Lee Chi Chung, Hu Yilin, Ribbe Markus W
Department of Molecular Biology and Biochemistry, University of California, Irvine, Irvine, CA 92697-3900 (USA).
Angew Chem Int Ed Engl. 2015 Jan 19;54(4):1219-22. doi: 10.1002/anie.201410412. Epub 2014 Nov 24.
Nitrogenase cofactors can be extracted into an organic solvent to catalyze the reduction of cyanide (CN(-)), carbon monoxide (CO), and carbon dioxide (CO2) without using adenosine triphosphate (ATP), when samarium(II) iodide (SmI2) and 2,6-lutidinium triflate (Lut-H) are employed as a reductant and a proton source, respectively. Driven by SmI2, the cofactors catalytically reduce CN(-) or CO to C1-C4 hydrocarbons, and CO2 to CO and C1-C3 hydrocarbons. The C-C coupling from CO2 indicates a unique Fischer-Tropsch-like reaction with an atypical carbonaceous substrate, whereas the catalytic turnover of CN(-), CO, and CO2 by isolated cofactors suggests the possibility to develop nitrogenase-based electrocatalysts for the production of hydrocarbons from these carbon-containing compounds.
当分别使用碘化钐(SmI2)和三氟甲磺酸2,6-二甲基吡啶鎓(Lut-H)作为还原剂和质子源时,固氮酶辅因子可被萃取到有机溶剂中,从而在不使用三磷酸腺苷(ATP)的情况下催化氰化物(CN(-))、一氧化碳(CO)和二氧化碳(CO2)的还原反应。在SmI2的驱动下,这些辅因子将CN(-)或CO催化还原为C1 - C4烃类,将CO2还原为CO和C1 - C3烃类。由CO2发生的C - C偶联反应表明了一种与非典型含碳底物发生的类似费托反应的独特反应,而分离出的辅因子对CN(-)、CO和CO2的催化周转表明了开发基于固氮酶的电催化剂以从这些含碳化合物生产烃类的可能性。