ISOMERIZATION OF TRANS-2,DELTA(5)-DIENOYL-COAS TO DELTA(3),DELTA(5)-DIENOYL-COAS IN THE BETA-OXIDATION OF DELTA(5)-UNSATURATED FATTY-ACIDS

Citation
Ls. Chen et al., ISOMERIZATION OF TRANS-2,DELTA(5)-DIENOYL-COAS TO DELTA(3),DELTA(5)-DIENOYL-COAS IN THE BETA-OXIDATION OF DELTA(5)-UNSATURATED FATTY-ACIDS, Biochemistry, 34(2), 1995, pp. 442-450
Citations number
24
Categorie Soggetti
Biology
Journal title
ISSN journal
00062960
Volume
34
Issue
2
Year of publication
1995
Pages
442 - 450
Database
ISI
SICI code
0006-2960(1995)34:2<442:IOTTD>2.0.ZU;2-X
Abstract
The NADPH-dependent reduction pathway for the metabolism of Delta(5)-u nsaturated fatty acids involves the isomerization of trans-2,Delta(5)- dienoyl-CoA, initially formed from the dehydrogenation of Delta(5)-eno yl-CoA, to isomeric Delta(3),Delta(5)-dienoyl-CoA. The latter intermed iates were then isomerized to trans-2,trans-4-dienoyl-CoA, which then follows the NADPH-dependent pathway mediated by 2,4-dienoyl-CoA reduct ase. The isomerization from trans-2,Delta(5)-dienoyl-CoA to Delta(3),D elta(5)-dienoyl-CoA is catalyzed by Delta(3),Delta(2)-enoyl-CoA isomer ase. In this investigation, we identified the stereoisomers of Delta(3 ),Delta(5)-dienoates that were formed in the reaction. Starting from t rans-2,cis-5-decadienoyl-CoA, the isomerization produced cis-3,cis-5- and trans-3,cis-5-decadienoates. On the other hand, trans-2,trans-5-de cadienoyl-CoA yielded cis-3,trans-5- and trans-3,trans-5-decadienoates . In addition to purified rat liver Delta(3),Delta(2)-enoyl-CoA isomer ase, acyl-CoA oxidase from Arthrobacter also catalyzed the isomerizati on from trans-2,cis-5-dienoyl-CoA. However, this acyl-CoA oxidase coul d not catalyze the similar isomerization of trans-2,trans-5-dienoyl-Co A. Delta(3),Delta(5)-t-2,t-4-Dienoyl-CoA isomerase used cis-3,cis-5-, trans-3,cis-5-, and cis-3,trans-5-dienoyl-CoA's as substrates and conv erted them to trans-2,trans-4-dienoyl-CoA. In contrast, trans-3,trans- 5-dienoyl-CoA was not a substrate for this isomerization. Extensive pu rification of acyl-CoA oxidase through column chromatography could not remove or diminish the isomerization activity associated with acyl-Co A oxidase. Acyl-CoA oxidases derived from Candida and rat liver also p ossess isomerization activity. In contrast, acyl-CoA dehydrogenases fr om beef liver could not catalyze the isomerization. The dehydrogenatio n and isomerization of cis-5-enoyl-CoA's catalyzed by commercially ava ilable acyl-CoA oxidase preparations render the preparation of Delta(3 ),Delta(5)-dienoyl-CoA's feasible. The data obtained so far tend to ru le out the possibility that the isomerase activity of acyl-CoA oxidase was due to contaminating enzymes.