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利什曼原虫的核糖体是氨基糖苷类药物的作用靶点。

Ribosomes of Leishmania are a target for the aminoglycosides.

作者信息

Maarouf M, Lawrence F, Croft S L, Robert-Gero M

机构信息

Institut de Chimie des Substances Naturelles, C.N.R.S., Gif-Yvette, France.

出版信息

Parasitol Res. 1995;81(5):421-5. doi: 10.1007/BF00931504.

Abstract

Ribosomes of Leishmania, a parasitic protozoan (member of the order of Kinetoplastidae), were purified on a sucrose density gradient. Two different types of ribosomes were isolated from the promastigotes: cytoplasmic (88S and 91S from L. tropica and L. donovani, respectively) and mitochondrial (75S in both species). Both types of ribosome dissociated into their subunits at low Mg2+ concentration (1-2 mM) as follows: 67S and 49S for the 91S cytoplasmic ribosomes of L. donovani and 61S and 43S for the 88S cytoplasmic ribosome of L. tropica; 55S and 34S for L. tropica and 60S and 39S for L. donovani mitochondrial ribosomes, respectively. Paromomycin (aminosidine), an aminoglycoside aminocyclitol antibiotic, interacted with the ribosomes to promote the association of the subunits. Under similar experimental conditions, spermidine and pentamidine were inactive.

摘要

利什曼原虫(一种寄生原生动物,动质体目成员)的核糖体在蔗糖密度梯度上进行了纯化。从前鞭毛体中分离出两种不同类型的核糖体:细胞质核糖体(分别来自热带利什曼原虫和杜氏利什曼原虫的88S和91S)和线粒体核糖体(两种物种均为75S)。在低镁离子浓度(1 - 2 mM)下,两种类型的核糖体均解离为亚基,具体如下:杜氏利什曼原虫91S细胞质核糖体解离为67S和49S,热带利什曼原虫88S细胞质核糖体解离为61S和43S;热带利什曼原虫线粒体核糖体解离为55S和34S,杜氏利什曼原虫线粒体核糖体解离为60S和39S。氨基糖苷类氨基环醇抗生素巴龙霉素(氨基脒)与核糖体相互作用,促进亚基的缔合。在类似的实验条件下,亚精胺和喷他脒无活性。

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