Siegel E C, Marmur J
J Virol. 1969 Nov;4(5):610-8. doi: 10.1128/JVI.4.5.610-618.1969.
In a temperature-sensitive mutant of Bacillus subtilis 168, induction of the defective phage PBSX occurred at 48 C. Cell lysis began after 90 min of growth at 48 C, and cell viability began to decrease after 10 to 30 min. The loss in viability at the nonpermissive temperature was prevented by azide or cyanide. Deoxyribonucleic acid (DNA), ribonucleic acid, and protein synthesis were not inhibited at 48 C. Temperature induction of the temperate phage SPO2 also occurred in this mutant. The temperature-sensitive mutation, designated tsi-23, was linked by transduction to purB6 and pig, the order being purB6 pig tsi-23. Mutation tsi-23 was transformable to wild type by B. subtilis 168 DNA but not by DNA from the closely related strains W23 or S31. DNA from the latter two strains transformed auxotrophic markers of strain 168 at frequencies close to those found with 168 donor DNA. Upon temperature induction, cellular DNA was broken to a size of 22S, characteristic of DNA in PBSX particles. The DNA isolated from temperature-induced PBSX did not give an increased Ade(+)/Met(+) transformant ratio relative to cellular DNA nor contain preferential break points as determined by transformation of four closely linked markers.
在枯草芽孢杆菌168的一个温度敏感突变体中,缺陷噬菌体PBSX在48℃时被诱导产生。在48℃下生长90分钟后细胞开始裂解,细胞活力在10至30分钟后开始下降。叠氮化物或氰化物可防止在非允许温度下活力的丧失。在48℃时,脱氧核糖核酸(DNA)、核糖核酸和蛋白质合成未受抑制。温和噬菌体SPO2在该突变体中也会发生温度诱导。这个被命名为tsi - 23的温度敏感突变通过转导与purB6和pig相连,顺序为purB6 pig tsi - 23。tsi - 23突变可被枯草芽孢杆菌168的DNA转化为野生型,但不能被密切相关菌株W23或S31的DNA转化。后两个菌株的DNA以接近168供体DNA的频率转化168菌株的营养缺陷型标记。温度诱导后,细胞DNA断裂为22S大小,这是PBSX颗粒中DNA的特征。相对于细胞DNA,从温度诱导的PBSX中分离出的DNA在Ade(+)/Met(+)转化子比例上没有增加,通过四个紧密连锁标记的转化测定也没有发现优先断裂点。