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一条涉及新型卡那霉素抗性转座子Tn4352的质粒NTP16的进化途径。

A pathway for the evolution of the plasmid NTP16 involving the novel kanamycin resistance transposon Tn4352.

作者信息

Wrighton C J, Strike P

出版信息

Plasmid. 1987 Jan;17(1):37-45. doi: 10.1016/0147-619x(87)90006-0.

Abstract

The kanamycin resistance determinant of the drug resistance plasmid NTP16 has been characterized by DNA sequencing and has been shown to possess all of the structural features of a transposable element. It is made up of a 1040-bp central region encoding a protein identical to the aminoglycoside 3'-phosphotransferase of Tn903, flanked by direct repeats of an element identical to IS26. This novel transposon has been designated Tn4352. Analysis of the host sequences flanking the transposon reveal that they are derived from a Tn3-like element, and contain no 8 base pair target size duplications which are normally created by the insertion of IS26-like elements. Comparison to the Tn3 sequence shows that the flanking sequences are noncontiguous within Tn3, with the clear implication that NTP16 has evolved from a similar plasmid encoding only ampicillin resistance (presumably NTP1) by the insertion of Tn4352 into the Tn3-like element, followed by a substantial deletion. The sequence analysis suggests that the initial insertion was into the tnpR gene of the ampicillin transposon, followed by a deletion extending to a specific site within tnpA.

摘要

耐药质粒NTP16的卡那霉素抗性决定簇已通过DNA测序进行了表征,并已显示具有转座元件的所有结构特征。它由一个1040bp的中心区域组成,该区域编码一种与Tn903的氨基糖苷3'-磷酸转移酶相同的蛋白质,两侧是与IS26相同元件的正向重复序列。这个新的转座子被命名为Tn4352。对转座子两侧宿主序列的分析表明,它们源自一个类似Tn3的元件,并且不包含通常由类似IS26元件插入产生的8个碱基对的靶标大小重复序列。与Tn3序列的比较表明,侧翼序列在Tn3内是不连续的,这清楚地表明NTP16是由一个仅编码氨苄青霉素抗性的类似质粒(可能是NTP1)通过将Tn4352插入到类似Tn3的元件中,随后进行大量缺失而进化而来的。序列分析表明,最初的插入是进入氨苄青霉素转座子的tnpR基因,随后是延伸到tnpA内特定位点的缺失。

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