Literature DB >> 2900141

The enantiomeric error frequency of aspartate aminotransferase.

S Kochhar1, P Christen.   

Abstract

The enantiomeric error frequency of aspartate aminotransferase (mitochondrial isoenzyme from chicken) was assessed by adding the enzyme in high concentration (0.89 mM) to a mixture of L-glutamate and 2-oxoglutarate (12 and 1.2 mM, respectively, at pH 7.5 and 25 degrees C). The substrates continuously undergo the transamination cycle under these conditions. Thereby, L-glutamate is progressively racemized, a 1:1 ratio of two enantiomers being reached within 240 h. The enantiomeric error frequency, i.e. the ratio of the rate of D-glutamate production and the rate of the transamination reaction with glutamate and 2-oxoglutarate as substrates, is 1.5 x 10(-7). D-Glutamate is also converted to a 1:1 racemic mixture. The racemizing activity of a mixture of free pyridoxal 5'-phosphate and pyridoxamine 5'-phosphate is about two orders of magnitude lower than that of aspartate aminotransferase. The error frequency of the enzyme in the case of the C4 substrate pair aspartate and oxalacetate is 3.4 x 10(-8), i.e. 4 times lower than that with the C5 substrate pair.

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Year:  1988        PMID: 2900141     DOI: 10.1111/j.1432-1033.1988.tb14213.x

Source DB:  PubMed          Journal:  Eur J Biochem        ISSN: 0014-2956


  2 in total

1.  Molecular evolution of B6 enzymes: binding of pyridoxal-5'-phosphate and Lys41Arg substitution turn ribonuclease A into a model B6 protoenzyme.

Authors:  Rosa A Vacca; Sergio Giannattasio; Guido Capitani; Ersilia Marra; Philipp Christen
Journal:  BMC Biochem       Date:  2008-06-19       Impact factor: 4.059

Review 2.  Oxygen reactivity with pyridoxal 5'-phosphate enzymes: biochemical implications and functional relevance.

Authors:  Giovanni Bisello; Carmen Longo; Giada Rossignoli; Robert S Phillips; Mariarita Bertoldi
Journal:  Amino Acids       Date:  2020-08-25       Impact factor: 3.520

  2 in total

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