Lipid Metabolism — Flashcards

_____ is a PUFA containing 6 double bonds

Abetalipoproteinemia is an _____ inherited malabsorption disorder that is caused by a mutation in the microsomal triglyceride transfer protein

In the cytosol, _____ may be converted to acetyl-CoA via the enzyme ATP citrate lyase (fatty acid synthesis)

17-hydroxypregnenolone may be converted to _____ via the enzyme 3-hydroxysteroid dehydrogenase

Each cycle of β-oxidation produces _____ molecule of FADH2 and one molecule of NADH

_____ deficiency is characterized by the accumulation of 8 to 10-carbon acyl carnitines in the blood

The phospholipid _____ is also known as phosphatidylethanolamine.

17-hydroxyprogesterone may be converted to _____ via the enzyme 17,20-lyase

_____ deficiency may cause dicarboxylic acidemia/aciduria due to omega-oxidation of fatty acids

In preparation for β-oxidation, fatty acids are converted to _____ via the enzyme fatty acyl-CoA synthetase