Harnessing Fluorescent Moenomycin A Antibiotics for Bacterial Cell Wall Imaging Studies.

Autor: Hsieh PY; Institute of Biological Chemistry, Academia Sinica, No. 128, Academia Road Sec. 2, Taipei, 115, Taiwan., Meng FC; Genomics Research Center, Academia Sinica, No. 128, Academia Road Sec. 2, Taipei, 115, Taiwan., Guo CW; Genomics Research Center, Academia Sinica, No. 128, Academia Road Sec. 2, Taipei, 115, Taiwan., Hu KH; Genomics Research Center, Academia Sinica, No. 128, Academia Road Sec. 2, Taipei, 115, Taiwan., Shih YL; Institute of Biological Chemistry, Academia Sinica, No. 128, Academia Road Sec. 2, Taipei, 115, Taiwan.; Institute of Biochemical Sciences, National Taiwan University, No. 1, Sec. 4, Roosevelt Rd., Taipei, 106, Taiwan.; Department of Microbiology, College of Medicine, National Taiwan University, No.1, Sec 1. Jen Ai Rd., Taipei, 100, Taiwan., Cheng WC; Genomics Research Center, Academia Sinica, No. 128, Academia Road Sec. 2, Taipei, 115, Taiwan.; Department of Chemistry, National Cheng Kung University, No.1, University Road, Tainan, 701, Taiwan.; Department of Applied Chemistry, National Chiayi University, No. 300, Syuefu Road, Chiayi, 600, Taiwan.; Department of Medicinal and Applied Chemistry, Kaohsiung Medical University, No.100, Shin-Chuan 1st Road, Kaohsiung, 807, Taiwan.
Jazyk: angličtina
Zdroj: Chembiochem : a European journal of chemical biology [Chembiochem] 2021 Dec 10; Vol. 22 (24), pp. 3462-3468. Date of Electronic Publication: 2021 Oct 14.
DOI: 10.1002/cbic.202100433
Abstrakt: The imaging of peptidoglycan (PGN) dynamics in living bacteria facilitates the understanding of PGN biosynthesis and wall-targeting antibiotics. The main tools for imaging bacterial PGN are fluorescent probes, such as the well-known PGN metabolic labeling probes. However, fluorescent small-molecule probes for labeling key PGN-synthesizing enzymes, especially for transglycosylases (TGases), remain to be explored. In this work, the first imaging probe for labeling TGase in bacterial cell wall studies is reported. We synthesized various fluorescent MoeA-based molecules by derivatizing the natural antibiotic moenomycin A (MoeA), and used them to label TGases in living bacteria, monitor bacterial growth and division cycles by time-lapse imaging, and study cell wall growth in the mecA-carrying methicillin-resistant Staphylococcus aureus (MRSA) strains when the β-lactam-based probes were unsuitable.
(© 2021 Wiley-VCH GmbH.)
Databáze: MEDLINE