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Expression of the nodulation gene nodA in Rhizobium meliloti and localization of the gene product in the cytosol
Author(s) -
Jürgen Schmidt,
Michael John,
Ursula Wieneke,
Heinz-Dieter Krüssmann,
Jeff Schell
Publication year - 1986
Publication title -
proceedings of the national academy of sciences of the united states of america
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.011
H-Index - 771
eISSN - 1091-6490
pISSN - 0027-8424
DOI - 10.1073/pnas.83.24.9581
Subject(s) - rhizobium , biology , gene product , fusion protein , polyclonal antibodies , biochemistry , sinorhizobium meliloti , gene , microbiology and biotechnology , gene expression , antibody , genetics , mutant , recombinant dna
ThenodA gene ofRhizobium meliloti encodes a 21.8-kDa protein, which is conserved in severalRhizobium species. We overproduced the nodA protein as a fusion product with a portion of the λc I repressor inEscherichia coli . This fusion protein was purified from inclusion bodies by gel and hydroxyapatite chromatography in the presence of NaDodSO4 . Monospecific polyclonal antibodies against the hybrid protein were used to detect the nodA protein in the cytosol ofE. coli andR. meliloti by immunoblotting. In contrast to experiments with antibodies against theR. meliloti nodC membrane protein, the alfalfa-R. meliloti nodulation was not affected by the addition of anti-nodA antibodies to medium and inoculum. This suggests that the nodA protein is located within the cell and is therefore not accessible to antibodies. The expression of thenodA gene is induced inR. meliloti by various compounds present in the exudate of leguminous plants, particularly by the flavone luteolin. We show that the plant hormone trigonelline also has some inducing activity. The nodC protein was further localized in the membrane fraction ofR. meliloti . Our experiments demonstrate that the nodC transmembrane protein is not necessary for the uptake of the compounds inducing the synthesis of the nodA protein. The nodA and the nodC proteins were also detected in mature nodules. During nodule development, the nodC protein may be processed to a 34-kDa protein.

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