Mechanism of O2 diffusion and reduction in FeFe hydrogenases

FeFe hydrogenases are the most efficient H 2 -producing enzymes. However, inactivation by O 2 remains an obstacle that prevents them being used in many biotechnological devices. Here, we combine electrochemistry, site-directed mutagenesis, molecular dynamics and quantum chemical calculations to uncover the molecular mechanism of O 2 diffusion within the enzyme and its reactions at the active site. We propose that the partial reversibility of the reaction with O 2 results from the four-electron reduction of O 2 to water. The third electron/proton transfer step is the bottleneck for water production, competing with formation of a highly reactive OH radical and hydroxylated cysteine. The rapid delivery of electrons and protons to the active site is therefore crucial to prevent the accumulation of these aggressive species during prolonged O 2 exposure. These findings should provide important clues for the design of hydrogenase mutants with increased resistance to oxidative damage. FeFe hydrogenases are highly efficient H 2 producing enzymes; however, they can be inactivated by O 2 . Now, a mechanism for O 2 diffusion within FeFe hydrogenases and its reactions at the active site of the enzyme has been proposed. These findings could help with the design of hydrogenase mutants with increased resistance to oxidative damage.