Goldstein S, Czapski G
Department of Physical Chemistry, Hebrew University of Jerusalem, Israel.
Free Radic Res Commun. 1991;12-13 Pt 1:205-10. doi: 10.3109/10715769109145787.
Using the direct method of pulse radiolysis to determine the superoxide dismutase like activity of copper(II) cimetidine complexes, it was found that the reaction rate constant with O2-, kcat, was (8.5 +/- 0.5) x 10(8) M-1s-1 independent of the cimetidine concentrations present in excess of 50-200 microM over the metal. The results suggest that either the 1:1 ligand to metal complex does not catalyze O2- dismutation at a comparable rate to that of the 2:1 complex, or that the stability constant of the last species is much higher than that determined earlier by Kimura et al., and only the 2:1 species is present in the solutions. With the indirect methods of cytochrome c and NBT for determining the ability of these complexes to catalyze O2 dismutation, these compounds exhibited a much lower SOD activity, and kcat was determined to be (5.0 +/- 0.3) x 10(6) and (7.6 +/- 0.4) x 10(7) M-1s-1, respectively using the two assays.
采用脉冲辐解直接法测定西咪替丁铜(II)配合物的超氧化物歧化酶样活性,结果发现与超氧阴离子(O₂⁻)的反应速率常数kcat为(8.5±0.5)×10⁸ M⁻¹s⁻¹,与超过金属50 - 200 μM的过量西咪替丁浓度无关。结果表明,要么1:1的配体与金属配合物催化O₂⁻歧化的速率与2:1配合物的速率不可比,要么最后一种物质的稳定常数远高于Kimura等人之前测定的数值,且溶液中仅存在2:1的物质。使用细胞色素c和NBT间接法测定这些配合物催化O₂歧化的能力时,这些化合物表现出低得多的超氧化物歧化酶(SOD)活性,使用这两种测定方法时,kcat分别确定为(5.0±0.3)×10⁶ M⁻¹s⁻¹和(7.6±0.4)×10⁷ M⁻¹s⁻¹。