Riva S, van Sluis C, Mastromei G, Attolini C, Mazza G, Polsinelli M, Falaschi A
Mol Gen Genet. 1975;137(3):185-202. doi: 10.1007/BF00333015.
We have isolated a new mutant of Bacillus subtilis temperature sensitive in DNA replication; its properties are those of an initiation mutant. When liquid cultures are shifted to 48 degrees DNA replication is the first macromolecular synthesis that stops, but only after synthesis of the amount of DNA predicted for the completion of one replication round. When spores of the mutant are germinated and shifted to 48 degrees at subsequent times, one round of DNA replication is observed only when the shift occurs between 60 and 100 min; earlier shifts do not allow replication to start, later shifts allow more than one replication. The DNA replicated after a shift to high temperature is enriched in markers close to the terminus. The reinitiation of DNA replication stopped by the high temperature, takes place following a shift to a permissive temperature only if protein synthesis is allowed. Examination of DNA replication following toluene treatment shows that the elongation of DNA chains is not affected at the non-permissive temperature. This mutant is shown by PBS-1 mapping to correspond to a new gene denominated dna P, which is located between the thy A and fur A genes and is distinct from all the mapped dna and rec genes of Bacillus subtilis. The mutation confers to the cells also a deficiency in the ability to be transformed, to be transfected with SPP1 phage DNA, and to survive treatment with methyl-methane sulfonate. These deficiencies, observed at the permissive temperature, are no more temperature dependent than in the parental strain. The ability to perform homologous and heterologous transduction with PBS-1 phage and the sensitivity to ultraviolet radiation or mitomycin C are normal.
我们分离出了一种枯草芽孢杆菌的新突变体,其在DNA复制方面对温度敏感;其特性属于起始突变体。当液体培养物转移至48℃时,DNA复制是首先停止的大分子合成,但仅在完成一轮复制所需的DNA量合成之后才停止。当突变体的孢子萌发并在随后的时间转移至48℃时,仅当在60至100分钟之间发生转移时才观察到一轮DNA复制;更早的转移不允许复制开始,更晚的转移允许进行一轮以上的复制。转移至高温后复制的DNA在靠近末端的标记物中富集。因高温而停止的DNA复制重新起始,只有在允许蛋白质合成的情况下,转移至允许温度后才会发生。甲苯处理后对DNA复制的检查表明,在非允许温度下DNA链的延伸不受影响。通过PBS - 1定位显示该突变体对应于一个名为dna P的新基因,它位于thy A和fur A基因之间,且与枯草芽孢杆菌所有已定位的dna和rec基因不同。该突变还使细胞在转化能力、用SPP1噬菌体DNA转染的能力以及对甲基磺酸甲酯处理的存活能力方面存在缺陷。在允许温度下观察到的这些缺陷与亲代菌株一样不再依赖温度。用PBS - 1噬菌体进行同源和异源转导的能力以及对紫外线辐射或丝裂霉素C的敏感性是正常的。