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在铜离子(Cu2+)存在的情况下,抗坏血酸引起的DNA损伤会诱发突变。

DNA damage caused by ascorbate in the presence of Cu2+ induces mutations.

作者信息

Kobayashi S, Yoshida K, Ueda K, Sakai H, Komano T

机构信息

Department of Agricultural Chemistry, Kyoto University, Japan.

出版信息

Nucleic Acids Symp Ser. 1988(19):29-32.

PMID:3067217
Abstract

The DNA damage induced by ascorbate in the presence of Cu2+ was analyzed by sequencing, and the mutagenic consequences of damages to plasmid pUC18 lacZ' were assayed in a forward repairing system in E. coli JM109 in vivo. Ascorbate induced two classes of DNA damage in the presence of Cu2+, one being non-base-specific direct strand cleavage, and the other being sequence-specific base modification labile to alkali treatment. Radicals generated from ascorbate hydroperoxide were involved in DNA damaging reactions. Ascorbate and Cu2+ caused mutations in pUC18 lacZ' gene. The mutation frequency by this method was about 10(-4) at 18% survivors when measured as a loss of alpha-complementation. All the mutations found were single-base substitutions that occurred in the structural part of the lacZ' gene. They were predominantly G:C----A:T transitions.

摘要

通过测序分析了抗坏血酸在Cu2+存在下诱导的DNA损伤,并在大肠杆菌JM109的体内正向修复系统中检测了对质粒pUC18 lacZ'的损伤所产生的诱变后果。抗坏血酸在Cu2+存在下诱导了两类DNA损伤,一类是非碱基特异性的直接链断裂,另一类是对碱处理不稳定的序列特异性碱基修饰。抗坏血酸氢过氧化物产生的自由基参与了DNA损伤反应。抗坏血酸和Cu2+导致pUC18 lacZ'基因发生突变。当以α-互补缺失来衡量时,用这种方法测得的突变频率在18%存活者中约为10(-4)。发现的所有突变都是发生在lacZ'基因结构部分的单碱基替换。它们主要是G:C----A:T转换。

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