin valorization strategies. John Wiley and Sons Inc. 2021-11-26 2022-02 /pmc/articles/PMC9299204/ /pubmed/34796477 http://dx.doi.org/10.1002/bit.27991 Text en © 2021 The Authors. Biotechnology and Bioengineering published by Wiley Periodicals LLC https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | ARTICLES A. Islam, Shams T. Zhang, Jie Tonin, Fabio Hinderks, Renske Deurloo, Yanthi N. Urlacher, Vlada B. Hagedoorn, Peter‐Leon Isothermal titration calorimetric assessment of lignin conversion by laccases |
title | Isothermal titration calorimetric assessment of lignin conversion by laccases |
title_full | Isothermal titration calorimetric assessment of lignin conversion by laccases |
title_fullStr | Isothermal titration calorimetric assessment of lignin conversion by laccases |
title_full_unstemmed | Isothermal titration calorimetric assessment of lignin conversion by laccases |
title_short | Isothermal titration calorimetric assessment of lignin conversion by laccases |
title_sort | isothermal titration calorimetric assessment of lignin conversion by laccases |
topic | ARTICLES |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9299204/ https://www.ncbi.nlm.nih.gov/pubmed/34796477 http://dx.doi.org/10.1002/bit.27991 |
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