Original Design of an Oxygen-Tolerant [NiFe] Hydrogenase: Major Effect of a Valine-to-Cysteine Mutation near the Active Site

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• 作者：Pierre-Pol Liebgott ; Antonio L. de Lacey ; B茅n茅dicte Burlat ; Laurent Cournac ; Pierre Richaud ; Myriam Brugna ; Victor M. Fernandez ; Bruno Guigliarelli ; Marc Rousset ; Christophe L茅ger ; S茅bastien Dementin
• 刊名：Journal of the American Chemical Society
• 出版年：2011
• 出版时间：February 2, 2011
• 年：2011
• 卷：133
• 期：4
• 页码：986-997
• 全文大小：1081K
• 年卷期：v.133,no.4(February 2, 2011)
• ISSN：1520-5126

文摘

Hydrogenases are efficient biological catalysts of H₂ oxidation and production. Most of them are inhibited by O₂, and a prerequisite for their use in biotechnological applications under air is to improve their oxygen tolerance. We have previously shown that exchanging the residue at position 74 in the large subunit of the oxygen-sensitive [NiFe] hydrogenase from Desulfovibrio fructosovorans could impact the reaction of the enzyme with O₂ (Dementinlass="NLM_x">, S.; J. Am. Chem. Soc.lass="NLM_x"> 2009lass="NLM_x">, 131lass="NLM_x">, 10156鈭?0164; Liebgottlass="NLM_x">, P. P.; Nat. Chem. Biol.lass="NLM_x"> 2010lass="NLM_x">, 6lass="NLM_x">, 63鈭?0). This residue, a valine in the wild-type enzyme, located at the bottleneck of the gas channel near the active site, has here been exchanged with a cysteine. A thorough characterization using a combination of kinetic, spectroscopic (EPR, FTIR), and electrochemical studies demonstrates that the V74C mutant has features of the naturally occurring oxygen-tolerant membrane-bound hydrogenases (MBH). The mutant is functional during several minutes under O₂, has impaired H₂-production activity, and has a weaker affinity for CO than the WT. Upon exposure to O₂, it is converted into the more easily reactivatable inactive form, Ni-B, and this inactive state reactivates about 20 times faster than in the WT enzyme. Control experiments carried out with the V74S and V74N mutants indicate that protonation of the position 74 residue is not the reason the mutants reactivate faster than the WT enzyme. The electrochemical behavior of the V74C mutant toward O₂ is intermediate between that of the WT enzyme from D. fructosovorans and the oxygen-tolerant MBH from Aquifex aeolicus.