Oriented Immobilization of Bacteriophages for Biosensor Applications

被引:91
作者
Tolba, M. [1 ]
Minikh, O. [1 ,2 ]
Brovko, L. Y. [1 ]
Evoy, S. [3 ,4 ]
Griffiths, M. W. [1 ]
机构
[1] Univ Guelph, Canadian Res Inst Food Safety, Guelph, ON N1G 2W1, Canada
[2] Moscow MV Lomonosov State Univ, Dept Chem Enzymol, Fac Chem, Moscow 119911, Russia
[3] Univ Alberta, Dept Elect & Comp Engn, Edmonton, AB T6G 2V4, Canada
[4] Univ Alberta, Natl Inst Nanotechnol, Edmonton, AB T6G 2V4, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
CARBOHYDRATE-BINDING MODULE; ESCHERICHIA-COLI; IN-VIVO; BIOTIN CARBOXYLASE; PHAGE-T4; PROTEINS; DISPLAY; SOC; BIOTINYLATION; SEPARATION;
D O I
10.1128/AEM.02294-09
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
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.
引用
收藏
页码:528 / 535
页数:8
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