Kaminski P A, Elmerich C
Unité de Physiologie Cellulaire and URA 1300 CNRS, Département des Biotechnologies, Institut Pasteur, Paris, France.
Mol Microbiol. 1998 May;28(3):603-13. doi: 10.1046/j.1365-2958.1998.00823.x.
The control of Azorhizobium caulinodans nifA expression in response to oxygen and ammonia involves FixLJ, FixK, NtrBC, NtrXY and the HF-I-like protein NrfA. The regulation is thus complex and possibly involves post-transcriptional regulation by NrfA. The coding region of nifA was determined using a translational lacZ fusion and by site-directed mutagenesis to identify which of four in frame AUG codons was used. The major NifA protein is translated from the second AUG codon and is predicted to consist of 613 amino acids. Primer extension analysis showed a major transcript starting 34 bp downstream from the anaerobox in wild-type, nifA, rpoN, ntrC and nrfA strains, but not in a fixK mutant. FixK- and oxygen-dependent transcription of nifA was confirmed by the analysis of four transcriptional nifA-lacZ fusions with fusion junctions at positions +1, +47, +110 and +181 with respect to the start site. Regulation by ammonia was independent of FixK and RpoN, NtrC being only partially required. Thus, there may be another type of nitrogen control that does not involve NtrC in A. caulinodans. NrfA is not required for the initiation of nifA transcription but, most probably, has an effect on nifA mRNA stability and/or translation. NrfA also restores the defect in rpoS translation to an Escherichia coli hfq mutant, indicating that HF-I and NrfA have similar activities in both A. caulinodans and E. coli.
茎瘤固氮根瘤菌nifA基因表达对氧气和氨的响应调控涉及FixLJ、FixK、NtrBC、NtrXY以及类HF-I蛋白NrfA。因此,这种调控较为复杂,可能涉及NrfA的转录后调控。利用翻译型lacZ融合以及定点诱变确定nifA的编码区,以识别四个读框内AUG密码子中哪一个被使用。主要的NifA蛋白由第二个AUG密码子翻译而来,预计由613个氨基酸组成。引物延伸分析表明,在野生型、nifA、rpoN、ntrC和nrfA菌株中,主要转录本起始于厌氧盒下游34 bp处,但在fixK突变体中则不然。通过分析四个转录nifA-lacZ融合体(融合位点相对于起始位点分别位于+1、+47、+110和+181位置),证实了nifA的FixK和氧气依赖性转录。氨的调控不依赖于FixK和RpoN,仅部分需要NtrC。因此,在茎瘤固氮根瘤菌中可能存在另一种不涉及NtrC的氮调控类型。NrfA不是nifA转录起始所必需的,但很可能对nifA mRNA的稳定性和/或翻译有影响。NrfA还能恢复大肠杆菌hfq突变体中rpoS翻译的缺陷,表明HF-I和NrfA在茎瘤固氮根瘤菌和大肠杆菌中具有相似的活性。