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Genome and proteome analysis of 7-7-1, a flagellotropic phage infecting Agrobacterium sp H13-3

机译:感染农杆菌sp H13-3的鞭毛噬菌体7-1-7-1的基因组和蛋白质组分析

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摘要

ABSTRACT: BACKGROUND: The flagellotropic phage 7-7-1 infects motile cells of Agrobacterium sp H13-3 by attaching to and traveling along the rotating flagellar filament to the secondary receptor at the base, where it injects its DNA into the host cell. Here we describe the complete genomic sequence of 69,391 base pairs of this unusual bacteriophage. METHODS: The sequence of the 7-7-1 genome was determined by pyro(454)sequencing to a coverage of 378-fold. It was annotated using MyRAST and a variety of internet resources. The structural proteome was analyzed by SDS-PAGE coupled electrospray ionization-tandem mass spectrometry (MS/MS). RESULTS: Sequence annotation and a structural proteome analysis revealed 127 open reading frames, 84 of which are unique. In six cases 7-7-1 proteins showed sequence similarity to proteins from the virulent Burkholderia myovirus BcepB1A. Unique features of the 7-7-1 genome are the physical separation of the genes encoding the small (orf100) and large (orf112) subunits of the DNA packaging complex and the apparent lack of a holin-lysin cassette. Proteomic analysis revealed the presence of 24 structural proteins, five of which were identified as baseplate (orf7), putative tail fibre (orf102), portal (orf113), major capsid (orf115) and tail sheath (orf126) proteins. In the latter case, the N-terminus was removed during capsid maturation, probably by a putative prohead protease (orf114).
机译:摘要:背景:鞭毛噬菌体7-7-1通过附着并沿着旋转的鞭毛丝行进至碱基的次级受体,并将其DNA注入宿主细胞,从而感染农杆菌H13-3的运动细胞。在这里,我们描述了这种不寻常的噬菌体的69,391个碱基对的完整基因组序列。方法:通过pyro(454)测序确定了7-7-1基因组的序列,覆盖率为378倍。使用MyRAST和各种Internet资源进行了注释。通过SDS-PAGE耦合电喷雾电离串联质谱(MS / MS)分析结构蛋白质组。结果:序列注释和结构蛋白质组分析揭示了127个开放阅读框,其中84个是独特的。在六种情况下,7-7-1蛋白与有毒的伯克霍尔德氏菌肌病毒BcepB1A的蛋白具有序列相似性。 7-7-1基因组的独特特征是编码DNA包装复合物的小(orf100)和大(orf112)亚基的基因的物理分离,以及明显缺乏霍林-溶素盒。蛋白质组学分析显示存在24种结构蛋白,其中5种被鉴定为基板(orf7),推定的尾纤维(orf102),门脉(orf113),主要衣壳(orf115)和尾鞘(orf126)蛋白。在后一种情况下,衣壳成熟过程中可能通过推定的前额蛋白酶(orf114)去除了N末端。

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