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Bioactive Compounds from an Endophytic Pezicula sp. Showing Antagonistic Effects against the Ash Dieback Pathogen.
- Source :
-
Biomolecules [Biomolecules] 2023 Nov 08; Vol. 13 (11). Date of Electronic Publication: 2023 Nov 08. - Publication Year :
- 2023
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Abstract
- A fungal endophyte originating from the Canary Islands was identified as a potent antagonist against the fungal phytopathogen Hymenoscyphus fraxineus , which causes the devastating ash dieback disease. This endophyte was tentatively identified as Pezicula cf. ericae , using molecular barcoding. Isolation of secondary metabolites by preparative high-performance liquid chromatography (HPLC) yielded the known compounds CJ-17,572 ( 1 ), mycorrhizin A ( 3 ) and cryptosporioptides A-C ( 4 - 6 ), besides a new N -acetylated dihydroxyphenylalanin derivative 2 , named peziculastatin. Planar structures were elucidated by NMR and HRMS data, while the relative stereochemistry of 2 was assigned by H,H and C,H coupling constants. The assignment of the unknown stereochemistry of CJ-17,572 ( 1 ) was hampered by the broadening of NMR signals. Nevertheless, after semisynthetic conversion of 1 into its methyl derivatives 7 and 8 , presumably preventing tautomeric effects, the relative configuration could be assigned, whereas comparison of ECD data to those of related compounds determined the absolute configuration. Metabolites 1 and 3 showed significant antifungal effects in vitro against H. fraxineus . Furthermore, 4 - 6 exhibited significant dispersive effects on preformed biofilms of S. aureus at concentrations up to 2 µg/mL, while the biofilm formation of C. albicans was also inhibited. Thus, cryptosporioptides might constitute a potential source for the development of novel antibiofilm agents.
- Subjects :
- Pyrrolidinones pharmacology
Staphylococcus aureus
Antifungal Agents
Subjects
Details
- Language :
- English
- ISSN :
- 2218-273X
- Volume :
- 13
- Issue :
- 11
- Database :
- MEDLINE
- Journal :
- Biomolecules
- Publication Type :
- Academic Journal
- Accession number :
- 38002314
- Full Text :
- https://doi.org/10.3390/biom13111632