Abstract
Lignin, composed predominantly of p-hydroxyphenyl (H), guaiacyl (G) and syringyl (S) subunits, is a major component of plant cell walls that imparts resistance toward chemical and microbial deconstruction of plant biomass, rendering its conversion inefficient and costly. Previous studies have shown that alterating lignin composition, i.e., the relative abundance of H, G and S subunits, promisesmore efficient extraction of sugars from plant biomass. Smaller and less branched lignin chains are more easily extracted during pretreatment, making cellulose more readily degradable. Here, using density functional theory calculations, we show that the incorporation of H subunits into lignin via b-b and b-5 interunit linkages reduces the degree of polymerization in lignin. Frontier molecularorbital analyses of lignin dimers and trimers show that H as a terminal subunit on a growing lignin polymer linked via b-b and b-5 linkage cannot undergo radical formation, preventing further chain growth by endwise polymerization resulting in lignin polymers with lower degree of polymerization. These results indicate that, for endwise polymerization in lignin synthesis, there exists a chemicalcontrol that may lay a significant role in determining the structure of lignin.
Original language | American English |
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State | Published - 2013 |
Event | American Chemical Society. 245th ACS National Meeting - New Orleans, Louisiana Duration: 7 Apr 2013 → 11 Apr 2013 |
Conference
Conference | American Chemical Society. 245th ACS National Meeting |
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City | New Orleans, Louisiana |
Period | 7/04/13 → 11/04/13 |
NREL Publication Number
- NREL/CP-5100-58868