Substrate specificity of polyphenol oxidase and its selectivity towards polyphenols: Unlocking the browning mechanism of fresh lotus root (Nelumbo nucifera Gaertn.)

被引:15
|
作者
Li, Jingfang [1 ]
Deng, Ze-yuan [1 ,2 ]
Dong, Huanhuan [3 ]
Tsao, Rong [4 ]
Liu, Xiaoru [1 ]
机构
[1] Nanchang Univ, State Key Lab Food Sci & Resources, Nanchang 330047, Jiangxi, Peoples R China
[2] Univ Nanchang, Inst Adv Study, Nanchang 330031, Jiangxi, Peoples R China
[3] Jiangxi Univ Tradit Chinese Med, Nanchang 330004, Jiangxi, Peoples R China
[4] Agr & Agrifood Canada, Guelph Res & Dev Ctr, Guelph, ON N1G 5C9, Canada
关键词
Lotus root browning; Polyphenol oxidase; Characterization; Inhibitors; Specific selectivity mechanism; PURIFICATION; APPLE; PEROXIDASE; METABOLISM; EXTRACTION;
D O I
10.1016/j.foodchem.2023.136392
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Polyphenol oxidase (PPO) causes the browning of lotus roots (LR), negatively affecting their nutrition and shelf-life. This study aimed to explore the specific selectivity of PPO toward polyphenol substrates, thus unlocking the browning mechanism of fresh LR. Results showed that two highly homologous PPOs were identified in LR and exhibited the highest catalytic activity at 35 celcius and pH 6.5. Furthermore, the substrate specificity study revealed (-)-epigallocatechin had the lowest Km among the polyphenols identified in LR, while (+)-catechin showed the highest Vmax. The molecular docking further clarified that (-)-epigallocatechin exhibited lower docking energy and formed more hydrogen bonds and Pi-Alkyl interactions with LR PPO than (+)-catechin, while (+)-catechin entered the active cavity of PPO more quickly due to its smaller structure, both of which enhance their affinity to PPO. Thus, (+)-catechin and (-)-epigallocatechin are the most specific substrates responsible for the browning mechanism of fresh LR.
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页数:10
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