Introduction of Methionines in the Gas Channel Makes [NiFe] Hydrogenase Aero-Tolerant

S. Dementin, F. Leroux, L. Cournac, A. De Lacey, A. Volbeda, C. Leger, B. Burlat, N. Martinez, S. Champ, L. Martin, O. Sanganas, M. Haumann, V. Fernandez, B. Guigliarelli, J. Fontecilla-Camps, M. Rousset.

J. Am. Chem. Soc., 131, 10156-10164 (2009) doi:10.1021/ja9018258

Hydrogenases catalyze the conversion between 2H+ + 2e− and H21. Most of these enzymes are inhibited by O2, which represents a major drawback for their use in biotechnological applications. Improving hydrogenase O2 tolerance is therefore a major contemporary challenge to allow the implementation of a sustainable hydrogen economy. We succeeded in improving O2 tolerance, which we define here as the ability of the enzyme to resist for several minutes to O2 exposure, by substituting with methionines small hydrophobic residues strongly conserved in the gas channel. Remarkably, the mutated enzymes remained active in the presence of an O2 concentration close to that found in aerobic solutions in equilibrium with air, while the wild type enzyme is inhibited in a few seconds. Crystallographic and spectroscopic studies showed that the structure and the chemistry at the active site are not affected by the mutations. Kinetic studies demonstrated that the inactivation is slower and reactivation faster in these mutants. We propose that in addition to restricting O2 diffusion to the active site of the enzyme, methionine may also interact with bound peroxide and provide an assisted escape route for H2O2 toward the gas channel. These results show for the first time that it is possible to improve O2-tolerance of [NiFe] hydrogenases, making possible the development of biohydrogen production systems.


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