Molecular cloning of CoA Synthase. The missing link in CoA biosynthesis |
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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 |
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Affiliation: | Department of Structure and Function of Nucleic Acid, The Institute of Molecular Biology and Genetics, 150 Zabolotnogo Street, Kyiv 143, Ukraine. |
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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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