Scientific Reports· 2026Q1
Phytochemical screening as an inhibitor of β-lactamases to overcome the carbapenem-resistant of Klebsiella pneumoniae
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- 2026year
Short summary
Quercetin, a phytochemical, enhanced carbapenem antibiotic activity against a carbapenem-resistant Klebsiella pneumoniae (CRKP) isolate by 2-fold at 2 µg/µL, suggesting its potential as a carbapenem adjuvant.
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Key points
- Quercetin, eriodictyol, and luteolin were identified via molecular docking as potential inhibitors of NDM-1 and KPC-2 β-lactamases.
- Quercetin exhibited favorable docking scores of -8.74 kcal/mol against NDM-1 and -9.1 kcal/mol against KPC-2.
- Quercetin at 2 µg/µL enhanced carbapenem activity against a CRKP isolate carrying both bla NDM-1 and bla KPC-2.
- Molecular dynamics simulations confirmed the conformational stability of quercetin-β-lactamase complexes.
AI-generated from the title and abstract; the full text is not read.
Abstract
The global emergence of carbapenem-resistant Klebsiella pneumoniae (CRKP) poses a major health challenge due to its resistance to carbapenem antibiotics, such as imipenem and meropenem, primarily mediated by β-lactamases, including NDM and KPC carbapenemases. This study aimed to identify phytochemicals predicted to interact with NDM-1 and KPC-2 β-lactamases, and to determine whether the most promising candidate could enhance carbapenem activity against CRKP. A library of phytochemicals selected for their reported potential to inhibit resistance enzymes rather than for direct antimicrobial activity was screened through ADMET (Absorption, Distribution, Metabolism, Excretion, Toxicity) profiling, followed by molecular docking against β-lactamase enzymes. Quercetin, eriodictyol, and luteolin showed favorable docking scores of − 9.1, − 8.32, and − 8.66 kcal/mol against KPC-2 and − 8.74, − 8.72, and − 8.73 kcal/mol against NDM-1, respectively. Molecular dynamics simulations were performed to evaluate the conformational behavior of the quercetin–NDM-1 and quercetin–KPC-2 complexes. In vitro assays showed that quercetin, at 2 µg/µL, enhanced the antibacterial activity of carbapenems against a CRKP isolate carrying both bla NDM-1 and bla KPC-2. However, these assays did not directly assess β-lactamase inhibition. These findings support the preliminary potential of quercetin as a carbapenem adjuvant, while the mechanism underlying the observed potentiation requires biochemical confirmation.
The authors' abstract, as published at the source. Scientific Reports, 2026 · DOI ↗
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Molecular MedicineBiochemistry, Genetics and Molecular Biology