Gatt S, Bremer J, Osmundsen H
Department of Membrane Biochemistry and Neurochemistry, Hebrew University-Hadassah School of Medicine, Jerusalem, Israel.
Biochim Biophys Acta. 1988 Jan 19;958(1):130-3. doi: 10.1016/0005-2760(88)90254-8.
Pyrenedodecanoyl-CoA was beta-oxidized by isolated rat liver peroxisomes at a rate which was about 50% of that observed with palmitoyl-CoA. Measurement of the quantity of NADH formed from a limiting amount of pyrenedodecanoyl-CoA suggested that it was subjected to two to three cycles of beta-oxidation. Pyrenedodecanoyl-CoA was a very poor substrate for carnitine palmitoyltransferase, exhibiting less than 1% of the rate obtained with palmitoyl-CoA; it also was a strong inhibitor of this enzyme. With rat liver microsomal alpha-glycerophosphate acyltransferase the rate of reaction with pyrenedodecanoyl-CoA was only 3-4% of that observed with palmitoyl-CoA.
芘十二烷酰辅酶A被分离的大鼠肝脏过氧化物酶体以约为棕榈酰辅酶A氧化速率50%的速度进行β-氧化。对由限量的芘十二烷酰辅酶A生成的NADH量的测定表明,它经历了两到三个β-氧化循环。芘十二烷酰辅酶A是肉碱棕榈酰转移酶的极差底物,其反应速率不到棕榈酰辅酶A的1%;它也是该酶的强抑制剂。对于大鼠肝脏微粒体α-甘油磷酸酰基转移酶,与芘十二烷酰辅酶A的反应速率仅为与棕榈酰辅酶A反应速率的3-4%。