Garner C C, Herrmann K M
J Biol Chem. 1985 Mar 25;260(6):3820-5.
The Escherichia coli aroF and aroG genes encode the tyrosine-sensitive and the phenylalanine-sensitive 3-deoxy-D-arabino-heptulosonate 7-phosphate synthases, respectively, two of the three isoenzymes that control carbon flow through the shikimate pathway. Transcription of aroF and aroG is repressed by the tyrR gene product complexed to tyrosine or phenylalanine, respectively. Constitutive aroF mutants with lesions linked to aroF were isolated. The nucleotide sequences in the regulatory regions of aroF from six such mutants and from the parental wild type strain were determined. The mutations were found in two 18-base pair imperfect palindromes, called aroFo1 and aroFo2, which are located upstream of the aroF transcription start by 61 and 113 base pairs, respectively. Nuclease S1 mapping and analysis of in vitro run-off transcripts identified the 5'-end of the aroF transcript 51 base pairs upstream of the aroF translation start. The -35 region of the aroF promoter overlaps aroFo1. The aroFo1 and aroFo2 sequences are homologous to a single 18-base pair DNA segment preceding the coding sequence of aroG.
大肠杆菌的aroF和aroG基因分别编码对酪氨酸敏感和对苯丙氨酸敏感的3-脱氧-D-阿拉伯庚酮糖酸7-磷酸合酶,这是控制碳流经莽草酸途径的三种同工酶中的两种。aroF和aroG的转录分别被与酪氨酸或苯丙氨酸复合的tyrR基因产物所抑制。分离出了与aroF相关的具有损伤的组成型aroF突变体。测定了来自六个此类突变体和亲本野生型菌株的aroF调控区的核苷酸序列。这些突变出现在两个18碱基对的不完全回文序列中,分别称为aroFo1和aroFo2,它们分别位于aroF转录起始位点上游61和113个碱基对处。核酸酶S1图谱分析和体外延伸转录本分析确定aroF转录本的5'端位于aroF翻译起始位点上游51个碱基对处。aroF启动子的-35区与aroFo1重叠。aroFo1和aroFo2序列与aroG编码序列之前的一个18碱基对DNA片段同源。