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Title: Ligand bound structures of a glycosyl hydrolase family 30 glucuronoxylan xylanohydrolase

Source: Journal of Molecular Biology

Author(s)St. Johns, Franz; Hurlbert, Jason C.; Rice, John D.; Preston, James F.; Pozharski, Edwin

Publication Year: 2011  View PDF »

Category: Journal Articles
Associated Research Project(s):   FPL-4712-3A

Abstract: Xylanases of glycosyl hydrolase family 30 (GH30) have been shown to cleave β-1,4 linkages of 4-O-methylglucuronoxylan (MeGXn) as directed by the position along the xylan chain of an α-1,2-linked 4-O-methylglucuronate (MeGA) moiety. Complete hydrolysis of MeGXn by these enzymes results in singly substituted aldouronates having a 4-O-methylglucuronate moiety linked to a xylose penultimate from the reducing terminal xylose and some number of xylose residues toward the nonreducing terminus. This novel mode of action distinguishes GH30 xylanases from the more common xylanase families that cleave MeGXn in accessible regions. To help understand this unique biochemical function, we have determined the structure of XynC in its native and ligand-bound forms. XynC structure models derived from diffraction data of XynC crystal soaks with the simple sugar glucuronate (GA) and the tetrameric sugar 4-O-methyl-aldotetrauronate resulted in models containing GA and 4-O-methyl-aldotriuronate, respectively. Each is observed in two locations within XynC surface openings. Ligand coordination occurs within the XynC catalytic substrate binding cleft and on the structurally fused side β-domain, demonstrating a substrate targeting role for this putative carbohydrate binding module. Structural data reveal that GA acts as a primary functional appendage for recognition and hydrolysis of the MeGXn polymer by the protein. This work compares the structure of XynC with a previously reported homologous enzyme, XynA, from Erwinia chrysanthemi and analyzes the ligand binding sites. Our results identify the molecular interactions that define the unique function of XynC and homologous GH30 enzymes.

Keywords: glycosyl hydrolase family 30; xylanase; glycosyl hydrolase family 5 xylanase; Bacillus subtilis XynC; glucuronic acid

Publication Review Process: Formally Refereed

File size: 2,140 kb(s)

Date posted: 09/30/2011

This publication is also viewable on Treesearch:  view
RITS Product ID: 40272
Current FPL Scientist associated with this product
St. Johns, Franz
Research Microbiologist
  

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