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A. W. B. Johnston - One of the best experts on this subject based on the ideXlab platform.

  • the genome of Rhizobium leguminosarum has recognizable core and accessory components
    Genome Biology, 2006
    Co-Authors: Peter J W Young, A. W. B. Johnston, Margaret Wexler, Lisa Crossman, Nicholas R Thomson, Zara Ghazoui, Katherine H Hull, Andrew R J Curson, Jonathan D Todd, Philip S Poole
    Abstract:

    Background Rhizobium leguminosarum is an α-proteobacterial N2-fixing symbiont of legumes that has been the subject of more than a thousand publications. Genes for the symbiotic interaction with plants are well studied, but the adaptations that allow survival and growth in the soil environment are poorly understood. We have sequenced the genome of R. leguminosarum biovar viciae strain 3841.

  • Structural studies of the Fur protein from Rhizobium leguminosarum
    Biochemical Society transactions, 2002
    Co-Authors: Olatomirin O. Kolade, A. W. B. Johnston, P. Bellini, Margaret Wexler, J. G. Grossmann, Andrew M. Hemmings
    Abstract:

    The X-ray crystal structure of the apo-form of the Fur protein from Rhizobium leguminosarum has been solved at 2.7 a resolution. Small-angle X-ray scattering was used to give information on the solution conformation of the protein. The Fur homodimer folds into two domains. The N-terminal domain is formed from the packing of two helix-turn-helix motifs while the C-terminal domain appears primarily to stabilize the dimeric state of the protein.

  • A Putative ECF σ Factor Gene, rpoI, Regulates Siderophore Production in Rhizobium leguminosarum
    Molecular plant-microbe interactions : MPMI, 1999
    Co-Authors: Kay H. Yeoman, Alex G. May, Nicola G. Deluca, Daniel B. Stuckey, A. W. B. Johnston
    Abstract:

    A cloned Rhizobium leguminosarum gene, termed rpoI, when transferred to wild-type strains, caused overproduction of the siderophore vicibactin. An rpoI mutant was defective in Fe uptake but was unaffected in symbiotic N2 fixation. The RpoI gene product was similar in sequence to extra-cytoplasmic σ factors of RNA polymerase. Transcription of rpoI was reduced in cells grown in medium that was replete with Fe.

  • The Rhizobium leguminosarum biovar viciae nodO gene can enable a nodE mutant of Rhizobium leguminosarum biovar trifolii to nodulate vetch
    Microbiology, 1994
    Co-Authors: Anastassios Economou, A. W. B. Johnston, A. E. Davies, J. A. Downie
    Abstract:

    Analysis of the nodulation characteristics of transposon-induced mutants of Rhizobium leguminosarum bv. viciae revealed that nodO and the closely-linked rhi genes contribute to nodulation of peas (Pisum sativum) and the vetch Vicia hirsuta. Although mutation of nodO alone had no significant effect on nodulation of either legume, a double mutant lacking both nodO and nodE nodulated both legumes very poorly. Similarly, a double mutant lacking nodE and either rhiA or rhiB nodulated peas less efficiently than a nodE mutant. Thus, although mutations affecting only the rhi genes normally have no observed effect on nodulation, these genes do appear to contribute to pea nodulation. When transferred to a wild-type strain of Rhizobium leguminosarum bv. trifolii, neither nodO nor the rhi gene region conferred pea or vetch nodulating ability. However, in a nodE mutant of R. I. bv. trifolii, nodO did confer a significant level of vetch nodulating ability, indicating that the secreted NodO protein can play a role in determining legume recognition by R. I. bv. viciae.

Jozef Vanderleyden - One of the best experts on this subject based on the ideXlab platform.

Martin Krehenbrink - One of the best experts on this subject based on the ideXlab platform.

Dietrich Werner - One of the best experts on this subject based on the ideXlab platform.

  • Application of subtraction hybridization for the development of a Rhizobium leguminosarum biovar phaseoli and Rhizobium tropici group-specific DNA probe
    FEMS Microbiology Ecology, 1993
    Co-Authors: Wolfgang R. Streit, Anthony J. Bjourson, J. E. Cooper, Dietrich Werner
    Abstract:

    A combined subtraction hybridization and polymerase chain reaction/amplification technique was used to develop a DNA probe which was specific for the Rhizobium leguminosarum biovar phaseoli and the Rhizobium tropici group. Total genomic DNA preparations from Rhizobium leguminosarum biovar viciae, Rhizobium leguminosarum biovar trifolii, Rhizobium sp., Agrobacterium tumefaciens, Rhizobium fredii, BradyRhizobium japonicum, BradyRhizobium ssp. and Rhizobium meliloti were pooled and used as subtracter DNA against total genomic DNA from the Rhizobium leguminosarum biovar phaseolo strain KIM5s. Only one round of subtraction hybridization at 65°C was necessary to remove all cross-hybridizing sequences. Dot blot hybridizations with total genomic DNA of the eight subtracter organisms and 29 bacteria of different groups confirmed the high specificity of the isolated DNA sequences. Dot blot hybridizations and total genomic DNA from ten different R. leguminosarum biovar phaseoli and R. tropici strains resulted in strong hybridization signals for all strains tested. The DNA probe for the R. tropici and R. leguminosarum biovar phaseoli group was used for dot blot hybridization with DNA extracts from three tropical and one boreal soil. When correlated with data from Most Probable Number analyses the probe was capable of detecting as low as 3 × 104 homologous indigenous rhizobia per g soil. The technique offers great benefits for the development of DNA probes for monitoring bacterial populations in environmental samples.

Philip S Poole - One of the best experts on this subject based on the ideXlab platform.