A New Subfamily of Glycoside Hydrolase Family 30 with Strict Xylobiohydrolase Function
Casey Crooks, Nathan J. Bechle, Franz J. St John
Abstract
The Acetivibrio clariflavus (basonym: Clostridium clariflavum ) glycoside hydrolase family 30 cellulosomal protein encoded by the Clocl_1795 gene was highly represented during growth on cellulosic substrates. In this report, the recombinantly expressed protein has been characterized and shown to be a non-reducing terminal (NRT)-specific xylobiohydrolase ( Ac Xbh30A). Biochemical function, optimal biophysical parameters, and phylogeny were investigated. The findings indicate that Ac Xbh30A strictly cleaves xylobiose from the NRT up until an α-1,2-linked glucuronic acid (GA)-decorated xylose if the number of xyloses is even or otherwise a single xylose will remain resulting in a penultimate GA-substituted xylose. Unlike recently reported xylobiohydrolases, Ac Xbh30A has no other detectable hydrolysis products under our optimized reaction conditions. Sequence analysis indicates that Ac Xbh30A represents a new GH30 subfamily. This new xylobiohydrolase may be useful for commercial production of industrial quantities of xylobiose.