Abstract
Melittin (ME) from honey-bee venom has a broad range of strong antimicrobial activity, but it has hemolytic activity against eukaryotic cells. In order to design peptides with powerful antifungal activity without cytotoxic property of ME and understand structure-antifungal activity relationships, the hybrid peptides derived from the sequences of ME and cecropin A (CA) or magainin 2 (MA), MA(10-17)ME(1-12) and CA(1-8)ME(1-12), were synthesized by solid phase method. MA(10-17)ME(1-12) showed potent antifungal activity comparable to ME against Fusarium oxysporum with no hemolytic activity against human red blood cells. The hybrid peptides showed strong inhibition of (1,3)-β-D-glucan synthase. This result indicates that the antifungal activity of the hybrid peptides against Fusarium oxysporum is attributed to the inhibition of cell wall synthesis. The results therefore showed a successful design of a peptide having antifungal activity without hemolytic property.
| Original language | English |
|---|---|
| Pages (from-to) | 529-533 |
| Number of pages | 5 |
| Journal | Korean Journal of Applied Microbiology and Biotechnology |
| Volume | 24 |
| Issue number | 5 |
| State | Published - 1996 |
Keywords
- β-1.3 glucan synthase
- Antifungal activity
- Hybrid peptide
- Melittin