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.
The preparation of natural product-inspired nucleoside analogs using solution-phase parallel synthesis is described.The key intermediates containing alkyne and N-protected amino moieties were developed to allow for further skeleton and substituent diversity using click chemistry and urea or amide bond formation. Rapid purification was accomplished using solidphase extraction. The obtained library comprised 80 molecules incorporating two diversity positions and one chiral center, each of which was efficiently prepared in good purity and acceptable overall yield. A bacterial morphology study was also performed.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.