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使用P4-质粒ColE1杂种对噬菌体P4进行遗传分析。

Genetic analysis of bacteriophage P4 using P4-plasmid ColE1 hybrids.

作者信息

Kahn M, Ow D, Sauer B, Rabinowitz A, Calendar R

出版信息

Mol Gen Genet. 1980 Feb;177(3):399-412. doi: 10.1007/BF00271478.

Abstract

A set of plasmids that contain fragments of the bacteriophage P4 genome has been constructed by deleting portions of a P4-ColE1 hybrid. A P4 genetic map has been established and related to the physical map by examining the ability of these plasmids to rescue various P4 mutations. The P4 virl mutation and P4 genes involved in DNA replication (alpha), activation of P2 helper genes (delta and epsilon), polarity suppression (psu) and head size determination (sid) have been mapped, as has the region responsible for synthesis of a nonessential P4 protein. One of the deleted plasmids contains only 5900 base pairs (52%) of P4 but will form plaques if additional DNA is added to increase its total size to near that of P4. This plasmid is also unique in that it will not form stable associations with P2 lysogens of E. coli which are recA+. P4 alpha mutants can be suppressed as a result of replication under control of the ColE1 part of the hybrid.

摘要

通过缺失P4 - ColE1杂种的部分片段构建了一组含有噬菌体P4基因组片段的质粒。通过检测这些质粒拯救各种P4突变的能力,已建立了P4遗传图谱并将其与物理图谱相关联。已对P4病毒突变以及参与DNA复制(α)、激活P2辅助基因(δ和ε)、极性抑制(psu)和头部大小确定(sid)的P4基因进行了定位,同时也对负责合成一种非必需P4蛋白的区域进行了定位。其中一个缺失的质粒仅含有P4的5900个碱基对(52%),但如果添加额外的DNA以将其总大小增加到接近P4的大小,它将形成噬菌斑。该质粒的独特之处还在于它不会与recA +的大肠杆菌P2溶原菌形成稳定的关联。由于在杂种的ColE1部分的控制下进行复制,P4α突变体可以被抑制。

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