16-03: Direct visualization of the enzymatic digestion of a single fiber of native cellulose in an aqueous environment by atomic force microscopy

Thursday, May 5, 2011: 2:00 PM
Grand Ballroom A, 2nd fl (Sheraton Seattle)
Amanda Quirk1, Jacek Lipkowski1, Chris Vandenende2, Darrell Cockburn2, Anthony J. Clarke2, John R. Dutcher3 and Sharon G. Roscoe4, (1)Chemistry, University of Guelph, Guelph, ON, Canada, (2)Molecular and Cellular Biology, University of Guelph, Guelph, ON, Canada, (3)Physics, University of Guelph, Guelph, ON, Canada, (4)Chemistry, Acadia University, Wolfville, NS, Canada
Atomic force microscopy (AFM) was used to study native cellulose films prepared from a bacterial cellulose source, Acetobacter xylinum, using a novel application of the Langmuir-Blodgett (LB) technique. These films allowed high-resolution AFM images of single fibers and their microfibril structure to be obtained. Two types of experiments were performed. First, the fibers were characterized using samples that were dried after LB deposition. Second, novel protocols that allowed us to image single fibers of cellulose in films that were never dried were developed. This procedure enabled us to perform in situ AFM imaging studies of the enzymatic hydrolysis of single cellulose fibers in solution using cellulolytic enzymes. The in situ degradation of cellulose fibers was monitored over several hours using AFM. These studies provided the first direct, real-time images of the enzymatic degradation of a single cellulose fiber. We have demonstrated the tremendous potential of AFM to study the mechanism of the enzymatic digestion of cellulose and to identify the most effective enzymes for the digestion of various cellulose structures or isomorphs.