Hommes F A, Eller A G, Scott D F, Carter A L
Enzyme. 1983;29(4):271-7. doi: 10.1159/000469647.
Several lines of evidence are presented that an entity is present in mitochondria which converts lysine and carbamylphosphate to homocitrulline, distinct from the ornithine transcarbamylase (OTC): lack of inhibition by lysine of OTC with ornithine as substrate at the pH of the mitochondrial matrix, a Km for lysine of 6.3 mmol/l in the crude mitochondrial extract, versus a Km of 55.3 mmol/l after partial purification of OTC, decrease of the specific activity of OTC with lysine as substrate and increase of the specific activity with ornithine as substrate after heat denaturation, and separation of the activities for ornithine and lysine after isoelectric focusing. This would explain the excretion of homocritrulline in the HHH-syndrome, saccharopinuria, citrullinemia and hyperlysinemia. The fact that homocitrulline excretion is not observed in OTC deficiency suggests that the activity responsible for homocitrulline excretion is closely related to OTC.
有几条证据表明,线粒体中存在一种将赖氨酸和氨甲酰磷酸转化为高瓜氨酸的实体,它与鸟氨酸转氨甲酰酶(OTC)不同:在线粒体基质的pH值下,以鸟氨酸为底物时,赖氨酸对OTC没有抑制作用;粗线粒体提取物中赖氨酸的Km值为6.3 mmol/l,而OTC部分纯化后的Km值为55.3 mmol/l;以赖氨酸为底物时OTC的比活性降低,热变性后以鸟氨酸为底物时比活性增加,以及等电聚焦后鸟氨酸和赖氨酸的活性分离。这可以解释HHH综合征、尿 saccharopinuria、瓜氨酸血症和高赖氨酸血症中高瓜氨酸的排泄情况。在OTC缺乏症中未观察到高瓜氨酸排泄这一事实表明,负责高瓜氨酸排泄的活性与OTC密切相关。