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来自谷氨酸棒杆菌的一个新插入序列IS14999。

A new insertion sequence, IS14999, from Corynebacterium glutamicum.

作者信息

Tsuge Yota, Ninomiya Kana, Suzuki Nobuaki, Inui Masayuki, Yukawa Hideaki

机构信息

Graduate School of Biological Sciences, Nara Institute of Science and Technology (NAIST), Ikoma, Nara 630-0101, Japan.

Research Institute of Innovative Technology for the Earth (RITE), 9-2 Kizugawadai, Kizu-cho Soraku-gun, Kyoto 619-0292, Japan.

出版信息

Microbiology (Reading). 2005 Feb;151(Pt 2):501-508. doi: 10.1099/mic.0.27567-0.

Abstract

A new insertion sequence from Corynebacterium glutamicum ATCC 14999 was isolated and characterized. This IS element, designated IS14999, comprised a 1149 bp nucleotide sequence with 22 bp imperfect terminal inverted repeats. IS14999 carries a single open reading frame of 345 amino acids encoding a putative transposase that appears to have partial homology to IS642, an IS630/Tc1 superfamily element, at the C-terminal region in the amino acid sequence. This indicated that IS14999 belonged to the IS630/Tc1 superfamily, which was first identified in C. glutamicum. IS14999 has a unique distance of 38 amino acid residues between the second and third amino acids in the DDE motif, which is well known as the catalytic centre of transposase. This suggested that IS14999 constituted a new subfamily of the IS630/Tc1 superfamily. A phylogenetic tree constructed on the basis of amino acid sequences of transposases revealed that this new transposable element was more similar to eukaryotic Tc1/mariner family elements than to prokaryotic IS630 family elements. Added to the fact that IS14999 was present in only a few C. glutamicum strains, this implies that IS14999 was probably acquired by a recent lateral transfer event from eukaryotic cells. Analysis of the insertion site in C. glutamicum R revealed that IS14999 appeared to transpose at random and always caused a target duplication of a 5'-TA-3' dinucleotide upon insertion, like the other IS630/Tc1 family elements. These findings indicated that IS14999 could be a powerful tool for genetic manipulation of corynebacteria and related species.

摘要

从谷氨酸棒杆菌ATCC 14999中分离并鉴定出一个新的插入序列。这个IS元件被命名为IS14999,由一个1149 bp的核苷酸序列组成,具有22 bp的不完全末端反向重复序列。IS14999携带一个由345个氨基酸组成的单一开放阅读框,编码一种假定的转座酶,该转座酶在氨基酸序列的C末端区域似乎与IS642(一种IS630/Tc1超家族元件)有部分同源性。这表明IS14999属于IS630/Tc1超家族,该超家族首次在谷氨酸棒杆菌中被鉴定出来。IS14999在DDE基序的第二个和第三个氨基酸之间有一个独特的38个氨基酸残基的距离,DDE基序是众所周知的转座酶催化中心。这表明IS14999构成了IS630/Tc1超家族的一个新亚家族。基于转座酶氨基酸序列构建的系统发育树表明,这个新的转座元件与真核Tc1/水手家族元件比与原核IS630家族元件更相似。再加上IS14999仅存在于少数谷氨酸棒杆菌菌株中这一事实,这意味着IS14999可能是最近通过横向转移事件从真核细胞中获得的。对谷氨酸棒杆菌R插入位点的分析表明,IS14999似乎随机转座,并且在插入时总是导致5'-TA-3'二核苷酸的靶标重复,这与其他IS630/Tc1家族元件一样。这些发现表明,IS14999可能是用于棒状杆菌及相关物种基因操作的有力工具。

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