Rutberg L
J Virol. 1973 Jul;12(1):9-12. doi: 10.1128/JVI.12.1.9-12.1973.
A mutant of Bacillus subtilis, dna-1, which cannot initiate new rounds of DNA replication (obtained from N. Sueoka) was lysogenized with wild-type phi 105 and with the heat-inducible mutant phi 105 cts23. Bacteria were incubated at the permissive temperature in the presence of chloramphenicol and then shifted to the nonpermissive temperature where induction of phi 105 cts23 occurs. DNA made after the shift was labeled with a density label, and the distribution of bacterial and phage markers in replicated and unreplicated DNA was determined. Similar experiments were performed with nonlysogenic dna-1 infected with phage phi 105 cts23 after the temperature shift. The results show that after induction of phi 105 cts23 prophage, bacterial markers on either side of the prophage replicate at an increased rate compared to more distant markers. No selective stimulation of bacterial DNA synthesis was observed on infection or after shifting bacteria lysogenic for noninducible phage to the higher temperature. Attempts to suppress the initiation mutation dna-1 by phage phi 105 were unsuccessful.
一种不能起始新一轮DNA复制的枯草芽孢杆菌突变体dna - 1(由N. 末冈提供),用野生型噬菌体φ105和热诱导突变体φ105 cts23进行了溶源化处理。细菌在允许温度下于氯霉素存在的条件下培养,然后转移至非允许温度,此时会发生φ105 cts23的诱导。转移后合成的DNA用密度标记进行标记,并测定细菌和噬菌体标记物在已复制和未复制DNA中的分布。对温度转移后用噬菌体φ105 cts23感染的非溶源化dna - 1进行了类似实验。结果表明,在诱导φ105 cts23原噬菌体后,与距离更远的标记物相比,原噬菌体两侧的细菌标记物复制速率增加。在感染时或对于非诱导性噬菌体的溶源菌转移至较高温度后,未观察到对细菌DNA合成的选择性刺激。用噬菌体φ105抑制起始突变dna - 1的尝试未成功。