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  • Isolation and characterization of dl

  • Add time:08/17/2019    Source:sciencedirect.com

    Certain amino acids and other compounds are metabolized via propionyl-CoA d-methylmalonyl-CoAl-methylmalonyl-CoAsuccinyl-CoA ↔ tricarboxylic acid cycle. d-Methylmalonyl-CoA can also be converted to methylmalonic acid and coenzyme A by a specific hydrolase that does not act on l-methylmalonyl-CoA [R. J. Kovachy, S. D. Copley, and R. H. Allen (1983) J. Biol. Chem.258, 11415–11421]. Because little is known about mammalian dl-methylmalonyl-CoA racemase and because it is involved in the flow of d-methylmalonyl-CoA to l-methylmalonyl-CoA → tricarboxylic acid cycle (versus to methylmalonic acid), we developed a new assay and purified rat liver racemase 23,000-fold to homogeneity. The molecular weight of the racemase is 32,000 and it contains two subunits of Mr 16,000 that are not connected by disulfide bonds. The rat liver and the rat and human white blood cell racemase are immunologically related. They are completely inactivated by EDTA and can be activated by the addition of Co+2, with 50% activation occurring at a concentration of 0.2 μm. Lower levels for maximal activation were obtained with higher concentrations of Co+3, Fe+2, and Mn+2. Other metals such as Zn+2, Cu+2, Cu+1, and Cd+2 completely inhibited racemase even in the presence of equal concentrations of Co+2. The purified racemase appears to bind 1 mol Co/mol subunit.

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    Prev:Purification and properties of methylmalonyl coenzyme A mutase from human liver
    Next:Methylmalonic aciduria: A variant form of methylmalonyl coenzyme A apomutase deficiency)

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