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Synthetic UDP-furanoses as potent inhibitors of mycobacterial galactan biogenesis.
- Source :
-
Chemistry & biology [Chem Biol] 2010 Dec 22; Vol. 17 (12), pp. 1356-66. - Publication Year :
- 2010
-
Abstract
- UDP-galactofuranose (UDP-Galf) is a substrate for two types of enzymes, UDP-galactopyranose mutase and galactofuranosyltransferases, which are present in many pathogenic organisms but absent from mammals. In particular, these enzymes are involved in the biosynthesis of cell wall galactan, a polymer essential for the survival of the causative agent of tuberculosis, Mycobacterium tuberculosis. We describe here the synthesis of derivatives of UDP-Galf modified at C-5 and C-6 using a chemoenzymatic route. In cell-free assays, these compounds prevented the formation of mycobacterial galactan, via the production of short "dead-end" intermediates resulting from their incorporation into the growing oligosaccharide chain. Modified UDP-furanoses thus constitute novel probes for the study of the two classes of enzymes involved in mycobacterial galactan assembly, and studies with these compounds may ultimately facilitate the future development of new therapeutic agents against tuberculosis.<br /> (Copyright © 2010 Elsevier Ltd. All rights reserved.)
- Subjects :
- Enzyme Inhibitors metabolism
Enzyme Inhibitors pharmacology
Galactans antagonists & inhibitors
Galactose biosynthesis
Galactose chemistry
Galactose pharmacology
Galactosyltransferases genetics
Galactosyltransferases metabolism
Intramolecular Transferases antagonists & inhibitors
Intramolecular Transferases metabolism
Klebsiella pneumoniae enzymology
Mycobacterium smegmatis enzymology
Recombinant Proteins antagonists & inhibitors
Recombinant Proteins genetics
Recombinant Proteins metabolism
Uridine Diphosphate biosynthesis
Uridine Diphosphate chemistry
Uridine Diphosphate pharmacology
Antitubercular Agents chemistry
Enzyme Inhibitors chemistry
Galactans biosynthesis
Galactose analogs & derivatives
Galactosyltransferases antagonists & inhibitors
Uridine Diphosphate analogs & derivatives
Subjects
Details
- Language :
- English
- ISSN :
- 1879-1301
- Volume :
- 17
- Issue :
- 12
- Database :
- MEDLINE
- Journal :
- Chemistry & biology
- Publication Type :
- Academic Journal
- Accession number :
- 21168771
- Full Text :
- https://doi.org/10.1016/j.chembiol.2010.10.014