Quantification of Native Lignin Structural Features with Gel‐Phase 2D‐HSQC0 Reveals Lignin Structural Changes During Extraction

Author:

Bourmaud Claire L.1ORCID,Bertella Stefania1ORCID,Bosch Rico Anna1,Karlen Steven D.2ORCID,Ralph John23ORCID,Luterbacher Jeremy S.1ORCID

Affiliation:

1. Laboratory of Sustainable and Catalytic Processing Institute of Chemical Sciences and Engineering École Polytechnique Fédérale de Lausanne (EPFL) CH-1015 Lausanne Switzerland

2. U.S. Department of Energy (DOE) Great Lakes Bioenergy Research Center Wisconsin Energy Institute University of Wisconsin Madison WI 53726 USA

3. Department of Biochemistry University of Wisconsin Madison WI 53706 USA

Abstract

AbstractOur ability to study and valorize the lignin fraction of biomass is hampered by the fundamental and still unmet challenge of precisely quantifying native lignin's structural features. Here, we developed a rapid elevated‐temperature 1H−13C Heteronuclear Single‐Quantum Coherence Zero (HSQC0) NMR method that enables this precise quantification of native lignin structural characteristics even with whole plant cell wall (WPCW) NMR spectroscopy, overcoming fast spin relaxation in the gel phase. We also formulated a Gaussian fitting algorithm to perform automatic and reliable spectral integration. By combining HSQC0 measurements with yield measurements following depolymerisation, we can confirm the combinatorial nature of radical coupling reactions during biosynthesis leading to a random sequential organization of linkages within a largely linear lignin chain. Such analyses illustrate how this analytical method can greatly facilitate the study of native lignin structure, which can then be used for fundamental studies or to understand lignin depolymerization methods like reductive catalytic fractionation or aldehyde‐assisted fractionation.

Funder

Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung

Publisher

Wiley

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