Electron paramagnetic resonance plastocyanin

We have mentioned earlier the dissimilarities between the spectral properties of chromophoric metal ions at the active sites of metalloen-zymes and the properties of simple bidentate model complexes of the same metals. Cobalt phosphatase has served well to illustrate such a dissimilarity and, in Figure 9, the data for phosphatase, representative of a cobalt enzyme, are shown again along with those for plastocyanin, a copper enzyme, and ferredoxin, an iron enzyme. Each enzyme spectrum is unusual compared with the simple model complexes shown at the bottom of the figure. More detailed spectral data as well as comparison of other physical properties of metalloenzymes—e.g., electron paramagnetic resonance spectra—with those of model complexes have been summarized previously (10). 

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