7 research outputs found

    O2_2 reduction and O2_2-induced damage at the active site of FeFe hydrogenase

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    International audienceFeFe hydrogenases are the most efficient H2_2-producing enzymes. However, inactivation by O2_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 O2_2 diffusion within the enzyme and its reactions at the active site. We propose that the partial reversibility of the reaction with O2_2 results from the four-electron reduction of O2_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 O2_2 exposure. These findings should provide important clues for the design of hydrogenase mutants with increased resistance to oxidative damage

    Structural basis for tRNA modification by Elp3 from Dehalococcoides mccartyi

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    International audienceDuring translation elongation, decoding is based on the recognition of codons by corresponding tRNA anticodon triplets. Molecular mechanisms that regulate global protein synthesis via specific base modifications in tRNA anticodons are receiving increasing attention. The conserved eukaryotic Elongator complex specifically modifies uridines located in the wobble base position of tRNAs. Mutations in Elongator subunits are associated with certain neurodegenerative diseases and cancer. Here we present the crystal structure of D. mccartyi Elp3 (DmcElp3) at 2.15-Å resolution. Our results reveal an unexpected arrangement of Elp3 lysine acetyltransferase (KAT) and radical S-adenosyl methionine (SAM) domains, which share a large interface and form a composite active site and tRNA-binding pocket, with an iron–sulfur cluster located in the dimerization interface of two DmcElp3 molecules. Structure-guided mutagenesis studies of yeast Elp3 confirmed the relevance of our findings for eukaryotic Elp3s and should aid in understanding the cellular functions and pathophysiological roles of Elongator

    Hydrogen and Biofuel Production in the Chloroplast

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