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DNA光解酶和模型系统对嘧啶二聚体的光修复

The photo repair of pyrimidine dimers by DNA photolyase and model systems.

作者信息

Heelis P F, Kim S T, Okamura T, Sancar A

机构信息

North East Wales Institute, Deeside, Clwyd, UK.

出版信息

J Photochem Photobiol B. 1993 Mar;17(3):219-28. doi: 10.1016/1011-1344(93)80019-6.

Abstract

Pyrimidine dimers are eliminated from DNA by a number of different mechanisms known as DNA repair. Photoreactivation, the reversal of the harmful effects of short wavelength radiation by subsequent exposure to longer wavelengths, is one such mechanism. In photoreactivation, the enzyme DNA photolyase utilises light in order to catalyse the cleavage of the cyclobutane ring of the pyrimidine dimer. The results of recent studies of E. coli DNA photolyase and model systems using techniques such as steady state and flash photolysis, time resolved fluorescence and photo CIDNP are surveyed. A mechanism is proposed for the in vitro reaction of E. coli DNA photolyase which involves photoreduction of the FAD radical cofactor followed by electron donation to the dimer from the excited singlet state of reduced FAD.

摘要

嘧啶二聚体通过多种被称为DNA修复的不同机制从DNA中消除。光复活作用,即通过随后暴露于较长波长来逆转短波长辐射的有害影响,就是这样一种机制。在光复活作用中,DNA光解酶利用光来催化嘧啶二聚体环丁烷环的裂解。本文综述了利用稳态和闪光光解、时间分辨荧光和光化学诱导动态核极化等技术对大肠杆菌DNA光解酶和模型系统的最新研究结果。本文提出了一种大肠杆菌DNA光解酶体外反应的机制,该机制涉及黄素腺嘌呤二核苷酸(FAD)自由基辅因子的光还原,随后从还原型FAD的激发单重态向二聚体供电子。

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