硫脲
化学
谷胱甘肽
半胱氨酸
氢键
分子动力学
对接(动物)
IC50型
立体化学
生物化学
酶
计算化学
分子
有机化学
体外
护理部
医学
作者
Hengle Zhou,Shenke Bie,Jian Li,Lei Yuan,Linyan Zhou
出处
期刊:Food Chemistry
[Elsevier BV]
日期:2022-08-30
卷期号:400: 134048-134048
被引量:32
标识
DOI:10.1016/j.foodchem.2022.134048
摘要
The inhibition mechanisms of soluble PPO (sPPO) by l-cysteine, reduced glutathione and thiourea, and membrane-bound (mPPO) by l-cysteine, reduced glutathione, thiourea, anisaldehyde and cinnamaldehyde were investigated by combining multispectroscopic analysis and computational simulations. Reduced glutathione showed the strongest inhibitory effect, with IC50 of 0.46 and 0.94 mM, respectively. The multispectral results showed that all inhibitors inhibited activity by destroying the secondary and tertiary structure, and the structure of sPPO were more easily affected. Docking showed that hydrogen bond and metal contact were the main driving force for inhibitors binding to sPPO and mPPO, respectively. Simulation showed that sPPO-inhibitor system had more fluctuation than mPPO-inhibitor system, indicating easier inhibition of sPPO activity. This work revealed that the structural differences between sPPO and mPPO led to different inhibition mechanisms of PPOs by inhibitors at the molecular level, which could provide the guidance for the selection of inhibitors in fruit and vegetable processing.
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