Kataoka M, Kuno N, Horiguchi T, Seki T, Yoshida T
International Center of Cooperative Research in Biotechnology, Japan, Osaka.
Mol Gen Genet. 1994 Jan;242(2):130-6. doi: 10.1007/BF00391005.
The replication of the 11 kb conjugative multicopy Streptomyces plasmid pSN22 was analyzed. Mutation and complementation analyses indicated that the minimal region essential for plasmid replication was located on a 1.9 kb fragment of pSN22, containing a transacting element encoding a replication protein and a cis-acting sequence acting as a replication origin. Southern hybridization showed that minimal replicon plasmids accumulated much more single-stranded plasmid molecules than did wild-type pSN22. Only one strand was accumulated. A 500 bp fragment from the pSN22 transfer region was identified which reduced the relative amount of single-stranded DNA, when added in the native orientation to minimal replicon plasmids. This 500 bp DNA sequence may be an origin for second-strand synthesis. It had no effect on the efficiency of co-transformation, plasmid incompatibility, or stability. The results indicate that pSN22 replicates via single-stranded intermediates by a rolling circle mechanism.
对11 kb的接合型多拷贝链霉菌质粒pSN22的复制进行了分析。突变和互补分析表明,质粒复制所必需的最小区域位于pSN22的一个1.9 kb片段上,该片段包含一个编码复制蛋白的反式作用元件和一个作为复制起点的顺式作用序列。Southern杂交显示,最小复制子质粒比野生型pSN22积累了更多的单链质粒分子。只积累了一条链。从pSN22转移区域鉴定出一个500 bp的片段,当以天然方向添加到最小复制子质粒中时,该片段减少了单链DNA的相对量。这个500 bp的DNA序列可能是第二链合成的起点。它对共转化效率、质粒不相容性或稳定性没有影响。结果表明,pSN22通过滚环机制经单链中间体进行复制。