Smith J M, Daum H A
J Biol Chem. 1986 Aug 15;261(23):10632-6.
5'-Phosphoribosyl-5-aminoimidazole synthetase (EC 6.3.3.1), encoded by the purM gene of Escherichia coli, catalyzes the synthesis of 5'-phosphoribosyl-5-aminoimidazole from 5'-phosphoribosylformylglycinamidine. The purM gene was subcloned from the Clarke and Carbon (Clarke, L., and Carbon, J. (1976) Cell 9, 91-99) plasmid pLC1-41 and the nucleotide sequence determined. The mature protein, as deduced from the purM structural gene sequence, contains 344 amino acid residues and has a calculated Mr of 36,726. The 5' end of the purM mRNA was determined by mung bean nuclease mapping to be 44-45 nucleotides up-stream of the proposed GTG translation initiation codon. A C-G-rich region characteristic of stringently controlled promoters is located immediately in front of the proposed purM promoter region. Comparison of the upstream sequences of the purM and the coregulated purF loci revealed a highly conserved (33 of 39 base pairs are identical) sequence. The presumptive purM promoter is located in this region, thus suggesting that both purine loci share a common mechanism of regulation mediated through this sequence.
5'-磷酸核糖-5-氨基咪唑合成酶(EC 6.3.3.1)由大肠杆菌的purM基因编码,催化从5'-磷酸核糖甲酰甘氨脒合成5'-磷酸核糖-5-氨基咪唑。purM基因从克拉克和卡尔文(克拉克,L.,和卡尔文,J.(1976年)《细胞》9卷,91 - 99页)的质粒pLC1 - 41中进行亚克隆并测定了核苷酸序列。从purM结构基因序列推导得出的成熟蛋白含有344个氨基酸残基,计算得出的分子量为36,726。通过绿豆核酸酶定位确定purM mRNA的5'端位于拟议的GTG翻译起始密码子上游44 - 45个核苷酸处。一个具有严格控制启动子特征的富含C - G的区域紧邻拟议的purM启动子区域。对purM和共同调控的purF基因座上游序列的比较揭示了一个高度保守的序列(39个碱基对中有33个相同)。推测的purM启动子位于该区域,因此表明这两个嘌呤基因座共享一种通过该序列介导的共同调控机制。