Investigating the impact of common migration substances found in milk packaging on proteases: A multispectral and molecular docking approach

被引:4
作者
Xiong, Zijian [1 ]
He, Yue [2 ]
Guan, Weiyan [1 ]
Lv, Xinguang [1 ]
Chen, Jing [5 ,6 ]
Ma, Da [1 ,3 ,4 ,7 ]
机构
[1] Jinan Univ, Coll Packaging Engn, Zhuhai 519070, Guangdong, Peoples R China
[2] Zhuhai Inst Food & Drug Control, Zhuhai 519000, Guangdong, Peoples R China
[3] Jinan Univ, Packaging Engn Inst, Zhuhai 519070, Guangdong, Peoples R China
[4] Jinan Univ, Guangdong Higher Educ Inst, Key Lab Prod Packaging & Logist, Zhuhai 519070, Guangdong, Peoples R China
[5] Jinan Univ, Inst Adv & Appl Chem Synth, Coll Pharm, Guangzhou 510632, Peoples R China
[6] 601 Huangpu Av West, Guangzhou, Guangdong, Peoples R China
[7] 206 Qianshan Rd, Zhuhai, Guangdong, Peoples R China
关键词
Milk packaging; Migrations; Digestive protease; Inhibitory kinetics; Molecular docking; N-ALKYL SULFATES; INTERACTION MECHANISM; ALOE-EMODIN; SPECTROSCOPY; PEPSIN; SIMULATION; STABILITY; AFFINITY; TRYPSIN; PAPAIN;
D O I
10.1016/j.saa.2024.124517
中图分类号
O433 [光谱学];
学科分类号
0703 ; 070302 ;
摘要
The effects of common migration substances in milk packaging on digestive protease were studied. We choose the common migrants found in eight types of multi-layer composite milk packaging. Enzyme activity experiments revealed that pepsin activity decreased by approximately 18 % at 500 mu g/mL of stearic acid and stearamide treatment, while trypsin activity decreased by approximately 18 % only by stearic acid treatment (500 mu g/mL). Subsequently, fluorescence spectroscopy, circular dichroism spectroscopy, and molecular docking technology were employed to investigate the inhibition mechanism of protease activity by migrating substances in three systems: stearic acid-trypsin, stearic acid-pepsin, and stearamide-pepsin. Results showed that the inhibitory effect of stearic acid on trypsin is a reversible mixed inhibition, whereas the inhibitory effects of stearic acid and stearamide on pepsin are non-competitive. In all three systems, Delta H < 0, Delta S < 0, and Delta G < 0, indicating the binding process between the migrant and the protease is a spontaneous exothermic process primarily driven by hydrogen bonding and van der Waals forces. In addition, their binding constants are all around 10(4) L/moL, indicating that there are moderate binding affinities exist between migrants and proteases. The binding process results in the quenching of the protease's endogenous fluorescence and induces alterations in the enzyme's secondary structure. Synchronized fluorescence spectroscopy showed that stearic acid enhanced the hydrophobicity near the Tyr residue of trypsin. The molecular docking results indicated that the binding affinity of stearic acid-trypsin, stearic acid-pepsin, and stearamide-pepsin was -22.51 kJ/mol, -12.35 kJ/mol, -19.28 kJ/mol respectively, which consistent with the trend in the enzyme activity results. This study can provide references for the selection of milk packaging materials and the use of processing additives, ensuring food health and safety.
引用
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页数:11
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