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体外组装具有生物活性的噬菌体λ原头部

Assembly of biologically active proheads of bacteriophage lambda in vitro.

作者信息

Murialdo H, Becker A

出版信息

Proc Natl Acad Sci U S A. 1977 Mar;74(3):906-10. doi: 10.1073/pnas.74.3.906.

Abstract

Bacteriophage lambda DNA can be packaged in vitro into preformed proheads to generate plaque-forming units. This complex set of reactions is initiated when lambda DNA is mixed with the product of the phage A gene, and proheads. Because proheads are an essential early reactant, the system has potential as an assay for the formation of biologically active proheads. When extracts of cells infected with certain lambda head mutants (for example, B--, C--, Nu3--, and E--) are used as the prohead donor, plaque-forming units are not produced. However, when extracts of E- - and Nu3- - infected cells are first reacted together the combination provides prohead-donor activity to the in vitro packaging system. In vitro assembled, biologically active proheads have the same sedimentation properties and electron micrsocopic appearance as "wild-type" proheads isolated from lambdaA-D- -infected cells. Centrifugation analysis shows that the Nu3- extract contributes gpE, the major capsid protein, to the reaction in the form of monomers or small polymers.

摘要

噬菌体λDNA可在体外包装到预先形成的原头部中以产生噬菌斑形成单位。当λDNA与噬菌体A基因的产物以及原头部混合时,这一系列复杂的反应就会启动。由于原头部是必不可少的早期反应物,该系统有潜力作为一种检测生物活性原头部形成的方法。当用感染了某些λ头部突变体(例如B--、C--、Nu3--和E--)的细胞提取物作为原头部供体时,不会产生噬菌斑形成单位。然而,当首先将E--和Nu3--感染细胞的提取物一起反应时,这种组合为体外包装系统提供了原头部供体活性。体外组装的具有生物活性的原头部具有与从λA-D--感染细胞中分离出的“野生型”原头部相同的沉降特性和电子显微镜外观。离心分析表明,Nu3--提取物以单体或小聚合物的形式为反应提供了主要衣壳蛋白gpE。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1843/430525/9f1a5d406f41/pnas00025-0115-a.jpg

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