甲酸脱氢酶
化学
格式化
三乙醇胺
光化学
小提琴手
卟啉
NAD+激酶
锌
电子转移
催化作用
无机化学
有机化学
酶
分析化学(期刊)
作者
Akimitsu Miyaji,Yutaka Amao
出处
期刊:ChemNanoMat
[Wiley]
日期:2021-03-26
卷期号:7 (6): 626-634
被引量:6
标识
DOI:10.1002/cnma.202100045
摘要
Abstract Visible‐light driven CO 2 reduction to formate with the system consisting of water‐soluble zinc tetraphneylporphyrin tetrasulfonate (ZnTPPS), formate dehydrogenase from Candida boidinii (CbFDH) and 1‐nicotinamidethy‐1’‐methyl‐4,4’‐ bipyridinium salt (NEMBP) in the presence of triethanolamine (TEOA) as an electron donor was investigated. NEMBP was prepared as the 4,4’‐BP with the nicotinamide‐group to promote the improvement of affinity with CbFDH. The properties of NEMBP were characterized by photochemical and electrochemical methods. In order to evaluate the affinity between cation radical of NEMBP (NEMBP +. ), as a co‐enzyme and CbFDH, the energy level based on simple docking simulation and density functional theory were estimated. It was speculated that NEMBP +. could bind near the substrate binding pocket of CbFDH as well as NAD + by docking simulation. In the visible‐light driven NEMBP reduction with the sensitization of ZnTPPS in the presence of TEOA, the yield for reduction of NEMBP to NEMBP +. was estimated to be 80%. In the CO 2 reduction to formate with the system consisting of TEOA, ZnTPPS, NEMBP and CbFDH, the turnover numbers of NEMBP and CbFDH were estimated to be 0.14 and 1.53 h −1 , respectively.
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