The Journal of Organic Chemistry · 2017 · 30 citations · 17 references
Life SciencesBiochemistryMolecular BiologyCarbohydrate ChemistryEnzymologyGlycobiologyCarbohydrate SynthesisChemoenzymatic SynthesisGlycan BiosynthesisGlycan StructureGlycosylation PathwaysProtein GlycosylationChemoenzymatic Carbohydrate SynthesisChemoenzymatic GlycosylationChemoenzymatic Oligosaccharide SynthesisChemoenzymatic Sugar SynthesisGlycosaminoglycan BiosynthesisHexosamine Biosynthetic PathwayN-linked Glycan BiosynthesisNucleotide-sugar Donor Synthesis
Unnatural uridine diphosphate (UDP)-sugar donors, UDP-4-deoxy-4-fluoro-N-acetylglucosamine (4FGlcNAc) and UDP-4-deoxy-4-fluoro-N-acetylgalactosamine (4FGalNAc), were prepared using both chemical and chemoenzymatic syntheses relying on N-acetylglucosamine-1-phosphate uridylyltransferase (GlmU). The resulting unnatural UDP-sugar donors were then tested as substrates in glycosaminoglycan synthesis catalyzed by various synthases. UDP-4FGlcNAc was transferred onto an acceptor by Pastuerella multocida heparosan synthase 1 and subsequently served as a chain terminator.
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Chemoenzymatic Design of Heparan Sulfate Oligosaccharides*
Renpeng Liu, Yongmei Xu, Miao Chen et al. · Journal of Biological Chemistry · 2010 · 157 citations · Full text
One-pot three-enzyme synthesis of UDP-GlcNAc derivatives
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