HIRAOKA T
J Biophys Biochem Cytol. 1957 Jul 25;3(4):525-44. doi: 10.1083/jcb.3.4.525.
A new extraction method for the quantitative determination of the fuchsin contained in a Feulgen-stained nucleoprotein sample has been introduced. The method is based on the following facts: (1) Treatment of a Feulgen-stained nucleoprotein sample with hot acid or alkali brings about a splitting of the linkage between fuchsin-SO(2) and the hydrolyzed nucleic acid moiety of nucleoprotein through aldehyde groups. (2) It also effectuates the formation of fuchsin from the liberated fuchsin-SO(2). (3) The fuchsin is made colorless by the treatment, but is restored to its original pink colored state when the pH of the acidic or alkaline medium is adjusted to 4.6. (4) The fuchsin, either pink colored or decolorized by alkali, can be extracted from an aqueous phase by amyl alcohol. A linear relationship was found to exist between the amount of fuchsin extracted by the FEM from a Feulgen-stained nucleoprotein sample and its DNA content. This relationship holds over a wide range of DNA concentration. From experiments utilizing this method, knowledge may be gained about the mechanism of the Feulgen reaction in situ which can lead to an improvement of the reaction in the field of cytochemistry.
一种用于定量测定福尔根染色核蛋白样品中品红含量的新提取方法已被引入。该方法基于以下事实:(1)用热酸或碱处理福尔根染色的核蛋白样品会导致品红 - SO(2) 与核蛋白水解核酸部分之间通过醛基的键断裂。(2)它还能使释放出的品红 - SO(2) 形成品红。(3)处理后品红变为无色,但当酸性或碱性介质的pH值调至4.6时,又恢复到原来的粉红色状态。(4)无论是粉红色的品红还是被碱脱色的品红,都可以用戊醇从水相中萃取出来。发现从福尔根染色核蛋白样品中用该方法萃取的品红量与其DNA含量之间存在线性关系。这种关系在很宽的DNA浓度范围内都成立。通过利用该方法进行的实验,可以了解原位福尔根反应的机制,这有助于在细胞化学领域改进该反应。