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肠贾第虫的脱氧核苷激酶

Deoxynucleoside kinases of Giardia intestinalis.

作者信息

Laoworawit P, Lee C S, O'Sullivan W J

机构信息

School of Biochemistry and Molecular Genetics, University of New South Wales, Kensington, Australia.

出版信息

Mol Biochem Parasitol. 1993 Jul;60(1):37-44. doi: 10.1016/0166-6851(93)90026-t.

Abstract

Giardia intestinalis lacks the ability to synthesise deoxyribonucleotides de novo and must rely on salvage synthesis. Two separate kinases, specific for purines (deoxyadenosine and deoxyguanosine) and pyrimidines (thymidine and deoxycytidine), respectively, are responsible for the incorporation of deoxyribonucleosides. A substantial degree of purification was achieved for the purine deoxynucleoside kinase by the combination of Mono Q anion exchange chromatography, preparative gel electrophoresis and Superose 12 gel filtration. An overall recovery of 4%, with 186- and 174-fold purification, for deoxyguanosine kinase and deoxyadenosine kinase activities, respectively, was observed. The molecular weight was found to be approximately 80,000 by gel filtration. Only a partial purification of thymidine/deoxycytidine kinase was achieved. However, both pyrimidine activities remained associated throughout various purification procedures and appeared to be associated with a protein of 44 kDa.

摘要

肠贾第虫缺乏从头合成脱氧核糖核苷酸的能力,必须依赖补救合成。两种分别对嘌呤(脱氧腺苷和脱氧鸟苷)和嘧啶(胸苷和脱氧胞苷)具有特异性的激酶负责脱氧核糖核苷的掺入。通过Mono Q阴离子交换色谱、制备性凝胶电泳和Superose 12凝胶过滤相结合的方法,对嘌呤脱氧核苷激酶进行了大量纯化。分别观察到脱氧鸟苷激酶和脱氧腺苷激酶活性的总回收率为4%,纯化倍数分别为186倍和174倍。通过凝胶过滤发现分子量约为80,000。胸苷/脱氧胞苷激酶仅得到部分纯化。然而,在各种纯化过程中,两种嘧啶活性始终相关,并且似乎与一种44 kDa的蛋白质相关。

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