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Biochemistry · Lipid metabolism: oxidation of unsaturated fatty acids
Sample itemDuring beta-oxidation of oleic acid, the cis double bond lies at an odd-numbered carbon and the usual hydratase step cannot proceed. Which additional enzyme repositions the bond?
Original practice item, not a recalled exam question. Nothing here is recorded.
The answer and the reasoning
D. Enoyl-CoA isomerase
Enoyl-CoA isomerase converts the cis-3 double bond to a trans-2 double bond, which is the substrate for enoyl-CoA hydratase. Acyl-CoA dehydrogenase is bypassed for that cycle, so slightly less FADH2 is made. Polyunsaturated acids with even-numbered bonds also need 2,4-dienoyl-CoA reductase.
Option by option
A. Thiolase
Thiolase cleaves acetyl-CoA from 3-ketoacyl-CoA and does not change double bonds.
B. Acyl-CoA dehydrogenase
Acyl-CoA dehydrogenase forms the trans-2 bond in saturated acids but is not the enzyme that shifts a cis bond.
C. Hydroxyacyl-CoA dehydrogenase
Hydroxyacyl-CoA dehydrogenase oxidises the 3-hydroxy group and is a regular step.
D. Enoyl-CoA isomerase (correct)
Correct. Enoyl-CoA isomerase shifts the cis-3 bond to the trans-2 position for hydration.
Source note: Original NextPrep sample item — pending expert review. This item is original practice material awaiting independent expert review, so confirm important facts in a standard textbook.
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