In order to efficiently convert biomass to other useful chemicals, it is necessary to understand and overcome its recalcitrance to enzymatic deconstruction processes. One key question involved in a biomass study is the correlation between the enzymatic activity and the cellulose structure. Although many experimental studies have been attempted previously to answer this fundamental question, the answer still remains elusive. The difficulty is that it requires molecular analysis of crystalline carbohydrate polymers (cellulose) in an amorphous matrix containing the same organic functional groups. Current analytical methods cannot provide sufficient details about crystalline cellulose in lignocellulosic biomass. In this EAGER project, the PIs Sunkyu Park from North Carolina State University and Seong H. Kim from Pennsylvania State University will explore the application of sum-frequency generation (SFG) vibration spectroscopy to find the influence of cellulose crystal structure on the enzymatic deconstruction process.

The unique crystal structure of cellulose allows it to demonstrate non-linear optical properties such as SFG which are absent in other biomass components. SFG is a second-order nonlinear optical response of a system without optical centrosymmetry when it is irradiated with high-intensity laser pulses. Based on this unique non-linear optical selection rule, amorphous components such as hemicellulose and lignin in biomass cannot generate SFG signals. Thus, SFG can detect the structure of crystalline cellulose in biomass without any chemical isolation and modification of the cellulose. Furthermore, the question of the relation between structure and enzymatic activity can be monitored by following changes in the cellulose SFG response.

There are a number of Broader technical impacts that result from this study. The molecular insights that will be obtained through this research will be valuable information to understand the biomass recalcitrance and develop more efficient biomass conversion processes. Specifically the expected outcomes include: (1) a significant step toward understanding of the crystalline structure of celluloses, (2) new tool development for cellulose characterization without separation, which is sensitive only to crystalline cellulose in lignocellulose biomass, (3) a molecular insight into the relationship between cellulose crystalline structure and enzymatic hydrolysis, and (4) student education in cross-disciplinary areas. This tool, SFG spectroscopy, is expected to be useful for other biomass applications such as cellulose dissolution, biomass thermal conversion, cellulose biosynthesis, etc.

Project Report

Enzymatic hydrolysis of biomass to produce sugars is essential to produce bioenergy and platform chemicals. The key question involved in the biomass study is the correlation between the enzymatic activity and the cellulose structure. Although many experimental studies have been attempted previously to answer this fundamental question, it still remains elusive. Whether the cellulose structure (distribution of polymorphs,crystal size and shape, microfibril assemly/aggregation) changes during enzymactic hydrolysis of biomass is an important question. Though these questions have been studied with XRD, NMR, FT-IR, and Raman, they were not able to provide unambiguous answers due to the lack of detection sensitivity. We are applying SFG spectroscopy which can selectively detect cellulose inside biomass without spectral interference from amorphous matrix. In this EAGER project, we proposed to explore the application of sum-frequency generation (SFG) vibration spectroscopy together with x-ray diffraction (XRD) to find the influence of cellulose crystal structure on enzymatic deconstruction process. XRD analyses of cellulose retrieved from enzymatic hydrolysis showed that cellulose polymorph (I-alpha and I-beta) and crystallinity in nano scale did not change. However, SFG analyses found changes in packing or assembly ofcrystalline cellulose microfibrils in the sample. This finding will provide new insights in understanding of enzymatic hydrolysis of biomass. We have published and presented the outcomes at the national meetings such as American Chemical Society (ACS) and America Institute of Chemical Engineer (AIChE). This was a collaborative project with Penn State University.

Project Start
Project End
Budget Start
2011-12-01
Budget End
2013-05-31
Support Year
Fiscal Year
2011
Total Cost
$50,000
Indirect Cost
Name
North Carolina State University Raleigh
Department
Type
DUNS #
City
Raleigh
State
NC
Country
United States
Zip Code
27695