Paper
Bacitracin: an inhibitor of the dephosphorylation of lipid pyrophosphate, an intermediate in the biosynthesis of the peptidoglycan of bacterial cell walls.
Published Mar 1, 1967 · G. Siewert, J. Strominger
Proceedings of the National Academy of Sciences of the United States of America
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Abstract
Bacitraciin is a polypeptide antibiotic produced by certain strainis of Bacillus licheniformis. It inhibits bacterial cell wall synthesis and induces the accumulation in Staphylococcus aureus of UDP-acetylmuramyl-pentapeptide,I a precursor of the cell wall. Recent studies of the detailed mechanism of biosynthesis of the peptidoglycaii of bacterial cell walls have revealed a process that occurs in three stages, viz.: (1) biosynthesis of the uridinie nucleotide precursors, (2) utilization of these precursors to form linear peptidoglycari strands, and (3) cross-linking of the liinearstrands.2 Each of these stages is specifically inhibited by different anti.biotics. Ristocetin, vancomycin, and bacitracin are all inhibitors of the second stage.3 This stage is a complex reaction sequence which occurs in the cell membralle as a consequence of which the sugar fragments of the uridine nucleotide precursors become attached to a phospholipid carrier in the membrane and are then modified. Studies of the individual reactions in this cycle (Fig. 1) have revealed that the re
Bacitracin inhibits the dephosphorylation of lipid pyrophosphate, an intermediate in the biosynthesis of bacterial cell wall peptidoglycan.
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