Conjugates of Iron-Transporting N-Hydroxylactams with Ciprofloxacin

• Published in: Molecules (Basel, Switzerland) Vol. 27; no. 12; p. 3910
• Main Authors: Bakulina, Olga, Bannykh, Anton, Levashova, Ekaterina, Krasavin, Mikhail
• Format: Journal Article
• Language: English
• Published: Basel MDPI AG 18.06.2022; MDPI
• Subjects: Acids; Antibacterial activity; Antibiotics; Bacteria; bacterial iron transport; Castagnoli-Cushman reaction; Ciprofloxacin; Conjugates; cyclic hydroxamic acids; Drug resistance; Enterobactin; Enzymes; Iron; Lead compounds; Mutants; Pyoverdines; Siderophores; Trojan horse antibiotics
• ISSN: 1420-3049; 1420-3049
• DOI: 10.3390/molecules27123910

Screening of a library of novel N-hydroxylactams amenable by the Castagnoli-Cushman reaction identified four lead compounds that facilitated 55Fe transport into P. aeruginosa cells (one of these synthetic siderophores was found to be as efficient at promoting iron uptake as the natural siderophores pyoverdine, pyochelin or enterobactin). Conjugates of the four lead siderophores with ciprofloxacin were tested for antibacterial activity against P. aeruginosa POA1 (wild type) and the ∆pvdF∆pchA mutant strain. The antibacterial activity was found to be pronounced against the ∆pvdF∆pchA mutant strain grown in CAA medium but not for the POA1 strain. This may be indicative of these compounds being ‘Trojan horse’ antibiotics. Further scrutiny of the mechanism of the antibacterial action of the newly developed conjugates is warranted.