Sumegi B, Porpaczy Z, Alkonyi I
University Medical School, Institute of Biochemistry, Pecs, Hungary.
Biochim Biophys Acta. 1991 Jan 28;1081(2):121-8. doi: 10.1016/0005-2760(91)90016-b.
Respiration-linked oxidation of 3-hydroxybutyryl-CoA, crotonyl-CoA and saturated fatty acyl (C4, C8 and C14)-CoA esters was studied in different mitochondrial preparations. Oxidation of acyl-CoA esters was poor in intact mitochondria; however, it was significant, as well as, NAD+ and CoA-dependent in gently and in vigorously sonicated mitochondria. The respiration-linked oxidation of crotonyl-CoA and 3-hydroxybutyryl-CoA proceeded at much higher rates (over 700%) in gently disrupted mitochondria than in completely disrupted mitochondria. The redox dye-linked oxidation of crotonyl-CoA (with inhibited respiratory chain) was also higher in gently disrupted mitochondria (149%) than in disrupted ones. During the respiration-linked oxidation of 3-hydroxybutyryl-CoA the steady-state NADH concentrations in the reaction chamber were determined, and found to be 8 microM in gently sonicated and 15 microM in completely sonicated mitochondria in spite of the observation that the gently sonicated mitochondria oxidized the 3-hydroxybutyryl-CoA much faster than the completely sonicated mitochondria. The NAD(+)-dependence of 3-hydroxybutyryl-CoA oxidation showed that a much smaller NAD+ concentration was enough to half-saturate the reaction in gently disrupted mitochondria than in completely disrupted ones. Thus, these observations indicate the positive kinetic consequence of organization of beta-oxidation enzymes in situ. Respiration-linked oxidation of butyryl-, octanoyl- and palmitoyl-CoA was also studied and these CoA intermediates were oxidized at approx. 50% of the rate of crotonyl- and 3-hydroxybutyryl-CoA in the gently disrupted mitochondria. In vigorously disrupted mitochondria the oxidation rate of these saturated acyl-CoA intermediates was hardly detectable indicating that the connection between the acyl-CoA dehydrogenase and the respiratory chain had been disrupted.
在不同的线粒体制剂中研究了与呼吸相关的3-羟基丁酰辅酶A、巴豆酰辅酶A和饱和脂肪酰基(C4、C8和C14)-辅酶A酯的氧化。完整线粒体中酰基辅酶A酯的氧化作用较弱;然而,在轻度和重度超声处理的线粒体中,其氧化作用显著,且依赖于NAD⁺和辅酶A。与呼吸相关的巴豆酰辅酶A和3-羟基丁酰辅酶A的氧化在轻度破碎的线粒体中比在完全破碎的线粒体中进行的速率要高得多(超过700%)。巴豆酰辅酶A(呼吸链受抑制时)与氧化还原染料相关的氧化在轻度破碎的线粒体中(149%)也高于破碎的线粒体。在3-羟基丁酰辅酶A与呼吸相关的氧化过程中,测定了反应室中的稳态NADH浓度,发现轻度超声处理的线粒体中为8微摩尔,完全超声处理的线粒体中为15微摩尔,尽管观察到轻度超声处理的线粒体氧化3-羟基丁酰辅酶A的速度比完全超声处理的线粒体快得多。3-羟基丁酰辅酶A氧化对NAD⁺的依赖性表明,与完全破碎的线粒体相比,在轻度破碎的线粒体中,要使反应达到半饱和所需的NAD⁺浓度要小得多。因此,这些观察结果表明了β-氧化酶原位组织的积极动力学后果。还研究了丁酰、辛酰和棕榈酰辅酶A与呼吸相关的氧化,在轻度破碎的线粒体中,这些辅酶A中间体的氧化速率约为巴豆酰和3-羟基丁酰辅酶A氧化速率的50%。在重度破碎的线粒体中,这些饱和酰基辅酶A中间体的氧化速率几乎检测不到,这表明酰基辅酶A脱氢酶与呼吸链之间的联系已被破坏。