Thomulka K W, Gots J S
J Bacteriol. 1982 Jul;151(1):153-61. doi: 10.1128/jb.151.1.153-161.1982.
Expression of the purE operon of Salmonella typhimurium was analyzed by using an Escherichia coli F' episome containing a purE-lac fusion. The fusion removes the lacOP and part of the lacZ genes of the lac operon and places the intact lacY and lacA genes under control of the purE operon as shown by inhibition of growth on melibiose (lacY) and repression of thiogalactoside transacetylase (lacA) by various purines. Two classes of regulatory-deficient mutants were found among those resistant to inhibition by purines. One class was trans active (chromosomal) and corresponded to previously described purR mutants involving a deficient cytoplasmic repressor substance. These were also altered in the expression of the purF, purD, purG amd purI genes as evidenced by loss of repressibility of the synthesis of glycinamide ribotide and aminoimidazole ribotide. The other class was cis active (episomal), specific for only purE expression, and thus corresponded to an altered purE operon signal (operator or promoter). The metabolic requirements for the expression of purE were also monitored by measuring repression of the transacetylase in strains with various genetically altered metabolic backgrounds. Repression by guanine required an intact guanine phosphorbosyltransferase (gpt) and repression by adenine and all nucleosides required purine nucleoside phosphorylase (deoD). Synthesis of cyclic AMP (cya) and its receptor protein (crp) were no longer required for the expression of the lac genes under purE control.
利用含有purE-lac融合基因的大肠杆菌F'附加体,分析了鼠伤寒沙门氏菌purE操纵子的表达。这种融合去除了lac操纵子的lacOP和部分lacZ基因,并将完整的lacY和lacA基因置于purE操纵子的控制之下,这可通过在蜜二糖(lacY)上生长受抑制以及各种嘌呤对硫代半乳糖苷转乙酰酶(lacA)的抑制来证明。在对嘌呤抑制有抗性的菌株中发现了两类调节缺陷型突变体。一类是反式作用(染色体)的,对应于先前描述的purR突变体,涉及一种缺陷的细胞质阻遏物质。这些突变体在purF、purD、purG和purI基因的表达上也发生了改变,这可通过甘氨酰胺核苷酸和氨基咪唑核苷酸合成的可阻遏性丧失来证明。另一类是顺式作用(附加体)的,仅对purE表达具有特异性,因此对应于改变的purE操纵子信号(操纵基因或启动子)。还通过测量具有各种遗传改变代谢背景的菌株中转乙酰酶的抑制情况,监测了purE表达的代谢需求。鸟嘌呤的抑制需要完整的鸟嘌呤磷酸核糖转移酶(gpt),腺嘌呤和所有核苷的抑制需要嘌呤核苷磷酸化酶(deoD)。在purE控制下,lac基因的表达不再需要环腺苷酸(cya)及其受体蛋白(crp)的合成。