1. A General O-Glycosylation System Important to the Physiology of a Major Human Intestinal Symbiont
- Author
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Fletcher, C. Mark, Coyne, Michael J., Villa, Otto F., Chatzidaki-Livanis, Maria, and Comstock, Laurie E.
- Subjects
Glycoproteins -- Physiological aspects ,Glycoproteins -- Analysis ,Wildlife conservation -- Physiological aspects ,Wildlife conservation -- Analysis ,Blood lipoproteins -- Physiological aspects ,Blood lipoproteins -- Analysis ,Lipoproteins -- Physiological aspects ,Lipoproteins -- Analysis ,Proteolipids -- Physiological aspects ,Proteolipids -- Analysis ,Deoxy sugars -- Physiological aspects ,Deoxy sugars -- Analysis ,Peptides -- Physiological aspects ,Peptides -- Analysis ,Blood lipids -- Physiological aspects ,Blood lipids -- Analysis ,Polysaccharides -- Physiological aspects ,Polysaccharides -- Analysis ,Biological sciences - Abstract
To link to full-text access for this article, visit this link: http://dx.doi.org/10.1016/j.cell.2009.02.041 Byline: C. Mark Fletcher (1), Michael J. Coyne (1), Otto F. Villa (2), Maria Chatzidaki-Livanis (1), Laurie E. Comstock (1) Keywords: MICROBIO Abstract: The Bacteroides are a numerically dominant genus of the human intestinal microbiota. These organisms harbor a rare bacterial pathway for incorporation of exogenous fucose into capsular polysaccharides and glycoproteins. The infrequency of glycoprotein synthesis by bacteria prompted a more detailed analysis of this process. Here, we demonstrate that Bacteroides fragilis has a general O-glycosylation system. The proteins targeted for glycosylation include those predicted to be involved in protein folding, protein-protein interactions, peptide degradation as well as surface lipoproteins. Protein glycosylation is central to the physiology of B. fragilis and is necessary for the organism to competitively colonize the mammalian intestine. We provide evidence that general O-glycosylation systems are conserved among intestinal Bacteroides species and likely contribute to the predominance of Bacteroides in the human intestine. Author Affiliation: (1) Channing Laboratory, Brigham & Women's Hospital, Harvard Medical School, 181 Longwood Avenue, Boston, MA 02115, USA (2) Pulmonary Critical Care and Sleep Division, Department of Medicine, Mount Sinai School of Medicine, 1468 Madison Avenue, New York, NY 10029, USA Article History: Received 8 October 2008; Revised 31 December 2008; Accepted 19 February 2009 Article Note: (miscellaneous) Published: April 16, 2009
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- 2009