M59
Unveiling ionic liquid deconstruction of lignocellulosic biomass using glycome profiling
Monday, April 28, 2014
Exhibit/Poster Hall, lower level (Hilton Clearwater Beach)
Jian Shi1, Sivakumar Pattathil2, Sivasankari Venkatachalam3, Michael G. Hahn2, Blake A. Simmons4 and Seema Singh5, (1)Deconstruction Division, Joint BioEnergy Institute/Sandia National Laboratories, Emeryville, CA, (2)Complex Carbohydrate Research Center, University of Georgia, Athens, GA, (3)BioEnergy Science Center, Complex Carbohydrate Research Center, University of Georgia, Athens, GA, (4)Vice-President, Deconstruction Division, Joint BioEnergy Institute, Emeryville, CA, (5)Deconstruction Division, Joint BioEnergy Institute, Emeryville, CA
Certain ionic liquids (ILs) are capable of effectively overcoming plant cell wall recalcitrance; however, the behind-the-scene mechanisms are not fully understood. To better understand how ionic liquids deconstruct biomass, we applied an immunological approach (“glycome profiling”) that employs a comprehensive suite of plant glycan-directed monoclonal antibodies to monitor cell wall structural/compositional/extractability changes in switchgrass biomass.  A range of ILs with very diverse chemical and solvent properties was tested under typical pretreatment conditions, with [C4mim][Cl] solubilizing and regenerating cellulose, [PAAA][H2PO4] and [Ch][Lys] extracting large fraction of lignin, and [C2mim][Ac] solubilizing both lignin and cellulose. Glycome profiling studies on pretreated biomass residues, in combination with wet chemistry quantification and spectrometric analysis, revealed distinct changes in the composition and extractability of non-cellulosic cell wall glycans, suggesting different deconstruction mechanisms caused by different ILs.  Interestingly, all ILs induced the disruption of lignin-polysaccharide interactions as reflected by a loss of pectins and arabinogalactan epitopes in less harsh extracts (oxalate and carbonate) and significantly increased extractability of hemicellulosic glycans in oxalate, carbonate, 1M KOH and 4M KOH extracts.  This study helps a better understanding of IL pretreatment and provides insights on the rational design of task-specific ILs for biomass deconstruction.