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[193纳米波长激光照射诱导的质粒DNA链断裂]

[Plasmid DNA strand breaks induced by laser irradiation of 193 nm wavelength].

作者信息

Gurzadian G G, Schulte-Frohlinde D

机构信息

Max-Planck Institute of Radiation Chemistry, Mühlheim-on-Ruhr, Germany.

出版信息

Biofizika. 1996 Sep-Oct;41(5):1033-7.

PMID:9011183
Abstract

DNA of plasmid pBR322 irradiated with laser at a wavelength of 193 mm was treated with an extract containing proteins from E.coli K12 AB1157 (wild-type). The enzymes were found to produce single- and double-strand DNA breaks, which was interpreted as a transformation of a portion of cyclobutane pyrimidine dimers and (6-4) photoproducts into nonrepairable single-strand DNA breaks. The products resulted from ionization of DNA, in particular, single-strand breaks, transform to double-strand breaks. A comparison of these data with the data on survival of plasmid upon transformation of E.coli K12 AB1157 enables one to assess the biological significance of single- and double-strand breaks. The inactivation of the plasmid (in AB1157) is mainly determined by the number of directly formed laser-induced single-strand breaks, whereas the contribution of enzymatically produced single- and double-strand breaks is insignificant.

摘要

用波长为193毫米的激光照射质粒pBR322的DNA,然后用含有来自大肠杆菌K12 AB1157(野生型)蛋白质的提取物处理。发现这些酶会产生单链和双链DNA断裂,这被解释为一部分环丁烷嘧啶二聚体和(6 - 4)光产物转化为不可修复的单链DNA断裂。这些产物是由DNA的电离产生的,特别是单链断裂会转化为双链断裂。将这些数据与大肠杆菌K12 AB1157转化时质粒存活的数据进行比较,能够评估单链和双链断裂的生物学意义。质粒(在AB1157中)的失活主要由直接形成的激光诱导单链断裂的数量决定,而酶促产生的单链和双链断裂的贡献微不足道。

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