Pfeifer F, Ghahraman P
Max-Planck-Institut für Biochemie, Martinsried, FRG.
Mol Gen Genet. 1993 Apr;238(1-2):193-200. doi: 10.1007/BF00279547.
The DNA sequence of the 5.7 kb plasmid pHH9 containing the replicon region of the 150 kb plasmid pHH1 from Halobacterium salinarium was determined. The minimal region necessary for stable plasmid maintenance lies within a 2.9 kb fragment, as defined by transformation experiments. The DNA sequence contained two open reading frames arranged in opposite orientations, separated by an unusually high AT-rich (60-70% A+T) sequence of 350 bp. All H. salinarium strains (H. halobium, H. cutirubrum) investigated harbour endogenous plasmids containing the pHH1 replicon; however, these pHH1-type plasmids differ by insertions and deletions. Adjacent to the replicon, and separated by a copy of each of the insertion elements ISH27 and ISH26, is the 9 kb p-vac region required for gas vesicle synthesis. Analysis of these and other ISH element copies in pHH1 revealed that most of them lack the target DNA duplication usually found with recently transposed ISH elements. These results underline the plasticity of plasmid pHH1.
测定了来自盐生盐杆菌的150 kb质粒pHH1复制子区域的5.7 kb质粒pHH9的DNA序列。通过转化实验确定,稳定维持质粒所需的最小区域位于一个2.9 kb的片段内。该DNA序列包含两个以相反方向排列的开放阅读框,由一段350 bp的异常富含AT(A+T含量为60-70%)的序列隔开。所研究的所有盐生盐杆菌菌株(盐生盐杆菌、红皮盐杆菌)都含有含有pHH1复制子的内源质粒;然而,这些pHH1型质粒因插入和缺失而有所不同。与复制子相邻,且被插入元件ISH27和ISH26各一个拷贝隔开的是气体囊泡合成所需的9 kb p-vac区域。对pHH1中这些及其他ISH元件拷贝的分析表明,它们中的大多数缺乏通常在最近转座的ISH元件中发现的靶DNA重复序列。这些结果突显了质粒pHH1的可塑性。