A new enzyme, i.e., Delta(3),Delta(5)-t-2,t-4-dienoyl-CoA isomerase, required in the NADPH-dependent metabolic pathway of odd-numbered double bond, unsaturated fatty acids, was isolated and purified to apparent homogeneity from rat liver. In the oxidation of odd-numbered double bond, unsaturated fatty acids, stepwise beta-oxidation leads to cis-5-enoyl-CoA, which is then dehydrogenated and isomerized to Delta(3),Delta(5)-dienoyl-CoA. Delta(3),Delta(5)-t-2,t-4-Dienoyl-CoA isomerase converts Delta(3),Delta(5)-dienoyl-CoA to trans-2,trans-4-dienoyl-CoA, which is a substrate for NADPH-dependent 2,4-dienoyl-CoA reductase. This enzyme was purified through Matrex gel red A, blue Sepharose, DEAE-cellulose, CM-cellulose, hydroxylapatite, and Sepharose CL6B column chromatography of an ammonium sulfate precipitated fraction (30-80%) of rat liver homogenate. A native molecular weight of 200 000 with four subunits of 55 000 each was determined. The isoelectric point was 6.5. This enzyme was located in mitochondria and was inducible by clofibrate treatment. Using Delta(3),Delta(5)-decadienoyl-CoA, Delta(3),Delta(5)-dodecadienoyl-CoA, and Delta(3),Delta(5)-tetradecadienoyl-CoA as substrates, the V-max ratio was 1:0.5:0.4 and the K-m's were 10.9, 5.9, and 1.4 mu M, respectively. The specific activity of purified enzyme was 7 units/mg using Delta(3),Delta(5)-decadienoyl-CoA as substrate. The mechanism of isomerization was studied by deuterium labeling. Consistent with the deuterium labeling pattern of the products, the isomerization from trans-2,cis-5-dienoyl-CoA to trans-2,trans-4-dienoyl-CoA was a two-step process through an intermediate Delta(3),Delta(5)-dienoyl-CoA. The contribution of this reductive pathway to the overall oxidation of odd-numbered double bond, unsaturated fatty acids is not known, but it is likely to be a major pathway since the dehydrogenation step is also accompanied by isomerization. Once isomerized to Delta(3),Delta(5)-dienoyl-CoA, the substrate is committed to the reduction pathway.