3-02: Constructing a mechanistic model for Cel7A processive action on cellulose from molecular simulation

Tuesday, April 20, 2010: 8:30 AM
Salon A-E (Hilton Clearwater Beach)
Gregg T. Beckham1, Yannick J. Bomble2, James F. Matthews2, Lintao Bu1, John W. Brady3, Mark R. Nimlos1, William S. Adney2, Michael E. Himmel2 and Michael F. Crowley2, (1)National Bioenergy Center, National Renewable Energy Laboratory, Golden, CO, (2)Biosciences Center, National Renewable Energy Laboratory, Golden, CO, (3)Department of Food Science, Cornell University, Ithaca, NY
The Family 7 processive cellulases are the basis of many enzyme cocktails for lignocellulosic biomass conversion. Despite their importance, a detailed mechanistic understanding of the Family 7 enzymes remains elusive. Here we present recent results illustrating our ongoing efforts to construct a molecular-level model of the action of a Family 7 cellulase, using the Trichoderma reesei Cel7A enzyme as the basis for study. The three sub-domains of Cel7A, namely the Family 1 carbohydrate-binding module, the O-glycosylated linker peptide, and the catalytic domain are studied independently to ascertain isolated structure-function relationships. The knowledge gained from studies of the individual domains is vital in developing a quantitative, mechanistic model of the processive action of Cel7A. Additionally, the free energy cost to decrystallize cellulose is an essential part of this model; thus, we also present a complementary study in which we measure the molecular-level basis for cellulose recalcitrance, which Cel7A (and other cellulase enzymes) must overcome to degrade the plant cell wall.