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胞内分枝杆菌质粒pLR7的限制性内切酶图谱分析与克隆

Restriction endonuclease mapping and cloning of Mycobacterium intracellulare plasmid pLR7.

作者信息

Crawford J T, Bates J H

出版信息

Gene. 1984 Mar;27(3):331-3. doi: 10.1016/0378-1119(84)90079-9.

Abstract

A restriction map of Mycobacterium intracellulare plasmid pLR7 was developed. This 15.3-kb plasmid had unique sites for BamHI, HindIII, and XbaI. Various large fragments of pLR7 were cloned into pBR322 or pHP34 and propagated in Escherichia coli. A hybrid pLR7 ::pBR322 plasmid carrying the complete pLR7 sequence was constructed by joining the plasmids at their HindIII sites. The construction of these hybrids will facilitate the analysis and manipulation of pLR7 and may allow the development of this plasmid as a model system for genetic analysis in mycobacteria.

摘要

构建了胞内分枝杆菌质粒pLR7的限制性酶切图谱。这个15.3kb的质粒具有BamHI、HindIII和XbaI的独特酶切位点。pLR7的各种大片段被克隆到pBR322或pHP34中,并在大肠杆菌中进行扩增。通过在它们的HindIII位点连接质粒,构建了携带完整pLR7序列的杂交质粒pLR7::pBR322。这些杂交质粒的构建将有助于对pLR7进行分析和操作,并可能使该质粒发展成为分枝杆菌遗传分析的模型系统。

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