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Characterization of a temperate actinophage,MPphiWR-1, capable of infectingMicromonospora purpurea ATCC 15835
Authors:Bruce C Tilley  Janise L Meyertons  Mary P Lechevalier
Institution:(1) Waksman Institute of Microbiology, Rutgers University, Piscataway, NJ, U.S.A.;(2) Present address: Lederle Labs, American Cyanamid Co., Middletown Rd., 10965 Pearl River, NY;(3) Present address: Cold Spring Harbor Laboratory, P.O. Box 100, 11724 Cold Spring Harbor, NY;(4) Waksman Institute of Microbiology, Rutgers University, P.O. Box 759, 08855-0759 Piscataway, NJ, U.S.A.
Abstract:Summary A temperate actinophage was isolated from soil using the gentamicin-producing microorganism,Micromonospora purpurea ATCC 15835 as host. The characterization of the phage represents the initial step in its development as a cloning vector. The phage isolated, MPphiWR-1, formed red- to purple-pigmented turbid plaques. Cells isolated from these plaques were resistant to superinfection with lytic mutants of MPphiWR-1. Southern blots of genomic DNA from a resistant culture showed that MPphiWR-1 integrated into the host genome. The phage was UV- or Mitomycin C-inducible. The integration, resistance to superinfection and inducibility indicated a lysogenic relationship with the host.Using MPphiE-RCPM, a lytic derivative, the phage host range was demonstrated to include members of three genera: one species each ofAmpullariella andCatellatospora, and 12 species ofMicromonospora. The phage belonged to Ackerman's B1 morphotype having an isometric head and a flexible noncontractile tail. The density of the phage was 1.525 g/cc. Restriction site mapping demonstrated that the phage DNA was 57.9 kb long and had cohesive ends. Using EDTA enrichment, viable mutants with deletions of at least 3.5 kb were isolated and mapped. Phage adsorption, sensitivities and plating efficiency were investigated. Non-liposome PEG-mediated transfection was demonstrated.
Keywords:Bacteriophage  Integration  Deletions  Cohesive ends  Gentamicin  Transfection
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