Buu A, Sonenshein A L
J Bacteriol. 1975 Oct;124(1):190-200. doi: 10.1128/jb.124.1.190-200.1975.
Nucleic acid synthesis was studied during germination and outgrowth of normal spores of Bacillus subtilis, as well as of spores carrying the genome of phage phie. In a system in which development was restricted to the spore-darkening phase, synthesis of ribonucleic acid (RNA), but not deoxyribonucleic acid (DNA), was detected. The extent of RNA synthesis and turnover, during this phase was similar for the two types of spores. In a partially darkened population of spores of either type, there was little RNA degradation, whereas there was considerable turnover in a fully darkened population. The DNA-dependent RNA polymerase of dormant or dark spores was not active in vitro with phi DNA as template, although a sigma-like factor could be separated from the polymerizing activity by zone centrifugation. Within 40 min after resuspension of dark spores in a medium that allows outgrowth, the enzyme acquired the ability to transcribe the phage DNA efficiently. During outgrowth, both normal and carrier spores synthesized DNA, but in carrier spores this DNA was almost entirely phage specific. The pattern of RNA accumulation in normal spores was in two distinct phase (0 to 60 min and 90 to 180 min). The second phase was absent in outgrowing carrier spores. The burst of phage in carrier spores occurred at 160 to 180 min.
对枯草芽孢杆菌正常孢子以及携带噬菌体phie基因组的孢子在萌发和生长过程中的核酸合成进行了研究。在一个发育仅限于孢子变暗阶段的系统中,检测到核糖核酸(RNA)的合成,但未检测到脱氧核糖核酸(DNA)的合成。在此阶段,两种类型的孢子RNA合成和周转的程度相似。在任何一种类型的部分变暗的孢子群体中,RNA降解很少,而在完全变暗的群体中则有相当程度的周转。休眠或暗色孢子的依赖DNA的RNA聚合酶在体外以phi DNA为模板时没有活性,尽管通过区带离心可以从聚合活性中分离出一种类sigma因子。在暗色孢子重悬于允许生长的培养基中后40分钟内,该酶获得了有效转录噬菌体DNA的能力。在生长过程中,正常孢子和携带孢子都合成DNA,但在携带孢子中,这种DNA几乎完全是噬菌体特异性的。正常孢子中RNA积累的模式分为两个不同阶段(0至60分钟和90至180分钟)。在生长的携带孢子中不存在第二阶段。携带孢子中的噬菌体爆发发生在160至180分钟。