Merrick M, Chambers S
AFRC Nitrogen Fixation Laboratory, University of Sussex, Brighton, United Kingdom.
J Bacteriol. 1992 Nov;174(22):7221-6. doi: 10.1128/jb.174.22.7221-7226.1992.
Residue Arg-383 in the proposed helix-turn-helix motif of the novel RNA polymerase sigma factor sigma 54 has been changed by site-directed mutagenesis to all possible alternative amino acids. Only two mutants, RK383 and RH383, are active in promoting transcription from either the glnAp2 promoter or the nifL promoter. We constructed a set of mutant derivatives of glnAp2 such that each base in the conserved GG and GC doublets at -24 and -12 was changed to all possible alternatives. All 12 mutant glnAp2 promoters showed a marked promoter-down phenotype with wild-type sigma 54, but RK383 suppressed changes of both G to C and G to T at -13. This result suggests that the sigma 54 helix-turn-helix is involved in recognition of the -13 region of sigma 54-dependent promoters.
新型RNA聚合酶σ因子σ54的拟螺旋-转角-螺旋基序中的精氨酸残基-383,已通过定点诱变被替换为所有可能的替代氨基酸。只有两个突变体RK383和RH383在促进从glnAp2启动子或nifL启动子转录方面具有活性。我们构建了一组glnAp2的突变衍生物,使得-24和-12位保守的GG和GC双联体中的每个碱基都被替换为所有可能的替代碱基。所有12个突变的glnAp2启动子与野生型σ54一起时都表现出明显的启动子下调表型,但RK383抑制了-13位从G到C和从G到T的变化。这一结果表明,σ54螺旋-转角-螺旋参与识别依赖于σ54的启动子的-13区域。