Wiegand R C, Godson G N, Radding C M
J Biol Chem. 1975 Nov 25;250(22):8848-55.
Conditions are described for digesting single-stranded DNA by S1 nuclease without introducing breaks in double-stranded DNA. The enzyme is inhibited by low concentrations of various compounds of phosphate. Under certain conditions S1 nuclease cleaves the strand opposite a nick in bacteriophage T5 DNA; under other conditions, the enzyme cleaves a loop in one strand of heteroduplex lambdaDNA while leaving the opposite strand intact. S1 nuclease makes many single strand breaks in ultraviolet-irradiated duplex lambdaDNA. Superhelical DNA of phiX174 (Form I) is converted first to a relaxed circular molecule (Form II), and then to a linear molecule (Form III) by cleavage at one site per molecule. Since the cleavage occurs at many sites in the population of molecules, the partially single-stranded regions in phiX174 superhelical DNA are not determined by specific nucleotide sequences.
本文描述了利用S1核酸酶消化单链DNA的条件,同时不会在双链DNA中引入断裂。该酶会被低浓度的各种磷酸盐化合物抑制。在特定条件下,S1核酸酶会切割噬菌体T5 DNA中与切口相对的链;在其他条件下,该酶会切割异源双链λDNA一条链中的环,而另一条链保持完整。S1核酸酶会在紫外线照射的双链λDNA中产生许多单链断裂。φX174的超螺旋DNA(形式I)首先转化为松弛的环状分子(形式II),然后通过每个分子在一个位点的切割转化为线性分子(形式III)。由于切割发生在分子群体的许多位点,因此φX174超螺旋DNA中的部分单链区域不是由特定的核苷酸序列决定的。