Activation Thermodynamics and H/D Kinetic Isotope Effect of the H-ox to HredH+ Transition in [FeFe] Hydrogenase

作者：Ratzloff Michael W; Wilker Molly B; Mulder David W; Lubner Carolyn E; Hamby Hayden; Brown Katherine A; Dukovic Gordana; King Paul W

来源：Journal of the American Chemical Society, 2017, 139(37): 12879-12882.

DOI：10.1021/jacs.7b04216

Molecular complexes between CdSe nanocrystals and Clostridium acetobutylicum [FeFe] hydrogenase I (CaI) enabled light-driven control of electron transfer for spectroscopic detection of redox intermediates during catalytic proton reduction. Here we address the route of electron transfer from CdSe -> CaI and activation thermodynamics of the initial step of proton reduction in CaI. The electron paramagnetic spectroscopy of illuminated CdSe:CaI showed how the CaI accessory FeS cluster chain (F-clusters) functions in electron transfer with CdSe. The H-ox -> HredH+ reduction step measured by Fourier-transform infrared spectroscopy showed an enthalpy of activation of 19 kJ mol(-1) and a similar to 2.5-fold kinetic isotope effect. Overall, these results support electron injection from CdSe into CaI involving F-clusters, and that the H-ox -> HredH+ step of catalytic proton reduction in CaI proceeds by a proton-dependent process.

• 出版日期2017-9-20