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鸟分枝杆菌质粒pLR7复制区域的分离与测序

Isolation and sequencing of the replication region of Mycobacterium avium plasmid pLR7.

作者信息

Beggs M L, Crawford J T, Eisenach K D

机构信息

Department of Pathology, University of Arkansas for Medical Sciences, Little Rock, USA.

出版信息

J Bacteriol. 1995 Sep;177(17):4836-40. doi: 10.1128/jb.177.17.4836-4840.1995.

Abstract

The Mycobacterium avium plasmid pLR7 is representative of a group of small plasmids that are common in isolates from AIDS patients with disseminated M. avium infections. Determination of the functions of these and other plasmids has been hampered by the lack of methods for genetic manipulation of M. avium. In this study, the region of pLR7 capable of replication was identified and sequenced. Fragments of pLR7 were cloned into a pUC18 derivative carrying a kanamycin resistance marker and introduced into a plasmid-free M. avium strain by electroporation. The origin of replication was located on a 1.8-kb PvuII-to-SmaI fragment. An open reading frame encoding a putative Rep protein was identified. Two other open reading frames were identified in this region. A shuttle vector, pMB351, was constructed with the pLR7 origin of replication, pUC18, and the kanamycin resistance gene from Tn5. This vector was successfully transformed into M. avium, Mycobacterium tuberculosis, and Mycobacterium bovis.

摘要

鸟分枝杆菌质粒pLR7是一组小质粒的代表,这些小质粒在患有播散性鸟分枝杆菌感染的艾滋病患者分离株中很常见。由于缺乏对鸟分枝杆菌进行基因操作的方法,这些质粒及其他质粒功能的确定受到了阻碍。在本研究中,鉴定并测序了pLR7中能够复制的区域。将pLR7的片段克隆到携带卡那霉素抗性标记的pUC18衍生物中,并通过电穿孔导入无质粒的鸟分枝杆菌菌株。复制起点位于一个1.8kb的PvuII至SmaI片段上。鉴定出一个编码假定Rep蛋白的开放阅读框。在该区域还鉴定出另外两个开放阅读框。用pLR7复制起点、pUC18和来自Tn5的卡那霉素抗性基因构建了穿梭载体pMB351。该载体成功转化到鸟分枝杆菌、结核分枝杆菌和牛分枝杆菌中。

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