Effect of non-covalent and covalent modification strategies on the structural assembly, antibacterial activity, and stability of gallic acid-mulberry leaf peptide complexes and their application in grape preservation
摘要
This study prepared, characterized, and applied synergistic antibacterial complexes of mulberry leaf peptide (MLP) and gallic acid (GA) for grape preservation. The complexes were formed through non-covalent binding (GA-MLP N), alkaline treatment (GA-MLP A), and free-radical grafting (GA-MLP F) to address the high usage concentration of MLP. The minimum inhibitory concentration of MLP in the synergistic combination was reduced by 87.5% against Staphylococcus aureus and Escherichia coli. GA-MLP A exhibited the highest binding capacity, surpassing GA-MLP N and GA-MLP F by 16.9% and 24.0%, respectively. The peptides in GA-MLP A refolded into stable α-helical structures, whereas the backbone and aromatic side chains of peptides in GA-MLP F were degraded due to the aggressive oxidative environment. Structural characterization indicated that particle size decreased, and a rigid molecular network formed under alkaline treatment and free-radical grafting, enhancing the stability of the complexes. GA-MLP A demonstrated the best antibacterial activity, particularly in disrupting phospholipid acyl chains and causing membrane damage. All complexes showed favorable biocompatibility, with GA-MLP A achieving the highest comprehensive quality index in grape preservation. Compared with the control group, the decay rate and weight loss in the GA-MLP A group were reduced by 77.2% and 36.2%, respectively. While maintaining higher firmness and nutrient content, thereby preserving superior sensory quality in grapes. Thus, base-induced covalent conjugation is a superior strategy to transform synergistic mixtures into stable and effective preservatives, facilitating molecular design of polyphenol-peptide complexes.