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
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.