Blake R D, Lefoley S G
Biochim Biophys Acta. 1978 Apr 27;518(2):233-46. doi: 10.1016/0005-2787(78)90180-6.
Derivative melting profiles of DNA have been obtained directly by recording the difference in absorbance between two identical solutions maintained at a small constant temperature differential. This deltaA is monitored continuously with increasing temperature in a ratio recording spectrophotometer. Resolution of complex hyperfine structure in the profiles of small homogeneous viral DNAs appears to be significantly better than has been produced by various numerical methods of differentiation. In addition, a spectral method has been modified that permits easy analysis for DNA base composition from the ratio of derivative melting curves obtained at 282 and 260 nm. Eight bacterial and three vertebrate DNAs have been analyzed for total base composition from the product of the instantaneous base composition at small temperature intervals (0.05 degrees C) throughout the entire melting region and the integrated area of the 282 nm profile. The results are in excellent agreement with values determined by traditional methods.
通过记录保持在微小恒定温差下的两种相同溶液之间的吸光度差异,可直接获得DNA的导数熔解曲线。在比率记录分光光度计中,随着温度升高持续监测这种ΔA。小型同源病毒DNA曲线中复杂超精细结构的分辨率似乎明显优于各种数值微分方法所产生的分辨率。此外,已对一种光谱方法进行了改进,该方法可根据在282和260nm处获得的导数熔解曲线的比率轻松分析DNA碱基组成。通过在整个熔解区域内小温度间隔(0.05℃)下的瞬时碱基组成产物以及282nm曲线的积分面积,对8种细菌DNA和3种脊椎动物DNA的总碱基组成进行了分析。结果与传统方法测定的值非常吻合。