Davis A W, Phillips D R
Biochem J. 1978 Jul 1;173(1):179-83. doi: 10.1042/bj1730179.
Concentrated solutions of low-molecular-weight DNA (Mw=35000) with a known molecular-weight distribution can be prepared in several hours, and require no additional fractionation procedures. This is achieved by sonication of the DNA in 1.0 M-NaCl at high power at 0--2 degrees C. No denaturation of the DNA is detectable, even after 8h of continuous sonication. After 2h, the molecular-weight distribution of the total DNA sample is that of the most probably Schulz distribution, described by-Mn:-Mw:-Mz ...=1:2:3 ...etc. Such a molecular-weight distribution is expected for a random break-up of indefinitely long macromolecules and indicates that the sonication process is essentially by random double-strand scission. DNA was also sonicated in the presence of ligands capable of modifying the DNA tertiary structure. The results support the idea that inflexibility of the DNA is required for efficient sonic degradation.
具有已知分子量分布的低分子量DNA(Mw = 35000)浓缩溶液可在数小时内制备完成,且无需额外的分级分离程序。这是通过在0 - 2摄氏度下以高功率对1.0 M - NaCl中的DNA进行超声处理来实现的。即使连续超声处理8小时后,也未检测到DNA变性。2小时后,总DNA样品的分子量分布符合最可能的舒尔茨分布,即-Mn:-Mw:-Mz ... = 1:2:3 ... 等。这种分子量分布是无限长的大分子随机断裂所预期的,表明超声处理过程本质上是通过随机双链断裂实现的。DNA也在能够修饰DNA三级结构的配体存在下进行超声处理。结果支持了高效超声降解需要DNA具有刚性的观点。