Collins C J, Guild W R
J Bacteriol. 1972 Jan;109(1):266-75. doi: 10.1128/jb.109.1.266-275.1972.
A marker-specific and strongly temperature-dependent reaction was observed to occur at a time during transformation in Diplococcus pneumoniae after the donor deoxyribonucleic acid (DNA) had acquired single-strand properties and immediately preceding the integration of these strands into the recipient chromosome. Operationally, it was observed as the prevention of an intracellular inactivation process, also described in this paper, which is specific for low molecular weight or for damaged DNA, and which occurs if the recipient cells are held at suboptimal temperatures after the DNA has entered. Brief exposure of the cells to a higher temperature stabilized the DNA against this inactivation, in a two step process. It is the first step which has a strong temperature dependence (DeltaHdouble dagger = 70 kcal/mole, DeltaSdouble dagger = 160 entropy units), is marker specific, and which appears to be reversible. The second step is much less temperature-dependent and overlaps in time the start of integration. The enthalpy and entropy of activation are both consistent with those needed to open a loop of six to eight base pairs in a DNA duplex. It is suggested that these observations may reflect, and provide an assay for, the kinetics of synapsis, which on this model is limited in rate by the appearance of unpaired regions on the recipient duplex.
在肺炎双球菌转化过程中,观察到一种标记特异性且强烈依赖温度的反应,该反应发生在供体脱氧核糖核酸(DNA)获得单链特性之后,且恰好在这些链整合到受体染色体之前。实际上,它表现为对一种细胞内失活过程的抑制,本文也对此进行了描述,这种失活过程针对低分子量或受损的DNA,并且如果在DNA进入后将受体细胞置于次优温度下就会发生。将细胞短暂暴露于较高温度下,可通过两步过程使DNA稳定以抵抗这种失活。第一步具有很强的温度依赖性(ΔH‡ = 70千卡/摩尔,ΔS‡ = 160熵单位),是标记特异性的,并且似乎是可逆的。第二步对温度的依赖性要小得多,并且在时间上与整合开始重叠。活化焓和活化熵都与打开DNA双链体中六到八个碱基对的环所需的数值一致。有人认为,这些观察结果可能反映了突触形成的动力学,并为其提供了一种检测方法,在此模型中,突触形成的速率受受体双链体上未配对区域出现的限制。