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从番茄大芽和澳大利亚植原体菌株中分离出的染色体外DNA。

Extrachromosomal DNA isolated from tomato big bud and Candidatus Phytoplasma australiense phytoplasma strains.

作者信息

Tran-Nguyen L T T, Gibb K S

机构信息

Charles Darwin University, Darwin, NT 0909, Australia.

出版信息

Plasmid. 2006 Nov;56(3):153-66. doi: 10.1016/j.plasmid.2006.05.009. Epub 2006 Aug 1.

Abstract

The nucleotide sequences of two extrachromosomal elements from tomato big bud (TBB) and one extrachromosomal element from Candidatus Phytoplasma australiense (Ca. P. australiense) phytoplasmas were determined. Both TBB plasmids (3319 and 4092 bp) contained an open reading frame ( approximately 570 bp) with homology to the rolling circle replication initiator protein (Rep). This gene was shorter than the rep genes identified from other phytoplasma plasmids, geminiviruses and bacterial plasmids. Both TBB extrachromosomal DNAs (eDNAs) encoded a putative DNA primase (dnaG) gene, a chromosomal gene required for DNA replication and which contains the conserved topoisomerase/primase domain. We speculate that the replication mechanism for the TBB phytoplasma eDNA involves the dnaG gene instead of the rep gene. The Ca. P. australiense eDNA (3773 bp) was shown to be circular and contained four open reading frames. The rep gene was encoded on ORF 1 and had homology to both plasmid (pLS1) and geminivirus-like domains.

摘要

测定了来自番茄巨芽病(TBB)的两个染色体外元件以及来自澳大利亚植原体(Ca. P. australiense)植原体的一个染色体外元件的核苷酸序列。两个TBB质粒(3319和4092 bp)均含有一个与滚环复制起始蛋白(Rep)具有同源性的开放阅读框(约570 bp)。该基因比从其他植原体质粒、双生病毒和细菌质粒中鉴定出的rep基因短。两个TBB染色体外DNA(eDNA)均编码一个假定的DNA引物酶(dnaG)基因,这是DNA复制所需的一个染色体基因,且含有保守的拓扑异构酶/引物酶结构域。我们推测,TBB植原体eDNA的复制机制涉及dnaG基因而非rep基因。澳大利亚植原体eDNA(3773 bp)呈环状,包含四个开放阅读框。rep基因在开放阅读框1上编码,与质粒(pLS1)和双生病毒样结构域均具有同源性。

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