He B, Shiau A, Choi K Y, Zalkin H, Smith J M
Department of Biochemistry, Purdue University, West Lafayette, Indiana 47907.
J Bacteriol. 1990 Aug;172(8):4555-62. doi: 10.1128/jb.172.8.4555-4562.1990.
Fusions of lacZ were constructed to genes in each of the loci involved in de novo synthesis of IMP. The expression of each pur-lacZ fusion was determined in isogenic purR and purR+ strains. These measurements indicated 5- to 17-fold coregulation of genes purF, purHD, purC, purMN, purL, and purEK and thus confirm the existence of a pur regulon. Gene purB, which encodes an enzyme involved in synthesis of IMP and in the AMP branch of the pathway, was not regulated by purR. Each locus of the pur regulon contains a 16-base-pair conserved operator sequence that overlaps with the promoter. The purR product, purine repressor, was shown to bind specifically to each operator. Thus, binding of repressor to each operator of pur regulon genes negatively coregulates expression.
构建了与参与肌苷酸(IMP)从头合成的每个基因座中的基因融合的lacZ。在同基因的purR和purR +菌株中测定每个pur-lacZ融合体的表达。这些测量表明基因purF、purHD、purC、purMN、purL和purEK有5至17倍的共调节,从而证实了嘌呤调节子的存在。编码参与IMP合成和该途径的AMP分支的一种酶的基因purB不受purR调节。嘌呤调节子的每个基因座都包含一个与启动子重叠的16个碱基对的保守操纵序列。嘌呤阻遏物purR产物被证明能特异性结合每个操纵子。因此,阻遏物与嘌呤调节子基因的每个操纵子结合会负向共调节表达。