Siddavattam D, Steibl H D, Kreutzer R, Klingmüller W
Institute for Genetics, University of Bayreuth, Germany.
Mol Gen Genet. 1995 Dec 20;249(6):629-36. doi: 10.1007/BF00418032.
The nucleotide sequence of a plasmid-borne 3.9 kb XhoI-SmaI fragment comprising the 3'-region of the nifM gene, the nifL and nifA genes and the 5'-region of nifB gene of Enterobacter agglomerans was determined. The genes were identified by their homology to the corresponding nif genes of Klebsiella pneumoniae. A typical sigma 54-dependent promoter and a consensus NtrC-binding motif were identified upstream of nifL. The predicted amino acid sequence of NifL showed close similarities to NifL of K. pneumoniae and Azotobacter vinelandii. However, no histidine residue was found to correspond to histidine-304 of A. vinelandii NifL, which had been proposed to be required for the repressor activity of NifL. The NifA sequence with a putative DNA binding motif (Q(x3) A(x3) G(x5)I) and an ATP binding site in the C-terminal and central domains, respectively, resembles that of other known NifA proteins. The function of the nifL and nifA genes was demonstrated in vivo using a binary plasmid system by their ability to activate a nifH promoter-lacZ fusion at different temperatures and concentrations of NH4+. Maximal promoter activity occurred at 25 degrees C, and it appears that the sensitivity of NifA to elevated temperatures is independent of NifL. The expression of nifL inhibited promoter activity in the presence of NifA when the initial NH4+ concentration in the medium exceeded 4 mM.
测定了成团肠杆菌质粒携带的一个3.9 kb XhoI - SmaI片段的核苷酸序列,该片段包含nifM基因的3'区域、nifL和nifA基因以及nifB基因的5'区域。这些基因通过与肺炎克雷伯菌相应nif基因的同源性得以鉴定。在nifL上游鉴定出一个典型的依赖于σ54的启动子和一个共有NtrC结合基序。预测的NifL氨基酸序列与肺炎克雷伯菌和棕色固氮菌的NifL有密切相似性。然而,未发现与棕色固氮菌NifL的组氨酸-304相对应的组氨酸残基,据推测该残基是NifL阻遏活性所必需的。NifA序列在C端和中央结构域分别具有一个假定的DNA结合基序(Q(x3)A(x3)G(x5)I)和一个ATP结合位点,与其他已知的NifA蛋白相似。利用二元质粒系统在体内证明了nifL和nifA基因的功能,它们能够在不同温度和NH4+浓度下激活nifH启动子 - lacZ融合。最大启动子活性出现在25℃,并且似乎NifA对温度升高的敏感性与NifL无关。当培养基中初始NH4+浓度超过4 mM时,在存在NifA的情况下,nifL的表达抑制了启动子活性。