Affiliation:
1. Wyeth-Ayerst Research, Pearl River, New York 10965
Abstract
ABSTRACT
Previous studies suggested that a Gly-containing branch of cell wall precursor [C
55
-MurNAc-(peptide)-GlcNAc], which is often referred to as lipid II, might serve as a nucleophilic acceptor in sortase-catalyzed anchoring of surface proteins in
Staphylococcus aureus.
To test this hypothesis, we first simplified the procedure for in vitro biosynthesis of Gly-containing lipid II by using branched UDP-MurNAc-hexapeptide isolated from the cytoplasm of
Streptomyces
spp. Second, we designed a thin-layer chromatography-based assay in which the mobility of branched but not linear lipid II is shifted in the presence of both sortase and LPSTG-containing peptide. These results and those of additional experiments presented in this study further suggest that lipid II indeed serves as a natural substrate in a sorting reaction.
Publisher
American Society for Microbiology
Subject
Molecular Biology,Microbiology
Cited by
79 articles.
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