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Identification and cloning of nodulation genes from the wide host range Rhizobium strain MPIK3030
Authors:Christian W B Bachem  Eva Kondorosi  Zsofia Banfalvi  Beatrix Horvath  Adam Kondorosi and Jeff Schell
Institution:(1) Abt. Schell, Max-Planck-Institut für Züchtungsforschung, D-5000 Köln 30, Federal Republic of Germany;(2) Institute of Biochemistry, Hungarian Academy of Sciences, POB 521, H-6701 Szeged, Hungary;(3) Institute of Genetics Biological Research Center, Hungarian Academy of Sciences, POB 521, H-6701 Szeged, Hungary
Abstract:Summary A 70 kbp segment of the megaplasmid from a broad host range Rhizobium strain (MPIK3030) was mapped with the aid of cosmid clones made in the vector pJB8. A 7.9 kbp EcoRI fragment from this region, 55 kbp away from the nif gene cluster, was shown to hybridize to the ldquocommonrdquo nod genes from R. meliloti. Using several R. meliloti nod probes it was possible to delimit an 830 bp region as being the center of greatest homology. Sequence data from two sections of this region gave a nucleotide homology of 73.7% to the nodC gene of R. meliloti. Using Tn5 mutagenesis a clone was isolated carrying Tn5 in the highly homologous region. When tested on Macroptilium atropurpureum, this MPIK3030 derivative was shown to have a Nod phenotype. When the wild-type allele was reintroduced into the Tn5 mutant, nodulation was restored. Interspecies complementation also showed that both R. meliloti and Rhizobium sp. MPIK3030 nod regions were able to restore nodulation to Tn5-induced nodC mutants from either strain.Dedicated to Professor Georg Melchers to celebrate his 50-year association with the journal
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