Meijer W J, Venema G, Bron S
Department of Genetics, Groningen Biomolecular Sciences and Biotechnology Institute, Haren, The Netherlands.
Nucleic Acids Res. 1995 Feb 25;23(4):612-9. doi: 10.1093/nar/23.4.612.
In this paper we describe the isolation and characterization of single strand origins (SSOs) of several cryptic Bacillus subtilis plasmids which use the rolling-circle mechanism of replication. The plasmids used in this study involved pTA1015, pTA1020, pTA1030, pTA1040, pTA1050 and pTA1060. The SSO of pTA1015 was isolated by shotgun cloning in a specially designed vector, pWM100, which has no SSO of its own. Sequence analysis revealed that the SSO of pTA1015 is almost identical to formerly described palT type SSOs. Also pTA1020 and pTA1060 were shown to contain SSOs highly homologous to palT. Using Southern hybridization with the palT of pTA1015 as a probe, the SSO of pTA1040 was cloned. Sequence analysis revealed a region of 200 bp which is 77% identical to the palT of pTA1015. The plasmids pTA1030 and pTA1050 contain an SSO which is highly homologous to the SSO of pTA1040. The majority of the SSOs of rolling-circle plasmids from B.subtilis seem to belong to two related families which we denote as palT1 (present on pTA1015, pTA1020 and pTA1060) and palT2 (present on pTA1030, pTA1040 and pTA1050). Both families of SSOs are highly efficient single-strand-conversion signals in B.subtilis.
在本文中,我们描述了几种利用滚环复制机制的枯草芽孢杆菌隐蔽质粒的单链起始位点(SSO)的分离和特性。本研究中使用的质粒包括pTA1015、pTA1020、pTA1030、pTA1040、pTA1050和pTA1060。pTA1015的SSO是通过在专门设计的载体pWM100中进行鸟枪法克隆分离出来的,该载体自身没有SSO。序列分析表明,pTA1015的SSO与先前描述的palT型SSO几乎相同。此外,pTA1020和pTA1060也被证明含有与palT高度同源的SSO。以pTA1015的palT为探针进行Southern杂交,克隆了pTA1040的SSO。序列分析揭示了一个200 bp的区域,它与pTA1015的palT有77%的同一性。质粒pTA1030和pTA1050含有一个与pTA1040的SSO高度同源的SSO。来自枯草芽孢杆菌的滚环质粒的大多数SSO似乎属于两个相关家族,我们将其分别命名为palT1(存在于pTA1015、pTA1020和pTA1060上)和palT2(存在于pTA1030、pTA1040和pTA1050上)。这两个SSO家族在枯草芽孢杆菌中都是高效的单链转换信号。