Evidence of Atypical Structural Flexibility of the Active Site Surrounding of an [FeFe] Hydrogenase from Clostridium beijerinkii .
Patrick S CorriganSean H MajerAlexey SilakovPublished in: Journal of the American Chemical Society (2023)
[FeFe] hydrogenase from Clostridium beijerinkii ( Cb HydA1) is an unusual hydrogenase in that it can withstand prolonged exposure to O 2 by reversibly converting into an O 2 -protected, inactive state (H inact ). It has been indicated in the past that an atypical conformation of the "SC 367 CP" loop near the [2Fe] H portion of the six-iron active site (H-cluster) allows the Cys367 residue to adopt an "off-H + -pathway" orientation, promoting a facile transition of the cofactor to H inact . Here, we investigated the electronic structure of the H-cluster in the oxidized state (H ox ) that directly converts to H inact under oxidizing conditions and the related CO-inhibited state (H ox -CO). We demonstrate that both states exhibit two distinct forms in electron paramagnetic resonance (EPR) spectroscopy. The ratio between the two forms is pH-dependent but also sensitive to the buffer choice. Our IR and EPR analyses illustrate that the spectral heterogeneity is due to a perturbation of the coordination environment of the H-cluster's [4Fe4S] H subcluster without affecting the [2Fe] H subcluster. Overall, we conclude that the observation of two spectral components per state is evidence of heterogeneity of the environment of the H-cluster likely associated with conformational mobility of the SCCP loop. Such flexibility may allow Cys367 to switch rapidly between off- and on-H + -pathway rotamers. Consequently, we believe such structural mobility may be the key to maintaining high enzymatic activity while allowing a facile transition to the O 2 -protected state.
Keyphrases
- metal organic framework
- optical coherence tomography
- molecular dynamics simulations
- single cell
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- hydrogen peroxide
- magnetic resonance imaging
- high resolution
- visible light
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- magnetic resonance
- molecular dynamics
- gold nanoparticles
- low density lipoprotein
- mass spectrometry
- reduced graphene oxide