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Synthesis of an analogue of the lipoglycopeptide membrane intermediate I of peptidoglycan biosynthesis
Authors:Geneviève Auger  Muriel Crouvoisier  Martine Caroff  Jean van Heijenoort and Didier Blanot
Institution:(1) URA 1131, CNRS, Bâtiment 432, Université de Paris-Sud, F-91405 Orsay, France;(2) URA 1116, CNRS, Bâtiment 432, Université de Paris-Sud, F-91405 Orsay, France
Abstract:agr-Dihydroheptaprenyl-pyrophosphoryl- N-acetylmuramoyl-L-Ala-gamma-D-Glu- meso-diaminopimeloyl(Nisin-dansyl)-D-Ala-D-Ala ( 1), an analogue of lipid I ofpeptidoglycan biosynthesis, was synthesized from natural UDP-N-acetylmuramoyl-pentapeptide in three steps. Compound 1 was shown to be asubstrate for the MurG transferase from Escherichia coli, even in theabsence of membranes. When membranes were present, dansylated peptidoglycanwas also formed.
Keywords:Dansyl group  agr-Dihydroheptaprenyl phosphate" target="_blank">gif" alt="agr" align="BASELINE" BORDER="0">-Dihydroheptaprenyl phosphate  MurG  Phosphoroimidazolidate method  Plasma desorption mass spectrometry  UDP-N-acetylmuramoyl-pentapeptide
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