Literature DB >> 8141

NADP+-specific isocitrate dehydrogenase of Excherichia coli. III. Two-step purification employing affinity chromatography.

M Hy, H C Reeves.   

Abstract

The NADP+-specific isocitrate dehydrogenase (threo-DS-isocitrate:NADP+ oxidoreductase (decarboxylating), EC 1.1.1.42) of Excherichia coli has been purified to electrophoretic homogeneity by a two-step purification procedure employing affinity chromatography. The overall yield of enzyme was 30% with specific activity 125 mumol/min per ng protein. Electrophoretic homogeneity of the isocitrate dehydrogenase was deterimed in analytical polyacrylamide gels in a Tris/acetate/EDTA buffer system at pH 7.5 and in a citrate/phosphate buffer system at pH 6.0.

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Year:  1976        PMID: 8141     DOI: 10.1016/0005-2744(76)90082-6

Source DB:  PubMed          Journal:  Biochim Biophys Acta        ISSN: 0006-3002


  1 in total

1.  Purification and structural properties of isozymes of isocitrate dehydrogenase from the mouse.

Authors:  B Pegoraro; J H Yuan; C Y Lee
Journal:  Mol Cell Biochem       Date:  1979-02-09       Impact factor: 3.396

  1 in total

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