Functional analysis of the Campylobacter jejuni N-linked protein glycosylation pathway.


Linton, D; Dorrell, N; Hitchen, PG; Amber, S; Karlyshev, AV; Morris, HR; Dell, A; Valvano, MA; Aebi, M; Wren, BW; (2005) Functional analysis of the Campylobacter jejuni N-linked protein glycosylation pathway. Molecular microbiology, 55 (6). pp. 1695-1703. ISSN 0950-382X DOI: https://doi.org/10.1111/j.1365-2958.2005.04519.x

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Abstract

Summary We describe in this report the characterization of the recently discovered N-linked glycosylation locus of the human bacterial pathogen Campylobacter jejuni, the first such system found in a species from the domain Bacteria. We exploited the ability of this locus to function in Escherichia coli to demonstrate through mutational and structural analyses that variant glycan structures can be transferred onto protein indicating the relaxed specificity of the putative oligosaccharyltransferase PglB. Structural data derived from these variant glycans allowed us to infer the role of five individual glycosyltransferases in the biosynthesis of the N-linked heptasaccharide. Furthermore, we show that C. jejuni- and E. coli-derived pathways can interact in the biosynthesis of N-linked glycoproteins. In particular, the E. coli encoded WecA protein, a UDP-GlcNAc: undecaprenylphosphate GlcNAc-1-phosphate transferase involved in glycolipid biosynthesis, provides for an alternative N-linked heptasaccharide biosynthetic pathway bypassing the requirement for the C. jejuni-derived glycosyltransferase PglC. This is the first experimental evidence that biosynthesis of the N-linked glycan occurs on a lipid-linked precursor prior to transfer onto protein. These findings provide a framework for understanding the process of N-linked protein glycosylation in Bacteria and for devising strategies to exploit this system for glycoengineering.

Item Type: Article
Faculty and Department: Faculty of Infectious and Tropical Diseases > Dept of Pathogen Molecular Biology
PubMed ID: 15752194
Web of Science ID: 227381000007
URI: http://researchonline.lshtm.ac.uk/id/eprint/13877

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