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瓜氨酸血症:遗传异质性的酶学证据。

Citrullinemia: enzymatic evidence for genetic heterogeneity.

作者信息

Kennaway N G, Harwood P J, Ramberg D A, Koler R D, Buist N R

出版信息

Pediatr Res. 1975 Jun;9(6):554-8. doi: 10.1203/00006450-197506000-00008.

Abstract

The specific activity of argininosuccinate synthetase (micromoles of 14CO2 per milligram of protein per hour) was 0.00104 and 0.00087 in fibroblasts derived from two patients with citrullinemia, and was undetectable in both fibroblasts and cultured lymphocytes from a third patient. In five obligate heterozygotes the specific activity in fibroblasts was 0.012-0.029 and in nine control subjects was 0.058 +/- 0.014 (0.030-0.076). In both control and patient cells, the maximum activity was obtained at pH 8.5 and there was no inhibition of normal argininosuccinate synthetase by any of the mutant cells.

摘要

在两名瓜氨酸血症患者的成纤维细胞中,精氨琥珀酸合成酶的比活性(每毫克蛋白质每小时产生的14CO2微摩尔数)分别为0.00104和0.00087,而在第三名患者的成纤维细胞和培养淋巴细胞中均未检测到该酶活性。在五名 obligate 杂合子中,成纤维细胞的比活性为0.012 - 0.029,在九名对照受试者中为0.058±0.014(0.030 - 0.076)。在对照细胞和患者细胞中,pH 8.5时均获得最大活性,且任何突变细胞均未抑制正常的精氨琥珀酸合成酶。

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