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Role of branched-chain 2-oxo acid dehydrogenase and pyruvate dehydrogenase in 2-oxobutyrate metabolism

TLDR
Both intramitochondrial complexes are responsible for oxidative decarboxylation of 2-oxobutyrate, but the BCODH is probably the more important complex, particularly in liver, on the basis of kinetic analyses, activity or phosphorylation state of both complexes, competition studies, and the apparent physiological concentration of pyruvate.
Abstract
Purified branched-chain 2-oxo acid dehydrogenase (BCODH) and pyruvate dehydrogenase (PDH) had apparent Km values (microM) for 2-oxobutyrate of 26 and 114, with a relative Vmax. (% of Vmax. for 3-methyl-2-oxobutyrate and pyruvate) of 38 and 45% respectively. The phosphorylation state of both complexes in extracts of mitochondria from rat liver, kidney, heart and skeletal muscle was shown to influence oxidative decarboxylation of 2-oxobutyrate. Inhibitory antibodies to BCODH and an inhibitor of PDH (3-fluoropyruvate) were used with mitochondrial extracts to determine the relative contribution of both complexes to oxidative decarboxylation of 2-oxobutyrate. Calculated rates of 2-oxobutyrate decarboxylation in mitochondrial extracts, based on the kinetic constants given above and the activities of both complexes, were the same as the measured rates. Hydroxyapatite chromatography of extracts of mitochondria from rat liver revealed only two peaks of oxidative decarboxylation of 2-oxobutyrate, with one peak associated with PDH and the other with BCODH. Competition studies with various 2-oxo acids revealed a different inhibition pattern with mitochondrial extracts from liver compared with those from heart or skeletal muscle. We conclude that both intramitochondrial complexes are responsible for oxidative decarboxylation of 2-oxobutyrate. However, the BCODH is probably the more important complex, particularly in liver, on the basis of kinetic analyses, activity or phosphorylation state of both complexes, competition studies, and the apparent physiological concentration of pyruvate, 2-oxobutyrate and the branched-chain 2-oxo acids.

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Emerging Perspectives on Essential Amino Acid Metabolism in Obesity and the Insulin-Resistant State

TL;DR: In this article, a model is proposed that links the FFA-rich environment of obesity/insulin resistance and type 2 diabetes mellitus with diminution of BCAA catabolic enzyme activity, changes in methionine oxidation and cysteine/cystine generation, and tissue redox balance.
Journal ArticleDOI

Serine Racemase Modulates Intracellular D-Serine Levels through an α,β-Elimination Activity

TL;DR: It is proposed that α,β-elimination provides a novel mechanism for regulating intracellular d-serine levels, especially in brain areas that do not possess d-amino acid oxidase activity.
Journal ArticleDOI

THE COMPLEX FATE OF α-KETOACIDS

TL;DR: The current status of knowledge of the biochemical, regulatory, structural, genomic, and evolutionary aspects of these fascinating multienzyme complexes are reviewed.
Journal ArticleDOI

THECOMPLEXFATE OFα-KETOACIDS

TL;DR: A review of the current status of knowledge of the biochemical, regulatory, structural, genomic, and evolutionary aspects of these fascinating multienzyme complexes are reviewed in this paper, where the alpha-ketoacid dehydrogenase complexes occupy key positions in intermediary metabolism.
Patent

Microorganisms for the production of adipic acid and other compounds

TL;DR: In this paper, a non-naturally occurring microbial organism having an adipate, 6-aminocaproic acid or caprolactam pathway was provided, where the microbial organism contained at least one exogenous nucleic acid encoding an enzyme in the respective pathway.
References
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Journal ArticleDOI

Methionine metabolism in mammals. Distribution of homocysteine between competing pathways.

TL;DR: Using an in vitro system which contained enzymes, substrates, and other reactants at concentrations which approximated the in vivo conditions in rat liver, it was demonstrated that the adaptation from a high protein diet to a low protein diet is achieved by a significant increase in betaine homocysteine methyltransferase, and 83% reduction in cystathionine synthase, which contributes significantly to the regulation of the pathway.
Journal ArticleDOI

Purification and characterization of branched chain α-keto acid dehydrogenase complex of bovine kidney

TL;DR: A branched chain alpha-keto acid dehydrogenase-dihydrolipoyl transacylase complex was purified to apparent homogeneity from bovine kidney mitochondria and apparently is not regulated by phosphorylation-dephosphorylation, subject to modulation by end-product inhibition.
Journal ArticleDOI

Active and inactive forms of pyruvate dehydrogenase in rat liver. Effect of starvation and refeeding and of insulin treatment on pyruvate-dehydrogenase interconversion.

TL;DR: It is concluded that in liver, similar to heart muscle and kidney, fatty acids play an important role in the control of pyruvate dehydrogenase interconversion.
Journal ArticleDOI

Pyruvate dehydrogenase, substrate specificity and product inhibition.

J. Bremmer
- 01 Apr 1969 - 
TL;DR: It is shown that pyruvate and α-ketobutyrate are oxidized by the same enzyme (pyruvates dehydrogenase), while α- ketovalerate is oxidizedBy a different enzyme (α-ketovalerate), which behaves mainly as a competitive inhibitor to NAD.
Journal ArticleDOI

Regulation of branched-chain α-ketoacid dehydrogenase kinase

TL;DR: Findings help explain the unique effects of Leu compared with Val and Ile on branched-chain amino acid metabolism and the differences between control of the kinases associated with pyruvate dehydrogenase and brancher-chain α-ketoacid dehydrogenases.
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