European Journal of Biochemistry · 1992 · 54 citations · 33 references
Natural SciencesBiochemistryChemistryCrystal StructureRedox BiochemistrySpectroscopyBioinorganic ChemistryX-ray CrystallographyX-ray DiffractionAscorbate OxidaseEpr States
The type-2 depleted form of ascorbate oxidase from zucchini has been prepared in crystals and characterised by X-ray crystallography and EPR spectroscopy. The X-ray structure analysis by difference-Fourier techniques and refinement shows that, on average, about 1.3 Cu atoms/ascorbate oxidase monomer are removed. The copper is lost from the trinuclear site whereby the EPR-active type-2 copper is depleted most; type-1 copper is not affected. This observation indicates preferential formation of a 1 Cu-depleted form with the hole equally distributed over all three copper sites. Each of these 1 Cu-depleted species may represent an anti-ferromagnetically coupled copper pair which is EPR-silent and could explain the disappearance of the type-2 EPR signal.
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Measurement of protein using bicinchoninic acid
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