作者:
DOI: 10.1016/S0021-9258(18)45161-7
关键词: Specific activity 、 Beta oxidation 、 Carnitine 、 Enzyme 、 Biology 、 Biochemistry 、 Endocrinology 、 Coenzyme A 、 Mitochondrion 、 Palmitoylcarnitine 、 Internal medicine 、 Thiolase
摘要: In an attempt to clarify why the brain oxidizes fatty acids poorly or not at all, activities of beta-oxidation enzymes present in rat and heart mitochondria were measured compared with each other. Although apparent Km values chain-length specificities are similar, specific all but one enzyme between 4 50% those observed mitochondria. The exception is 3-ketoacyl-CoA thiolase (EC 2.3.1.16) whose activity 125 times lower than partially purified was shown be catalytically immunologically identical enzyme. low rate acid oxidation mitochondria, estimated on basis palmitoylcarnitine-supported respiration [1-14C]palmitoylcarnitine degradation less 0.5 nmol/min/mg protein, may consequence thiolase. Inhibition by 4-bromocrotonic proves dependent thus occur via beta-oxidation. Since reactions catalyzed carnitine palmitoyltransferase 2.3.1.21) acyl-CoA synthetase 6.2.1.3) do seem restrict brain, it concluded that limited mitochondrial 3-keto-acyl-CoA