Aerobic Damage to [FeFe]‐Hydrogenases: Activation Barriers for the Chemical Attachment of O21. (11th March 2014)

• Record Type: Journal Article
• Authors: Kubas, Adam; De Sancho, David; Best, Robert B.; Blumberger, Jochen
• Is Part Of: Angewandte Chemie. Volume 126:Number 16(2014)
• Page Start: 4165
• Page End: 4168
• Publication Date: 2014-03-11
• Subjects: Chemistry -- Periodicals; 540
• DOI: 10.1002/ange.201400534
• Languages: English
• ISSNs: 0044-8249

Abstract

<abstract abstract-type="main" xml:lang="en"> <title>Abstract</title> <p>[FeFe]‐hydrogenases are the best natural hydrogen‐producing enzymes but their biotechnological exploitation is hampered by their extreme oxygen sensitivity. The free energy profile for the chemical attachment of O₂ to the enzyme active site was investigated by using a range‐separated density functional re‐parametrized to reproduce high‐level ab initio data. An activation free‐energy barrier of 13 kcal mol⁻¹ was obtained for chemical bond formation between the di‐iron active site and O₂, a value in good agreement with experimental inactivation rates. The oxygen binding can be viewed as an inner‐sphere electron‐transfer process that is strongly influenced by Coulombic interactions with the proximal cubane cluster and the protein environment. The implications of these results for future mutation studies with the aim of increasing the oxygen tolerance of this enzyme are discussed.</p> </abstract>