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Synthetic UDP-furanoses as potent inhibitors of mycobacterial galactan biogenesis.

Authors :
Peltier P
Beláňová M
Dianišková P
Zhou R
Zheng RB
Pearcey JA
Joe M
Brennan PJ
Nugier-Chauvin C
Ferrières V
Lowary TL
Daniellou R
Mikušová K
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.)

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