Belfaiza J, Guillou Y, Margarita D, Perrin D, Saint Girons I
J Bacteriol. 1987 Feb;169(2):670-4. doi: 10.1128/jb.169.2.670-674.1987.
The Escherichia coli metF gene codes for 5,10-methylene-tetrahydrofolate reductase, the enzyme that leads to the formation of N-methyltetrahydrofolate, supplying the methyl group of methionine. Transcription of metF, as well as most of the methionine genes, is repressed by the metJ gene product complexed with S-adenosylmethionine. A metF'-'lacZ gene fusion was used to isolate mutants that have altered expression from the metF promoter. The nucleotide sequences of the metF regulatory region from five such mutants were determined. The mutations were located in the region previously defined as the potential target of the methionine repressor by its similarity to other binding sites. The mutationally defined metF operator thus consists of a 40-base-pair-long region, with five 8-base-pair imperfect palindromes spanning the metF transcription start. The altered operators do not recognize the purified repressor in an in vitro transcription-translation system, although the repressor binds efficiently to the metF wild-type operator.
大肠杆菌的metF基因编码5,10-亚甲基四氢叶酸还原酶,该酶可导致N-甲基四氢叶酸的形成,为甲硫氨酸提供甲基。metF以及大多数甲硫氨酸基因的转录会被与S-腺苷甲硫氨酸复合的metJ基因产物所抑制。利用metF'-'lacZ基因融合技术分离出了一些在metF启动子处表达发生改变的突变体。测定了来自五个此类突变体的metF调控区域的核苷酸序列。这些突变位于先前因其与其他结合位点的相似性而被定义为甲硫氨酸阻遏物潜在靶点的区域。通过突变定义的metF操纵子因此由一个40个碱基对长的区域组成,有五个8个碱基对的不完全回文序列跨越metF转录起始位点。尽管阻遏物能有效地结合到metF野生型操纵子上,但在体外转录-翻译系统中,改变后的操纵子无法识别纯化的阻遏物。