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PMID: 2363500 Published · ppublish English Comparative Study Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

An acyl-coenzyme A dehydrogenase assay utilizing the ferricenium ion.

Analytical biochemistry ·Vol. 186 ·No. 2 ·1990-05-01 ·Pages 280-4

Lehman TC, Hale DE, Bhala A, Thorpe C

Abstract

A sensitive assay for medium chain acyl-CoA dehydrogenase has been developed by substituting ferricenium hexafluorophosphate for the physiological acceptor, electron transferring flavoprotein. The ferricenium ion is a facile oxidant of the octanoyl-CoA-reduced enzyme with a Vmax of 1400 min-1 and a KM of 55 microM at pH 7.6. The ferricenium assay does not require additional mediator dyes, exhibits low background rates, and avoids the necessity of purifying substantial amounts of electron transferring flavoprotein. Unlike the fluorescence-based electron transferring flavoprotein assay, this new procedure can be performed aerobically. Both assays give comparable results when tested with crude fibroblast homogenates from normal and medium chain acyl-CoA dehydrogenase deficient patients. The convenience of the ferricenium method suggests it may be generally useful as a screening assay for a number of acyl-CoA dehydrogenases.

MeSH Terms
Acyl-CoA Dehydrogenase Acyl-CoA Dehydrogenases/analysis,deficiency Aerobiosis Cells, Cultured Electron Transport Ferrous Compounds/therapeutic use Fibroblasts/enzymology Humans Oxidation-Reduction
Chemicals
Ferrous Compounds ferrocenium Acyl-CoA Dehydrogenases Acyl-CoA Dehydrogenase
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Lehman T C
Department of Chemistry, University of Delaware, Newark 19716.
Hale D E
Bhala A
Thorpe C
Article Info
Journal
Analytical biochemistry
Abbr.
Anal Biochem
ISSN
0003-2697
Published
1990-05-01
Pages
280-4
Language
English
Region
United States
NLM ID
0370535
Subset
IM
Grants
NIGMS NIH HHS · GM 26643 · United States
NINDS NIH HHS · NS 17752 · United States
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