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对梨火疫病菌及其他革兰氏阴性菌中携带链霉素抗性基因的转座子(Tn5393)进行核苷酸序列分析。

Nucleotide sequence analysis of a transposon (Tn5393) carrying streptomycin resistance genes in Erwinia amylovora and other gram-negative bacteria.

作者信息

Chiou C S, Jones A L

机构信息

Department of Botany and Plant Pathology, Michigan State University, East Lansing 48824-1312.

出版信息

J Bacteriol. 1993 Feb;175(3):732-40. doi: 10.1128/jb.175.3.732-740.1993.

Abstract

A class II Tn3-type transposable element, designated Tn5393 and located on plasmid pEa34 from streptomycin-resistant strain CA11 of Erwinia amylovora, was identified by its ability to move from pEa34 to different sites in plasmids pGEM3Zf(+) and pUCD800. Nucleotide sequence analysis reveals that Tn5393 consists of 6,705 bp with 81-bp terminal inverted repeats and generates 5-bp duplications of the target DNA following insertion. Tn5393 contains open reading frames that encode a putative transposase (tnpA) and resolvase (tnpR) of 961 and 181 amino acids, respectively. The two open reading frames are separated by a putative recombination site (res) consisting of 194 bp. Two streptomycin resistance genes, strA and strB, were identified on the basis of their DNA sequence homology to streptomycin resistance genes in plasmid RSF1010. StrA is separated from tnpR by a 1.2-kb insertion element designated IS1133. The tnpA-res-tnpR region of Tn5393 was detected in Pseudomonas syringae pv. papulans Psp36 and in many other gram-negative bacteria harboring strA and strB. Except for some strains of Erwinia herbicola, these other gram-negative bacteria lacked insertion sequence IS1133. The prevalence of strA and strB could be accounted for by transposition of Tn5393 to conjugative plasmids that are then disseminated widely among gram-negative bacteria.

摘要

一种II类Tn3型转座元件,命名为Tn5393,位于来自解淀粉欧文氏菌链霉素抗性菌株CA11的质粒pEa34上,通过其从pEa34转移到质粒pGEM3Zf(+)和pUCD800不同位点的能力得以鉴定。核苷酸序列分析表明,Tn5393由6705 bp组成,具有81 bp的末端反向重复序列,插入后会在靶DNA上产生5 bp的重复序列。Tn5393包含开放阅读框,分别编码推定的转座酶(tnpA)和解离酶(tnpR),它们分别由961和181个氨基酸组成。这两个开放阅读框由一个由194 bp组成的推定重组位点(res)隔开。基于它们与质粒RSF1010中链霉素抗性基因的DNA序列同源性,鉴定出两个链霉素抗性基因strA和strB。StrA与tnpR被一个名为IS1133的1.2 kb插入元件隔开。在丁香假单胞菌pv. papulans Psp36以及许多其他携带strA和strB的革兰氏阴性细菌中检测到了Tn5393的tnpA-res-tnpR区域。除了一些草本欧文氏菌菌株外,这些其他革兰氏阴性细菌缺乏插入序列IS1133。strA和strB的普遍存在可能是由于Tn5393转座到接合性质粒上,然后在革兰氏阴性细菌中广泛传播所致。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ad2/196212/26c4e9cda6ca/jbacter00045-0172-a.jpg

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