Chatfield L K, Wilkins B M
Mol Gen Genet. 1984;197(3):461-6. doi: 10.1007/BF00329943.
DNA primase of ColIb-P9drd-1 generates RNA primers that are thought to initiate DNA synthesis on the conjugatively transferred strand of the plasmid. To examine whether plasmid-specified primase is transferred during conjugation, we exploited the property of the enzyme to promote bacterial DNA replication in dnaG (primase-defective) mutants of Escherichia coli. It was found that dnaG3 recipient cells, treated with rifampicin to inhibit transcription, recovered ability to synthesise bacterial DNA by a process requiring an active plasmid primase gene in donor cells and a functional conjugation system. A non-transferable primase gene in the donor strain complemented a primase-negative derivative of ColIb-P9drd-1, confirming that the enzyme responsible for recovery was supplied by donor cells. The implication is that certain proteins are transmitted from donor cells to promote conjugative metabolism of plasmid DNA in the recipients.
ColIb-P9drd-1的DNA引发酶产生RNA引物,据认为这些引物可启动质粒接合转移链上的DNA合成。为了检测在接合过程中质粒特异性引发酶是否会转移,我们利用该酶促进大肠杆菌dnaG(引发酶缺陷型)突变体中细菌DNA复制的特性。结果发现,用利福平处理以抑制转录的dnaG3受体细胞,通过一个需要供体细胞中具有活性质粒引发酶基因和功能性接合系统的过程,恢复了合成细菌DNA的能力。供体菌株中一个不可转移的引发酶基因补充了ColIb-P9drd-1的引发酶阴性衍生物,证实负责恢复的酶是由供体细胞提供的。这意味着某些蛋白质从供体细胞传递过来,以促进受体中质粒DNA的接合代谢。