Literature DB >> 2061287

Phylogenetic relationships among Frankia genomic species determined by use of amplified 16S rDNA sequences.

S Nazaret1, B Cournoyer, P Normand, P Simonet.   

Abstract

Actinomycetes of the genus Frankia establish a nitrogen-fixing symbiosis with a large number of woody dicotyledonous plants. Hundreds of strains isolated from various actinorhizal plants growing in different geographical areas have recently been classified into at least nine genomic species by use of the DNA-DNA hybridization technique (M.P. Fernandez, H. Meugnier, P.A.D. Grimont, and R. Bardin, Int. J. Syst. Bacteriol. 39:424-429, 1989). A protocol based on the amplification and sequencing of 16S ribosomal DNA segments was used to classify and estimate the phylogenetic relationships among eight different genomic species. A good correlation was established between the grouping of strains according to their 16S ribosomal DNA sequence homology and that based on total DNA homology, since most genomic species could be characterized by a specific sequence. The phylogenetic tree showed that strains belonging to the Alnus infectivity group are closely related to strains belonging to the Casuarina infectivity group and that strains of these two infectivity groups are well separated from strains of the Elaeagnus infectivity group, which also includes atypical strains isolated from the Casuarina group. This phylogenetic analysis was also very efficient for classifying previously unclassified pure cultures or unisolatable strains by using total DNA extracted directly from nodules.

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Year:  1991        PMID: 2061287      PMCID: PMC208055          DOI: 10.1128/jb.173.13.4072-4078.1991

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


  17 in total

1.  Rapid determination of 16S ribosomal RNA sequences for phylogenetic analyses.

Authors:  D J Lane; B Pace; G J Olsen; D A Stahl; M L Sogin; N R Pace
Journal:  Proc Natl Acad Sci U S A       Date:  1985-10       Impact factor: 11.205

2.  Conservation of nif sequences in Frankia.

Authors:  P Normand; P Simonet; R Bardin
Journal:  Mol Gen Genet       Date:  1988-08

3.  The neighbor-joining method: a new method for reconstructing phylogenetic trees.

Authors:  N Saitou; M Nei
Journal:  Mol Biol Evol       Date:  1987-07       Impact factor: 16.240

4.  An improved method for directly sequencing PCR amplified material using dimethyl sulphoxide.

Authors:  P R Winship
Journal:  Nucleic Acids Res       Date:  1989-02-11       Impact factor: 16.971

Review 5.  Construction of phylogenetic trees.

Authors:  W M Fitch; E Margoliash
Journal:  Science       Date:  1967-01-20       Impact factor: 47.728

Review 6.  Detailed analysis of the higher-order structure of 16S-like ribosomal ribonucleic acids.

Authors:  C R Woese; R Gutell; R Gupta; H F Noller
Journal:  Microbiol Rev       Date:  1983-12

7.  Gene organization and primary structure of a ribosomal RNA operon from Escherichia coli.

Authors:  J Brosius; T J Dull; D D Sleeter; H F Noller
Journal:  J Mol Biol       Date:  1981-05-15       Impact factor: 5.469

8.  Identification of Frankia strains in nodules by hybridization of polymerase chain reaction products with strain-specific oligonucleotide probes.

Authors:  P Simonet; P Normand; A Moiroud; R Bardin
Journal:  Arch Microbiol       Date:  1990       Impact factor: 2.552

9.  Organization and nucleotide sequence analysis of a ribosomal RNA gene cluster from Streptomyces ambofaciens.

Authors:  J L Pernodet; F Boccard; M T Alegre; J Gagnat; M Guérineau
Journal:  Gene       Date:  1989-06-30       Impact factor: 3.688

10.  Isolation and Cultivation in vitro of the Actinomycete Causing Root Nodulation in Comptonia.

Authors:  D Callaham; P Deltredici; J G Torrey
Journal:  Science       Date:  1978-02-24       Impact factor: 47.728

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  18 in total

1.  Characterization of natural populations of Nitrobacter spp. using PCR/RFLP analysis of the ribosomal intergenic spacer.

Authors:  E Navarro; P Simonet; P Normand; R Bardin
Journal:  Arch Microbiol       Date:  1992       Impact factor: 2.552

2.  New nucleotide sequence data on the EMBL File Server.

Authors: 
Journal:  Nucleic Acids Res       Date:  1992-01-11       Impact factor: 16.971

3.  Hypervariable spacer regions are good sites for developing specific PCR-RFLP markers and PCR primers for screening actinorhizal symbionts.

Authors:  Rajani Varehese; Vineeta S Chauhan; Arvind K Misra
Journal:  J Biosci       Date:  2003-06       Impact factor: 1.826

4.  New nucleotide sequence data on the EMBL File Server.

Authors: 
Journal:  Nucleic Acids Res       Date:  1991-11-25       Impact factor: 16.971

5.  Whole-Cell Hybridization of Frankia Strains with Fluorescence- or Digoxigenin-Labeled, 16S rRNA-Targeted Oligonucleotide Probes.

Authors:  D Hahn; R I Amann; J Zeyer
Journal:  Appl Environ Microbiol       Date:  1993-06       Impact factor: 4.792

6.  Morphological and molecular characterization of Frankia sp. isolates from nodules of Alnus nepalensis Don.

Authors:  G Ganesh; A K Misra; C Chapelon; P Normand
Journal:  Arch Microbiol       Date:  1994       Impact factor: 2.552

7.  Analysis of partial sequences of genes coding for 16S rRNA of actinomycetes isolated from Casuarina equisetifolia nodules in Mexico.

Authors:  B M Niner; J P Brandt; M Villegas; C R Marshall; A M Hirsch; M Valdés
Journal:  Appl Environ Microbiol       Date:  1996-08       Impact factor: 4.792

8.  Diversity of frankia strains in root nodules of plants from the families elaeagnaceae and rhamnaceae

Authors: 
Journal:  Appl Environ Microbiol       Date:  1998-09       Impact factor: 4.792

9.  Frankia genus-specific characterization by polymerase chain reaction.

Authors:  P Simonet; M C Grosjean; A K Misra; S Nazaret; B Cournoyer; P Normand
Journal:  Appl Environ Microbiol       Date:  1991-11       Impact factor: 4.792

10.  Evidence that some Frankia sp. strains are able to cross boundaries between Alnus and Elaeagnus host specificity groups.

Authors:  M Bosco; M P Fernandez; P Simonet; R Materassi; P Normand
Journal:  Appl Environ Microbiol       Date:  1992-05       Impact factor: 4.792

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