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酶激活的4-羟基氨基喹啉1-氧化物产生的可修复致死性DNA损伤。

Reparable lethal DNA damage produced by enzyme-activated 4-hydroxyaminoquinoline 1-oxide.

作者信息

Tanooka H, Tada M

出版信息

Chem Biol Interact. 1975 Jan;10(1):11-8. doi: 10.1016/0009-2797(75)90042-3.

Abstract

4-Hydroxyaminoquinoline 1-oxide (4HAQO), the proximate form of a carcinogen 4-nitroquinoline 1-oxide (4NQO), was activated by 4HAQO-activating enzyme to react with transforming DNA of Bacillus subtilis. Inactivation of the transforming activity proceeded in parallel with the extent of binding of enzyme-activated 4HAQO to DNA. The inactivated DNA was susceptible to host-cell reactivation (Hcr) as judged from the difference in the surviving activity assayed with Hcr plus and Hcr- hosts, indicating the reparability of the DNA damage. The enzymatic binding of 4HAQO did not induce strand breaks in DNA as measured by its sedimentation rate in alkaline sucrose density gradient. It is estimated that the activated 4HAQO binding has almost the same efficiency of inactivating the transforming DNA as pyrimidine dimers induced by UV radiation. The results indicate that the activating enzyme is responsible for intracellular reaction of 4HAQO with DNA.

摘要

4-羟基氨基喹啉1-氧化物(4HAQO)是致癌物4-硝基喹啉1-氧化物(4NQO)的直接前体形式,它被4HAQO激活酶激活后与枯草芽孢杆菌的转化DNA发生反应。转化活性的失活与酶激活的4HAQO与DNA的结合程度平行进行。从用Hcr+和Hcr-宿主测定的存活活性差异判断,失活的DNA易于被宿主细胞再激活(Hcr),这表明DNA损伤具有可修复性。通过其在碱性蔗糖密度梯度中的沉降速率测量,4HAQO的酶促结合未诱导DNA链断裂。据估计,激活的4HAQO结合使转化DNA失活的效率与紫外线辐射诱导的嘧啶二聚体几乎相同。结果表明,激活酶负责4HAQO在细胞内与DNA的反应。

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