Rep-PCR of tropical rhizobia for strain fingerprinting, biodiversity appraisal and as a taxonomic and phylogenetic tool |
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Authors: | Pâmela Menna Alan Alves Pereira Eliane Villamil Bangel Mariangela Hungria |
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Affiliation: | 1. Embrapa Soja, Cx. Postal 231, 86001-970, Londrina, Paraná, Brazil 2. Department of Microbiology, Universidade Estadual de Londrina, Cx. Postal 60001, 86051-990, Londrina, Brazil 3. ConselhoNacional de Desenvolvimento Cientifico e Tecnol6gico (CNPq-MCT), Brasilia, Federal District, Brazil 4. FEPAGRO, Rua Goncalves Dias 579, 90130-060, Porto Alegre, Rio Grande do Sui, Brazil
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Abstract: | With more than 30 million doses of rhizobial inoculants marketed per year, it is probable that Brazilian agriculture benefits more than any other country from symbiotic N2 fixation. As a result of strain-selection programs, 142 strains of rhizobia are officially recommended for use in commercial inoculants for ninety-six leguminous crops. In this study, sixty-eight of these elite strains were characterized by rep-PCR with the BOX-primer. Reproducibility of the DNA profiles was confirmed, suggesting efficacy of BOX-PCR both for control of quality of inoculants and for preliminary characterization of rhizobial culture collections. Strains of different species never showed similarity higher than 70% in the BOX-PCR analysis, however, some strains of the same species fit into more than one cluster, and correlation between BOX-PCR products and l6S rRNA sequences was low (7.6%). On the other hand, a polyphasic approach — 20%∶80% of BOX-PCR:16S rRNA which correlated well with the l6S rRNA analysis (95%), and provided higher definition of the genotypes, resulting in clearer indications of the taxonomic groups — might expedite rhizobial diversity studies. |
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