Contador Carolina A, Rizk Matthew L, Asenjo Juan A, Liao James C
Department of Chemical and Biomolecular Engineering, University of California, Los Angeles, Los Angeles, CA 90095-1592, USA.
Metab Eng. 2009 Jul-Sep;11(4-5):221-33. doi: 10.1016/j.ymben.2009.04.002. Epub 2009 Apr 18.
One of the main strategies to improve the production of relevant metabolites has been the manipulation of single or multiple key genes in the metabolic pathways. This kind of strategy requires several rounds of experiments to identify enzymes that impact either yield or productivity. The use of mathematical tools to facilitate this process is desirable. In this work, we apply the Ensemble Modeling (EM) framework, which uses phenotypic data (effects of enzyme overexpression or genetic knockouts on the steady-state production rate) to screen for potential models capable of describe existing data and thus gaining insight to improve strains for l-lysine production. Described herein is a strategy to generate a set of kinetic models that describe a set of enzyme overexpression phenotypes previously determined in an Escherichia coli strain that produces increased levels of l-lysine in an industrial laboratory. This final ensemble of models captures the kinetic characteristics of the cell through screening of phenotypes after sequential overexpression of enzymes. Furthermore, these models demonstrate some predictive capability, as starting from the reference producing strain (overexpressing desensitized dihydrodipicolinate synthetase (dapA*)) this set of models is able to predict that the desensitization of aspartate kinase (lysC*) is the next rate-controlling step in the l-lysine pathway. Moreover, this set of models allows for the generation of further targets for testing, for example, phosphoenolpyruvate (Ppc), aspartate aminotransferase (AspC), and glutamate dehydrogenase (GdhA). This work demonstrates the usefulness, applicability, and scope that the Ensemble Modeling framework offers to build production strains.
提高相关代谢产物产量的主要策略之一是对代谢途径中的单个或多个关键基因进行调控。这种策略需要进行多轮实验,以确定影响产量或生产率的酶。使用数学工具来促进这一过程是很有必要的。在这项工作中,我们应用了集成建模(EM)框架,该框架使用表型数据(酶过表达或基因敲除对稳态生产率的影响)来筛选能够描述现有数据的潜在模型,从而深入了解如何改进L-赖氨酸生产菌株。本文描述了一种生成一组动力学模型的策略,这些模型描述了先前在工业实验室中确定的一组酶过表达表型,该表型存在于一株L-赖氨酸产量增加的大肠杆菌菌株中。这组最终的模型通过对酶进行顺序过表达后的表型筛选,捕捉了细胞的动力学特征。此外,这些模型还展示了一定的预测能力,从参考生产菌株(过表达脱敏二氢吡啶二羧酸合酶(dapA*))开始,这组模型能够预测天冬氨酸激酶(lysC*)的脱敏是L-赖氨酸途径中的下一个速率控制步骤。此外,这组模型还可以生成进一步的测试靶点,例如磷酸烯醇丙酮酸(Ppc)、天冬氨酸转氨酶(AspC)和谷氨酸脱氢酶(GdhA)。这项工作证明了集成建模框架在构建生产菌株方面的有用性、适用性和范围。