Suppr超能文献

肠出血性大肠杆菌噬菌体VT-2 dam甲基转移酶的克隆

Cloning of enterohemorrhagic Escherichia coli phage VT-2 dam methyltransferase.

作者信息

Radlinska M, Bujnicki J M

机构信息

Institute of Microbiology, University of Warsaw, Warszawa, Poland.

出版信息

Acta Microbiol Pol. 2001;50(2):161-7.

Abstract

Enterobacterial GATC-specific DNA adenine methyltransferase (Dam) plays an essential role in regulation of DNA replication, methyl-directed mismatch repair, transposition and gene expression. In Salmonella typhimurium it has been shown to directly control virulence. In this paper we report cloning and expression of the dam gene from the Shiga toxin-producing VT2-Sa prophage of enterohemorrhagic Escherichia coli O157. Comparisons of the predicted amino acid sequence indicates that Dam methyltransferases of E. coli phages VT2-Sa, 933W, T1 and Haemophilus influenzae phage HP1 make up a separate subgroup of adenine-N6 methyltransferases. These proteins are similar to the gamma subfamily of amino-methyltransferases in respect to the linear order of sequence motifs and the presence of the hallmark "NPPY" tetrapeptide. However, they apparently lack an autonomous target-recognizing domain at the C-terminus of the catalytic domain and therefore we propose to dub them as a "mini-gamma" subfamily.

摘要

肠道细菌特异性GATC DNA腺嘌呤甲基转移酶(Dam)在DNA复制、甲基定向错配修复、转座和基因表达的调控中发挥着重要作用。在鼠伤寒沙门氏菌中,它已被证明可直接控制毒力。在本文中,我们报道了从产志贺毒素的肠出血性大肠杆菌O157的VT2-Sa原噬菌体中克隆和表达dam基因。预测氨基酸序列的比较表明,大肠杆菌噬菌体VT2-Sa、933W、T1和流感嗜血杆菌噬菌体HP1的Dam甲基转移酶构成了腺嘌呤-N6甲基转移酶的一个独立亚组。就序列基序的线性顺序和标志性“NPPY”四肽的存在而言,这些蛋白质类似于氨基甲基转移酶的γ亚家族。然而,它们在催化结构域的C末端显然缺乏一个自主的靶标识别结构域,因此我们建议将它们称为“微型γ”亚家族。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验