Notley-McRobb Lucinda, Death Alison, Ferenci Thomas
Department of Microbiology G08, University of Sydney, Sydney, New South Wales 2006, Australia.
Microbiology (Reading). 1997 Jun;143 ( Pt 6):1909-1918. doi: 10.1099/00221287-143-6-1909.
The concentration of glucose in the medium influences the regulation of cAMP levels in Escherichia coli. Growth in minimal medium with micromolar glucose results in 8- to 10-fold higher intracellular cAMP concentrations than observed during growth with excess glucose. Current models would suggest that the difference in cAMP levels between glucose-rich and glucose-limited states is due to altered transport flux through the phosphoenolpyruvate: glucose phosphotransferase system (PTS), which in turn controls adenylate cyclase. A consequence of this model is that cAMP levels should be inversely related to the saturation of the PTS transporter. To test this hypothesis, the relationship between external glucose concentration and cAMP levels inside E. coli were investigated in detail, both through direct cAMP assay and indirectly through measurement of expression of cAMP-regulated genes. Responses were followed in batch, dialysis and glucose-limited continuous culture. A sharp rise in intracellular cAMP occurred when the nutrient concentration in minimal medium dropped to approximately 0.3 mM glucose. Likewise, addition of > 0.3 mM glucose, but not < 0.3 mM glucose, sharply reduced the intracellular cAMP level of starving bacteria. There was no striking shift in growth rate or [14C] glucose assimilation in bacteria passing through the 0.5 to 0.3 mM concentration threshold influencing cAMP levels, suggesting that neither metabolic flux nor transporter saturation influenced the sensing of nutrient levels. The (IIA/IIBC)Glc PTS is 96-97% saturated at 0.3 mM glucose so these results are not easily reconcilable with current models of cAMP regulation. Aside from the transition in cAMP levels initiated above 0.3 mM, a second shift occurred below 1 muM glucose. Approaching starvation, well below saturation of the PTS, cAMP levels either increased or decreased depending on unknown factors that differ between common E. coli K-12 strains.
培养基中葡萄糖的浓度会影响大肠杆菌中cAMP水平的调节。在含有微摩尔浓度葡萄糖的基本培养基中生长时,细胞内cAMP浓度比在葡萄糖过量时生长时高出8至10倍。目前的模型表明,富含葡萄糖和葡萄糖受限状态之间cAMP水平的差异是由于通过磷酸烯醇丙酮酸:葡萄糖磷酸转移酶系统(PTS)的转运通量改变所致,而这又反过来控制腺苷酸环化酶。该模型的一个结果是cAMP水平应与PTS转运体的饱和度呈负相关。为了验证这一假设,通过直接cAMP测定以及间接通过测量cAMP调节基因的表达,详细研究了大肠杆菌外部葡萄糖浓度与细胞内cAMP水平之间的关系。在分批培养、透析培养和葡萄糖受限连续培养中跟踪反应。当基本培养基中的营养物浓度降至约0.3 mM葡萄糖时,细胞内cAMP急剧上升。同样,添加>0.3 mM葡萄糖而非<0.3 mM葡萄糖会显著降低饥饿细菌的细胞内cAMP水平。在通过影响cAMP水平的0.5至0.3 mM浓度阈值的细菌中,生长速率或[14C]葡萄糖同化没有明显变化,这表明代谢通量和转运体饱和度均未影响营养水平的感知。(IIA/IIBC)Glc PTS在0.3 mM葡萄糖时饱和度为96 - 97%,因此这些结果与当前的cAMP调节模型难以协调一致。除了在0.3 mM以上引发的cAMP水平转变外,在葡萄糖浓度低于1 μM时还发生了第二次转变。接近饥饿状态时,远低于PTS的饱和度,cAMP水平根据常见大肠杆菌K - 12菌株之间不同的未知因素而升高或降低。