Please use this identifier to cite or link to this item: http://hdl.handle.net/10497/23940
Title: 
Authors: 
Keywords: 
Marine sponge
Psammaplin
Marine natural products
Quorum sensing inhibitor
Pseudomonas aeruginosa
Inhibitor of biofilm formation
Elastase inhibitor
Issue Date: 
2022
Citation: 
Oluwabusola, E. T., Katermeran, N. P., Poh, W. H., Goh, T. M., Tan, L. T., Diyaolu, O., Tabudravu, J., Ebel, R., Rice, S. A., & Jaspars, M. (2022). Inhibition of the quorum sensing system, elastase production and biofilm formation in Pseudomonas aeruginosa by psammaplin A and bisaprasin. Molecules, 27(5), Article 1721. https://doi.org/10.3390/molecules27051721
Journal: 
Molecules
Abstract: 
Natural products derived from marine sponges have exhibited bioactivity and, in some cases, serve as potent quorum sensing inhibitory agents that prevent biofilm formation and attenuate virulence factor expression by pathogenic microorganisms. In this study, the inhibitory activity of the psammaplin-type compounds, psammaplin A (1) and bisaprasin (2), isolated from the marine sponge, Aplysinellarhax, are evaluated in quorum sensing inhibitory assays based on the Pseudomonas aeruginosa PAO1 lasB-gfp(ASV) and rhlA-gfp(ASV) biosensor strains. The results indicate that psammaplin A (1) showed moderate inhibition on lasB-gfp expression, but significantly inhibited the QS-gene promoter, rhlA-gfp, with IC50 values at 14.02 μM and 4.99 μM, respectively. In contrast, bisaprasin (2) displayed significant florescence inhibition in both biosensors, PAO1 lasB-gfp and rhlA-gfp, with IC50 values at 3.53 μM and 2.41 μM, respectively. Preliminary analysis suggested the importance of the bromotyrosine and oxime functionalities for QSI activity in these molecules. In addition, psammaplin A and bisaprasin downregulated elastase expression as determined by the standard enzymatic elastase assay, although greater reduction in elastase production was observed with 1 at 50 μM and 100 μM. Furthermore, the study revealed that bisaprasin (2) reduced biofilm formation in P. aeruginosa.
URI: 
ISSN: 
1420-3049 (online)
DOI: 
Grant ID: 
MSRDP-P15
MSRDP-P34
grant agreement no-312184
Funding Agency: 
National Research Foundation, Singapore
Prime Minister's Office (PMO), Singapore
PharmaSea
File Permission: 
Open
File Availability: 
With file
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