A REVIEW OF ELECTRON TRANSPORT MECHANISMS IN PARASITIC PROTOZOA

A REVIEW OF ELECTRON TRANSPORT MECHANISMS IN PARASITIC PROTOZOA
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DOI:
10.2307/3275663
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发表时间:
1963-01-01
影响因子:
1.3
通讯作者:
BAERNSTEIN, HD
BAERNSTEIN, HD
中科院分区:
医学4区
文献类型:
--
作者:
BAERNSTEIN, HD

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本文综述了寄生原生动物电子传递的研究进展。疟原虫含有对氰化物、叠氮化物和一氧化碳敏感的氧化酶,表明存在细胞色素氧化酶。琥珀氧化酶和其他黄素蛋白的存在,通过氧摄取研究中靛酚和甲酚蓝的减少来判断。中间载体的存在是从萘醌对氧摄取的抑制推断的。毛滴虫具有有限的氧利用能力,这对氰化物不敏感,并且导致过氧化氢积累,除非过氧化氢酶也存在。一种黄素蛋白末端氧化酶被指出,但氧利用的重要性是未知的。一些菌株产生氢气,这可能与电子传递有关。生物体基本上是厌氧的,因此依赖于由吡啶和黄素蛋白介导的偶联反应,导致还原化合物的产生。锥虫显示了多种与氧相连的电子传递系统。多年来,氰化物被用来区分两种类型的氧化酶,一种是敏感的,一种是不敏感的。一般来说,所有锥虫的无脊椎动物或培养形式都具有氰化物敏感呼吸,而脊椎动物形式有两种类型:路易氏锥虫对氰化物敏感,布氏锥虫不敏感。所有组均显示传统的糖酵解途径,但只有敏感组显示活跃的柠檬酸循环反应和血红素蛋白谱。后者的性质知之甚少,似乎在某些方面与哺乳动物的类似因素不同。对氧的敏感途径与哺乳动物相似,但不敏感途径具有一些独特的特征。还原型烟酰胺腺嘌呤二核苷酸(NADH)1主要被磷酸二羟基丙酮再氧化生成甘油磷酸。它被脱氢酶氧化,脱氢酶可能是一种黄素蛋白,含有巯基和通过丙酮可溶因子与氧连接的金属。过氧化氢没有发现,因为它通常是在其他氰化物不敏感的氧化酶。
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