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The O-glycosylated linker from the Trichoderma reesei Family 7 cellulase is a flexible, disordered protein
Authors:Beckham Gregg T  Bomble Yannick J  Matthews James F  Taylor Courtney B  Resch Michael G  Yarbrough John M  Decker Steve R  Bu Lintao  Zhao Xiongce  McCabe Clare  Wohlert Jakob  Bergenstråhle Malin  Brady John W  Adney William S  Himmel Michael E  Crowley Michael F
Institution: National Bioenergy Center, National Renewable Energy Laboratory, Golden, Colorado
Department of Chemical Engineering, Colorado School of Mines, Golden, Colorado
§ Renewable and Sustainable Energy Institute, University of Colorado at Boulder, Boulder, Colorado
Biosciences Center, National Renewable Energy Laboratory, Golden, Colorado
Department of Chemical and Biomolecular Engineering, Vanderbilt University, Nashville, Tennessee
∗∗ Department of Chemistry, Vanderbilt University, Nashville, Tennessee
†† Center for Nanophase Materials Science, Oak Ridge National Laboratory, Oak Ridge, Tennessee
‡‡ Department of Food Science, Cornell University, Ithaca, New York
§§ Wallenberg Wood Science Center, Royal Institute of Technology, Stockholm, Sweden
Abstract:Fungi and bacteria secrete glycoprotein cocktails to deconstruct cellulose. Cellulose-degrading enzymes (cellulases) are often modular, with catalytic domains for cellulose hydrolysis and carbohydrate-binding modules connected by linkers rich in serine and threonine with O-glycosylation. Few studies have probed the role that the linker and O-glycans play in catalysis. Since different expression and growth conditions produce different glycosylation patterns that affect enzyme activity, the structure-function relationships that glycosylation imparts to linkers are relevant for understanding cellulase mechanisms. Here, the linker of the Trichoderma reesei Family 7 cellobiohydrolase (Cel7A) is examined by simulation. Our results suggest that the Cel7A linker is an intrinsically disordered protein with and without glycosylation. Contrary to the predominant view, the O-glycosylation does not change the stiffness of the linker, as measured by the relative fluctuations in the end-to-end distance; rather, it provides a 16 Å extension, thus expanding the operating range of Cel7A. We explain observations from previous biochemical experiments in the light of results obtained here, and compare the Cel7A linker with linkers from other cellulases with sequence-based tools to predict disorder. This preliminary screen indicates that linkers from Family 7 enzymes from other genera and other cellulases within T. reesei may not be as disordered, warranting further study.
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