Staphylococcus aureus Penicillin‐Binding Protein 2 Can Use Depsi‐Lipid II Derived from Vancomycin‐Resistant Strains for Cell Wall Synthesis. Issue 36 (19th July 2013)

• Record Type: Journal Article
• Authors: Nakamura, Jun; Yamashiro, Hidenori; Miya, Hiroto; Nishiguchi, Kenzo; Maki, Hideki; Arimoto, Hirokazu
• Is Part Of: Chemistry. Volume 19:Issue 36(2013)
• Page Start: 12104
• Page End: 12112
• Publication Date: 2013-07-19
• Subjects: Chemistry -- Periodicals; 540
• DOI: 10.1002/chem.201301074
• Languages: English
• ISSNs: 0947-6539

Abstract

<abstract abstract-type="main" xml:lang="en"> <title>Abstract</title> <p>Vancomycin‐resistant <italic>Staphylococcus aureus</italic> (<italic>S. aureus</italic>) (VRSA) uses depsipeptide‐containing modified cell‐wall precursors for the biosynthesis of peptidoglycan. Transglycosylase is responsible for the polymerization of the peptidoglycan, and the penicillin‐binding protein 2 (PBP2) plays a major role in the polymerization among several transglycosylases of wild‐type <italic>S. aureus.</italic> However, it is unclear whether VRSA processes the depsipeptide‐containing peptidoglycan precursor by using PBP2. Here, we describe the total synthesis of depsi‐lipid I, a cell‐wall precursor of VRSA. By using this chemistry, we prepared a depsi‐lipid II analogue as substrate for a cell‐free transglycosylation system. The reconstituted system revealed that the PBP2 of <italic>S. aureus</italic> is able to process a depsi‐lipid II intermediate as efficiently as its normal substrate. Moreover, the system was successfully used to demonstrate the difference in the mode of action of the two antibiotics moenomycin and vancomycin.</p> </abstract>