Improved methods for breaking down cellulose nanofibers are central to cost-effective biofuel production.
Improved methods for breaking down cellulose nanofibers are central to cost-effective biofuel production and the subject of new research from Los Alamos National Laboratory (LANL) and the Great Lakes Bioenergy Research Center (GLBRC). Scientists are investigating the unique properties of crystalline cellulose nanofibers to develop novel chemical pretreatments and designer enzymes for biofuel production from cellulosic—or non-food—plant derived biomass.
“Cellulose is laid out in plant cell walls as crystalline nanofibers, like steel reinforcements embedded in concrete columns,” says GLBRC’s Shishir Chundawat. “The key to cheaper biofuel production is to unravel these tightly packed nanofibers more efficiently into soluble sugars using fewer enzymes.”
An article published this week in the Proceedings of the National Academy of Sciences suggests—counter-intuitively—that increased binding of enzymes to cellulose polymers doesn’t always lead to faster breakdown into simple sugars. In fact, Chundawat’s research team found that using novel biomass pretreatments to convert cellulose to a unique crystalline structure called cellulose III reduced native enzyme binding while increasing sugar yields by as much as five times.
“The ability of this unconventional pretreatment strategy, currently under development at GLBRC, to selectively alter the cellulose crystal structure may lead to an order of magnitude reduction in enzyme usage. This will be critical for cost-effective cellulosic biofuel production,” says Bruce Dale of Michigan State University, who leads GLBRC’s biomass deconstruction research area.
The researchers had previously demonstrated that altering the crystal structure of native cellulose to cellulose III accelerates enzymatic deconstruction; however, the recent observation that cellulose III increased sugar yields with reduced levels of bound enzyme was unexpected. To explain this finding, Chundawat and a team of LANL researchers led by Gnana Gnanakaran and Anurag Sethi developed a mechanistic kinetic model indicating that the relationship between enzyme affinity for cellulose and catalytic efficiency is more complex than previously thought.
Cellulose III was found to have a less sticky surface that makes it harder for native enzymes to get stuck non-productively on it, unlike untreated cellulose surfaces. The model further predicts that the enhanced enzyme activity, despite reduced binding, is due to the relative ease with which enzymes are able to pull out individual cellulose III chains from the pretreated nanofiber surface and then break them apart into simple sugars.
“These findings are exciting because they may catalyze future development of novel engineered enzymes that are further tailored for conversion of cellulose III rich pretreated biomass to cheaper fuels and other useful compounds that are currently derived from non-renewable fossil fuels,” says Gnanakaran.
Online link to paper: “Increased enzyme binding to substrate is not necessary for more efficient cellulose hydrolysis” PNAS 2013; published ahead of print June 19, 2013, doi:10.1073/pnas.1213426110.
This research was funded by the Great Lakes Bioenergy Research Center (supported by the U.S. Department of Energy, Office of Science, Office of Biological and Environmental Research through Cooperative Agreement DE-FC02-07ER64494 between the Board of Regents of the University of Wisconsin System and the U.S. Department of Energy). The LANL team was supported by the National Advanced Biofuels Consortium (NABC), the Center for Non-Linear Studies, and the Laboratory Directed Research & Development (LDRD) program at LANL.
The Great Lakes Bioenergy Research Center (GLBRC) is one of three Department of Energy funded Bioenergy Research Centers that were founded by DOE’s Office of Science in 2007 to conduct the basic research that will form the foundation of new cellulosic biofuels technology. The GLBRC is headed by the University of Wisconsin (Madison, WI) with Michigan State University (East Lansing, MI) as the major partner. Additional scientific partners are DOE national laboratories, other universities and a biotechnology company.
Source: Los Alamos National Laboratory
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