Abstract
AbstractTrans-translation is a crucial bacterial process and a target for new antibiotics. We developed twoPseudomonas aeruginosabiosensor strains that detecttrans-translation inhibitors by exploiting the bacterium’s natural red fluorescence, linked to protoporphyrin IX accumulation. The first biosensor monitors tmRNA-SmpB-mediated tagging, while the second serves as control for biosensor 1 by keeping track of ClpP1-related proteolysis and porphyrin biosynthesis. Validation through gene deletions and complementation confirmed their specificity. These biosensors were effective in screening antibiotics and designed inhibitors, demonstrating their potential for high-throughput identification oftrans-translation inhibitors in drug-resistantP. aeruginosa.
Publisher
Cold Spring Harbor Laboratory