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大肠杆菌的NADP特异性异柠檬酸脱氢酶。IV. 通过Affi-Gel Blue柱层析法进行纯化

NADP-specific isocitrate dehydrogenase of Escherichia coli. IV. Purification by chromatography on Affi-Gel Blue.

作者信息

Vasquez B, Reeves H C

出版信息

Biochim Biophys Acta. 1979 May 23;578(1):31-40. doi: 10.1016/0005-2795(79)90109-0.

Abstract

Affinity chromatography on Affi-Gel Blue has been used to purify the NADP-specific isocitrate dehydrogenase (EC 1.1.1.42) from Escherichia coli. The protocol permits rapid purification of the enzyme in milligram quantities with a yield of 50% and is carried out almost entirely at room temperature. The preparation was judged to be homogeneous by non-denaturing electrophoresis at pH 7.5 and denaturing electrophoresis in the presence of sodium dodecyl sulfate. The subunit molecular weight of 53 000, determined by sodium dodecyl sulfate gel electrophoresis, is in reasonable agreement with the value of 46 900 estimated from the amino acid composition data.

摘要

利用Affi-Gel Blue亲和层析法从大肠杆菌中纯化了NADP特异性异柠檬酸脱氢酶(EC 1.1.1.42)。该方案能够快速纯化出毫克量的酶,产率为50%,并且几乎完全在室温下进行。通过在pH 7.5下的非变性电泳和在十二烷基硫酸钠存在下的变性电泳判断该制剂是均一的。通过十二烷基硫酸钠凝胶电泳测定的亚基分子量为53000,与根据氨基酸组成数据估计的46900的值合理相符。

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