Abstract
A reversible temperature-dependent high-spin to low-spin transition with T 1/2 =-60 °C has been observed in the resonance Raman spectra of the equilibrium reduced and photoreduced heme a 3 of the thermophilic ba 3 heme-copper oxidoreductase. The transition is based on the frequency shifts of the spin-state marker bands ν 2 (C b C b ) and ν 10 (C a C m ) and is attributed to the displacement of the heme iron along the heme normal as a consequence of the Fe-Np repulsion at temperature below-40 °C which will increase the ligand field strength forcing the pairing of d electrons into the lower energy orbitals.
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CITATION STYLE
Nicolaides, A., Soulimane, T., & Varotsis, C. (2019). Reversible temperature-dependent high-to low-spin transition in the heme Fe-Cu binuclear center of cytochrome: Ba 3 oxidase. RSC Advances, 9(9), 4776–4780. https://doi.org/10.1039/c8ra09954e
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