Flavonoid derivatives from red propolis : In silico predictions of their interactions with Staphylococcus aureus sortase A and studies on their antibiofilm potential
Sarker, Dipto Kumer and Ratcliffe, Emma and Burnett, Fraser and Uddin, Shaikh Jamal and Shilpi, Jamil A. and Efthimiou, Georgios and Seidel, Veronique (2025) Flavonoid derivatives from red propolis : In silico predictions of their interactions with Staphylococcus aureus sortase A and studies on their antibiofilm potential. Zeitschrift fur Naturforschung C. ISSN 1865-7125 (https://doi.org/10.1515/znc-2024-0270)
Preview |
Text.
Filename: Sarker-etal-ZNC-2025-Flavonoid-derivatives-from-red-propolis.pdf
Accepted Author Manuscript License:
Download (1MB)| Preview |
Abstract
Sortase A (SrtA) is an enzyme essential for biofilm formation in Gram-positive bacteria including Staphylococcus aureus. In silico investigations were conducted to investigate the interactions of flavonoid derivatives from red propolis with S. aureus SrtA (PDB ID:1T2P). Molecular docking, MD and ADME/drug-likeness predictions used Autodock Vina, GROMACS-2021 and SwissADME, respectively. Chrysin, galangin, thevetiaflavone and vestitone showed the best size-independent ligand efficiency (SILE) scores–higher than those of the control ligand. The chrysin- and thevetiaflavone-protein complexes showed the most stable behaviour and compactness in MD analysis. Chrysin and thevetiaflavone exhibited high binding free energy values towards SrtA. Chrysin interacted strongly with eight active site residues (including two from the catalytic triad) while thevetiaflavone interacted with four active site residues (including one from the catalytic triad). An in vitro crystal violet staining assay confirmed that chrysin and galangin showed significant antibiofilm activity against S. aureus. It remains to be seen if thevetiaflavone displays any similar activity. Further studies are warranted to confirm if the binding of these flavonoids to sortase A is a possible mechanism of their antibiofilm activity. As such, they may prove useful for the discovery of new antibiofilm agents against S. aureus.
ORCID iDs
Sarker, Dipto Kumer, Ratcliffe, Emma, Burnett, Fraser, Uddin, Shaikh Jamal, Shilpi, Jamil A., Efthimiou, Georgios and Seidel, Veronique
ORCID: https://orcid.org/0000-0003-3880-5261;
-
-
Item type: Article ID code: 94516 Dates: DateEvent14 October 2025Published28 August 2025Accepted12 May 2025SubmittedSubjects: Science > Microbiology
Medicine > Pharmacy and materia medicaDepartment: Faculty of Science > Strathclyde Institute of Pharmacy and Biomedical Sciences Depositing user: Pure Administrator Date deposited: 24 Oct 2025 11:44 Last modified: 30 Jan 2026 17:11 Related URLs: URI: https://strathprints.strath.ac.uk/id/eprint/94516
Tools
Tools






