Blekkenhorst G H, Eales L, Pimstone N R
S Afr Med J. 1979 Nov 24;56(22):918-20.
Uroporphyrinogen decarboxylase was measured in the presence of ferrous iron, using mitochondria-free rat liver extracts as enzyme source. The activity of the enzyme was found to be increased at concentrations of ferrous iron from 0,01 mM, with maximal activity exhibited from 0,1 mM. Enzyme kinetics indicate that uroporphyrinogen decarboxylase reversibly binds ferrous iron, with a binding constant of approximately 5 x 10(4) mol-1. It is proposed that the effect of phlebotomy on patients with porphyria cutanea tarda is to mobilze storage iron in the liver to the active ferrous form, which activates hepatic uroporphyrinogen decarboxylase, the enzyme which is defective in this syndrome, with resultant clinical and biochemical remission.
在亚铁存在的情况下,使用无线粒体的大鼠肝脏提取物作为酶源来测定尿卟啉原脱羧酶。发现该酶的活性在亚铁浓度为0.01 mM时增加,在0.1 mM时表现出最大活性。酶动力学表明尿卟啉原脱羧酶与亚铁可逆结合,结合常数约为5×10⁴ mol⁻¹。有人提出,放血疗法对迟发性皮肤卟啉症患者的作用是将肝脏中储存的铁动员到活性亚铁形式,从而激活肝脏尿卟啉原脱羧酶,该酶在该综合征中存在缺陷,从而导致临床和生化缓解。