Abstract

The bacteriostatic concentration of essential oil (EO) in practical application is usually higher than the flavor threshold, resulting in a lack of balance between bacteriostatic concentration and flavor, which has become the bottleneck of its application in the field of agriculture products. One of the effective ways to solve this problem is the synergistic antibacterial effect of the active components of EO. In this paper, molecular docking , independent gradient model (IGM) and symmetric matching perturbation theory (SAPT) are combined for the first time to investigated the molecular mechanism of eugenol and citral small molecules (E AC ) against Aspergillus niger . The results show that E AC can combine with β-(1,3)-glucan synthase and chitin synthase proteins, and then destroy the integrity of cell wall, in which the trans -citral has the best affinity with these two enzyme proteins. In addition, E AC can bind to tryptophan , tyrosine and phenylalanine in cell membrane. The binding of citral small molecules to these three amino acids is mainly hydrogen bond, while the binding force of eugenol to them is mainly van der Waals force or π-π interaction. Finally, the synergistic antifungal effect of E AC was confirmed by the damage of membrane proteins and the leakage of cell contents. In this combination, citral binds to the cell wall, which promotes the interaction between eugenol and cell membrane, and finally leads to the serious destruction of cell membrane. The above results show that E AC has the potential to be developed into a new type of agriculture products preservative with synergistic antifungal effect. • Eugenol and citral (E AC ) can combine with chitin synthase and β-(1,3)-glucan synthase to destroy the integrity of cell wall. • Trans-Citral has the best affinity with chitin synthase and β-(1,3)-glucan synthase. • Static electricity is the main contribution to the stability of essential oils molecules and amino acids. • The E AC could cause damages to Aspergillus niger cell membrane that led to a loss of cell viability.

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