del Solar G, Moscoso M, Espinosa M
Centro de Investigaciones Biológicas, CSIC, Madrid, Spain.
Mol Gen Genet. 1993 Feb;237(1-2):65-72. doi: 10.1007/BF00282785.
We have defined the minimal origin of replication of the plasmid pLS1 leading strand, as comprised within a 247 bp region, by in vivo deletion analyses. Cloning of pLS1 DNA regions containing its oriV(+) into a compatible replicon resulted in weak incompatibility towards pLS1, but only when the cloned fragment included the entire pLS1 oriV(+). Plasmids lacking a functional repB gene (which encodes the pLS1 initiator of replication RepB protein) could be established in Streptococcus pneumoniae only when RepB was supplied in trans. We conclude that all the pLS1-encoded gene products involved in its replication and control are efficient trans-complementing plasmid elements.
我们通过体内缺失分析,将质粒pLS1前导链的最小复制起点定义为一个247 bp的区域。将含有其oriV(+)的pLS1 DNA区域克隆到一个相容的复制子中,会导致对pLS1的弱不相容性,但只有当克隆片段包含整个pLS1 oriV(+)时才会出现这种情况。只有在反式提供RepB时,缺乏功能性repB基因(编码pLS1复制起始蛋白RepB)的质粒才能在肺炎链球菌中建立。我们得出结论,所有参与pLS1复制和控制的pLS1编码基因产物都是有效的反式互补质粒元件。