Nalin R, Domenach A M, Normand P
Laboratoire d'Ecologie Microbienne du Sol, URA CNRS 1977, Université Claude Bernard Lyon I, Villeurbanne, France.
Mol Ecol. 1995 Aug;4(4):483-91. doi: 10.1111/j.1365-294x.1995.tb00242.x.
The nifD-K intergenic spacer (IGS) of ArI3 and ACoN24d were found to have a length 265 and 199 nucleotides, respectively. They are markedly less conserved than the two neighbouring genes and have, in some instances, a repeated structure reminiscent of an insertion event. The repeated sequence and the IGSs have no detectable homology with sequences in DNA databanks. The IGS has a stem-loop structure with a low folding energy, lower than that between nifH and nifD. No convincing alignment of IGS sequences could be obtained among Frankia strains. Only between ACoN24d and ArI3, which belong to the same genomic species, was the alignment good enough to permit detection of a doubly repeated structure. No promoter could be detected in the IGSs. The putative nifK open reading frame (ORF) in Frankia strain ArI3 has a length of 1587 nucleotides, starting with a GTG codon, preceded by a ribosome binding site of a structure similar to that of nifH (GGAGGN7). The codon usage was similar to that of previously sequenced Frankia genes with a strong bias toward G- and C-ending codons except in the case of glycine where GGT is frequent. Alignment of the three Frankia nifK sequences (EUN1f; ArI3 and ACoN24d) with those of other nitrogen-fixing bacteria permitted detection of a sequence conserved among the three Frankia strains but absent in the other sequences. A primer targeted to that region in combination with FGPD807-85 amplified the nifD-KIGS sequences of all Frankia strains (except the non-nitrogen-fixing Frankia strains CN3 and AgB1-9) and yet failed to amplify DNA of all other nitrogen-fixing bacteria.(ABSTRACT TRUNCATED AT 250 WORDS)
发现ArI3和ACoN24d的nifD-K基因间隔区(IGS)长度分别为265和199个核苷酸。它们的保守性明显低于两个相邻基因,并且在某些情况下具有类似于插入事件的重复结构。重复序列和IGS与DNA数据库中的序列没有可检测到的同源性。IGS具有低折叠能的茎环结构,低于nifH和nifD之间的折叠能。在弗兰克氏菌菌株之间无法获得令人信服的IGS序列比对。只有属于同一基因组种的ACoN24d和ArI3之间的比对足够好,能够检测到双重重复结构。在IGS中未检测到启动子。弗兰克氏菌菌株ArI3中假定的nifK开放阅读框(ORF)长度为1587个核苷酸,起始于GTG密码子,前面有一个与nifH结构相似的核糖体结合位点(GGAGGN7)。密码子使用情况与先前测序的弗兰克氏菌基因相似,除了甘氨酸中GGT频繁出现外,强烈偏向于以G和C结尾的密码子。将三个弗兰克氏菌nifK序列(EUN1f;ArI3和ACoN24d)与其他固氮细菌的序列进行比对,能够检测到三个弗兰克氏菌菌株中保守但在其他序列中不存在的序列。靶向该区域的引物与FGPD807-85结合,扩增了所有弗兰克氏菌菌株(除了非固氮弗兰克氏菌菌株CN3和AgB1-9)的nifD-K IGS序列,但未能扩增所有其他固氮细菌的DNA。(摘要截断于250字)