PT  - JOURNAL ARTICLE
AU  - Hokin Chio
AU  - Ellen E Guest
AU  - Jon L Hobman
AU  - Tania Dottorini
AU  - Jonathan D Hirst
AU  - Dov J Stekel
TI  - Predicting bioactivity of antibiotic metabolites by molecular docking and dynamics
AID  - 10.1101/2022.09.06.506739
DP  - 2022 Jan 01
TA  - bioRxiv
PG  - 2022.09.06.506739
4099  - http://biorxiv.org/content/early/2022/09/06/2022.09.06.506739.short
4100  - http://biorxiv.org/content/early/2022/09/06/2022.09.06.506739.full
AB  - Antibiotics enter the environment through waste streams, where they can exert selective pressure for antimicrobial resistance in bacteria. However, many antibiotics are excreted as partly metabolized forms, or can be subject to partial breakdown in wastewater treatment, soil, or through natural processes in the environment. If a metabolite is bioactive, even at sub-lethal levels, and also stable in the environment, then it could provide selection pressure for resistance. (5S)-penicilloic acid of piperacillin has previously been found complexed to the binding pocket of penicillin binding protein 3 (PBP3) of Pseudomonas aeruginosa. Here, we predicted the affinities of all potentially relevant antibiotic metabolites of ten different penicillins to that target protein, using molecular docking and molecular dynamics simulations. Docking predicts that, in addition to penicilloic acid, pseudopenicillin derivatives of these penicillins, as well as 6-aminopenicillanic acid (6APA), could also bind to this target. Molecular dynamics simulations further confirmed that (5R)-pseudopenicillin and 6APA bind the target protein, in addition to (5S)-penicilloic acid. Thus, it is possible that these metabolites are bioactive, and, if stable in the environment, could be contaminants selective for antibiotic resistance. This could have considerable significance for environmental surveillance for antibiotics as a means to reduce antimicrobial resistance, because targeted mass spectrometry could be required for relevant metabolites as well as the native antibiotics.Competing Interest StatementThe authors have declared no competing interest.