Cargando…

NMR Study on Laccase Polymerization of Kraft Lignin Using Different Enzymes Source

The usage of laccases is a sustainable and environmentally friendly approach to modifying the Kraft lignin structure for use in certain applications. However, the inherent structure of Kraft lignin, as well as that resulting from laccase modification, still presents challenges for fundamental compre...

Descripción completa

Detalles Bibliográficos
Autores principales: Ibarra, David, García-Fuentevilla, Luisa, Domínguez, Gabriela, Martín-Sampedro, Raquel, Hernández, Manuel, Arias, María E., Santos, José I., Eugenio, María E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9917248/
https://www.ncbi.nlm.nih.gov/pubmed/36768678
http://dx.doi.org/10.3390/ijms24032359
_version_ 1784886325183250432
author Ibarra, David
García-Fuentevilla, Luisa
Domínguez, Gabriela
Martín-Sampedro, Raquel
Hernández, Manuel
Arias, María E.
Santos, José I.
Eugenio, María E.
author_facet Ibarra, David
García-Fuentevilla, Luisa
Domínguez, Gabriela
Martín-Sampedro, Raquel
Hernández, Manuel
Arias, María E.
Santos, José I.
Eugenio, María E.
author_sort Ibarra, David
collection PubMed
description The usage of laccases is a sustainable and environmentally friendly approach to modifying the Kraft lignin structure for use in certain applications. However, the inherent structure of Kraft lignin, as well as that resulting from laccase modification, still presents challenges for fundamental comprehension and successful lignin valorization. In this study, bacterial and fungal laccases were employed to modify eucalypt Kraft lignin. To evaluate the type and range of the chemical and structural changes of laccase-treated lignins, different NMR techniques, including solution (1)H and 2D NMR (heteronuclear single quantum correlation (HSQC)), and solid-state (13)C NMR, were applied. Size exclusion chromatography and infrared spectroscopy were also used. Interestingly, HSQC analysis showed substantial changes in the oxygenated aliphatic region of lignins, showing an almost complete absence of signals corresponding to side-chains due to laccase depolymerization. Simultaneously, a significant loss of aromatic signals was observed by HSQC and (1)H NMR, which was attributed to a deprotonation of the lignin benzenic rings due to polymerization/condensation by laccase reactions. Then, condensed structures, such as α-5′, 5-5′, and 4-O-5′, were detected by HSQC and (13)C NMR, supporting the increment in molecular weight, as well as the phenolic content reduction determined in lignins.
format Online
Article
Text
id pubmed-9917248
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-99172482023-02-11 NMR Study on Laccase Polymerization of Kraft Lignin Using Different Enzymes Source Ibarra, David García-Fuentevilla, Luisa Domínguez, Gabriela Martín-Sampedro, Raquel Hernández, Manuel Arias, María E. Santos, José I. Eugenio, María E. Int J Mol Sci Article The usage of laccases is a sustainable and environmentally friendly approach to modifying the Kraft lignin structure for use in certain applications. However, the inherent structure of Kraft lignin, as well as that resulting from laccase modification, still presents challenges for fundamental comprehension and successful lignin valorization. In this study, bacterial and fungal laccases were employed to modify eucalypt Kraft lignin. To evaluate the type and range of the chemical and structural changes of laccase-treated lignins, different NMR techniques, including solution (1)H and 2D NMR (heteronuclear single quantum correlation (HSQC)), and solid-state (13)C NMR, were applied. Size exclusion chromatography and infrared spectroscopy were also used. Interestingly, HSQC analysis showed substantial changes in the oxygenated aliphatic region of lignins, showing an almost complete absence of signals corresponding to side-chains due to laccase depolymerization. Simultaneously, a significant loss of aromatic signals was observed by HSQC and (1)H NMR, which was attributed to a deprotonation of the lignin benzenic rings due to polymerization/condensation by laccase reactions. Then, condensed structures, such as α-5′, 5-5′, and 4-O-5′, were detected by HSQC and (13)C NMR, supporting the increment in molecular weight, as well as the phenolic content reduction determined in lignins. MDPI 2023-01-25 /pmc/articles/PMC9917248/ /pubmed/36768678 http://dx.doi.org/10.3390/ijms24032359 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Ibarra, David
García-Fuentevilla, Luisa
Domínguez, Gabriela
Martín-Sampedro, Raquel
Hernández, Manuel
Arias, María E.
Santos, José I.
Eugenio, María E.
NMR Study on Laccase Polymerization of Kraft Lignin Using Different Enzymes Source
title NMR Study on Laccase Polymerization of Kraft Lignin Using Different Enzymes Source
title_full NMR Study on Laccase Polymerization of Kraft Lignin Using Different Enzymes Source
title_fullStr NMR Study on Laccase Polymerization of Kraft Lignin Using Different Enzymes Source
title_full_unstemmed NMR Study on Laccase Polymerization of Kraft Lignin Using Different Enzymes Source
title_short NMR Study on Laccase Polymerization of Kraft Lignin Using Different Enzymes Source
title_sort nmr study on laccase polymerization of kraft lignin using different enzymes source
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9917248/
https://www.ncbi.nlm.nih.gov/pubmed/36768678
http://dx.doi.org/10.3390/ijms24032359
work_keys_str_mv AT ibarradavid nmrstudyonlaccasepolymerizationofkraftligninusingdifferentenzymessource
AT garciafuentevillaluisa nmrstudyonlaccasepolymerizationofkraftligninusingdifferentenzymessource
AT dominguezgabriela nmrstudyonlaccasepolymerizationofkraftligninusingdifferentenzymessource
AT martinsampedroraquel nmrstudyonlaccasepolymerizationofkraftligninusingdifferentenzymessource
AT hernandezmanuel nmrstudyonlaccasepolymerizationofkraftligninusingdifferentenzymessource
AT ariasmariae nmrstudyonlaccasepolymerizationofkraftligninusingdifferentenzymessource
AT santosjosei nmrstudyonlaccasepolymerizationofkraftligninusingdifferentenzymessource
AT eugeniomariae nmrstudyonlaccasepolymerizationofkraftligninusingdifferentenzymessource