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甘露糖苷贮积症:培养的成纤维细胞中特定α-甘露糖苷酶成分缺乏。

Mannosidosis: deficiency of a specific alpha-mannosidase component in cultured fibroblasts.

作者信息

Taylor H A, Thomas G H, Aylsworth A, Stevenson R E, Reynolds L W

出版信息

Clin Chim Acta. 1975 Feb 22;59(1):93-9. doi: 10.1016/0009-8981(75)90223-5.

Abstract

Evidence is prisented which shows that the enzymatic defect in mannosidosis, the deficiency of alpha-mannosidase, is expressed in cultured skin fibroblasts from patients with mannosidosis. Additionally, by Cellogel electrophoresis, the enzyme can be separated into two major components (a heat stable component missing in mannosidosis fibroblasts with a pH optimum of 3.6-4.0 and a heat labile component present in mannosidosis fibroblasts with a pH optimum of 5.6-6.0). The specific activity and electrophoresis of alpha-mannosidase from cultured amniotic fluid cells are also shown to be similar to cultured skin fibroblasts.

摘要

有证据表明,甘露糖苷贮积症中的酶缺陷,即α-甘露糖苷酶缺乏,在甘露糖苷贮积症患者的培养皮肤成纤维细胞中有所体现。此外,通过Cellogel电泳,该酶可被分离为两个主要成分(一个在甘露糖苷贮积症成纤维细胞中缺失的热稳定成分,其最适pH为3.6 - 4.0,以及一个在甘露糖苷贮积症成纤维细胞中存在的热不稳定成分,其最适pH为5.6 - 6.0)。培养羊水细胞中的α-甘露糖苷酶的比活性和电泳也显示与培养的皮肤成纤维细胞相似。

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