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将顺反子定位到F性因子DNA的EcoRI片段上。

Assignment of tra cistrons to EcoRI fragments of F sex factor DNA.

作者信息

Achtman M, Skurray R A, Thompson R, Helmuth R, Hall S, Beutin L, Clark A J

出版信息

J Bacteriol. 1978 Mar;133(3):1383-92. doi: 10.1128/jb.133.3.1383-1392.1978.

Abstract

We describe here the cloning of single EcoRI fragments from the tra region of F DNA using ColE1::Tn3 as vector. These plasmids, as well as the series of Skurray et al. (Proc. Natl. Acad. Sci. U.S.A. 73:64-68, 1976), have been used to refine the map positions of tra cistrons on the F factor as well as to define a new DNA transfer cistron, traM. The current map of the tra cistrons is presented. None of the known tra cistrons, with the exception of traG, straddles an EcoRI site. The EcoRI site at 82 kilobases splits the traG cistron into two portions, an operator-proximal portion necessary for F pilus synthesis and an operator distal portion involved in conjugation itself. The operon structure of the tra cistrons was reevaluated, and we found that traI is at least partially independent of transcription of the traA to traD operon.

摘要

我们在此描述了以ColE1::Tn3为载体从F因子的tra区域克隆单个EcoRI片段的过程。这些质粒以及Skurray等人(《美国国家科学院院刊》73:64 - 68, 1976)的系列质粒已被用于精确确定F因子上tra顺反子的图谱位置,并定义了一个新的DNA转移顺反子traM。文中给出了tra顺反子的当前图谱。除traG外,已知的tra顺反子均不跨越EcoRI位点。位于82千碱基处的EcoRI位点将traG顺反子分成两部分,一部分是F菌毛合成所需的靠近操纵子的部分,另一部分是参与接合本身的远离操纵子的部分。我们重新评估了tra顺反子的操纵子结构,发现traI至少部分独立于traA至traD操纵子的转录。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0864/222176/9dd2aefaeb13/jbacter00298-0347-a.jpg

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