Literature DB >> 2651865

R-body-producing bacteria.

F R Pond, I Gibson, J Lalucat, R L Quackenbush.   

Abstract

Until 10 years ago, R bodies were known only as diagnostic features by which endosymbionts of paramecia were identified as kappa particles. They were thought to be limited to the cytoplasm of two species in the Paramecium aurelia species complex. Now, R bodies have been found in free-living bacteria and other Paramecium species. The organisms now known to form R bodies include the cytoplasmic kappa endosymbionts of P. biaurelia and P. tetraurelia, the macronuclear kappa endosymbionts of P. caudatum, Pseudomonas avenae (a free-living plant pathogen), Pseudomonas taeniospiralis (a hydrogen-oxidizing soil microorganism), Rhodospirillum centenum (a photosynthetic bacterium), and a soil bacterium, EPS-5028, which is probably a pseudomonad. R bodies themselves fall into five distinct groups, distinguished by size, the morphology of the R-body ribbons, and the unrolling behavior of wound R bodies. In recent years, the inherent difficulties in studying the organization and assembly of R bodies by the obligate endosymbiont kappa, have been alleviated by cloning and expressing genetic determinants for these R bodies (type 51) in Escherichia coli. Type 51 R-body synthesis requires three low-molecular-mass polypeptides. One of these is modified posttranslationally, giving rise to 12 polypeptide species, which are the major structural subunits of the R body. R bodies are encoded in kappa species by extrachromosomal elements. Type 51 R bodies, produced in Caedibacter taeniospiralis, are encoded by a plasmid, whereas bacteriophage genomes probably control R-body synthesis in other kappa species. However, there is no evidence that either bacteriophages or plasmids are present in P. avenae or P. taeniospiralis. No sequence homology was detected between type 51 R-body-encoding DNA and DNA from any R-body-producing species, except C. varicaedens 1038. The evolutionary relatedness of different types of R bodies remains unknown.

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Year:  1989        PMID: 2651865      PMCID: PMC372716          DOI: 10.1128/mr.53.1.25-67.1989

Source DB:  PubMed          Journal:  Microbiol Rev        ISSN: 0146-0749


  60 in total

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Authors:  J E SMITH-SONNEBORN; W J VANWAGTENDONK
Journal:  Exp Cell Res       Date:  1964-01       Impact factor: 3.905

2.  Cytological observations on the cytoplasmic factor "kappa" in Paramecium aurelia.

Authors:  J R PREER; P STARK
Journal:  Exp Cell Res       Date:  1953-12       Impact factor: 3.905

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Authors:  J R Preer; R W Siegel; P S Stark
Journal:  Proc Natl Acad Sci U S A       Date:  1953-12       Impact factor: 11.205

4.  Mutation of the killer cytoplasmic factor in Paramecium aurelia.

Authors:  R V DIPPELL
Journal:  Heredity (Edinb)       Date:  1950-08       Impact factor: 3.821

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Authors:  H J Schmidt; H D Görtz; F R Pond; R L Quackenbush
Journal:  Exp Cell Res       Date:  1988-01       Impact factor: 3.905

Review 6.  Kappa and other endosymbionts in Paramecium aurelia.

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Journal:  Bacteriol Rev       Date:  1974-06

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Journal:  Biosystems       Date:  1978-04       Impact factor: 1.973

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Authors:  J R Preer; L B Preer; B Rudman; A Jurand
Journal:  Mol Gen Genet       Date:  1971

Review 9.  Symbiotic theory of the origin of eukaryotic organelles; criteria for proof.

Authors:  L Margulis
Journal:  Symp Soc Exp Biol       Date:  1975

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Authors:  J R Preer
Journal:  Symp Soc Exp Biol       Date:  1975
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9.  The Toxic Symbiont Caedibacter caryophila in the Cytoplasm of Paramecium novaurelia.

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10.  Characterization of genetic determinants for R body synthesis and assembly in Caedibacter taeniospiralis 47 and 116.

Authors:  D P Heruth; F R Pond; J A Dilts; R L Quackenbush
Journal:  J Bacteriol       Date:  1994-06       Impact factor: 3.490

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