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PMID: 16286454 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Functional characterization of dehydratase/aminotransferase pairs from Helicobacter and Campylobacter: enzymes distinguishing the pseudaminic acid and bacillosamine biosynthetic pathways.

The Journal of biological chemistry ·Vol. 281 ·No. 2 ·2006-01-13 ·Pages 723-32

Schoenhofen IC, McNally DJ, Vinogradov E, Whitfield D, Young NM, Dick S, Wakarchuk WW, Brisson JR, Logan SM

Abstract

Helicobacter pylori and Campylobacter jejuni have been shown to modify their flagellins with pseudaminic acid (Pse), via O-linkage, while C. jejuni also possesses a general protein glycosylation pathway (Pgl) responsible for the N-linked modification of at least 30 proteins with a heptasaccharide containing 2,4-diacetamido-2,4,6-trideoxy-alpha-D-glucopyranose, a derivative of bacillosamine. To further define the Pse and bacillosamine biosynthetic pathways, we have undertaken functional characterization of UDP-alpha-D-GlcNAc modifying dehydratase/aminotransferase pairs, in particular the H. pylori and C. jejuni flagellar pairs HP0840/HP0366 and Cj1293/Cj1294, as well as the C. jejuni Pgl pair Cj1120c/Cj1121c using His(6)-tagged purified derivatives. The metabolites produced by these enzymes were identified using NMR spectroscopy at 500 and/or 600 MHz with a cryogenically cooled probe for optimal sensitivity. The metabolites of Cj1293 (PseB) and HP0840 (FlaA1) were found to be labile and could only be characterized by NMR analysis directly in aqueous reaction buffer. The Cj1293 and HP0840 enzymes exhibited C6 dehydratase as well as a newly identified C5 epimerase activity that resulted in the production of both UDP-2-acetamido-2,6-dideoxy-beta-L-arabino-4-hexulose and UDP-2-acetamido-2,6-dideoxy-alpha-D-xylo-4-hexulose. In contrast, the Pgl dehydratase Cj1120c (PglF) was found to possess only C6 dehydratase activity generating UDP-2-acetamido-2,6-dideoxy-alpha-D-xylo-4-hexulose. Substrate-specificity studies demonstrated that the flagellar aminotransferases HP0366 and Cj1294 utilize only UDP-2-acetamido-2,6-dideoxy-beta-L-arabino-4-hexulose as substrate producing UDP-4-amino-4,6-dideoxy-beta-L-AltNAc, a precursor in the Pse biosynthetic pathway. In contrast, the Pgl aminotransferase Cj1121c (PglE) utilizes only UDP-2-acetamido-2,6-dideoxy-alpha-D-xylo-4-hexulose producing UDP-4-amino-4,6-dideoxy-alpha-D-GlcNAc (UDP-2-acetamido-4-amino-2,4,6-trideoxy-alpha-D-glucopyranose), a precursor used in the production of the Pgl glycan component 2,4-diacetamido-2,4,6-trideoxy-alpha-D-glucopyranose.

MeSH Terms
Campylobacter jejuni/enzymology Carbohydrate Sequence DNA/metabolism Dose-Response Relationship, Drug Electrophoresis, Capillary Electrophoresis, Polyacrylamide Gel Helicobacter pylori/enzymology Hexosamines/chemistry,metabolism Histidine/chemistry Hydro-Lyases/chemistry Kinetics Magnetic Resonance Spectroscopy Models, Chemical Molecular Sequence Data Mutation Oligonucleotides/chemistry Plasmids/metabolism Substrate Specificity Time Factors Transaminases/chemistry Uridine Diphosphate N-Acetylglucosamine/chemistry
Chemicals
Hexosamines Oligonucleotides Histidine Uridine Diphosphate N-Acetylglucosamine 4-deoxyneosamine C DNA Transaminases Hydro-Lyases
Authors & Affiliations
9 authors, click to expand affiliations / ORCID
Schoenhofen Ian C
Institute for Biological Sciences, National Research Council, Ottawa, Ontario, Canada.
McNally David J
Vinogradov Evgeny
Whitfield Dennis
Young N Martin
Dick Scott
Wakarchuk Warren W
Brisson Jean-Robert
Logan Susan M
Article Info
Journal
The Journal of biological chemistry
Abbr.
J Biol Chem
ISSN
0021-9258
Published
2006-01-13
Epub
2005-00-11
Pages
723-32
Language
English
Region
United States
NLM ID
2985121R
Subset
IM
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