68 results on '"Horch, Marius"'
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52. Revealing the Absolute Configuration of the CO and CN− Ligands at the Active Site of a [NiFe] Hydrogenase.
53. Untersuchung des katalytischen Zentrums der O2-toleranten NAD+-reduzierenden [NiFe]-Hydrogenase von Ralstonia eutropha H16 mit In-situ-EPR- und -FTIR-Spektroskopie.
54. Probing the Active Site of an O2-Tolerant NAD+-Reducing [NiFe]-Hydrogenase from Ralstonia eutropha H16 by In Situ EPR and FTIR Spectroscopy.
55. Probing the Active Site of an O2‐Tolerant NAD+‐Reducing [NiFe]‐Hydrogenase from Ralstonia eutrophaH16 by In Situ EPR and FTIR Spectroscopy
56. Untersuchung des katalytischen Zentrums der O2‐toleranten NAD+‐reduzierenden [NiFe]‐Hydrogenase von Ralstonia eutrophaH16 mit In‐situ‐EPR‐ und ‐FTIR‐Spektroskopie
57. A Beginner's Guide to Thermodynamic Modelling of [FeFe] Hydrogenase.
58. Electrocatalysis by Heme Enzymes—Applications in Biosensing.
59. Investigation of the NADH/NAD+ ratio in Ralstonia eutropha using the fluorescence reporter protein Peredox.
60. Light-Induced Electron Transfer in a [NiFe] Hydrogenase Opens a Photochemical Shortcut for Catalytic Dihydrogen Cleavage.
61. Understanding the [NiFe] Hydrogenase Active Site Environment through Ultrafast Infrared and 2D-IR Spectroscopy of the Subsite Analogue K[CpFe(CO)(CN) 2 ] in Polar and Protic Solvents.
62. Exploring Structure and Function of Redox Intermediates in [NiFe]-Hydrogenases by an Advanced Experimental Approach for Solvated, Lyophilized and Crystallized Metalloenzymes.
63. X-ray Crystallography and Vibrational Spectroscopy Reveal the Key Determinants of Biocatalytic Dihydrogen Cycling by [NiFe] Hydrogenases.
64. Enzymatic and spectroscopic properties of a thermostable [NiFe]‑hydrogenase performing H 2 -driven NAD + -reduction in the presence of O 2 .
65. An S-Oxygenated [NiFe] Complex Modelling Sulfenate Intermediates of an O 2 -Tolerant Hydrogenase.
66. Nuclear resonance vibrational spectroscopy reveals the FeS cluster composition and active site vibrational properties of an O 2 -tolerant NAD + -reducing [NiFe] hydrogenase.
67. Resonance Raman spectroscopy as a tool to monitor the active site of hydrogenases.
68. Probing the active site of an O2-tolerant NAD+-reducing [NiFe]-hydrogenase from Ralstonia eutropha H16 by in situ EPR and FTIR spectroscopy.
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