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布氏锥虫血液和培养形式中的线粒体核糖体、细胞质核糖体及其活性

Mitochondrial and cytoplasmic ribosomes and their activity in blood and culture form Trypanosoma brucei.

作者信息

Hanas J, Linden G, Stuart K

出版信息

J Cell Biol. 1975 Apr;65(1):103-11. doi: 10.1083/jcb.65.1.103.

Abstract

Ribosomes of Trypanosoma brucei, a parasitic, flagellated protozoan (order Kinetoplastida), were identified on sucrose density gradients by their radioactively labeled nascent peptides. Ultraviolet absorption revealed only cytoplasmic ribosomes which served as internal sedimentation markers. Synthesis on cytoplasmic ribosomes was completely inhibited by cycloheximide. In the presence of this antibiotic, nascent peptides were associated with ribosomes of lower sedimentation coefficient than the cytoplasmic ribosomes. Chloramphenicol blocked synthesis on these ribosomes which are probably the mitochondrial ribosomes. These ribosomes differed from the cytoplasmic ribosomes in several ways. Their sedimentation coefficient was about 72S rather than 84S. The stability of the 72S ribosomes was less sensitive to pancreatic ribonuclease and low Mg-++ concentrations, dissociating below 0.1 mM Mg++. The 72S ribosomes were more sensitive to elevated KCl concentrations, dissociation above 0.25 M. Protein synthetic activity associated with the 72S class of ribosomes was found in trypanosomes grown in rats. Under these conditions no cytochromes or fully active Krebs cycle is present in these cells and respiration is insensitive to cyanide.

摘要

布氏锥虫是一种寄生的、具鞭毛的原生动物(动基体目),其核糖体通过放射性标记的新生肽在蔗糖密度梯度上得以鉴定。紫外线吸收显示仅存在细胞质核糖体,其作为内部沉降标记物。细胞质核糖体上的合成被环己酰亚胺完全抑制。在这种抗生素存在的情况下,新生肽与沉降系数低于细胞质核糖体的核糖体相关联。氯霉素阻断了这些可能是线粒体核糖体上的合成。这些核糖体在几个方面与细胞质核糖体不同。它们的沉降系数约为72S而非84S。72S核糖体的稳定性对胰核糖核酸酶和低镁离子浓度不太敏感,在镁离子浓度低于0.1 mM时会解离。72S核糖体对氯化钾浓度升高更敏感,在高于0.25 M时会解离。在大鼠体内生长的锥虫中发现了与72S核糖体类别相关的蛋白质合成活性。在这些条件下,这些细胞中不存在细胞色素或完全活跃的三羧酸循环,呼吸对氰化物不敏感。

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Mitochondrial ribosomes.线粒体核糖体
FEBS Lett. 1971 Feb 19;13(2):73-88. doi: 10.1016/0014-5793(71)80204-1.
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Mitochondrial nucleic acids.线粒体核酸
Annu Rev Biochem. 1972;41:333-76. doi: 10.1146/annurev.bi.41.070172.002001.

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