Hiszczyńska-Sawicka E, Kur J
Department of Microbiology, Technical University of Gdańsk, Poland.
Plasmid. 1997;38(3):174-9. doi: 10.1006/plas.1997.1307.
Four isogenic strains (himAhimD double mutant, himA and himD single mutants, and their wild type counterpart) harboring orip15A plasmid (pACYC184 or pACYC184Amp or pACYC177) show different copy numbers of that plasmid in the early stationary phase of cultivation. The copy number of orip15A plasmid increases about four times in the himAhimD double (65-70 copies per cell) and himD single mutant cells (50-56 copies per cell) and was almost the same in himA mutant (17-18 copies per cell) and wild type cells (14-16 copies per cell). The results suggest that HimD can form homodimers, which are functionally competent for the regulation of orip15A plasmid copy number. Complementation experiments of himAhimD double mutant cells using plasmid carrying himA and himD genes (pPLhiphimA-5) confirm the effect of integration host factor (IHF) absence on increasing the copy number of orip15A plasmid (plasmid producing IHF complemented the defect of IHF mutant). The absence of IHF (using himAhimD double mutant as host) had no effect on the copy number of the pBR322 (oripMB1) plasmid.
四种同基因菌株(himAhimD双突变体、himA单突变体、himD单突变体及其野生型对应物)携带orip15A质粒(pACYC184或pACYC184Amp或pACYC177),在培养的早期稳定期显示出该质粒的不同拷贝数。orip15A质粒的拷贝数在himAhimD双突变体细胞(每个细胞65 - 70个拷贝)和himD单突变体细胞(每个细胞50 - 56个拷贝)中增加了约四倍,而在himA突变体细胞(每个细胞17 - 18个拷贝)和野生型细胞(每个细胞14 - 16个拷贝)中几乎相同。结果表明,HimD可以形成同源二聚体,其在功能上能够调节orip15A质粒的拷贝数。使用携带himA和himD基因的质粒(pPLhiphimA - 5)对himAhimD双突变体细胞进行互补实验,证实了整合宿主因子(IHF)缺失对增加orip15A质粒拷贝数的影响(产生IHF的质粒弥补了IHF突变体的缺陷)。IHF的缺失(以himAhimD双突变体为宿主)对pBR322(oripMB1)质粒的拷贝数没有影响。