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The generalized transducing Salmonella bacteriophage ES18: Complete genome sequence and DNA packaging strategy

机译:广义转导沙门氏菌噬菌体ES18:完整的基因组序列和DNA包装策略

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摘要

The generalized transducing double-stranded DNA bacteriophage ES18 has an icosahedral head and a long noncontractile tail, and it infects both rough and smooth Salmonella enterica strains. We report here the complete 46,900-bp genome nucleotide sequence and provide an analysis of the sequence. Its 79 genes and their organization clearly show that ES18 is a member of the lambda-like (lambdoid) phage group; however, it contains a novel set of genes that program assembly of the virion head. Most of its integration-excision, immunity, Nin region, and lysis genes are nearly identical to those of the short-tailed Salmonella phage P22, while other early genes are nearly identical to Escherichia coli phages λ and HK97, S. enterica phage ST64T, or a Shigella flexneri prophage. Some of the ES18 late genes are novel, while others are most closely related to phages HK97, lambda, or N15. Thus, the ES18 genome is mosaically related to other lambdoid phages, as is typical for all group members. Analysis of virion DNA showed that it is circularly permuted and about 10% terminally redundant and that initiation of DNA packaging series occurs across an approximately 1-kbp region rather than at a precise location on the genome. This supports a model in which ES18 terminase can move substantial distances along the DNA between recognition and cleavage of DNA destined to be packaged. Bio-informatic analysis of large terminase subunits shows that the different functional classes of phage-encoded terminases can usually be predicted from their amino acid sequence.
机译:通用的转导双链DNA噬菌体ES18具有二十面体头部和长长的不收缩尾巴,可同时感染粗糙和光滑的肠沙门氏菌菌株。我们在这里报告了完整的46,900-bp基因组核苷酸序列,并对序列进行了分析。它的79个基因及其组织清楚地表明,ES18是λ样(lambdoid)噬菌体组的成员。然而,它包含了一套新的基因,可对病毒体头部的装配进行编程。它的大部分整合切除,免疫,Nin区和裂解基因与短尾沙门氏菌噬菌体P22几乎相同,而其他早期基因则与大肠杆菌噬菌体λ和HK97,肠炎沙门氏菌噬菌体ST64T几乎相同。或弗氏志贺氏菌的预言。 ES18晚期基因中的一些是新基因,而其他一些与噬菌体HK97,λ或N15最相关。因此,ES18基因组与其他lambdoid噬菌体在马赛克上相关,这对于所有小组成员都是典型的。对病毒粒子DNA的分析表明,它是环状排列的,末端约有10%冗余,DNA包装序列的起始发生在大约1-kbp区域,而不是基因组上的精确位置。这支持了一种模型,在该模型中,ES18末端酶可以在DNA的识别和切割之间注定要沿包装的DNA方向移动相当长的距离。大型末端酶亚基的生物信息学分析表明,通常可以从它们的氨基酸序列预测噬菌体编码的末端酶的不同功能类别。

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