Belogurov A A, Yussifov T N, Kotova V U, Zavilgelsky G B
Mol Gen Genet. 1985;198(3):509-13. doi: 10.1007/BF00332948.
The host-controlled K restriction of unmodified phage lambda was 10-100-fold alleviated in the wild-type strain E. coli K12, carrying plasmid pKM101 of incompability group N. pKM101-mediated release of K restriction was also observed in lexA-, recA-, and recB- strains of E. coli K12. By restriction mapping Tn5 insertions in pKM101, which reduced pKM101-mediated alleviation of restriction, were shown to be located within the BglIIB fragment approximately 11 kb anticlockwise from the RI site of pKM101. We have termed the gene(s) promoting the alleviation of K restriction of phage lambda ard (alleviation of restriction of DNA). It was shown (1) that ard function affected only the EcoK restriction system and not the EcoB, EcoRI, EcoRIII, or EcoPI systems, (2) ard gene(s) did not mediate EcoK type modification of lambda DNA and did not increase the modification activity of the EcoK system in a way similar to that observed with gene ral of bacteriophage lambda.
在携带不相容群N的质粒pKM101的野生型大肠杆菌K12菌株中,未修饰的噬菌体λ的宿主控制的K限制被减轻了10至100倍。在大肠杆菌K12的lexA -、recA -和recB -菌株中也观察到了pKM101介导的K限制的释放。通过对pKM101中Tn5插入进行限制酶切图谱分析,发现降低pKM101介导的限制减轻作用的Tn5插入位于pKM101的RI位点逆时针方向约11 kb处的BglIIB片段内。我们将促进噬菌体λ的K限制减轻的基因称为ard(DNA限制减轻)。结果表明:(1)ard功能仅影响EcoK限制系统,而不影响EcoB、EcoRI、EcoRIII或EcoPI系统;(2)ard基因不介导λ DNA的EcoK型修饰,也不会以类似于噬菌体λ的ral基因所观察到的方式增加EcoK系统的修饰活性。