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在分段双链RNA噬菌体phi 6的原衣壳中重建活性复制酶。

Reconstitution of active replicase in procapsids of the segmented dsRNA bacteriophage phi 6.

作者信息

Casini G, Qiao X, Mindich L

机构信息

Department of Microbiology, Public Health Research Institute, New York, New York 10016.

出版信息

Virology. 1994 Oct;204(1):251-3. doi: 10.1006/viro.1994.1529.

Abstract

Bacteriophage phi 6 has a genome of three segments of double-stranded RNA enclosed in a procapsid composed of four different proteins. The preformed procapsid is capable of packaging plus strand transcripts of the genomic segments in an in vitro reaction. The plus strands then serve as templates for in vitro minus strand synthesis. Procapsids that are missing protein P2 are incapable of minus strand synthesis. In this report we show that incubation with a cell extract containing P2 results in particles with normal amounts of attached P2 and with packaging and replicase activity. Particles lacking P7 have reduced replicase activity which can be augmented by incubation with extracts containing P7, but the amount of attached P7 is small.

摘要

噬菌体φ6具有由三段双链RNA组成的基因组,这些双链RNA被包裹在一个由四种不同蛋白质构成的原衣壳中。预先形成的原衣壳能够在体外反应中包装基因组片段的正链转录本。然后正链作为体外负链合成的模板。缺失蛋白质P2的原衣壳无法进行负链合成。在本报告中,我们表明,与含有P2的细胞提取物一起孵育会产生具有正常量附着P2且具有包装和复制酶活性的颗粒。缺乏P7的颗粒复制酶活性降低,通过与含有P7的提取物一起孵育可增强其活性,但附着的P7量很少。

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