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Reversible temperature-dependent high- to low-spin transition in the heme Fe–Cu binuclear center of cytochrome ba(3) oxidase
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...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9060599/ https://www.ncbi.nlm.nih.gov/pubmed/35514640 http://dx.doi.org/10.1039/c8ra09954e |
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author | Nicolaides, Antonis Soulimane, Tewfik Varotsis, Constantinos |
author_facet | Nicolaides, Antonis Soulimane, Tewfik Varotsis, Constantinos |
author_sort | Nicolaides, Antonis |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-9060599 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-90605992022-05-04 Reversible temperature-dependent high- to low-spin transition in the heme Fe–Cu binuclear center of cytochrome ba(3) oxidase Nicolaides, Antonis Soulimane, Tewfik Varotsis, Constantinos RSC Adv Chemistry 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. The Royal Society of Chemistry 2019-02-06 /pmc/articles/PMC9060599/ /pubmed/35514640 http://dx.doi.org/10.1039/c8ra09954e Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/ |
spellingShingle | Chemistry Nicolaides, Antonis Soulimane, Tewfik Varotsis, Constantinos Reversible temperature-dependent high- to low-spin transition in the heme Fe–Cu binuclear center of cytochrome ba(3) oxidase |
title | Reversible temperature-dependent high- to low-spin transition in the heme Fe–Cu binuclear center of cytochrome ba(3) oxidase |
title_full | Reversible temperature-dependent high- to low-spin transition in the heme Fe–Cu binuclear center of cytochrome ba(3) oxidase |
title_fullStr | Reversible temperature-dependent high- to low-spin transition in the heme Fe–Cu binuclear center of cytochrome ba(3) oxidase |
title_full_unstemmed | Reversible temperature-dependent high- to low-spin transition in the heme Fe–Cu binuclear center of cytochrome ba(3) oxidase |
title_short | Reversible temperature-dependent high- to low-spin transition in the heme Fe–Cu binuclear center of cytochrome ba(3) oxidase |
title_sort | reversible temperature-dependent high- to low-spin transition in the heme fe–cu binuclear center of cytochrome ba(3) oxidase |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9060599/ https://www.ncbi.nlm.nih.gov/pubmed/35514640 http://dx.doi.org/10.1039/c8ra09954e |
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