Abstract
The ratio of syringyl (S) and guaiacyl (G) units in lignin has been regarded as a major factor in determining the maximum monomer yield from lignin depolymerization. This limit arises from the notion that G units are prone to C-C bond formation during lignin biosynthesis, resulting in less ether linkages that generate monomers. This study uses reductive catalytic fractionation (RCF) in flow-through reactors as an analytical tool to depolymerize lignin in poplar with naturally varying S/G ratios, and directly challenges the common conception that the S/G ratio predicts monomer yields. Rather, this work suggests that the plant controls C-O and C-C bond content by regulating monomer transport during lignin biosynthesis. Overall, our results indicate that additional factors beyond the monomeric composition of native lignin are important in developing a fundamental understanding of lignin biosynthesis.
Original language | American English |
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Article number | 2033 |
Number of pages | 10 |
Journal | Nature Communications |
Volume | 10 |
Issue number | 1 |
DOIs | |
State | Published - 1 Dec 2019 |
Bibliographical note
Publisher Copyright:© 2019, The Author(s).
NREL Publication Number
- NREL/JA-2A00-73032
Keywords
- biomass pretreatment
- flow-through extraction
- lignin conversion
- lignin first
- reductive catalysis
- S/G ratio
- semi-continuous processing