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Genotypic Characterisation of Indigenous Soybean Rhizobia by PCR-RFLP of 16S rDNA, rep-PCR and RAPD Analysis (CROSBI ID 99611)

Prilog u časopisu | izvorni znanstveni rad | međunarodna recenzija

Sikora, Sanja ; Redžepović, Sulejman Genotypic Characterisation of Indigenous Soybean Rhizobia by PCR-RFLP of 16S rDNA, rep-PCR and RAPD Analysis // Food technology and biotechnology, 41 (2003), 1; 61-67-x

Podaci o odgovornosti

Sikora, Sanja ; Redžepović, Sulejman

engleski

Genotypic Characterisation of Indigenous Soybean Rhizobia by PCR-RFLP of 16S rDNA, rep-PCR and RAPD Analysis

The taxonomy of nitrogen fixing bacteria that form symbiotic associations with leguminous plants has been deeply changed in recent years. the use of very senssitive and accurate molecular methods has enabled the detection of large rhizobial diversity, particularly among natural field populations of these soil bacteria. The aim of the presentinvestigation was to identify and characterise the indigenous soybean rhizobia isolatedfrom different soil types in eastern Croatia that are regularly used for agricultural production. The actual composition and genetic diversity of natural field population aws studied by using different PCR fingerprinting methods such as 16S rDNA PCR-RFLP, rep-PCR and RAPD analysis. Eighteen rhizobial strains, isolated from soybean nodules, were characterised and compared with reference and/or type strains representing Bradyrhizobium japonicum, B. elkanii, and Sinorhizobium fredii. Cluster analysis of combined RFLP patterns obtained with six restriction endonuclease revealed taht all soybean isolates differ significantly from B. elkanii and S. fredii type strains, while they were closely related to B. japonicum type strains. however, a considerable levele of genetic diversity was determined among B. japonicum isolates. PCR-RFLP of 16S rDNA clearly showed the existaence of two divergent groups among indigenous bradyrhizobia. After identification at the species level, all isolates were further characterised by RAPD and rep-PCR. Both RAPD and rep-PCR generated highly specific and reproduciblepatterns that enabled accurate strain differentiation. among B. japonicum strains a high level of diversity was found with these two fingerprinting methods. Dendrograms derived from RAPD, REP and ERIC profiles showed that all indigenous strains could be divided into three main gropus. The grouping of strains was consistent with all methods used in this study.

nitrogen fixation; rhizobia; soybean; indigenous strains; Bradyrhizobium japonicum; DNA fingerprinting; genetic diversity

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Podaci o izdanju

41 (1)

2003.

61-67-x

objavljeno

1330-9862

Povezanost rada

Poljoprivreda (agronomija)

Indeksiranost