Hasunuma K, Sekiguchi M
J Bacteriol. 1979 Mar;137(3):1095-9. doi: 10.1128/jb.137.3.1095-1099.1979.
Escherichia coli strains with mutations in genes dnaB, dnaC, and dnaG were tested for their capacity to replicate pSC101 deoxyribonucleic acid (DNA) at a nonpermissive temperature. Only a small amount of radioactive thymine was incorporated into pSC101 DNA in the dna mutants at 42 degrees C, whereas active incorporation into plasmid DNA took place in wild-type strains under the same conditions. The effects of the dnaB and dnaC mutations were greater on plasmid DNA synthesis than on host chromosomal DNA synthesis, suggesting that these gene products are directly involved in the process of pSC101 DNA replication. In dnaG mutants, both plasmid and chromosomal DNA synthesis were blocked soon after the shift to high temperature; although the extent of inhibition of the plasmid DNA synthesis was greater during the early period of temperature shift to 42 degrees C as compared with that of the host DNA synthesis, during the later period it was less. It was found that the number of copies of pSC101 per chromosome in dnaA and dnaC strains, grown at 30 degrees C, was considerably lower than that in wildtype strains, suggesting that the replication of pSC101 in these mutant strains was partially suppressed even under the permissive conditions. No correlation was found between the number of plasmid copies and the tetracycline resistance level of the host bacterium.
对在基因dnaB、dnaC和dnaG中发生突变的大肠杆菌菌株,测试了它们在非允许温度下复制pSC101脱氧核糖核酸(DNA)的能力。在42℃时,只有少量放射性胸腺嘧啶掺入dna突变体中的pSC101 DNA,而在相同条件下野生型菌株中则发生了活跃的胸腺嘧啶掺入质粒DNA的情况。与宿主染色体DNA合成相比,dnaB和dnaC突变对质粒DNA合成的影响更大,这表明这些基因产物直接参与了pSC101 DNA复制过程。在dnaG突变体中,转移到高温后不久,质粒和染色体DNA合成均被阻断;尽管在温度转移到42℃的早期,质粒DNA合成的抑制程度比宿主DNA合成的抑制程度更大,但在后期则较小。研究发现,在30℃下生长的dnaA和dnaC菌株中,每条染色体上pSC101的拷贝数明显低于野生型菌株,这表明即使在允许条件下,这些突变菌株中pSC101的复制也受到部分抑制。未发现质粒拷贝数与宿主细菌的四环素抗性水平之间存在相关性。