Literature DB >> 36923

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

B Vasquez, H C Reeves.   

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.

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Year:  1979        PMID: 36923     DOI: 10.1016/0005-2795(79)90109-0

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


  3 in total

1.  Characterizing Lysine Acetylation of Isocitrate Dehydrogenase in Escherichia coli.

Authors:  Sumana Venkat; Hao Chen; Alleigh Stahman; Denver Hudson; Paige McGuire; Qinglei Gan; Chenguang Fan
Journal:  J Mol Biol       Date:  2018-05-04       Impact factor: 5.469

2.  Partial Purification and Characterization of NADP-Isocitrate Dehydrogenase from Immature Pod Walls of Chickpea (Cicer arietinum L.).

Authors:  V K Gupta; R Singh
Journal:  Plant Physiol       Date:  1988-07       Impact factor: 8.340

3.  Novel NADP-linked isocitrate dehydrogenase present in peroxisomes of n-alkane-utilizing yeast, Candida tropicalis: comparison with mitochondrial NAD-linked isocitrate dehydrogenase.

Authors:  S Yamamoto; H Atomi; M Ueda; A Tanaka
Journal:  Arch Microbiol       Date:  1995-02       Impact factor: 2.552

  3 in total

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