Skip to Main Content
Ligand bound structures of a glycosyl hydrolase family 30 glucuronoxylan xylanohydrolaseAuthor(s): Franz St. Johns; Jason C. Hurlbert; John D. Rice; James F. Preston; Edwin Pozharski
Source: Journal of Molecular Biology
Publication Series: Scientific Journal (JRNL)
Station: Forest Products Laboratory
View PDF (2.09 MB)
DescriptionXylanases 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.
- We recommend that you also print this page and attach it to the printout of the article, to retain the full citation information.
- This article was written and prepared by U.S. Government employees on official time, and is therefore in the public domain.
CitationSt John, Franz J.; Hurlbert, Jason C.; Rice, John D.; Preston, James F.; Pozharski, Edwin. 2011. Ligand bound structures of a glycosyl hydrolase family 30 glucuronoxylan xylanohydrolase. Journal of Molecular Biology. 407: 92-109.
Keywordsglycosyl hydrolase family 30, xylanase, glycosyl hydrolase family 5 xylanase, Bacillus subtilis XynC, glucuronic acid
- A novel member of glycoside hydrolase family 30 subfamily 8 with altered substrate specificity
- Engineering the Xylan Utilization System in Bacillus subtilis for Production of Acidic Xylooligosaccharides
- Xylanase 30 A from Clostridium thermocellum functions as a glucuronoxylan xylanohydrolase
XML: View XML