Resolving a Natural Product Cold Case: Elucidation of Fusapyrone Structure and Absolute Configuration and Demonstration of Their Fungal Biofilm Disrupting Properties.
Yun-Seo KilJianlan YouKaren L WendtJarrod B KingRobert H CichewiczPublished in: The Journal of organic chemistry (2023)
Fusapyrones are fungal metabolites, which have been reported to have broad-spectrum antibacterial and antifungal properties. Despite the first members of this chemical class being described three decades prior, many aspects of their structures have remained unresolved, thereby constraining efforts to fully understand structure-activity relationships within this metabolite family and impeding the design of streamlined syntheses. Among the main challenges posed by fusapyrones is the incorporation of several single and groups of stereocenters separated by atoms with freely rotating bonds, which have proven unyielding to spectroscopic analyses. In this study, we obtained a series of new ( 2 - 5 and 7 - 9 ) and previously reported fusapyrones ( 1 and 6 ), which were subjected to a combination of spectroscopic, chemical, and computational techniques enabling us to offer proposals for their full structures, as well as provide a pathway to reinterpreting the absolute configurations of other published fusapyrone metabolites. Biological testing of the fusapyrones revealed their abilities to inhibit and disrupt biofilms made by the human fungal pathogen, Candida albicans . These results show that fusapyrones reduce hyphae formation in C. albicans , as well as decrease the surface adherence capabilities of planktonic cells and cells transitioning into early-stage biofilm formation.
Keyphrases
- candida albicans
- biofilm formation
- induced apoptosis
- early stage
- cell cycle arrest
- endothelial cells
- molecular docking
- ms ms
- signaling pathway
- high resolution
- single cell
- pseudomonas aeruginosa
- randomized controlled trial
- oxidative stress
- radiation therapy
- escherichia coli
- skeletal muscle
- squamous cell carcinoma
- staphylococcus aureus
- cell death
- metabolic syndrome
- wound healing