<p><b>A</b>. Schematic representation of analyzed hybrid proteins. <i>B. pertussis</i> adenylate cyclase fragments T18 and T25 (oval shaped) were translationaly fused to σ factor EcfF (black rectangle) and anti-σ factor OsrA (grey rectangle; wild-type (wt) or mutant variants), respectively. Plasmids encoding respective proteins were transformed into <i>E. coli</i> BTH101 in the indicated combinations to yield strains 1 to 4. <b>B</b>. <i>E. coli</i> cultures were grown for 18 h at 30°C and assayed for β-galactosidase activity. Control strain 5 containing vectors pKT25 and pUT18C was used to determine background activity. Shown are mean values and standard deviations derived from a representative experiment with four independent cultures per strain.</p
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