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鸟氨酸转氨甲酰酶缺乏症一例的酶缺陷研究。

Study of enzyme defect in a case of ornithine transcarbamylase deficiency.

作者信息

Qureshi I A, Letarte J, Quellet R

出版信息

Diabete Metab. 1978 Dec;4(4):239-41.

PMID:729890
Abstract

Activity of liver ornithine transcarbamylase was measured in a biopsy obtained from a seven years old girl, suffering from chronic hyperammonemia and orotic aciduria. The activity of the defective enzyme was only 17% of that of a control. pH optimum was 8.1 in the patient and the control. However, the pH curves were different between 7.0 and 8.1. Km (ornithine) of the patient's ornithine transcarbamylase was within the normal range (0.41 nM), but the Km (carbamyl phosphate) was low (0.18 mM). The girl seems to be a heterozygote carrier of ornithine transcarbamylase deficiency due to an abnormal liver enzyme.

摘要

在一名患有慢性高氨血症和乳清酸尿症的7岁女孩的肝脏活检样本中,检测了鸟氨酸转氨甲酰酶的活性。缺陷酶的活性仅为对照的17%。患者和对照的最适pH均为8.1。然而,在7.0至8.1之间,pH曲线有所不同。患者鸟氨酸转氨甲酰酶的Km(鸟氨酸)在正常范围内(0.41 nM),但Km(氨甲酰磷酸)较低(0.18 mM)。由于肝脏酶异常,该女孩似乎是鸟氨酸转氨甲酰酶缺乏症的杂合子携带者。

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