Literature DB >> 1846148

The genomes of the family Rhizobiaceae: size, stability, and rarely cutting restriction endonucleases.

B W Sobral1, R J Honeycutt, A G Atherly.   

Abstract

The lack of high-resolution genetic or physical maps for the family Rhizobiaceae limits our understanding of this agronomically important bacterial family. On the basis of statistical analyses of DNA sequences of the Rhizobiaceae and direct evaluation by pulsed-field agarose gel electrophoresis (PFE), five restriction endonucleases with AT-rich target sites were identified as the most rarely cutting: AseI (5'-ATTAAT-3'), DraI (5'-TTTAAA-3'), SpeI (5'-ACTAGT-3'), SspI (5'-AATAAT-3'), and XbaI (5'-TCTAGA-3'). We computed the sizes of the genomes of Bradyrhizobium japonicum USDA 424 and Rhizobium meliloti 1021 by adding the sizes of DNA fragments generated by SpeI digests. The genome sizes of R. meliloti 1021 and B. japonicum USDA 424 were 5,379 +/- 282.5 kb and 6,195 +/- 192.4 kb, respectively. We also compared the organization of the genomes of free-living and bacteroid forms of B. japonicum. No differences between the PFE-resolved genomic fingerprints of free-living and mature (35 days after inoculation) bacteroids of B. japonicum USDA 123 and USDA 122 were observed. Also, B. japonicum USDA 123 genomic fingerprints were unchanged after passage through nodules and after maintenance on a rich growth medium for 100 generations. We conclude that large-scale DNA rearrangements are not seen in mature bacteroids or during free-living growth on rich growth media under laboratory conditions.

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Year:  1991        PMID: 1846148      PMCID: PMC207062          DOI: 10.1128/jb.173.2.704-709.1991

Source DB:  PubMed          Journal:  J Bacteriol        ISSN: 0021-9193            Impact factor:   3.490


  30 in total

1.  Genome analysis of Bradyrhizobium japonicum serocluster 123 field isolates by using field inversion gel electrophoresis.

Authors:  B W Sobral; M J Sadowsky; A G Atherly
Journal:  Appl Environ Microbiol       Date:  1990-06       Impact factor: 4.792

2.  A rapid and cost-effective method for preparing genomic DNA from gram-negative bacteria in agarose plugs for pulsed-field gel electrophoresis.

Authors:  B W Sobral; A G Atherly
Journal:  Biotechniques       Date:  1989-10       Impact factor: 1.993

Review 3.  Why do bacterial plasmids carry some genes and not others?

Authors:  W G Eberhard
Journal:  Plasmid       Date:  1989-05       Impact factor: 3.466

4.  A physical map of the Escherichia coli K12 genome.

Authors:  C L Smith; J G Econome; A Schutt; S Klco; C R Cantor
Journal:  Science       Date:  1987-06-12       Impact factor: 47.728

5.  Genomic instability in Rhizobium phaseoli.

Authors:  M Flores; V González; M A Pardo; A Leija; E Martínez; D Romero; D Piñero; G Dávila; R Palacios
Journal:  J Bacteriol       Date:  1988-03       Impact factor: 3.490

6.  Constitution of the cell envelope of Haemophilus influenzae in relation to competence for genetic transformation.

Authors:  K C Zoon; J J Scocca
Journal:  J Bacteriol       Date:  1975-08       Impact factor: 3.490

7.  Genetic map of Rhizobium meliloti megaplasmid pRmeSU47b.

Authors:  T C Charles; T M Finan
Journal:  J Bacteriol       Date:  1990-05       Impact factor: 3.490

8.  Reiteration of genes involved in symbiotic nitrogen fixation by fast-growing Rhizobium japonicum.

Authors:  R K Prakash; A G Atherly
Journal:  J Bacteriol       Date:  1984-11       Impact factor: 3.490

9.  The development of plasmid-free strains of Agrobacterium tumefaciens by using incompatibility with a Rhizobium meliloti plasmid to eliminate pAtC58.

Authors:  M F Hynes; R Simon; A Pühler
Journal:  Plasmid       Date:  1985-03       Impact factor: 3.466

10.  Reiterated DNA sequences in Rhizobium and Agrobacterium spp.

Authors:  M Flores; V González; S Brom; E Martínez; D Piñero; D Romero; G Dávila; R Palacios
Journal:  J Bacteriol       Date:  1987-12       Impact factor: 3.490

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  8 in total

1.  Molecular cloning, purification, and biochemical characterization of hydantoin racemase from the legume symbiont Sinorhizobium meliloti CECT 4114.

Authors:  Sergio Martínez-Rodríguez; Francisco Javier Las Heras-Vázquez; Lydia Mingorance-Cazorla; Josefa María Clemente-Jiménez; Felipe Rodríguez-Vico
Journal:  Appl Environ Microbiol       Date:  2004-01       Impact factor: 4.792

2.  Fructose uptake in Sinorhizobium meliloti is mediated by a high-affinity ATP-binding cassette transport system.

Authors:  A Lambert; M Østerås; K Mandon; M C Poggi; D Le Rudulier
Journal:  J Bacteriol       Date:  2001-08       Impact factor: 3.490

3.  Presence of two independent chromosomes in the Brucella melitensis 16M genome.

Authors:  S Michaux; J Paillisson; M J Carles-Nurit; G Bourg; A Allardet-Servent; M Ramuz
Journal:  J Bacteriol       Date:  1993-02       Impact factor: 3.490

4.  Physical map of the genome of Rhizobium meliloti 1021.

Authors:  R J Honeycutt; M McClelland; B W Sobral
Journal:  J Bacteriol       Date:  1993-11       Impact factor: 3.490

5.  Electrophoretic separation of the three Rhizobium meliloti replicons.

Authors:  B W Sobral; R J Honeycutt; A G Atherly; M McClelland
Journal:  J Bacteriol       Date:  1991-08       Impact factor: 3.490

6.  Conserved symbiotic plasmid DNA sequences in the multireplicon pangenomic structure of Rhizobium etli.

Authors:  Víctor González; José L Acosta; Rosa I Santamaría; Patricia Bustos; José L Fernández; Ismael L Hernández González; Rafael Díaz; Margarita Flores; Rafael Palacios; Jaime Mora; Guillermo Dávila
Journal:  Appl Environ Microbiol       Date:  2010-01-04       Impact factor: 4.792

7.  Correlated physical and genetic map of the Bradyrhizobium japonicum 110 genome.

Authors:  C Kündig; H Hennecke; M Göttfert
Journal:  J Bacteriol       Date:  1993-02       Impact factor: 3.490

8.  Stability and asymmetric replication of the Bacillus subtilis 168 chromosome structure.

Authors:  M Itaya
Journal:  J Bacteriol       Date:  1993-02       Impact factor: 3.490

  8 in total

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