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一种能够检测插入DNA的ColE1-Apr克隆载体的构建。

The generation of a ColE1-Apr cloning vehicle which allows detection of inserted DNA.

作者信息

So M, Gill R, Falkow S

出版信息

Mol Gen Genet. 1975 Dec 30;142(3):239-49. doi: 10.1007/BF00425649.

Abstract

A 3.2 Mdal sequence of DNA, TnA, which contains the ampicillin (Ap) resistance determinant has been translocated from an R plasmid to the plasmid ColE1. A total of 12 isolates were studied. There are at least 8 sites in ColE1 at which TnA has inserted. Insertion at five of these has resulted in a Col-phenotype. One ColE1-Apr plasmid, RSF2124, was examined further and its replication properties are found to be similar to that of the parent plasmid. RSF2124 appears to be a useful plasmid vehicle for the molecular cloning of DNA from diverse prokaryotic sources: it codes for readily detectable Ap resistance and contains a single EcoRI site in a gene affecting colicin biosynthesis so that it is unable to produce colicin upon ligation to other DNA.

摘要

一段包含氨苄青霉素(Ap)抗性决定簇的3.2兆道尔顿DNA序列TnA,已从R质粒转移至质粒ColE1。共研究了12个分离株。ColE1中至少有8个TnA插入位点。其中5个位点的插入导致了Col-表型。对一个ColE1-Apr质粒RSF2124进行了进一步研究,发现其复制特性与亲本质粒相似。RSF2124似乎是一种用于从多种原核生物来源进行DNA分子克隆的有用质粒载体:它编码易于检测的Ap抗性,并且在影响大肠杆菌素生物合成的基因中含有一个单一的EcoRI位点,因此在与其他DNA连接后无法产生大肠杆菌素。

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