Institute of Molecular System Biology, ETH Zurich, 8093 Zurich, Switzerland.
Proc Natl Acad Sci U S A. 2013 Jan 15;110(3):1130-5. doi: 10.1073/pnas.1202582110. Epub 2012 Dec 31.
Regulation of metabolic operation in response to extracellular cues is crucial for cells' survival. Next to the canonical nutrient sensors, which measure the concentration of nutrients, recently intracellular "metabolic flux" was proposed as a novel impetus for metabolic regulation. According to this concept, cells would have molecular systems ("flux sensors") in place that regulate metabolism as a function of the actually occurring metabolic fluxes. Although this resembles an appealing concept, we have not had any experimental evidence for the existence of flux sensors and also we have not known how these flux sensors would work in detail. Here, we show experimental evidence that supports the hypothesis that Escherichia coli is indeed able to measure its glycolytic flux and uses this signal for metabolic regulation. Combining experiment and theory, we show how this flux-sensing function could emerge from an aggregate of several molecular mechanisms: First, the system of reactions of lower glycolysis and the feedforward activation of fructose-1,6-bisphosphate on pyruvate kinase translate flux information into the concentration of the metabolite fructose-1,6-bisphosphate. The interaction of this "flux-signaling metabolite" with the transcription factor Cra then leads to flux-dependent regulation. By responding to glycolytic flux, rather than to the concentration of individual carbon sources, the cell may minimize sensing and regulatory expenses.
细胞为了生存,必须根据细胞外信号调控代谢活动。除了经典的营养传感器(用于测量营养物质浓度),最近还提出了“代谢流”作为代谢调控的新动力。根据这一概念,细胞内应该存在分子系统(“代谢流传感器”),可根据实际发生的代谢流来调节代谢。尽管这一概念很有吸引力,但我们还没有任何关于代谢流传感器存在的实验证据,也不知道这些代谢流传感器的具体工作机制。在这里,我们提供了实验证据,表明大肠杆菌确实能够测量其糖酵解流,并利用该信号进行代谢调控。通过实验和理论相结合,我们展示了这种通量感应功能如何从几种分子机制的集合中产生:首先,低聚糖酵解反应系统和对丙酮酸激酶的果糖-1,6-二磷酸的前馈激活将通量信息转化为代谢物果糖-1,6-二磷酸的浓度。这种“通量信号代谢物”与转录因子 Cra 的相互作用导致了依赖通量的调节。通过响应糖酵解流,而不是单个碳源的浓度,细胞可以最小化感应和调节的成本。