Darr D, Fridovich I
Biochem J. 1985 Mar 15;226(3):781-7. doi: 10.1042/bj2260781.
3,3'-Diaminobenzidine strongly inhibits bovine liver catalase in two distinct ways. One of these was competitive with respect to H2O2, approached a limit of 100% inhibition and was rapidly reversed by dilution or by dialysis. The other was dependent upon H2O2, approached a limit of 60% and was not reversed by dilution or dialysis. Exposure to diaminobenzidine followed by dialysis did not modify the electrophoretic mobility of the enzyme, its Km for H2O2 or its optical spectrum, although Vmax. was halved. Diaminobenzidine protects catalase against the irreversible inactivation imposed by 3-amino-1,2,4-triazole plus H2O2. CN-protected catalase against the apparently irreversible inhibition by diaminobenzidine, and dialysis against CN- reversed this inhibition. Ethanol was similarly protective, and ethanol plus H2O2 reversed the inhibition by diaminobenzidine. Several other aromatic diamines inhibited in a fashion similar to that of diaminobenzidine, but were less effective. A scheme of reactions that accounts for these observations is proposed.
3,3'-二氨基联苯胺以两种不同方式强烈抑制牛肝过氧化氢酶。其中一种对过氧化氢具有竞争性,抑制极限接近100%,通过稀释或透析可迅速逆转。另一种依赖于过氧化氢,抑制极限接近60%,不能通过稀释或透析逆转。经透析处理后接触二氨基联苯胺,虽然最大反应速度减半,但酶的电泳迁移率、对过氧化氢的米氏常数或其光谱并未改变。二氨基联苯胺可保护过氧化氢酶免受3-氨基-1,2,4-三唑加过氧化氢所致的不可逆失活。氰化物可保护过氧化氢酶免受二氨基联苯胺明显的不可逆抑制,透析除去氰化物可逆转这种抑制。乙醇同样具有保护作用,乙醇加过氧化氢可逆转二氨基联苯胺的抑制作用。其他几种芳香族二胺的抑制方式与二氨基联苯胺相似,但效果较差。本文提出了一个解释这些观察结果的反应方案。