Corbomycin blocks autolysins by attaching to the peptidoglycancell wall. As a result, the bacterium cannot divide, as division requires the wall to be broken down and remodeled.[2] Ordinary glycopeptides instead block cell wall formation.[1]
It can block infections caused by the drug-resistant strain of Staphylococcus aureus that cause serious infections.[1] As of 2020 it had not been approved by any regulatory body for human use.[citation needed]
The antibiotic was discovered in 2020. Researchers found the substance while studying the biosynthetic genesofglycopeptides that lacked self-resistance mechanisms. Researcher Beth Culp worked with Yves Brun and his team to image the cells to identify the action site. Culp's later team found other antibiotics that employed the same method of action. Complestatin is an existing antibiotic that was shown to use the same mechanism of action.[2][1]
