Orrego C, Arnaud M, Halvorsen H O
J Bacteriol. 1978 Jun;134(3):973-81. doi: 10.1128/jb.134.3.973-981.1978.
Transforming activity released in sequential genetic order during the first synchronous cycle of DNA replication during outgrowth of spores of Bacillus subtilis 168 was investigated. A transformation assay was used consisting of outgrowing spores as DNA donors and multiply marked competent cells as recipients. DNA synthesis inhibitors known to stop DNA release were used during and subsequent to DNA transfer to recipient cells. The released DNA sedimented with the outgrowing cells after low-speed centrifugation, and it was discovered that markers released both early and late were resistant to up to 500 microgram of deoxyribonuclease per ml under conditions in which the transforming capacity of purified DNA was eliminated by 5 microgram of the nuclease per ml. Inaccessibility to deoxyribonuclease was increased and maintained during the transformation event while detergents and proteolytic attack did not expose the released chromosome to nuclease action. The results indicate that tight physical contact between outgrowing spores and competent cells is required for transformation in this system.
研究了枯草芽孢杆菌168孢子萌发过程中,在DNA复制的第一个同步周期按顺序遗传释放的转化活性。采用了一种转化试验,以萌发的孢子作为DNA供体,以多重标记的感受态细胞作为受体。在DNA转移至受体细胞期间及之后,使用了已知能阻止DNA释放的DNA合成抑制剂。低速离心后,释放的DNA与萌发的细胞一起沉淀,并且发现在每毫升5微克核酸酶可消除纯化DNA转化能力的条件下,早期和晚期释放的标记物对每毫升高达500微克的脱氧核糖核酸酶具有抗性。在转化过程中,脱氧核糖核酸酶的不可及性增加并得以维持,而洗涤剂和蛋白水解攻击并未使释放的染色体暴露于核酸酶作用之下。结果表明,该系统中的转化需要萌发的孢子与感受态细胞之间紧密的物理接触。