Analytical Biochemistry 2012-11-15

Simultaneous high-performance liquid chromatography determination of coenzyme A, dephospho-coenzyme A, and acetyl-coenzyme A in normal and pantothenic acid-deficient rats.

Katsumi Shibata, Takumi Nakai, Tsutomu Fukuwatari

Index: Anal. Biochem. 430(2) , 151-5, (2012)

Full Text: HTML

Abstract

We describe here a simultaneous high-performance liquid chromatography method for practical and rapid determination of coenzyme A (CoA), dephospho-CoA, and acetyl-CoA in tissues. These coenzymes are biosynthesized from the vitamin pantothenic acid (PaA), which is involved in the metabolism of fatty acids, amino acid catabolism, and several other nutrients. The method employed a Tosoh TSK-GEL ODS-100 V column (250×4.6mm i.d., particle size 5μm) eluted with 100mmol/L NaH(2)PO(4) and 75mmol/L CH(3)COONa (pH was adjusted to 4.6 by the addition of concentrated H(3)PO(4))-acetonitrile (94:6, v/v) at a flow rate of 1.0ml/min. The ultraviolet detector was set at 259nm. The limits of detection for CoA, dephospho-CoA, and acetyl-CoA all were 10pmol. The method was applied to the analysis of several tissues of rats fed normal and PaA-free diets. The results clearly showed that the method was suitable for the simultaneous determination of CoA, dephospho-CoA, and acetyl-CoA in the liver, heart, kidney, spleen, testis, large colon, and muscle, but not for the small intestine, of rats.Copyright © 2012 Elsevier Inc. All rights reserved.


Related Compounds

Related Articles:

Identification of the active site of phosphoribosyl-dephospho-coenzyme A transferase and relationship of the enzyme to an ancient class of nucleotidyltransferases.

2000-10-31

[Biochemistry 39(43) , 13233-40, (2000)]

Purification and characterization of phosphopantetheine adenylyltransferase from Escherichia coli.

1999-09-17

[J. Biol. Chem. 274(38) , 27105-11, (1999)]

Hydrolysis and absorption of pantothenate and its coenzymes in the rat small intestine.

1983-10-01

[J. Nutr. 113(10) , 2107-15, (1983)]

Coenzyme A affects firefly luciferase luminescence because it acts as a substrate and not as an allosteric effector.

2005-10-01

[FEBS J. 272(20) , 5206-16, (2005)]

Pantothenic acid transport and metabolism in the central nervous system.

1986-02-01

[Am. J. Physiol. 250(2 Pt 2) , R292-7, (1986)]

More Articles...