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铜离子(II)使pBR322质粒DNA对UV - B(280 - 315纳米)诱导的失活作用敏感。

Cu(II) sensitizes pBR322 plasmid DNA to inactivation by UV-B (280-315 nm).

作者信息

Lloyd R E, Larson R A, Adair T L, Tuveson R W

机构信息

Department of Microbiology, University of Illinois at Urbana-Champaign 61801.

出版信息

Photochem Photobiol. 1993 Jun;57(6):1011-7. doi: 10.1111/j.1751-1097.1993.tb02964.x.

Abstract

Copper(II), in the presence of UV-B radiation (280-315 nm), can generate single-strand breaks in the sugar-phosphate backbone of pBR322 plasmid DNA. A low level of single-strand backbone breaks occurs in the presence of Cu(II) alone, but UV-B irradiation increases the rate by the more than 100-fold. Concomitant with the damage to the DNA backbone is a loss of transforming activity. Oxygen is required for generation of the single-strand breaks but not for the loss of transforming activity. A DNA glycosylase (Fpg), which participates in the repair of certain DNA nitrogenous base damage, does not repair plasmid DNA damaged by Cu(II). The hydroxyl radical scavenging compound DMSO is only somewhat effective at protecting the physical and biological properties of the DNA. These results with Cu(II) are compared to those obtained previously with pBR322 plasmid DNA in the presence of Fe(III) and UV-A.

摘要

在紫外线B辐射(280 - 315纳米)存在的情况下,铜(II)可在pBR322质粒DNA的糖 - 磷酸主链上产生单链断裂。仅在铜(II)存在时会发生低水平的单链主链断裂,但紫外线B照射会使断裂速率增加100倍以上。与DNA主链损伤相伴的是转化活性的丧失。产生单链断裂需要氧气,但转化活性的丧失不需要氧气。一种参与修复某些DNA含氮碱基损伤的DNA糖基化酶(Fpg),不能修复被铜(II)损伤的质粒DNA。羟基自由基清除化合物二甲基亚砜在保护DNA的物理和生物学特性方面仅略有成效。将这些铜(II)的实验结果与之前在铁(III)和紫外线A存在的情况下用pBR322质粒DNA所获得的结果进行了比较。

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