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Published on: January 26, 2016
Fungicidal properties, sterol binding, and proteolytic resistance of the synthetic peptide D4E1
A J De Lucca1, J M Bland, C Grimm
1Southern Regional Research Center, United States Department of Agriculture, New Orleans, LA 70124, USA. adelucca@nola.srrc.usda.gov
Abstract:
The fungicidal properties of the synthetic peptide D4E1 were studied with nongerminated and germinating conidia of Aspergillus flavus, Aspergillus fumigatus, Aspergillus niger, Fusarium moniliforme, and Fusarium oxysporum. The minimal lethal concentrations (MLC) needed to kill 100% of germinating conidia of A. fumigatus, A. flavus, and A. niger were 12.5, 12.5, and 25 microM, respectively. The MLC value for nongerminated and germinating conidia of both Fusarium spp. was 3.0 microM. Except for A. fumigatus, D4E1 was inactive against the nongerminated conidia of the Aspergillus spp. Physicochemical studies showed D4E1 complexed with ergosterol, a sterol present in conidial walls. Cholesterol, present in nongerminated conidia of F. moniliforme, had a greater affinity for D4E1 than did ergosterol. D4E1 was more resistant to fungal and plant protease degradation than the natural peptide, cecropin A. These in vitro results suggest D4E1 is a candidate for transgenic expression in plants to enhance host resistance to fungal infection.
Insights
The synthetic peptide D4E1 shows potent fungicidal activity against key plant pathogens like Aspergillus and Fusarium species. Its ability to target conidial walls suggests potential for enhancing plant disease resistance.
Area of Science:
- Agricultural Science
- Biochemistry
- Mycology
Background:
- Fungal infections pose a significant threat to crop yields and food security.
- Developing novel antifungal agents is crucial for sustainable agriculture.
- Synthetic peptides offer a promising alternative to conventional fungicides.
Purpose of the Study:
- To evaluate the fungicidal efficacy of the synthetic peptide D4E1 against important plant pathogenic fungi.
- To elucidate the mechanism of action of D4E1, including its interaction with fungal cell components.
- To assess the stability of D4E1 against proteolytic degradation.
Main Methods:
- Minimal lethal concentrations (MLC) were determined for germinating and non-germinating conidia of Aspergillus and Fusarium species.
- Physicochemical studies investigated the interaction of D4E1 with ergosterol and cholesterol.
- Protease degradation assays compared D4E1 stability with the natural peptide cecropin A.
Main Results:
- D4E1 exhibited potent fungicidal activity against germinating conidia of Aspergillus (12.5-25 microM) and Fusarium (3.0 microM) species.
- D4E1 was largely inactive against non-germinating Aspergillus conidia but effective against both states of Fusarium.
- Complexation with ergosterol and a higher affinity for cholesterol were observed, suggesting a specific interaction with fungal and plant sterols.
- D4E1 demonstrated greater resistance to protease degradation than cecropin A.
Conclusions:
- The synthetic peptide D4E1 possesses significant in vitro fungicidal properties against key plant pathogens.
- Its mechanism involves interaction with sterols in conidial walls.
- D4E1's stability and efficacy make it a strong candidate for developing enhanced host resistance in plants via transgenic expression.
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