TY - JOUR
T1 - Hemicellulose Modulates Nanoscale Lignin Architecture in Synthetic Plant Cell Walls
AU - Snyder, Patrick J.
AU - Allard, Valentin
AU - Bhagia, Samarthya
AU - Farahi, Rubye H.
AU - Lereu, Aude L.
AU - Backlund, Mikael P.
AU - Passian, Ali
N1 - This work was supported by the Office of Biological and Environmental Research (BER) in the U.S. Department of Energy (DOE) Office of Science, under grant DE-SC0023167. The s-SNOM measurements were carried out at the Illinois Materials Research Laboratory Central Research Facilities, University of Illinois Urbana–Champaign. ORNL is managed by UT-Battelle, LLC, for the U.S. DOE under Contract No. DE-AC05-00OR22725. This paper has been authored by UT- Battelle, LLC under Contract No. DE-AC05-00OR22725 with the U.S. Department of Energy. The United States Government retains and the publisher, by accepting the article for publication, acknowledges that the United States Government retains a nonexclusive, paid-up, irrevocable, worldwide license to publish or reproduce the published form of this paper or allow others to do so, for United States Government purposes.
PY - 2025/12/2
Y1 - 2025/12/2
N2 - Cellulose, hemicellulose, and lignin─the most abundant biopolymers on Earth─compose the structural matrix of plant biomass, providing renewable resources critical to bioenergy and sustainable materials. Despite their importance, the nanoscale mechanochemical processes underlying lignocellulose assembly during plant secondary cell wall formation remain poorly understood, hindering advancements in biomass conversion technologies. Here, we synthesize a biomimetic model system comprising cellulose–hemicellulose nanofibrils (CHN) to examine guaiacyl lignin polymerization in a physiologically relevant context. Using advanced nanocharacterization─scattering-type scanning near-field optical microscopy (s-SNOM) with infrared nanospectroscopy coupled to solid-state nuclear magnetic resonance (NMR)─we reveal that hemicellulose presence considerably modulates lignin deposition and alters its interunit bond distribution. Specifically, hemicellulose-rich environments dramatically reduce lignin deposition by approximately 50% and yield highly condensed lignin structures characterized by severely reduced β–O–4′ linkages (<2%) and suppressed β–β′ linkages. Conversely, cellulose-alone scaffolds support notably higher β–O–4′ content (∼10%), resulting in a more uniform nanoscale lignin coating. Our work helps explain how accessible hemicellulose sites, both sterically and chemically, direct radical coupling during lignification, fundamentally reshaping lignin’s nanoscale architecture. These findings deepen our mechanistic understanding of plant cell wall biosynthesis and inform strategies aimed at enhancing biomass deconstruction efficiency for sustainable bioenergy applications.
AB - Cellulose, hemicellulose, and lignin─the most abundant biopolymers on Earth─compose the structural matrix of plant biomass, providing renewable resources critical to bioenergy and sustainable materials. Despite their importance, the nanoscale mechanochemical processes underlying lignocellulose assembly during plant secondary cell wall formation remain poorly understood, hindering advancements in biomass conversion technologies. Here, we synthesize a biomimetic model system comprising cellulose–hemicellulose nanofibrils (CHN) to examine guaiacyl lignin polymerization in a physiologically relevant context. Using advanced nanocharacterization─scattering-type scanning near-field optical microscopy (s-SNOM) with infrared nanospectroscopy coupled to solid-state nuclear magnetic resonance (NMR)─we reveal that hemicellulose presence considerably modulates lignin deposition and alters its interunit bond distribution. Specifically, hemicellulose-rich environments dramatically reduce lignin deposition by approximately 50% and yield highly condensed lignin structures characterized by severely reduced β–O–4′ linkages (<2%) and suppressed β–β′ linkages. Conversely, cellulose-alone scaffolds support notably higher β–O–4′ content (∼10%), resulting in a more uniform nanoscale lignin coating. Our work helps explain how accessible hemicellulose sites, both sterically and chemically, direct radical coupling during lignification, fundamentally reshaping lignin’s nanoscale architecture. These findings deepen our mechanistic understanding of plant cell wall biosynthesis and inform strategies aimed at enhancing biomass deconstruction efficiency for sustainable bioenergy applications.
KW - NMR
KW - biomimetic plant cell wall model
KW - cellulose−hemicellulose nanofibrils
KW - infrared nanospectroscopy
KW - lignin polymerization
KW - nanoscale chemical mapping
KW - scattering-type scanning near-field optical microscopy (s-SNOM)
UR - https://www.scopus.com/pages/publications/105023489580
UR - https://www.scopus.com/pages/publications/105023489580#tab=citedBy
U2 - 10.1021/acsnano.5c09006
DO - 10.1021/acsnano.5c09006
M3 - Article
C2 - 41248213
AN - SCOPUS:105023489580
SN - 1936-0851
VL - 19
SP - 40364
EP - 40382
JO - ACS Nano
JF - ACS Nano
IS - 47
ER -