A Site-Differentiated [4Fe-4S] Cluster Controls Electron Transfer Reactivity of Clostridium acetobutylicum [FeFe]-hydrogenase I

Carolyn Lubner, Jacob Artz, David Mulder, Aisha Oza, Rachel Ward, S. Garrett Williams, Anne Jones, John Peters, Ivan Smalyukh, Vivek Bharadwaj, Paul King

Research output: Contribution to journalArticlepeer-review

9 Scopus Citations


One of the many functions of reduction-oxidation (redox) cofactors is to mediate electron transfer in biological enzymes catalyzing redox-based chemical transformation reactions. There are numerous examples of enzymes that utilize redox cofactors to form electron transfer relays to connect catalytic sites to external electron donors and acceptors. The compositions of relays are diverse and tune transfer thermodynamics and kinetics towards the chemical reactivity of the enzyme. Diversity in relay design is exemplified among different members of hydrogenases, enzymes which catalyze reversible H2 activation, which also couple to diverse types of donor and acceptor molecules. The [FeFe]-hydrogenase I from Clostridium acetobutylicum (CaI) is a member of a large family of structurally related enzymes where interfacial electron transfer is mediated by a terminal, non-canonical, His-coordinated, [4Fe-4S] cluster. The function of His coordination was examined by comparing the biophysical properties and reactivity to a Cys substituted variant of CaI. This demonstrated that His coordination strongly affected the distal [4Fe-4S] cluster spin state, spin pairing, and spatial orientations of molecular orbitals, with a minor effect on reduction potential. The deviations in these properties by substituting His for Cys in CaI, correlated with pronounced changes in electron transfer and reactivity with the native electron donor-acceptor ferredoxin. The results demonstrate that differential coordination of the surface localized [4Fe-4S]His cluster in CaI is utilized to control intermolecular and intramolecular electron transfer where His coordination creates a physical and electronic environment that enables facile electron exchange between electron carrier molecules and the iron-sulfur cluster relay for coupling to reversible H2 activation at the catalytic site.

Original languageAmerican English
Pages (from-to)4581-4588
Number of pages8
JournalChemical Science
Issue number16
StatePublished - 2022

Bibliographical note

Publisher Copyright:
© 2022 The Royal Society of Chemistry

NREL Publication Number

  • NREL/JA-2700-81667


  • electron transfer
  • hydrogenase
  • iron-sulfur protein
  • metalloenzyme
  • site-differentiated ligand


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