Canadian Research Institute for Food Safety, University of Guelph, 43 McGilvray Street, Guelph, Ontario N1G 2W1, Canada.
Appl Environ Microbiol. 2010 Jan;76(2):528-35. doi: 10.1128/AEM.02294-09. Epub 2009 Nov 30.
A method was developed for oriented immobilization of bacteriophage T4 through introduction of specific binding ligands into the phage head using a phage display technique. Fusion of the biotin carboxyl carrier protein gene (bccp) or the cellulose binding module gene (cbm) with the small outer capsid protein gene (soc) of T4 resulted in expression of the respective ligand on the phage head. Recombinant bacteriophages were characterized in terms of infectivity. It was shown that both recombinant phages retain their lytic activity and host range. However, phage head modification resulted in a decreased burst size and an increased latent period. The efficiency of bacteriophage immobilization with streptavidin-coated magnetic beads and cellulose-based materials was investigated. It was shown that recombinant bacteriophages form specific and strong bonds with their respective solid support and are able to specifically capture and infect the host bacterium. Thus, the use of immobilized BCCP-T4 bacteriophage for an Escherichia coli B assay using a phage multiplication approach and real-time PCR allowed detection of as few as 800 cells within 2 h.
开发了一种方法,通过噬菌体展示技术将特定结合配体引入噬菌体头部,从而实现噬菌体 T4 的定向固定化。将生物素羧基载体蛋白基因 (bccp) 或纤维素结合模块基因 (cbm) 与 T4 的小外壳蛋白基因 (soc) 融合,导致相应配体在噬菌体头部表达。对重组噬菌体的感染力进行了表征。结果表明,两种重组噬菌体均保持其裂解活性和宿主范围。然而,噬菌体头部的修饰导致爆发大小减小,潜伏期增加。研究了用链霉亲和素包被的磁性珠和基于纤维素的材料固定噬菌体的效率。结果表明,重组噬菌体与其各自的固相载体形成特异性强的结合,并能够特异性地捕获和感染宿主菌。因此,使用固定化 BCCP-T4 噬菌体通过噬菌体增殖法和实时 PCR 对大肠杆菌 B 进行检测,在 2 小时内可检测到低至 800 个细胞。