Abstract
Labeled UDP-GlcNAc and chitooligosaccharides should be powerful tools for studies of N-acetylglucosaminyltransferase such as chitin synthases. We describe here a rapid, inexpensive and a common strategie for the chemoenzymatic synthesis of uridine 5′-diphospho-N-[2H]-acetyl-glucosamine and the chemical preparation of N-[2H]-acetyl chitooligosaccharides (from 2 to 5 mers). Deuterated UDP-GlcNAc analogue was tested as chitin synthase substrate and it exhibited an incorporation level in chitin as the natural substrate. Deuterium labeling of carbohydrates present different advantages: it is a stable isotope and allows glycosyltransferase mechanism studies by a mass spectrometry approach.
| Original language | English |
|---|---|
| Pages (from-to) | 687-692 |
| Number of pages | 6 |
| Journal | Glycoconjugate Journal |
| Volume | 23 |
| Issue number | 9 |
| DOIs | |
| Publication status | Published - 1 Dec 2006 |
| Externally published | Yes |
Keywords
- Chemoenzymatic synthesis
- Chitooligosaccharides
- N-acetylation
- UDP-N-acetyl-glucosamine
- Uridylation
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