Nanchen Annik, Schicker Alexander, Sauer Uwe
Institute of Molecular Systems Biology, ETH Zürich, CH-8093 Zürich, Switzerland.
Appl Environ Microbiol. 2006 Feb;72(2):1164-72. doi: 10.1128/AEM.72.2.1164-1172.2006.
A novel mini-scale chemostat system was developed for the physiological characterization of 10-ml cultures. The parallel operation of eight such mini-scale chemostats was exploited for systematic 13C analysis of intracellular fluxes over a broad range of growth rates in glucose-limited Escherichia coli. As expected, physiological variables changed monotonously with the dilution rate, allowing for the assessment of maintenance metabolism. Despite the linear dependence of total cellular carbon influx on dilution rate, the distribution of almost all major fluxes varied nonlinearly with dilution rate. Most prominent were the distinct maximum of glyoxylate shunt activity and the concomitant minimum of tricarboxylic acid cycle activity at low to intermediate dilution rates of 0.05 to 0.2 h(-1). During growth on glucose, this glyoxylate shunt activity is best understood from a network perspective as the recently described phosphoenolpyruvate (PEP)-glyoxylate cycle that oxidizes PEP (or pyruvate) to CO2. At higher or extremely low dilution rates, in vivo PEP-glyoxylate cycle activity was low or absent. The step increase in pentose phosphate pathway activity at around 0.2 h(-1) was not related to the cellular demand for the reduction equivalent NADPH, since NADPH formation was 20 to 50% in excess of the anabolic demand at all dilution rates. The results demonstrate that mini-scale continuous cultivation enables quantitative and parallel characterization of intra- and extracellular phenotypes in steady state, thereby greatly reducing workload and costs for stable-isotope experiments.
开发了一种新型的小型恒化器系统,用于对10毫升培养物进行生理特性分析。利用八个这样的小型恒化器并行运行,对葡萄糖受限的大肠杆菌在广泛生长速率范围内的细胞内通量进行系统的13C分析。正如预期的那样,生理变量随稀释率单调变化,从而能够评估维持代谢。尽管总细胞碳流入量与稀释率呈线性相关,但几乎所有主要通量的分布都随稀释率非线性变化。最显著的是在0.05至0.2 h(-1)的低至中等稀释率下,乙醛酸循环活性有明显最大值,而三羧酸循环活性则相应出现最小值。在葡萄糖上生长期间,从网络角度来看,这种乙醛酸循环活性最好理解为最近描述的磷酸烯醇丙酮酸(PEP)-乙醛酸循环,该循环将PEP(或丙酮酸)氧化为CO2。在较高或极低稀释率下,体内PEP-乙醛酸循环活性较低或不存在。在约0.2 h(-1)时磷酸戊糖途径活性的阶跃增加与细胞对还原当量NADPH的需求无关,因为在所有稀释率下,NADPH的形成都比合成代谢需求高出20%至50%。结果表明,小型连续培养能够在稳态下对细胞内和细胞外表型进行定量和并行表征,从而大大减少稳定同位素实验的工作量和成本。