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1. (Article ID: 4770)
Li Z, Hwang S, Ericson J, Bowler K, Bar-Peled M
Pen and Pal Are Nucleotide-Sugar Dehydratases That Convert UDP-GlcNAc to UDP-6-Deoxy-D-GlcNAc-5,6-ene and Then to UDP-4-Keto-6-deoxy-L-AltNAc for CMP-Pseudaminic Acid Synthesis in Bacillus thuringiensis
Journal of Biological Chemistry 290(2) (2015)
691-704
CMP-pseudaminic acid is a precursor required for the O-glycosylation of flagellin in some pathogenic Gram-negative bacteria, a process known to be critical in bacterial motility and infection. However, little is known about flagellin glycosylation in Gram-positive bacteria. Here, we identified and functionally characterized an operon, named Bti_pse, in Bacillus thuringiensis israelensis ATCC 35646, which encodes seven different enzymes that together convert UDP-GlcNAc to CMP-pseudaminic acid. In contrast, Gram-negative bacteria complete this reaction with six enzymes. The first enzyme, which we named Pen, converts UDP-D-GlcNAc to an uncommon UDP-sugar, UDP-6-deoxy-D-GlcNAc-5,6-ene. Pen contains strongly bound NADP+ and has distinct UDP-GlcNAc 4-oxidase, 5,6-dehydratase, and 4-reductase activities. The second enzyme, which we named Pal, converts UDP-6-deoxy-D-GlcNAc-5,6-ene to UDP-4-keto-6-deoxy-L-AltNAc. Pal is NAD+-dependent and has distinct UDP-6-deoxy-D-GlcNAc-5,6-ene 4-oxidase, 5,6-reductase, and 5-epimerase activities. We also show here using NMR spectroscopy and mass spectrometry that in B. thuringiensis, the enzymatic product of Pen and Pal, UDP-4-keto-6-deoxy-L-AltNAc, is converted to CMP-pseudaminic acid by the sequential activities of a C4?-transaminase (Pam), a 4-N-acetyltransferase (Pdi), a UDP-hydrolase (Phy), an enzyme (Ppa) that adds phosphoenolpyruvate to form pseudaminic acid, and finally a cytidylyltransferase that condenses CTP to generate CMP-pseudaminic acid. Knowledge of the distinct dehydratase-like enzymes Pen and Pal and their role in CMP-pseudaminic acid biosynthesis in Gram-positive bacteria provides a foundation to investigate the role of pseudaminic acid and flagellin glycosylation in Bacillus and their involvement in bacterial motility and pathogenicity.
pseudaminic acid, Bacillus, aminotransferase, CMP-pseudaminic acid, flagellin glycosylation, dehydratase, enzyme catalysis, bacterial metabolism, Bacillus thuringiensis, carbohydrate biosynthesis, glycobiology, UDP-GlcNAc
NCBI PubMed ID: 25414257Publication DOI: 10.1074/jbc.M114.612747Journal NLM ID: 2985121RPublisher: Baltimore, MD: American Society for Biochemistry and Molecular Biology
Correspondence: peled

ccrc.uga.edu
Institutions: Complex Carbohydrate Research Center, University of Georgia, Athens, GA, USA, From the Department of Plant Biology and Complex Carbohydrate Research Center, University of Georgia, Athens, GA, USA
Methods: 13C NMR, 1H NMR, gel filtration, NMR-2D, PCR, SDS-PAGE, DNA techniques, kinetics assays, NMR-1D, genetic methods, biochemical methods, HPLC, UV, enzymatic analysis, LC-ESI-MS/MS, HILIC-HPLC-UV, HILIC-ESI-MS
The publication contains the following compound(s):
- Compound ID: 7507
Structure type: monomer
Trivial name: CMP-5,7-diacetamido-3,5,7,9-tetradeoxy-L-glycero-α-L-manno-non-2-ulosonic (CMP-Pse5Ac7AC), CMP-pseudaminic acid
- Compound ID: 11950
|
a-D-Sugp2Ac-(1---P---P---5)-U
Sug = 2-amino-2,6-deoxy-xylo-5,6-en-hexose = SMILES O{1}[C@@H]1{2}[C@@H]([C@H]([C@@H](C(O1)=C)O)O)N |
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Structure type: monomer
Trivial name: UDP-6-deoxy-D-GlcNAc-5,6-ene (UDP-2-acetamido-6-deoxy-α-D-xylo-hexopyranose-5,6-ene)
- Compound ID: 11951
|
b-L-6daraHexpNAc-4-ulo-(1---P---P---5)-U
6daraHexpN-4-ulo = 2-amino-2,6-dideoxy-β-L-arabino-hex-4-ulose |
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Structure type: monomer
Trivial name: UDP-4-keto-6-deoxy-L-AltNAc (UDP-2-acetamido-2,6-dideoxy-β-L-arabino-hex-4-ulose)
- Compound ID: 11952
|
b-L-Sugp2Ac-(1---P---P---5)-U
Sug = 2-amino-2,6-dideoxy-arabino-hex-4-ulose (hydrated) = SMILES O{1}[C@@H]1{2}[C@@H]([C@H](C([C@H](C)O1)(O)O)O)N |
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Structure type: monomer
Trivial name: UDP-4-keto-6-deoxy-L-AltNAc-hydrated (UDP-2-acetamido-2,6-dideoxy-β-L-arabino-hex-4-ulose hydrated form)
- Compound ID: 11953
|
a-D-Sugp2Ac-(1---P---P---5)-U
Sug = 2-amino-2,6-dideoxy-xylo-hex-4-ulose (hydrated) = SMILES O{1}[C@@H]1{2}[C@@H]([C@H](C([C@@H](C)O1)(O)O)O)N |
Show graphically |
Structure type: monomer
Trivial name: UDP-4-keto-6-deoxy-D-GlcNAc-hydrated (UDP-2-acetamido-6-deoxy-α-D-xylo-hex-4-ulose hydrated form)
- Compound ID: 11954
Structure type: monomer
Trivial name: UDP-4-amino-6-deoxy-L-AltNAc (UDP-4-amino-4,6-dideoxy-N-acetyl-β-L-altrosamine)
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