Pfeifer F, Blaseio U, Ghahraman P
Max-Planck-Institut für Biochemie, Martinsried, Federal Republic of Germany.
J Bacteriol. 1988 Aug;170(8):3718-24. doi: 10.1128/jb.170.8.3718-3724.1988.
Deletion events occurring in the major 150-kilobase-pair (kb) plasmid pHH1 of the archaebacterium Halobacterium halobium were investigated. We found four deletion derivatives of pHH1 in gas-vacuole-negative mutants, two of which (pHH23) [65 kb] and pHH4 [36 kb]) we analyzed. Both plasmids incurred more than one deletion, leading to the fusion of noncontiguous pHH1 sequences. pHH23 and pHH4 overlapped by only 4 kb of DNA sequence. A DNA fragment derived from this region was used to monitor the production of further deletion variants of pHH4. A total of 25 single colonies were characterized, 23 of which contained various smaller pHH4 derivatives. Of the 25 colonies investigated, 2 had lost pHH4 entirely and contained only large (greater than or equal to 100-kb) minor covalently closed circular DNAs. One colony contained the 17-kb deletion derivative pHH6 without any residual pHH4. The sizes of the pHH4 deletion derivatives, produced during the development of a single colony, ranged from 5 to 20 kb. In five colonies, pHH4 was altered by the integration of an additional insertion element. These insertions, as well as copies of the various insertion elements already present in pHH4, presumably serve as hot spots for recombination events which result in deletions. A second enrichment procedure led to the identification of colonies containing either a 16-kb (pHH7) or a 5-kb (pHH8) deletion derivative of pHH4 as the major plasmid. pHH8, the smallest plasmid found, contained the 4 kb of unique DNA sequence shared by pHH23 and pHH4, as well as some flanking pHH4 sequences. This result indicates that the 4-kb region contains the necessary sequences for plasmid maintenance and replication.
对嗜盐古菌嗜盐栖热菌(Halobacterium halobium)主要的150千碱基对(kb)质粒pHH1中发生的缺失事件进行了研究。我们在气胞缺失突变体中发现了pHH1的四种缺失衍生物,其中两种(pHH23 [65 kb] 和pHH4 [36 kb])进行了分析。两种质粒都发生了不止一次缺失,导致非相邻的pHH1序列融合。pHH23和pHH4仅重叠4 kb的DNA序列。源自该区域的一个DNA片段用于监测pHH4进一步缺失变体的产生。总共对25个单菌落进行了表征,其中23个含有各种较小的pHH4衍生物。在研究的25个菌落中,有2个完全丢失了pHH4,仅含有大的(大于或等于100 kb)次要共价闭合环状DNA。一个菌落含有17 kb的缺失衍生物pHH6,没有任何残留的pHH4。在单个菌落发育过程中产生的pHH4缺失衍生物的大小范围为5至20 kb。在五个菌落中,pHH4因额外插入元件的整合而发生改变。这些插入以及pHH4中已经存在的各种插入元件的拷贝,可能作为重组事件的热点,导致缺失。第二个富集程序导致鉴定出以pHH4的16 kb(pHH7)或5 kb(pHH8)缺失衍生物作为主要质粒的菌落。pHH8是发现的最小质粒,包含pHH23和pHH4共有的4 kb独特DNA序列以及一些侧翼pHH4序列。这一结果表明,4 kb区域包含质粒维持和复制所需的序列。