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In vivo studies on the positive control function of NifA: a conserved hydrophobic amino acid patch at the central domain involved in transcriptional activation
Author(s) -
González Víctor,
Olvera Leticia,
Soberón Xavier,
Morett Enrique
Publication year - 1998
Publication title -
molecular microbiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.857
H-Index - 247
eISSN - 1365-2958
pISSN - 0950-382X
DOI - 10.1046/j.1365-2958.1998.00772.x
Subject(s) - biology , in vivo , function (biology) , domain (mathematical analysis) , amino acid , microbiology and biotechnology , biochemistry , genetics , mathematical analysis , mathematics
The eubacterial enhancer‐binding proteins activate transcription by binding to distant sites and, simultaneously, contacting the RNA polymerase σ 54 promoter complex (Eσ 54 ). The positive control function is located at the central domain of these proteins, but it is not know which specific region has the determinants for the interaction with Eσ 54 . Here, we present genetic evidence that a small region of hydrophobic amino acids, previously denominated C3, at the central domain of Bradyrhizobium japonicum NifA is involved in positive control. We obtained 26 missense mutants along this conserved region. Among these, only strains expressing the NifA F307→Y and NifA A310→S mutant proteins retained some of the transcriptional activity (< 20%), whereas those carrying NifA E298→D and NifA T308→S had very low but detectable activity (< 1.0%). The rest of the NifA mutants did not induce any measurable transcriptional activity. When expressed in the presence of wild‐type NifA, the great majority of the mutants displayed a dominant phenotype, suggesting that their oligomerization determinants were not altered. In vivo dimethyl‐sulphate footprinting experiments for a subset of the NifA mutants showed that they were still able to bind specifically to DNA. Analysis of intragenic supressors highlight the functional role of a hydroxyl group at position 308 to activate transcription.

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