The mutation Met121 arrow right His creates a type-1.5 copper site in Alcaligenes denitrificans azurin
The Cu ligand Met121 in azurin of Alcaligenes denitrificans was mutated to His. The spectroscopic and mechanistic properties of [M121H]azurin appear to be pH dependent with a pK sub(a) of 3.8 due to the ionization of His121. The [M121H]azurin mutant exhibits two major distinct metal-site-coordinatio...
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Veröffentlicht in: | European journal of biochemistry 1996-09, Vol.240 (2), p.342-351 |
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Sprache: | eng |
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Zusammenfassung: | The Cu ligand Met121 in azurin of Alcaligenes denitrificans was mutated to His. The spectroscopic and mechanistic properties of [M121H]azurin appear to be pH dependent with a pK sub(a) of 3.8 due to the ionization of His121. The [M121H]azurin mutant exhibits two major distinct metal-site-coordination geometries which coexist in solution according to a pH-dependent equilibrium. Both species have been spectroscopically characterized by ultraviolet-visible, EPR and resonance Raman spectroscopies. At neutral pH, His121 is deprotonated and acts as the fourth ligand of the Cu; the spectroscopic characteristics of the Cu site at this pH are halfway between those of a type-1 anti a type-2 Cu site, and the site is referred to as a type-1.5 or intermediate Cu site. The spectral data are compatible with a tetrahedral geometry of this site. At low pH, the spectroscopic data indicate that [M121H]azurin has a trigonal type-1 rhombic Cu site. |
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ISSN: | 0014-2956 |