Doshi Rupak, Day Philip J R, Tirelli Nicola
School of Translational Medicine, Manchester Interdisciplinary Biocentre, University of Manchester, Manchester, UK.
Biochem Soc Trans. 2009 Apr;37(Pt 2):466-70. doi: 10.1042/BST0370466.
Nucleic acids are routinely and readily analysed using the A(260)/A(280) ratio, although this method is known to be prone to erroneous results owing to contaminants in solution that absorb at similar wavelengths. The aim of the present review, while highlighting the problems and alternatives of using UV spectrophotometry for nucleic acid measurements, is to bring forth an observational result from our recent studies, namely that DO (dissolved oxygen) and nitrogen can alter the A(260) of aqueous DNA solutions. Our finding is of importance because DO is highly variable between protocols and storage conditions of DNA preparations. The physicochemical nature of the oxygen-DNA interactions is briefly discussed.
核酸通常很容易通过A(260)/A(280)比值进行分析,尽管已知该方法由于溶液中在相似波长处有吸收的污染物而容易产生错误结果。本综述的目的,在强调使用紫外分光光度法进行核酸测量的问题和替代方法的同时,是要提出我们最近研究的一个观察结果,即溶解氧(DO)和氮会改变DNA水溶液的A(260)。我们的发现很重要,因为溶解氧在DNA制备的方案和储存条件之间变化很大。本文简要讨论了氧与DNA相互作用的物理化学性质。