醇脱氢酶
化学
酒
戒毒(替代医学)
辅因子
乙醇
活性氧
电子传输链
氧气
酶
基质(水族馆)
生物化学
肉桂醇
组合化学
新陈代谢
降级(电信)
还原剂
生物物理学
活动站点
醛脱氢酶
电子转移
乙醇代谢
催化作用
氧化还原酶
生物转化
立体化学
NAD+激酶
代谢途径
代谢工程
金属
纳米技术
氧化还原
八面体
再生(生物学)
作者
Yinjun Tang,Pengcheng Qi,Yifei Chen,Li J,Wenxuan Jiang,Hongcheng Sun,Wenling Gu,Yao Sun,Chengzhou Zhu
摘要
Acute alcohol intoxication causes severe damage to the liver, nervous system and metabolic processes while inducing inflammatory responses. Current therapeutic strategies targeting ethanol metabolism through alcohol or aldehyde dehydrogenase activation face critical limitations of NADH accumulation and excessive reactive oxygen species (ROS) generation. Herein, by introducing a topology-controlled Pt atomic site into Co3O4 lattices, the geometric structure diversification of Pt was achieved for alcohol detoxification by coenzyme regeneration. In comparison with octahedral PtOhCo/O and pure Co3O4, PtTdCo/O (atomic Pt sites within tetrahedral topology) exhibits 3.59- and 3.83-fold higher NOX-like activity, and preferentially catalyzes 4e⁻ oxygen reduction, improving electron utilization while minimizing ROS production. Mechanistic studies indicate that the introduction of PtTd sites improves substrate adsorption, enhances electron utilization efficiency and lowers the energy of reactions, thereby promoting alcohol degradation and reducing the release of ROS. This work on topological structure engineering offers new insights into designing high-performance biocatalysts for biological applications.
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