Aim: Several kinds of harmful yeasts may cause spoilage of foods and even endanger health. As a natural active ingredient, cordycepin has been found to be effective against bacteria. However, the antifungal mechanism of the cordycepin is uncertain. In this work, the antifungal activity and mechanism of cordycepin against yeasts has been studied.
Methods and results: The effects of cordycepin on cell structure, biomacromolecule substances, respiratory metabolism, and nucleic acid were analyzed through scanning electron microscopy (SEM), ultraviolet-visible (UV-vis) spectrophotometer, fluorescence titration, etc. The results indicated that cordycepin was more effective in antifungal activity against Saccharomyces cerevisiae, Candida albicans and Zygosaccharomyces rouxii, compared to potassium sorbate. SEM observations revealed irreversible damage to the cell wall and membrane, leading to intracellular biological macromolecules leakage, which was proved by the quantification of biological macromolecular substances. Moreover, it was found that cordycepin inhibited respiratory metabolic pathways of S. cerevisiae, C. albicans and Z. rouxii by affecting the HMP and TCA pathways. In addition, cordycepin had intercalated binding and electrostatic interaction with DNA.
Conclusions: Cordycepin exhibited high antifungal activity with a minimum inhibitory concentration of 0.125-0.05 mg/ml against Saccharomyces cerevisiae, Candida albicans and Zygosaccharomyces rouxii. Cordycepin exerted antibacterial effects through damaging cell membranes, inhibiting respiratory metabolism and binding DNA to affect fungal physiological functions.
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Evidence ID | Analyze ID | Gene/Complex | Systematic Name/Complex Accession | Qualifier | Gene Ontology Term ID | Gene Ontology Term | Aspect | Annotation Extension | Evidence | Method | Source | Assigned On | Reference |
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Evidence ID | Analyze ID | Gene | Gene Systematic Name | Phenotype | Experiment Type | Experiment Type Category | Mutant Information | Strain Background | Chemical | Details | Reference |
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Evidence ID | Analyze ID | Gene | Gene Systematic Name | Disease Ontology Term | Disease Ontology Term ID | Qualifier | Evidence | Method | Source | Assigned On | Reference |
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Evidence ID | Analyze ID | Regulator | Regulator Systematic Name | Target | Target Systematic Name | Direction | Regulation of | Happens During | Regulator Type | Direction | Regulation Of | Happens During | Method | Evidence | Strain Background | Reference |
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Site | Modification | Modifier | Source | Reference |
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Evidence ID | Analyze ID | Interactor | Interactor Systematic Name | Interactor | Interactor Systematic Name | Allele | Assay | Annotation | Action | Phenotype | SGA score | P-value | Source | Reference | Note |
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Evidence ID | Analyze ID | Interactor | Interactor Systematic Name | Interactor | Interactor Systematic Name | Assay | Annotation | Action | Modification | Source | Reference | Note |
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Complement ID | Locus ID | Gene | Species | Gene ID | Strain background | Direction | Details | Source | Reference |
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Evidence ID | Analyze ID | Dataset | Description | Keywords | Number of Conditions | Reference |
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