Moreno S N, Stolze K, Janzen E G, Mason R P
Laboratory of Molecular Biophysics, National Institute of Environmental Health Sciences, Research Triangle Park, North Carolina 27709.
Arch Biochem Biophys. 1988 Sep;265(2):267-71. doi: 10.1016/0003-9861(88)90127-0.
The cyanyl radical was formed during the oxidation of potassium or sodium cyanide by horseradish peroxidase, lactoperoxidase, chloroperoxidase, NADH peroxidase, or methemoglobin in the presence of hydrogen peroxide. The spin adducts of the cyanyl radical with 5,5-dimethyl-1-pyrroline-N-oxide and N-tert-butyl-alpha-phenylnitrone were quite stable at neutral pH. The identity of these spin adducts could be demonstrated using 13C-labeled cyanide and by comparison with the spin adducts of the formamide radical, a hydrolysis product of the cyanyl radical adduct. The enzymatic conversion of cyanide to cyanyl radical by peroxidases should be considered in addition to its well-known role as a metal ligand. Furthermore, since cyanide is used routinely as an inhibitor of peroxidases, some consideration should be given to the biochemical consequences of this formation of the cyanyl radical by the catalytic activity of these enzymes.
在过氧化氢存在的情况下,辣根过氧化物酶、乳过氧化物酶、氯过氧化物酶、NADH过氧化物酶或高铁血红蛋白氧化氰化钾或氰化钠时会形成氰基自由基。氰基自由基与5,5-二甲基-1-吡咯啉-N-氧化物和N-叔丁基-α-苯基硝酮的自旋加合物在中性pH下相当稳定。使用13C标记的氰化物并与氰基自由基加合物的水解产物甲酰胺自由基的自旋加合物进行比较,可以证明这些自旋加合物的身份。除了氰化物作为金属配体的众所周知的作用外,还应考虑过氧化物酶将氰化物酶促转化为氰基自由基的过程。此外,由于氰化物通常用作过氧化物酶的抑制剂,因此应考虑这些酶的催化活性形成氰基自由基的生化后果。