Literature DB >> 4110105

Isolation and characterization of a bacteriophage tail-like bacteriocin from a strain of Rhizobium.

W Lotz, F Mayer.   

Abstract

Bacterial strain 16-3 spontaneously produces a bacteriocin which inhibits the growth of closely related strain 16-2. Both strains were newly isolated from root nodules of lupines and probably belong to the species Rhizobium lupini. Production of infectious progeny of newly isolated virulent phage 16-2-4 in strain 16-2 is inhibited completely if complexes are bacteriocin-treated during the first half of the latent period. Treatment begun during the second half leads to premature lysis of complexes and inactivates only those progeny phages which were not yet fully matured at the moment of the particle-induced lysis. Examination by electron microscope of the bacteriocin enrichment revealed the presence of particles 123 nm in length which resemble the tails of T-even bacteriophages. Since the particles sediment together with the bactericidal activity in the sucrose gradient and adsorb specifically to bacteriocin-sensitive cells, it is concluded that they are identical with the bactericidal agent. The particles are not found attached to phage heads and cannot self-propagate; they are regarded as incomplete and are named INCO particles. INCO particles consist of a core enveloped by a contractile sheath. One end of the sheath is connected to a baseplate to which six fibers, each 32 nm in length, are attached. These connect the baseplate of an adsorbing particle to the cell surface. Since INCo cores are probably empty, it is concluded that specific adsorption of the particles to the bacterial surface is sufficient to inactive sensitive cells irreversibly.

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Year:  1972        PMID: 4110105      PMCID: PMC356273     

Source DB:  PubMed          Journal:  J Virol        ISSN: 0022-538X            Impact factor:   5.103


  15 in total

1.  A negative staining method for high resolution electron microscopy of viruses.

Authors:  S BRENNER; R W HORNE
Journal:  Biochim Biophys Acta       Date:  1959-07

2.  STUDIES OF A PYOCIN. III. BIOLOGICAL PROPERTIES OF THE PYOCIN.

Authors:  M KAGEYAMA; K IKEDA; F EGAMI
Journal:  J Biochem       Date:  1964-01       Impact factor: 3.387

3.  The fine structure of a pyocin.

Authors:  S I Ishii; Y Nishi; F Egami
Journal:  J Mol Biol       Date:  1965-09       Impact factor: 5.469

4.  Conjugation in starforming Rhizobium lupini.

Authors:  W Heumann
Journal:  Mol Gen Genet       Date:  1968

5.  The infection of Escherichia coli by T2 and T4 bacteriophages as seen in the electron microscope. I. Attachment and penetration.

Authors:  L D Simon; T F Anderson
Journal:  Virology       Date:  1967-06       Impact factor: 3.616

6.  Defective bacteriophages.

Authors:  A J Garro; J Marmur
Journal:  J Cell Physiol       Date:  1970-12       Impact factor: 6.384

7.  Selective medium for growth of Rhizobium.

Authors:  P H Graham
Journal:  Appl Microbiol       Date:  1969-05

Review 8.  Rhizobia (with particular reference to relationships with host plants).

Authors:  R O Dixon
Journal:  Annu Rev Microbiol       Date:  1969       Impact factor: 15.500

9.  Morphological studies on relaxed and contracted forms of purified pyocin particles.

Authors:  T B Higerd; C A Baechler; R S Berk
Journal:  J Bacteriol       Date:  1969-06       Impact factor: 3.490

10.  The intracellular growth of bacteriophages. I. Liberation of intracellular bacteriophage T4 by premature lysis with another phage or with cyanide.

Authors:  A H DOERMANN
Journal:  J Gen Physiol       Date:  1952-03       Impact factor: 4.086

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  13 in total

1.  Attachment of a long-tailed Rhizobium bacteriophage to the pili of its host.

Authors:  W Lotz; H Pfister
Journal:  J Virol       Date:  1975-09       Impact factor: 5.103

2.  Production of Antimicrobial and Bacteriocin-Like Substances by Rhizobium trifolii.

Authors:  M V Joseph; J D Desai; A J Desai
Journal:  Appl Environ Microbiol       Date:  1983-02       Impact factor: 4.792

3.  Possible Involvement of Phage-Like Structures in Antagonism of Cowpea Rhizobia by Rhizobium trifolii.

Authors:  M V Joseph; J D Desai; A J Desai
Journal:  Appl Environ Microbiol       Date:  1985-02       Impact factor: 4.792

4.  Characterization of serracin P, a phage-tail-like bacteriocin, and its activity against Erwinia amylovora, the fire blight pathogen.

Authors:  Abdelhamid Jabrane; Ahmed Sabri; Philippe Compère; Philippe Jacques; Isabel Vandenberghe; Jozef Van Beeumen; Philippe Thonart
Journal:  Appl Environ Microbiol       Date:  2002-11       Impact factor: 4.792

5.  Genetic studies on rhizobiophage 16-3. I. Genes and functions on the chromosome.

Authors:  L Orosz; Z Sváb; A Kondorosi; T Sik
Journal:  Mol Gen Genet       Date:  1973-09-27

6.  Cloning and characterization of a Rhizobium leguminosarum gene encoding a bacteriocin with similarities to RTX toxins.

Authors:  I J Oresnik; S Twelker; M F Hynes
Journal:  Appl Environ Microbiol       Date:  1999-07       Impact factor: 4.792

7.  Bacteriocin-like substances produced by Rhizobium japonicum and other slow-growing rhizobia.

Authors:  D C Gross; A K Vidaver
Journal:  Appl Environ Microbiol       Date:  1978-12       Impact factor: 4.792

8.  [Intracellular organisation of bacteriophage tail-like bacteriocins of group A in Serratia marcescens (author's transl)].

Authors:  G Acker
Journal:  Arch Microbiol       Date:  1976-12-01       Impact factor: 2.552

9.  F-Type Bacteriocins of Listeria monocytogenes: a New Class of Phage Tail-Like Structures Reveals Broad Parallel Coevolution between Tailed Bacteriophages and High-Molecular-Weight Bacteriocins.

Authors:  Grace Lee; Urmi Chakraborty; Dana Gebhart; Gregory R Govoni; Z Hong Zhou; Dean Scholl
Journal:  J Bacteriol       Date:  2016-09-22       Impact factor: 3.490

10.  Electron microscopy study of length and partial denaturation of Rhizobium bacteriophage DNA.

Authors:  F Mayer; W Lotz; D Lang
Journal:  J Virol       Date:  1973-06       Impact factor: 5.103

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