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The effect of several nucleic acid binding drugs on the cleavage of d(GGAATTCC) and pBR 322 by the Eco RI restriction endonuclease.

机译:几种核酸结合药物对Eco RI限制性内切核酸酶切割d(GGAATTCC)和pBR 322的影响。

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摘要

The endonucleolytic action of the EcoRI restriction enzyme on the double-stranded oligonucleotide d(GGAATTCC) and the supercoiled plasmid DNA pBR 233 is inhibited by actinomycin D, ethidium bromide, proflavin, distamycin A and netropsin. Half-maximal inhibition is observed at around 100 microM concentrations for the intercalating drugs, and around 0.1 to 1 microM concentrations for netropsin and distamycin A. The inhibitory activity of these drugs can be correlated with their affinity to the oligonucleotide and the plasmid DNA. Since at high concentrations of the drugs a complete inhibition is observed, it is concluded that the effect of the drugs on the stereochemistry of the EcoRI site is such that recognition is excluded.
机译:EcoRI限制性内切酶对双链寡核苷酸d(GGAATTCC)和超螺旋质粒DNA pBR 233的内切核酸作用受到放线菌素D,溴化乙锭,前黄素,双霉素A和Netropsin的抑制。对于插层药物,在约100 microM的浓度下观察到最大抑制作用的一半,对于Netropsin和Distamycin A,约有0.1至1 microM的浓度观察到。这些药物的抑制活性可能与它们对寡核苷酸和质粒DNA的亲和力有关。由于在高浓度的药物中观察到了完全的抑制作用,因此得出结论,药物对EcoRI位点的立体化学的影响使得识别被排除。

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