Institute of Systems and Synthetic Biology, University of Evry Val d'Essonne , Evry , France ; Institute of Biochemistry, Biological Research Centre of the Hungarian Academy of Sciences , Szeged , Hungary.
Institute of Systems and Synthetic Biology, University of Evry Val d'Essonne , Evry , France ; Paris Diderot University , Paris , France.
Front Bioeng Biotechnol. 2015 Apr 8;3:46. doi: 10.3389/fbioe.2015.00046. eCollection 2015.
Production of value-added chemicals in microorganisms is regarded as a viable alternative to chemical synthesis. In the past decade, several engineered pathways producing such chemicals, including plant secondary metabolites in microorganisms have been reported; upscaling their production yields, however, was often challenging. Here, we analyze a modular device designed for sensing malonyl-CoA, a common precursor for both fatty acid and flavonoid biosynthesis. The sensor can be used either for high-throughput pathway screening in synthetic biology applications or for introducing a feedback circuit to regulate production of the desired chemical. Here, we used the sensor to compare the performance of several predicted malonyl-CoA-producing pathways, and validated the utility of malonyl-CoA reductase and malonate-CoA transferase for malonyl-CoA biosynthesis. We generated a second-order dynamic linear model describing the relation of the fluorescence generated by the sensor to the biomass of the host cell representing a filter/amplifier with a gain that correlates with the level of induction. We found the time constants describing filter dynamics to be independent of the level of induction but distinctively clustered for each of the production pathways, indicating the robustness of the sensor. Moreover, by monitoring the effect of the copy-number of the production plasmid on the dose-response curve of the sensor, we managed to coarse-tune the level of pathway expression to maximize malonyl-CoA synthesis. In addition, we provide an example of the sensor's use in analyzing the effect of inducer or substrate concentrations on production levels. The rational development of models describing sensors, supplemented with the power of high-throughput optimization provide a promising potential for engineering feedback loops regulating enzyme levels to maximize productivity yields of synthetic metabolic pathways.
在微生物中生产增值化学品被认为是替代化学合成的可行方法。在过去的十年中,已经报道了几种产生此类化学物质的工程途径,包括微生物中的植物次生代谢物;然而,提高它们的生产产量通常具有挑战性。在这里,我们分析了一种用于感应丙二酰辅酶 A 的模块化设备,丙二酰辅酶 A 是脂肪酸和类黄酮生物合成的常见前体。该传感器可用于合成生物学应用中的高通量途径筛选,或用于引入反馈回路以调节所需化学物质的生产。在这里,我们使用该传感器比较了几种预测的丙二酰辅酶 A 产生途径的性能,并验证了丙二酰辅酶 A 还原酶和丙二酸盐-CoA 转移酶用于丙二酰辅酶 A 生物合成的实用性。我们生成了一个二阶动态线性模型,该模型描述了传感器产生的荧光与代表滤波器/放大器的宿主细胞生物量之间的关系,该放大器的增益与诱导水平相关。我们发现,描述滤波器动力学的时间常数与诱导水平无关,但对于每种生产途径都有明显的聚类,这表明传感器具有鲁棒性。此外,通过监测生产质粒的拷贝数对传感器剂量-反应曲线的影响,我们设法对途径表达的水平进行粗调,以最大化丙二酰辅酶 A 的合成。此外,我们还提供了一个示例,说明该传感器用于分析诱导物或底物浓度对生产水平的影响。描述传感器的模型的合理开发,加上高通量优化的功能,为工程反馈回路提供了有希望的潜力,该反馈回路可调节酶水平以最大化合成代谢途径的生产力产量。