Department of Chemical Engineering, The Pennsylvania State University, University Park, PA 16802, United States.
Department of Chemical Engineering, The Pennsylvania State University, University Park, PA 16802, United States.
Curr Opin Biotechnol. 2015 Dec;36:57-64. doi: 10.1016/j.copbio.2015.08.011. Epub 2015 Aug 28.
Several modeling frameworks for describing and redirecting cellular metabolism have been developed keeping pace with the rapid development in high-throughput data generation and advances in metabolic engineering techniques. The incorporation of kinetic information within stoichiometry-only modeling techniques offers potential advantages for improved phenotype prediction and consequently more precise computational strain design. In addition to substrate-level kinetic regulatory information, the integration of a number of additional layers of regulation at the transcription, translation, and post-translation levels is sought after by many research groups. However, the practical integration of these complex biological processes into a unified framework amenable to design remains an ongoing challenge.
随着高通量数据生成和代谢工程技术的进步,已经开发出了几种用于描述和重定向细胞代谢的建模框架。在仅基于化学计量学的建模技术中纳入动力学信息为改善表型预测提供了潜在优势,从而可以更精确地进行计算菌株设计。除了底物水平的动力学调节信息外,许多研究小组还寻求在转录、翻译和翻译后水平整合许多其他调节层。然而,将这些复杂的生物过程实际整合到一个统一的、适合设计的框架中仍然是一个持续的挑战。