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通过分析T5和BF23的杂交噬菌体来鉴定宿主受体特异性的噬菌体基因。

Identification of the phage gene for host receptor specificity by analyzing hybrid phages of T5 and BF23.

作者信息

Heller K J

出版信息

Virology. 1984 Nov;139(1):11-21. doi: 10.1016/0042-6822(84)90325-8.

Abstract

The closely related coliphages T5 and BF23 differ in the receptor used for adsorption to cells. In order to identify phage genes encoding host receptor specificity, hybrid phages were isolated from crosses of T5 and BF23. These hybrid phages were analyzed for their protein composition, kinetics of adsorption to various bacterial strains, and DNA restriction maps. Analyses of the protein compositions of purified tails suggested that only one tail protein was involved in the expression of host specificity. In T5 tails this protein was identified as a minor tail protein of an apparent molecular weight of 67K. A corresponding BF23 protein could not be detected. The DNA region encoding structural proteins was analyzed by digestion with the restriction enzymes BamHI, HindIII, and PstI. The distribution of restriction sites in these recombinants implied that the region affecting host specificity was located at ca. 90% of the T5 genome length. Evidence is presented that this gene is identical to the oad gene previously described (K.J. Heller and D. Bryniok (1984), J. Virol. 49, 20-25). The location of other genes encoding tail proteins is discussed.

摘要

密切相关的大肠杆菌噬菌体T5和BF23在吸附细胞所使用的受体方面存在差异。为了鉴定编码宿主受体特异性的噬菌体基因,从T5和BF23的杂交中分离出了杂交噬菌体。对这些杂交噬菌体进行了蛋白质组成分析、对各种细菌菌株的吸附动力学分析以及DNA限制性图谱分析。对纯化尾部的蛋白质组成分析表明,只有一种尾部蛋白质参与宿主特异性的表达。在T5尾部,这种蛋白质被鉴定为一种表观分子量为67K的次要尾部蛋白质。未检测到相应的BF23蛋白质。通过用限制性内切酶BamHI、HindIII和PstI消化来分析编码结构蛋白质的DNA区域。这些重组体中限制性位点的分布表明,影响宿主特异性的区域位于T5基因组长度的约90%处。有证据表明,该基因与先前描述的oad基因相同(K.J. 赫勒和D. 布里尼奥克(1984年),《病毒学杂志》49卷,20 - 25页)。还讨论了其他编码尾部蛋白质的基因的位置。

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