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[体内作用于细菌DNA的N-亚硝基甲基脲和N-亚硝基乙基脲诱变效力的差异]

[Differences in the mutagenic effectiveness of N-nitrosomethyl- and N-nitrosoethylurea acting on bacterial DNA in vivo].

作者信息

Vasil'eva S V

出版信息

Genetika. 1976;12(5):149-56.

PMID:789181
Abstract

Chemically induced lethals and reversion frequencies of two mutants of Salmonella typhimurium LT-2 1530 and 1532 were examined. Prototrophic mutants to histidine independence occurred by two different mechanisms and were induced by nitrous acid, hydroxylamine, N-nitrosomethylurea (NMU), N-nitrosoethylurea (NEU) and N, N, nitrosodimethylurea (NDMU). The ability of the mutants to revert was affected by the chemical structure (in the row of N-nitrosoalkylurea - by alkyl group) of the mutagen. NEU is found to induce in bacterial DNA only base pair substitutions; NMU and NDMU - deletions and base pair substitutions. An original model of deletion mechanism with Goldwait endonuclease II participation is proposed.

摘要

对鼠伤寒沙门氏菌LT-2的两个突变体1530和1532的化学诱导致死率和回复突变频率进行了检测。对组氨酸不依赖的原养型突变体通过两种不同机制产生,并由亚硝酸、羟胺、N-亚硝基甲基脲(NMU)、N-亚硝基乙基脲(NEU)和N,N-亚硝基二甲基脲(NDMU)诱导。突变体的回复能力受诱变剂化学结构(在N-亚硝基烷基脲系列中 - 受烷基影响)的影响。发现NEU仅在细菌DNA中诱导碱基对替换;NMU和NDMU - 缺失和碱基对替换。提出了一种有戈德韦特内切核酸酶II参与的缺失机制原始模型。

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