
An 800 bp AccI-PUCII DNA containing promoter region of nodABC (P1) from A. caulinodans ORS571 was cloned and used as a hybridization probe against the chromosome DNA, which led to the identification of another 8.4-kb EcoRI fragment showing homology to P1. A corresponding clone of 8.4-kb DNA was isolated from a pLAFI gene bank (pRG90). The restriction enzyme analysis and DNA-DNA hybridization of 8.4-kb DNA indicated the P1 homology was located in the 450-bp SmaI-SphI region (P2 region). omega insertion deletion of 8.4 kb DNA resulted in a mutant strain ORS571-5 that delayed to nodulate the stems of S. rostrata. This phenotype was complemented by the introduction of pRK84 carrying nod locus 5 DNA.
Base Sequence, Genes, Bacterial, Rhizobiaceae, Molecular Sequence Data, Nucleic Acid Hybridization, Cloning, Molecular, DNA Probes, Promoter Regions, Genetic
Base Sequence, Genes, Bacterial, Rhizobiaceae, Molecular Sequence Data, Nucleic Acid Hybridization, Cloning, Molecular, DNA Probes, Promoter Regions, Genetic
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