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[解脂假丝酵母氰化物抗性线粒体中电子传递替代途径活性丧失的原因]

[Cause of the activity loss of the alternative pathway of electron transport in cyanide-resistant mitochondria of the yeast Candida lipolytica].

作者信息

Akimenko V K, Medentsev A G

出版信息

Biokhimiia. 1981 Jan;46(1):140-7.

PMID:6788097
Abstract

The cause of the activity loss of alternative pathway of electron transport in mitochondria of the yeast Candida lipolytica has been investigated. Incubation of cyanide-resistant mitochondria at 25 degrees was shown to cause the loss by mitochondria of their ability to oxidize substrates in the presence of 1 mM cyanide. This suggests that in the course of incubation the alternative pathway loses its activity. Repeated washing of mitochondria with a solution containing 2,5 mM EDTA inhibits, while Ca2+, Mn2+, Cu2+ and Zn2+ (but not Sr2+) enhance the process of the activity loss of the alternative pathway. The loss of the cyanide-resistant respiration is also observed during incubation of mitochondria in the presence of phospholipases A, C and D or lysolecithin. In all cases studied the reactivation of the cyanide-resistant respiration of mitochondria is attained by addition of azolectin. The loss of cyanide-resistant respiration is accompanied by the activity reduction of the main respiratory chain, which is restored by addition of cytochrome c and Mg2+. These data indicate that the activity loss of the alternative pathway is not related to inactivation of any components in the alternative pathway itself or in the main respiratory chain. The most probable cause of the activity loss in the destruction of reducing equivalents in the alternative pathway of a donor as a result of a break of the structural entity of the internal membrane of mitochondria due to the detersive action of the phospholipid lysoforms produced either by endogenic or exogenic phospholipases.

摘要

对解脂假丝酵母线粒体中电子传递替代途径活性丧失的原因进行了研究。结果表明,在25℃下孵育抗氰线粒体,会导致线粒体在存在1 mM氰化物的情况下氧化底物的能力丧失。这表明在孵育过程中替代途径丧失了其活性。用含有2.5 mM EDTA的溶液反复洗涤线粒体可抑制替代途径活性丧失的过程,而Ca2+、Mn2+、Cu2+和Zn2+(但不是Sr2+)会增强该过程。在磷脂酶A、C和D或溶血卵磷脂存在的情况下孵育线粒体时,也会观察到抗氰呼吸的丧失。在所有研究的情况下,通过添加偶氮卵磷脂可使线粒体的抗氰呼吸重新激活。抗氰呼吸的丧失伴随着主呼吸链活性的降低,添加细胞色素c和Mg2+可使其恢复活性。这些数据表明,替代途径活性的丧失与替代途径本身或主呼吸链中任何成分的失活无关。活性丧失最可能的原因是由于内源性或外源性磷脂酶产生的磷脂溶形式的去污作用,导致线粒体内膜结构实体破裂,从而破坏了替代途径中供体的还原当量。

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