Isolation and characterization of a hydroxyacid-oxoacid transhydrogenase from rat kidney mitochondria.

EE Kaufman, T Nelson, HM Fales, DM Levin - Journal of Biological …, 1988 - Elsevier
EE Kaufman, T Nelson, HM Fales, DM Levin
Journal of Biological Chemistry, 1988Elsevier
A transhydrogenase that catalyzes the oxoacid-dependent oxidation of specific
hydroxyacids has been found in rat kidney, liver, and brain. The hydroxyacids that have
been found to be substrates for this enzyme are gamma-hydroxybutyrate, D-alpha-
hydroxyglutarate, and L-beta-hydroxybutyrate. The oxoacids that are the best substrates for
this enzyme are alpha-ketoglutarate and succinic semialdehyde; alpha-ketoadipate and
oxalacetate are also substrates. This enzyme is located in the mitochondrial fraction of the …
A transhydrogenase that catalyzes the oxoacid-dependent oxidation of specific hydroxyacids has been found in rat kidney, liver, and brain. The hydroxyacids that have been found to be substrates for this enzyme are gamma-hydroxybutyrate, D-alpha-hydroxyglutarate, and L-beta-hydroxybutyrate. The oxoacids that are the best substrates for this enzyme are alpha-ketoglutarate and succinic semialdehyde; alpha-ketoadipate and oxalacetate are also substrates. This enzyme is located in the mitochondrial fraction of the cell and is not dependent on added NAD+ or NADP+.
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