Brown S E, Ausubel F M
J Bacteriol. 1984 Jan;157(1):143-7. doi: 10.1128/jb.157.1.143-147.1984.
Starting with plasmid pSA30 which contains an intact nifHDKY operon, we selected mutants that no longer inhibited nitrogen fixation in Klebsiella pneumoniae. Three categories of mutants were found among eight mutant plasmids examined in detail. Three mutant plasmids carried a single-base-pair (bp) change at position -12 or -14 relative to the nifH transcription start site. These mutations were located in a previously described consensus sequence found in the -10 to -15 region of nif promoters. Four of the mutant plasmids contain lesions considerably upstream from the start point of transcription. Two of these upstream mutations are identical 112-bp deletions of nucleotides -72 to -184, and two others are a single-bp change at position -136. The final plasmid does not contain a mutation within a 525-bp region which includes 289 bp upstream from the nifH ATG initiation codon and which extends 69 codons into the nifH gene. All eight of the mutant pSA30 plasmids failed to complement a chromosomal nifH mutation, suggesting that the mutations that block inhibition of nif expression also prevent transcription of the nifHDKY operon.
从含有完整固氮酶操纵子(nifHDKY operon)的质粒pSA30开始,我们筛选出了不再抑制肺炎克雷伯菌中固氮作用的突变体。在详细检测的8个突变体质粒中发现了三类突变体。3个突变体质粒在相对于nifH转录起始位点的-12或-14位置发生了单碱基对(bp)变化。这些突变位于先前描述的nif启动子-10至-15区域中的共有序列中。4个突变体质粒在转录起始点上游有明显的损伤。其中两个上游突变是核苷酸-72至-184的相同112 bp缺失,另外两个是-136位置的单碱基对变化。最后一个质粒在一个525 bp区域内没有突变,该区域包括nifH ATG起始密码子上游289 bp,并延伸到nifH基因内69个密码子。所有8个突变的pSA30质粒都不能互补染色体nifH突变,这表明阻止nif表达抑制的突变也会阻止nifHDKY操纵子的转录。