Eichel J, Chang Y Y, Riesenberg D, Cronan J E
Hans-Knöll Institute for Natural Products Research, Jena, Germany.
J Bacteriol. 1999 Jan;181(2):572-6. doi: 10.1128/JB.181.2.572-576.1999.
Strains of Escherichia coli carrying mutations at the relA locus are deficient in cyclopropane fatty acid (CFA) synthesis, a phospholipid modification that occurs as cultures enter stationary phase. RelA protein catalyzes the synthesis of guanosine-3',5'-bisdiphosphate (ppGpp); therefore, ppGpp was a putative direct regulator of CFA synthesis. The nucleotide could act by increasing either the activity or the amount of CFA synthase, the enzyme catalyzing the lipid modification. We report that the effect of RelA on CFA synthesis is indirect. In vitro and in vivo experiments show no direct interaction between ppGpp and CFA synthase activity. The relA effect is due to ppGpp-engendered stimulation of the synthesis of the alternative sigma factor, RpoS, which is required for function of one of the two promoters responsible for expression of CFA synthase.
携带relA位点突变的大肠杆菌菌株在环丙烷脂肪酸(CFA)合成方面存在缺陷,CFA合成是一种在培养物进入稳定期时发生的磷脂修饰。RelA蛋白催化鸟苷-3',5'-双二磷酸(ppGpp)的合成;因此,ppGpp被认为是CFA合成的直接调节因子。该核苷酸可能通过增加CFA合酶的活性或数量来发挥作用,CFA合酶是催化脂质修饰的酶。我们报告RelA对CFA合成的影响是间接的。体外和体内实验表明ppGpp与CFA合酶活性之间没有直接相互作用。relA的作用是由于ppGpp对替代西格玛因子RpoS合成的刺激,RpoS是负责CFA合酶表达的两个启动子之一的功能所必需的。