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Profiling Redox and Energy Coenzymes in Whole Blood, Tissue and Cells Using NMR Spectroscopy [PDF]

open access: yesMetabolites, 2018
Coenzymes of cellular redox reactions and cellular energy, as well as antioxidants mediate biochemical reactions fundamental to the functioning of all living cells.
G A Nagana Gowda
exaly   +2 more sources

Electrochemical synthesis of coenzymes Q n by oxidation of tetramethoxy precursors [PDF]

open access: yesJournal of Applied Electrochemistry, 2009
The electrochemical oxidation of tetramethoxy precursors (2) to coenzymes Q (n) (1) at a carbon anode was investigated both in a bench-scale batch electrochemical reactor and in a continuous recirculation reaction system equipped with a parallel-plate ...
Alessandro Galia   +2 more
exaly   +2 more sources
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Structure of Coenzyme A

Nature, 1953
CHEMICAL1 and enzymic2 studies from these two laboratories suggested that coenzyme A is best represented by formula (I) (cf. ref. 3). While the synthesis of various fragments of the molecule4 has lent considerable support to this structure, the enzymic and chemical evidence did not agree on one point.
J, BADDILEY   +3 more
openaire   +2 more sources

Coenzyme A metabolism

American Journal of Physiology-Endocrinology and Metabolism, 1985
The metabolism of coenzyme A and control of its synthesis are reviewed. Pantothenate kinase is an important rate-controlling enzyme in the synthetic pathway of all tissues studied and appears to catalyze the flux-generating reaction of the pathway in cardiac muscle. This enzyme is strongly inhibited by coenzyme A and all of its acyl esters.
J D, Robishaw, J R, Neely
openaire   +2 more sources

Coenzyme A: to make it or uptake it?

Nature Reviews Molecular Cell Biology, 2016
The consensus has been that intracellular coenzyme A (CoA) is obtained exclusively by de novo biosynthesis via a universal, conserved five-step pathway in the cell cytosol. However, old and new evidence suggest that cells (and some microorganisms) have several strategies to obtain CoA, with 4'-phosphopantetheine (P-PantSH; the fourth intermediate in ...
Sibon, Ody C. M., Strauss, Erick
openaire   +2 more sources

Coenzymes I: Organic Coenzymes

2007
Most enzymatic reactions proceed with chemical changes that cannot be brought about by the side chains of amino acid residues. These enzymes function in cooperation with coenzymes and cofactors, which lend physicochemical potentialities not found in amino acids.
Perry A. Frey, Adrian D. Hegeman
openaire   +1 more source

Synthesis of coenzyme A

Biochimica et Biophysica Acta (BBA) - General Subjects, 1961
Abstract An improved procedure for the chemical synthesis of coenzyme A by anhydride-anion exchange is described. A mixture of the 2′,5′- and 3′,5′-diphosphastes of adenosine is treated with diphenylphosphorochloridate to give P 1 -adenosine (2′3′-cyclic phosphate)-5′- P 2 -diphenylpyrophosphate quantitatively. This is then treated with pantethine
openaire   +3 more sources

Coenzymes as coribozymes

Biochimie, 2002
Coenzymes are small organic molecules that supply a varied set of reactive groups to protein enzymes, thereby diversifying catalysis beyond the chemistries of amino acid sidechains. As RNA structures begin with a more limited chemical diversity than proteins, it seems likely that RNA enzymes would also use functional groups from other molecules to ...
Vasant R, Jadhav, Michael, Yarus
openaire   +2 more sources

Requirement of acetyl-coenzyme A carboxylase kinase for coenzyme A

Archives of Biochemistry and Biophysics, 1983
Phosphorylation and inactivation of acetyl-coenzyme A (CoA) carboxylase by acetyl-CoA carboxylase kinase in the presence of ATP and Mg2+ requires coenzyme A. Coenzyme A did not enhance the phosphorylation of alternative substrates of the carboxylase kinase such as protamine or histones.
B A, Lent, K H, Kim
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Synthesis of arachidonoyl coenzyme A and docosahexaenoyl coenzyme A in retina

Current Eye Research, 1984
The synthesis of 14C-labeled arachidonoyl coenzyme A (CoA) and docosahexaenoyl CoA was studied in the human, bovine, rat and frog retina. The synthesis of arachidonoyl CoA was two- to fourfold higher than that of docosahexaenoyl CoA in the retinal membranes examined.
T S, Reddy, N G, Bazan
openaire   +2 more sources

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