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Applied and Environmental Microbiology
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Microorganism-Plant Interactions

Rapid Identification of Rhizobia by Restriction Fragment Length Polymorphism Analysis of PCR-Amplified 16S rRNA Genes

Gisèle Laguerre, Marie-Reine Allard, Françoise Revoy, Noelle Amarger
Gisèle Laguerre
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Marie-Reine Allard
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Françoise Revoy
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Noelle Amarger
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ABSTRACT

Forty-eight strains representing the eight recognized Rhizobium species, two new Phaseolus bean Rhizobium genomic species, Bradyrhizobium spp., Agrobacterium spp., and unclassified rhizobia from various host plants were examined by restriction fragment length polymorphism (RFLP) analysis of 16S rRNA genes amplified by polymerase chain reaction (PCR). Twenty-one composite genotypes were obtained from the combined data of the RFLP analysis with nine endonucleases. Species assignments were in full agreement with the established taxonomic classification. Estimation from these data of genetic relationships between and within genera and species correlated well with previously published data based on DNA-rRNA hybridizations and sequence analysis of 16S rRNA genes. This PCR-RFLP method provides a rapid tool for the identification of root nodule isolates and the detection of new taxa.

FOOTNOTES

  • ↵* Corresponding author. Mailing address: Laboratoire de Microbiologie des Sols, INRA, 17 rue Sully, Dijon, France BV 1540 21034 cedex. Phone: (33) 80-633093. Fax: (33) 80-633224.

  • Copyright © 1994, American Society for Microbiology
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Rapid Identification of Rhizobia by Restriction Fragment Length Polymorphism Analysis of PCR-Amplified 16S rRNA Genes
Gisèle Laguerre, Marie-Reine Allard, Françoise Revoy, Noelle Amarger
Applied and Environmental Microbiology Jan 1994, 60 (1) 56-63; DOI:

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Rapid Identification of Rhizobia by Restriction Fragment Length Polymorphism Analysis of PCR-Amplified 16S rRNA Genes
Gisèle Laguerre, Marie-Reine Allard, Françoise Revoy, Noelle Amarger
Applied and Environmental Microbiology Jan 1994, 60 (1) 56-63; DOI:
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