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Dioxygenases copper complexes

NON-IRON MODEL STUDIES ON DIOXYGENASES 4.6. Copper Complexes... [Pg.187]

Peptide Amidation by Metal Complexes. 16.6 A COPPER DIOXYGENASE ENZYME... [Pg.395]

Mechanisms have rarely been elucidated unambiguously, especially for easily oxidizable ligands, where alternative explanations are difficult to rule out. In fact, closer examination of some of these so-called transfer reactions has revealed that free hydrogen peroxide is the oxidant (55). Moreover, this type of reaction is restricted to the heavier transition metals which form Jt-type peroxo complexes (7) with dioxygen and are therefore scarcely models for the iron- and copper-containing dioxygenases. [Pg.198]

Nearly all dioxygenases contain iron or copper, which in most cases is a direct constituent of the enzyme protein. Iron may also be part of ferroprotoporphyrin IX (heme, D 10.1 Table 15). The metal activates the oxygen linked to the enzyme, a process which is associated with polarization of the complex. In the case of the iron-containing enzymes this may be formulated as follows ... [Pg.95]


See other pages where Dioxygenases copper complexes is mentioned: [Pg.469]    [Pg.504]    [Pg.3290]    [Pg.153]    [Pg.181]    [Pg.33]    [Pg.1163]    [Pg.3495]    [Pg.670]    [Pg.520]    [Pg.1162]    [Pg.3494]    [Pg.6047]    [Pg.186]    [Pg.423]    [Pg.295]    [Pg.251]    [Pg.250]    [Pg.276]    [Pg.105]    [Pg.158]   
See also in sourсe #XX -- [ Pg.5 , Pg.721 ]




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