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鉴定乳球菌 936 组噬菌体中的双受体结合蛋白系统。

Identification of Dual Receptor Binding Protein Systems in Lactococcal 936 Group Phages.

机构信息

School of Microbiology & APC Microbiome Ireland, University College Cork, Western Road, Cork T12 YT20, Ireland.

Architecture et Fonction des Macromolécules Biologiques, Centre National de la Recherche Scientifique (CNRS), Campus de Luminy, 13288 Marseille, France.

出版信息

Viruses. 2018 Nov 27;10(12):668. doi: 10.3390/v10120668.

Abstract

of the lactococcal 936 group are the most commonly encountered bacteriophages in the dairy processing environment. The 936 group phages possess a discrete baseplate at the tip of their tail-a complex harbouring the Receptor Binding Protein (RBP) which is responsible for host recognition and attachment. The baseplate-encoding region is highly conserved amongst 936 phages, with 112 of 115 publicly available phages exhibiting complete synteny. Here, we detail the three exceptions (Phi4.2, Phi4R15L, and Phi4R16L), which differ from this genomic architecture in possessing an apparent second RBP-encoding gene upstream of the "classical" gene. The newly identified RBP possesses an elongated neck region relative to currently defined 936 phage RBPs and is genetically distinct from defined 936 group RBPs. Through detailed characterisation of the representative phage Phi4.2 using a wide range of complementary techniques, we demonstrated that the above-mentioned three phages possess a complex and atypical baseplate structure. Furthermore, the presence of both RBPs in the tail tip of the mature virion was confirmed, while the anticipated host-binding capabilities of both proteins were also verified.

摘要

乳球菌 936 组噬菌体是乳制品加工环境中最常见的噬菌体。936 组噬菌体在其尾部末端具有离散的基板——一个包含受体结合蛋白 (RBP) 的复杂结构,负责宿主识别和附着。基板编码区域在 936 噬菌体中高度保守,115 个公开可用的噬菌体中有 112 个表现出完全的同线性。在这里,我们详细介绍了三个例外(Phi4.2、Phi4R15L 和 Phi4R16L),它们与这种基因组结构不同,在“经典”基因的上游具有明显的第二个 RBP 编码基因。新鉴定的 RBP 相对于目前定义的 936 噬菌体 RBPs 具有更长的颈区,并且在遗传上与定义的 936 组 RBPs 不同。通过使用多种互补技术对代表性噬菌体 Phi4.2 进行详细表征,我们证明了上述三种噬菌体具有复杂且非典型的基板结构。此外,还证实了成熟病毒粒子的尾部末端存在两个 RBP,同时还验证了这两种蛋白质的预期宿主结合能力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/593b/6315561/67559a96b5d5/viruses-10-00668-g001.jpg

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