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一种大肠杆菌-分枝杆菌穿梭粘粒载体,pMSC1。

An Escherichia coli-Mycobacterium shuttle cosmid vector, pMSC1.

作者信息

Hinshelwood S, Stoker N G

机构信息

Bacterial Molecular Genetics Unit, Department of Clinical Sciences, London School of Hygiene and Tropical Medicine, U.K.

出版信息

Gene. 1992 Jan 2;110(1):115-8. doi: 10.1016/0378-1119(92)90453-v.

Abstract

A shuttle cosmid vector, pMSC1, has been constructed which replicates in Escherichia coli and Mycobacterium smegmatis. The vector was mainly derived from the lambda ori cosmid, Lawrist4, and the Mycobacterium fortuitum cryptic plasmid, pAL5000, which replicates in M. smegmatis and Mycobacterium bovis BCG. The vector contains two cos sites which facilitates library construction, unique BamHI and HindIII sites for cloning, and a kanamycin-resistance-encoding gene for selection in mycobacteria. After packaging, the vector sequences comprise 10.3 kb, so that the theoretical size limits for inserts are 30-42 kb. A genomic library from M. smegmatis was constructed in E. coli; clones from this library were transferred into M. smegmatis by electroporation, and back again to E. coli, without any apparent rearrangements. This vector will be useful in cloning genes encoding complex pathways in mycobacteria.

摘要

已构建了一种穿梭黏粒载体pMSC1,它能在大肠杆菌和耻垢分枝杆菌中复制。该载体主要来源于λ ori黏粒Lawrist4和偶然分枝杆菌隐蔽质粒pAL5000,pAL5000能在耻垢分枝杆菌和牛分枝杆菌卡介苗中复制。该载体包含两个有助于文库构建的黏粒位点、用于克隆的独特BamHI和HindIII位点,以及一个用于在分枝杆菌中进行选择的卡那霉素抗性编码基因。包装后,载体序列为10.3 kb,因此插入片段的理论大小限制为30 - 42 kb。在大肠杆菌中构建了耻垢分枝杆菌的基因组文库;该文库中的克隆通过电穿孔转移到耻垢分枝杆菌中,然后再转回大肠杆菌,未出现明显重排。该载体将有助于克隆编码分枝杆菌复杂途径的基因。

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