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[志贺氏菌甲基化过程及DNA甲基化酶特异性研究]

[Study of the methylation process and DNA methylase specificity in Shigella].

作者信息

Nikol'skaia I I, Tediashvili M I, Chanishvili T G, Debov S S

出版信息

Biokhimiia. 1978 Jul;43(7):1228-32.

PMID:359056
Abstract

The nature and content of minor bases in DNA of 3 Shigella strains are investigated. DNAs from Shigella stutzeri 2, Sh. sonnei 1188 and Sh. sonnei 311 are found to contain 0.43, 0.56 and 0.45 mol.% of N6-methyladenine respectively. 5-methylcytosine (0.16 mol.%) is discovered in Sh. sonnei 311. Substrate specificity of adenine methylase from Sh. sonnei 1188 with respect to phage DNAs of different host modification is investigated. Recognition sites for guanine methylase of DDVI phage and for adenine methylase of Sh. sonnei 1188 turned to be different. DNA of DDII phage grown in Sh. stutzeri 2 cells does not accept methyl groups under the treatment with Sh. sonnei 1188 extracts, but it is methylated by Escherichia coli extract. Adenine methylases of Sh. sonnei 1188 and Sh. stutzeri 2 are suggested to be either the same enzyme, or enzymes, which recognition sites are partially overlapped.

摘要

对3株志贺氏菌DNA中微量碱基的性质和含量进行了研究。发现斯氏志贺氏菌2、宋内氏志贺氏菌1188和宋内氏志贺氏菌311的DNA分别含有0.43、0.56和0.45摩尔%的N6-甲基腺嘌呤。在宋内氏志贺氏菌311中发现了5-甲基胞嘧啶(0.16摩尔%)。研究了宋内氏志贺氏菌1188的腺嘌呤甲基化酶对不同宿主修饰的噬菌体DNA的底物特异性。DDVI噬菌体的鸟嘌呤甲基化酶和宋内氏志贺氏菌1188的腺嘌呤甲基化酶的识别位点不同。在斯氏志贺氏菌2细胞中生长的DDII噬菌体DNA在用宋内氏志贺氏菌1188提取物处理时不接受甲基基团,但它被大肠杆菌提取物甲基化。推测宋内氏志贺氏菌1188和斯氏志贺氏菌2的腺嘌呤甲基化酶要么是同一种酶,要么是识别位点部分重叠的酶。

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