Multi-frequency e.p.r. studies of a mercury-containing mixed-metal derivative of laccase
- 14 April 1986
- journal article
- research article
- Published by Portland Press Ltd. in Biochemical Journal
- Vol. 235 (2) , 415-420
- https://doi.org/10.1042/bj2350415
Abstract
Multi-frequency e.p.r. studies of a derivative of laccase containing one mercury atom and three of copper were carried out at -150.degree. C. The e.p.r. signal of the mercury derivative and fluoride-binding studies establish that a type 2-like copper centre is present. The signal suffers broadening, owing to g-strain, but at low frequencies (S-band) ligand hyperfine splitting can be resolved, and it can be explained in terms of coupling to three nitrogen atoms. The g values and the effect of solvent deuteration on the line width suggest that the fourth ligand in the equatorial plane is a water molecule. Simulations of the e.p.r. spectrum reveal that the site is slightly rhombic at -150.degree. C, a finding in accord with the proposed N3O donor set. Finally, it is emphasized that a structural reorganization of the type-2 copper site occurs with the binding of fluoride at low temperature. The reorganization may be linked to a conformational change which has previously been claimed to occur on cooling; however, this transition is not necessarily relevant to the temperature-dependence of fluoride binding.This publication has 36 references indexed in Scilit:
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