Chawla M, Das Gupta S K
Department of Microbiology, Bose Institute (Centenary Building), P1/12 C.I.T. Scheme VIIM, Calcutta, 700054, India.
Plasmid. 1999 Mar;41(2):135-40. doi: 10.1006/plas.1998.1384.
Escherichia coli-mycobacteria shuttle vectors, derived from pAL5000 (a mycobacterial plasmid) and pUC19, were frequently found to undergo structural alterations due to transposition of IS1096, a Mycobacterium smegmatis transposable element, at a cluster of sites located within a small region of 60 bp, immediately upstream of a kanamycin resistance gene present in these vectors. The structural alterations led to deletion of large regions of the vector which, in several cases, were found to extend into the ORF2 (RepB) coding sequences of the pAL5000 replication region without affecting its replication capability. This suggests that the entire ORF2 coding sequences of the pAL5000 replication region may not be essential for replication of pAL5000-derived vectors. The deletion derivatives, which contain the minimal sequences required for replication and selection in mycobacteria, were found to be structurally stable and therefore these could be potentially used as stable vector systems for the transformation of mycobacteria.
源自pAL5000(一种分枝杆菌质粒)和pUC19的大肠杆菌-分枝杆菌穿梭载体,经常被发现会由于IS1096(耻垢分枝杆菌转座元件)的转座而发生结构改变,转座发生在这些载体中卡那霉素抗性基因上游紧邻的一个60 bp小区域内的一组位点上。结构改变导致载体大片段缺失,在几种情况下,发现缺失延伸到了pAL5000复制区域的ORF2(RepB)编码序列中,但不影响其复制能力。这表明pAL5000复制区域的整个ORF2编码序列对于pAL5000衍生载体的复制可能不是必需的。缺失衍生物含有分枝杆菌复制和选择所需的最小序列,被发现结构稳定,因此这些衍生物有可能用作分枝杆菌转化的稳定载体系统。