Akrigg A, Mandelstam J
Biochem J. 1978 Apr 15;172(1):63-7. doi: 10.1042/bj1720063.
A considerable amount of Mn2+-stimulated DNAase (deoxyribonuclease) activity is released by Bacillus subtilis 168 during sporulation in a glucose-deficient medium; much smaller amounts are released during starvation for phosphate or nitrogen. Protein synthesis is required. Two forms of evidence are presented that production of the DNAase is associated with events late in stage II of sporulation. 19 Thymidine starvation, which inhibits the biochemical events associated with sporulation, also inhibits release of the DNAase. 2. Several asporogenous mutants blocked at stage II or earlier and unable to produce alkaline phosphatase (a stage-II event) do not produce the enzyme. Mutants blocked towards the end of stage II or later produce both enzymes. During sporulation of the wild-type strain, the DNAase appears about 1 h after alkaline phosphatase. The results suggest that production of the DNAase is controlled by a still-undiscovered stage-II genetic locus.
在缺乏葡萄糖的培养基中,枯草芽孢杆菌168在芽孢形成过程中会释放出大量受锰离子刺激的脱氧核糖核酸酶(DNA酶)活性;在磷酸盐或氮饥饿期间释放的量则少得多。这一过程需要蛋白质合成。有两种证据表明,DNA酶的产生与芽孢形成第二阶段后期的事件有关。1. 胸腺嘧啶饥饿会抑制与芽孢形成相关的生化事件,同时也会抑制DNA酶的释放。2. 几个在第二阶段或更早阶段受阻且无法产生碱性磷酸酶(第二阶段事件)的无芽孢突变体不会产生这种酶。在第二阶段接近尾声或更晚阶段受阻的突变体则会产生这两种酶。在野生型菌株的芽孢形成过程中,DNA酶在碱性磷酸酶出现约1小时后出现。结果表明,DNA酶的产生受一个尚未发现的第二阶段遗传位点控制。