A Cell-Surface GH9 Endo-Glucanase Coordinates with Surface Glycan-Binding Proteins to Mediate Xyloglucan Uptake in the Gut Symbiont Bacteroides ovatus. Issue 5 (1st March 2019)

• Record Type: Journal Article
• Authors: Foley, Matthew H.; Déjean, Guillaume; Hemsworth, Glyn R.; Davies, Gideon J.; Brumer, Harry; Koropatkin, Nicole M.
• Is Part Of: Journal of molecular biology. Volume 431:Issue 5(2019)
• Page Start: 981
• Page End: 995
• Publication Date: 2019-03-01
• Subjects: Bacteroidetes -- xyloglucan utilization locus -- polysaccharide utilization system -- Sus-like system -- lipoprotein; GH glycoside hydrolase -- PUL polysaccharide utilization loci -- Sus starch utilization system -- TBDT TonB-dependent transporter -- SGBP surface glycan-binding protein -- XyGs xyloglucans -- XyGUL xyloglucan utilization locus -- HEC hydroxyethylcellulose -- CMC carboxymethylcellulose -- MM minimal media -- aTC anhydrotetracycline; Molecular biology -- Periodicals; Biology -- Periodicals; Biochemistry -- Periodicals; Bacteriology -- Periodicals; Molecular Biology -- Periodicals; Biochemistry -- Periodicals; Biologie moléculaire -- Périodiques; Biologie -- Périodiques; Biochimie -- Périodiques; Moleculaire biologie; Biochemistry; Biology; Molecular biology; Periodicals; 572.805
• DOI: 10.1016/j.jmb.2019.01.008
• Languages: English
• ISSNs: 0022-2836

Abstract

Abstract: Dietary fiber is an important food source for members of the human gut microbiome. Members of the dominant Bacteroidetes phylum capture diverse polysaccharides via the action of multiple cell surface proteins encoded within polysaccharide utilization loci (PUL). The independent activities of PUL-encoded glycoside hydrolases (GHs) and surface glycan-binding proteins (SGBPs) for the harvest of various glycans have been studied in detail, but how these proteins work together to coordinate uptake is poorly understood. Here, we combine genetic and biochemical approaches to discern the interplay between the BoGH9 endoglucanase and the xyloglucan-binding proteins SGBP-A and SGBP-B from the Bacteroides ovatus xyloglucan utilization locus (XyGUL). The expression of BoGH9, a weakly active xyloglucanase in isolation, is required in a strain that expresses a non-binding version of SGBP-A (SGBP-A*). The crystal structure of the BoGH9 enzyme suggests the molecular basis for its robust activity on mixed-linkage β-glucan compared to xyloglucan. However, catalytically inactive site-directed mutants of BoGH9 fail to complement the deletion of the active BoGH9 in a SGBP-A* strain. We also find that SGBP-B is needed in an SGBP-A* background to support growth on xyloglucan, but that the non-binding SGBP-B* protein acts in a dominant negative manner to inhibit growth on xyloglucan. We postulate a model whereby the SGBP-A, SGBP-B, and BoGH9 work together at the cell surface, likely within a discrete complex, and that xyloglucan binding by SGBP-B and BoGH9 may facilitate the orientation of the xyloglucan for transfer across the outer membrane. Graphical Abstract: Unlabelled Image Highlights: Xyloglucan (Xyg) is a dietary fiber utilized by the gut symbiont Bacteroides ovatus . How XyG is captured at the cell surface by SGBP-A, SGBP-B, and BoGH9 is unclear. The BoGH9 structure reveals the molecular basis for activity. Functional BoGH9 and SGBP-B are required for XyG uptake in an SGBPA mutant. SGBP-A, SGBP-B, and BoGH9 work together, and SGBP-B and BoGH9 may orient XyG for uptake.