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Gisèle Laguerre

Researcher at Institut national de la recherche agronomique

Publications -  43
Citations -  3759

Gisèle Laguerre is an academic researcher from Institut national de la recherche agronomique. The author has contributed to research in topics: Rhizobium leguminosarum & Rhizobia. The author has an hindex of 28, co-authored 43 publications receiving 3613 citations. Previous affiliations of Gisèle Laguerre include SupAgro.

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Classification of rhizobia based on nodC and nifH gene analysis reveals a close phylogenetic relationship among Phaseolus vulgaris symbionts.

TL;DR: The results support the view that lateral genetic transfer across rhizobial species and, in some instances, across Rhizobia and Sinorhizobium genera plays a role in diversification and in structuring the natural populations of rhizobia.
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Rapid Identification of Rhizobia by Restriction Fragment Length Polymorphism Analysis of PCR-Amplified 16S rRNA Genes.

TL;DR: This PCR-RFLP method provides a rapid tool for the identification of root nodule isolates and the detection of new taxa.
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Rhizobium gallicum sp. nov. and Rhizobium giardinii sp. nov., from Phaseolus vulgaris Nodules

TL;DR: Thirty-one strains of two new genomic species of rhizobia isolated from root nodules of Phaseolus vulgaris and originating from various locations in France were compared with reference strains by performing a numerical analysis of 64 phenotypic features, revealing that each genomic species formed a lineage independent of the lineages formed by the previously recognized species of Rhizobia.
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Typing of rhizobia by PCR DNA fingerprinting and PCR-restriction fragment length polymorphism analysis of chromosomal and symbiotic gene regions: application to Rhizobium leguminosarum and its different biovars.

TL;DR: Characterization of 43 strains of Rhizobium leguminosarum biovars viciae, trifolii, and phaseoli was performed by two methodologies based on PCR amplification, i.e., PCR DNA fingerprinting of interrepeat sequences and restriction fragment length polymorphism (RFLP) analysis of PCR -amplified chromosomal and symbiotic gene regions.
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Evaluation of denaturing gradient gel electrophoresis in the detection of 16S rDNA sequence variation in rhizobia and methanotrophs

TL;DR: The ability of denaturing gradient gel electrophoresis technique to resolve 16S rDNA products generated from two different collections of bacteria using universal 16S primers was investigated and the difference in sequence divergence within the two groups members allowed therefore to scale the resolution ability of the DGGE technique.