Durland R H, Helinski D R
Department of Biology, University of California, San Diego, La Jolla 92093.
Plasmid. 1987 Sep;18(2):164-9. doi: 10.1016/0147-619x(87)90044-8.
The trfA gene of the broad-host-range plasmid RK2 encodes two proteins of 43- and 32-kDa by initiating translation at either of two in-phase AUG codons in a single open reading frame. At least one of these proteins is essential for replication of RK2 derivatives. In order to study the role of the 43-kDa protein, Bal31 deletions into the 5' end of the trfA gene were constructed and incorporated into minimal RK2 replicons. When examined in Escherichia coli, replication and maintenance properties of plasmids encoding only the 32-kDa protein were indistinguishable from those of plasmids encoding both the 43- and the 32-kDa proteins. In four other gram-negative hosts deletion of sequences encoding only the 43-kDa protein did not have a substantial effect on plasmid establishment or stable maintenance. However, in Pseudomonas aeruginosa, deletion of 43-kDa coding sequences greatly reduced the efficiency of plasmid maintenance, suggesting a host-specific role for the 43-kDa TrfA protein in RK2 replication.
广宿主范围质粒RK2的trfA基因通过在单个开放阅读框中的两个同相位AUG密码子之一处起始翻译,编码两种蛋白质,分子量分别为43 kDa和32 kDa。这些蛋白质中至少有一种对于RK2衍生物的复制至关重要。为了研究43 kDa蛋白质的作用,构建了trfA基因5'端的Bal31缺失片段,并将其整合到最小的RK2复制子中。在大肠杆菌中检测时,仅编码32 kDa蛋白质的质粒的复制和维持特性与编码43 kDa和32 kDa蛋白质的质粒没有区别。在其他四种革兰氏阴性宿主中,仅缺失编码43 kDa蛋白质的序列对质粒的建立或稳定维持没有实质性影响。然而,在铜绿假单胞菌中,缺失43 kDa编码序列大大降低了质粒维持的效率,表明43 kDa的TrfA蛋白在RK2复制中具有宿主特异性作用。