FeFe hydrogenases are the most efficient H2 producing enzymes, but inactivation by O2 is an obstacle to using them in biotechnological devices. Here we combine electrochemistry, site-directed mutagenesis, molecular dynamics and quantum chemical calculations to uncover the molecular mechanism of O2 diffusion within the enzyme and its reactions at the active site. We find that the partial reversibility of the reaction with O2 results from the four-electron reduction of O2 to water. The third electron/proton transfer step is the bottleneck for water production, competing with formation of the highly reactive OH radical and hydroxylated cysteine, consistent with recent crystallographic evidence. The rapid delivery of electrons and protons to the active site is therefore crucial to prevent the accumulation of these aggressive species at prolonged O2 exposure. These findings should provide important clues for the design of hydrogenase mutants with increased resistance to oxidative damage.
The mechanism of reaction of FeFe hydrogenases with oxygen has been debated. It is complex, apparently very dependent on the details of the protein structure, and difficult to study using conventional kinetic techniques. Here we build on our recent work on the anaerobic inactivation of the enzyme [Fourmond et al. Nat. Chem. 2014, 4, 336-342] to propose and apply a new method for studying this reaction. Using electrochemical measurements of the turnover rate of hydrogenase, we could resolve the first steps of the inhibition reaction and accurately determine their rates. We show that the two most studied FeFe hydrogenases, from Chlamydomonas reinhardtii and Clostridium acetobutylicum, react with O2 according to the same mechanism, despite the fact that the former is much more O2 sensitive than the latter. Unlike often assumed, both enzymes are reversibly inhibited by a short exposure to O2. This will have to be considered to elucidate the mechanism of inhibition, before any prediction can be made regarding which mutations will improve oxygen resistance. We hope that the approach described herein will prove useful in this respect.
International audienceIron–thiolate complexes of the type [Fe2(μ-bdt)(CO)6−xP(OMe3)x] (bdt=S2C6H4=benzenedithiolate, x≤2) are simplified models of iron–iron hydrogenase enzymes. Recently, we have shown that these water-insoluble organometallic complexes, when included into micelles formed by sodium dodecyl sulfate (SDS), are good catalysts for the electrochemical production of hydrogen in aqueous solutions at pH<6. We herein report that the all-CO derivative [Fe2(μ-bdt)(CO)6] (1), owing to its comparatively low reduction potential, is also a robust molecular catalyst for visible-light-driven production of H2 in aqueous SDS solutions at pH 10.5. Irradiation at λ=455 nm of a system consisting of complex 1, Eosin Y as a sensitizer, and triethylamine as an electron donor produced up to 0.86 mL of H2 in 4.5 h, corresponding to a turnover number of 117 mol of H2 per mol of catalyst. In the presence of a large excess of sensitizer, the production of H2 lasted for more than 30 h, stressing the relative stability of complex 1 under the photocatalytic conditions used herein. Thermodynamic considerations and UV/Vis spectroscopy experiments suggest that the catalytic cycle begins with the photo-driven reduction of complex 1. The reduced intermediate reacts with a proton source to yield iron hydride. Subsequent reduction and protonation steps produce H2, regenerating the starting complex. As a result, the iron–thiolate complex 1 is a versatile proton reduction catalyst that can utilize either solar or electrical energy inputs, providing a starting point for the construction of noble metal-free molecular systems for renewable H2 production
Many enzymes that produce or transform small molecules such as O, H, and CO embed inorganic cofactors based on transition metals. Their active site, where the chemical reaction occurs, is buried in and protected by the protein matrix, and connected to the solvent in several ways: chains of redox cofactors mediate long-range electron transfer; static or dynamic tunnels guide the substrate, product and inhibitors; amino acids and water molecules transfer protons. The catalytic mechanism of these enzymes is therefore delocalized over the protein and involves many different steps, some of which determine the response of the enzyme under conditions of stress (extreme redox conditions, presence of inhibitors, light), the catalytic rates in the two directions of the reaction and their ratio (the "catalytic bias"). Understanding all the steps in the catalytic cycle, including those that occur on sites of the protein that are remote from the active site, requires a combination of biochemical, structural, spectroscopic, theoretical, and kinetic methods. Here we argue that kinetics should be used to the fullest extent, by extracting quantitative information from the comparison of data and kinetic models and by exploring the combination of experimental kinetics and theoretical chemistry. In studies of these catalytic mechanisms, direct electrochemistry, the technique which we use and contribute to develop, has become unescapable. It simply consists in monitoring the changes in activity of an enzyme that is wired to an electrode by recording an electric current. We have described kinetic models that can be used to make sense of these data and to learn about various aspects of the mechanism that are difficult to probe using more conventional methods: long-range electron transfer, diffusion along gas channels, redox-driven (in)activations, active site chemistry and photoreactivity under conditions of turnover. In this Account, we highlight a few results that illustrate our approach. We describe how electrochemistry can be used to monitor substrate and inhibitor diffusion along the gas channels of hydrogenases and we discuss how the kinetics of intramolecular diffusion relates to global properties such as resistance to oxygen and catalytic bias. The kinetics and/or thermodynamics of intramolecular electron transfer may also affect the catalytic bias, the catalytic potentials on either side of the equilibrium potential, and the overpotentials for catalysis (defined as the difference between the catalytic potentials and the open circuit potential). This is understood by modeling the shape of the steady-state catalytic response of the enzyme. Other determinants of the catalytic rate, such as domain motions, have been probed by examining the transient catalytic response recorded at fast scan rates. Last, we show that combining electrochemical investigations and MD, DFT, and TD-DFT calculations is an original way of probing the reactivity of the H-cluster of hydrogenase, in particular its reactions with CO, O, and light. This approac...
Two new Cu complexes bearing a 6-ethynyl bis-(methyl-pyridyl)amine (6eBMPA) moiety, as an electroclickable function linked to a ferrocenylbased triazolyl arm (ligands 3 and 4) have been synthetized and characterized by UV-Visible, EPR spectroscopies and cyclic voltammetry in acetonitrile. Two different spacer groups between the terminal ferrocene and the triazolyl group were inserted: an hexyl chain in the case of the complex Cu-3, an ethenyl-bridged diferrocenyl system for the complex Cu-4. The monoelectronic oxidation of the diferrocenyl species yields a stable mixed-valence complex. NIR-Visible spectroscopic studies show a moderate interaction between ferrocenyl units (class II according to the Robin-Day classification). The immobilization of these systems as SAMs on an azidoundecanethiol modified gold electrode has been successfully operated by using the "self-induced electroclick" procedure. The voltammetric characterization of the surface-tagged Cu complexes indicates that good surface coverage was achieved, with moderately fast electron-transfer reaction between the electrode and the redox active immobilized systems (k 0 (Cu) = 2-4 s −1 , k 0 (Fc) = 20-90 s −1). Remarkably, the rate of charge transport is significantly controlled by the nature of the spacer on the ferrocenyl triazole arm.
A novel and general strategy for the immobilisation of functional objects onto electrodes is described. The concept is based on the addition of two pendant ethynyl groups onto a bis(pyridyl)amine derivative, which acts as a molecular platform. This platform is pre-functionalised with an N(3)-tagged object of interest by Huisgen cycloaddition to one of the ethynyl groups in biphasic conditions. Hence, when complexed by Cu(II) , this molecular-object holder can be immobilised, by a "self-induced electroclick", through the second ethynyl group onto N(3)-alkanethiol self-assembled monolayers on a gold electrode. Two different functional groups, a redox innocent ((CH(2))(3)-Ph) and an electrochemical probe (ferrocene), were immobilised by following this strategy. The in situ electrochemical grafting showed, for both systems, that the kinetics of immobilisation is fast. The voltammetric characterisation of the surface-tagged functionalised copper complexes indicated that a good surface coverage was achieved and that a moderately fast electron-transfer reaction occurs. Remarkably, in the case of the redox-active ferrocenyl-immobilised system, the electrochemical response highlighted the involvement of the copper ion of the platform in the kinetics of the electron transfer to the ferrocene moiety. This platform is a promising candidate for applications in surface addressing in areas as diverse as biology and materials.
Localized "electroclick" was achieved on azido-terminated self-assembled monolayers using Scanning Electrochemical Microscopy (SECM) in feedback mode, in which the substrate is not electrically connected (unbiased conditions). The method allows both the local immobilization of diverse functional moieties and the monitoring of each modification step at a micrometer scale. Conditions of the "click" coupling reaction were optimized especially to avoid the deposit of metallic copper by the choice of a specific ligand to stabilize the Cu(I) species. The catalytic efficiency in localized "electroclick" reaction of Cu(II)TMPA (TMPA: tris(2-pyridylmethyl)amine) as the "click" catalyst was compared with a derivative containing an alkyne group Cu(II)6eTMPA, the same molecule playing the role of the catalyst and the substrate. Evidences for surface self-catalysis propagation are demonstrated through SECM imaging showing a random 2D progression of the catalytic modification.
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