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Molecular cloning of CoA Synthase. The missing link in CoA biosynthesis
Authors:Zhyvoloup Alexander  Nemazanyy Ivan  Babich Aleksei  Panasyuk Ganna  Pobigailo Natalya  Vudmaska Mariya  Naidenov Valeriy  Kukharenko Oleksandr  Palchevskii Sergiy  Savinska Liliya  Ovcharenko Galina  Verdier Frederique  Valovka Taras  Fenton Tim  Rebholz Heike  Wang Mong-Lien  Shepherd Peter  Matsuka Genadiy  Filonenko Valeriy  Gout Ivan T
Affiliation:Department of Structure and Function of Nucleic Acid, The Institute of Molecular Biology and Genetics, 150 Zabolotnogo Street, Kyiv 143, Ukraine.
Abstract:Coenzyme A functions as a carrier of acetyl and acyl groups in living cells and is essential for numerous biosynthetic, energy-yielding, and degradative metabolic pathways. There are five enzymatic steps in CoA biosynthesis. To date, molecular cloning of enzymes involved in the CoA biosynthetic pathway in mammals has been only reported for pantothenate kinase. In this study, we present cDNA cloning and functional characterization of CoA synthase. It has an open reading frame of 563 aa and encodes a protein of approximately 60 kDa. Sequence alignments suggested that the protein possesses both phosphopantetheine adenylyltransferase and dephospho-CoA kinase domains. Biochemical assays using wild type recombinant protein confirmed the gene product indeed contained both these enzymatic activities. The presence of intrinsic phosphopantetheine adenylyltransferase activity was further confirmed by site-directed mutagenesis. Therefore, this study describes the first cloning and characterization of a mammalian CoA synthase and confirms this is a bifunctional enzyme containing the last two components of CoA biosynthesis.
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