Purification of a diketo acid hydrolase from rat liver and its use for the enzymic determination of 3,5-dioxohexanoate (triacetate)

Author:

Brock D. J. H.1,Williamson D. H.1

Affiliation:

1. Medical Research Council Unit for Research in Cell Metabolism, Department of Biochemistry, University of Oxford

Abstract

1. A diketo acid hydrolase was purified about 100-fold from rat liver and some of its properties were studied. 2. Comparison of its activity with 3,5-dioxohexanoate (triacetate) and fumarylacetoacetate at various stages during the purification suggests that it is identical with 4-fumarylacetoacetate fumarylhydrolase. 3. The acetoacetate formed on cleavage of 3,5-dioxohexanoate by the hydrolase can be determined either with 3-hydroxybutyrate dehydrogenase or with 3-oxo acid CoA-transferase and 3-hydroxyacyl-CoA dehydrogenase. These reactions form the basis of enzymic assays for 3,5-dioxohexanoate.

Publisher

Portland Press Ltd.

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