Guo Weihua, Sheng Jiayuan, Feng Xueyang
Department of Biological Systems Engineering, Virginia Polytechnic Institute and State University, Blacksburg, VA 24061, USA.
Bioengineering (Basel). 2015 Dec 25;3(1):3. doi: 10.3390/bioengineering3010003.
Metabolic engineering of various industrial microorganisms to produce chemicals, fuels, and drugs has raised interest since it is environmentally friendly, sustainable, and independent of nonrenewable resources. However, microbial metabolism is so complex that only a few metabolic engineering efforts have been able to achieve a satisfactory yield, titer or productivity of the target chemicals for industrial commercialization. In order to overcome this challenge, C Metabolic Flux Analysis (C-MFA) has been continuously developed and widely applied to rigorously investigate cell metabolism and quantify the carbon flux distribution in central metabolic pathways. In the past decade, many C-MFA studies have been performed in academic labs and biotechnology industries to pinpoint key issues related to microbe-based chemical production. Insightful information about the metabolic rewiring has been provided to guide the development of the appropriate metabolic engineering strategies for improving the biochemical production. In this review, we will introduce the basics of C-MFA and illustrate how C-MFA has been applied via integration with metabolic engineering to identify and tackle the rate-limiting steps in biochemical production for various host microorganisms.
对各种工业微生物进行代谢工程改造以生产化学品、燃料和药物,因其环境友好、可持续且不依赖不可再生资源而备受关注。然而,微生物代谢非常复杂,只有少数代谢工程研究能够实现目标化学品在工业商业化方面令人满意的产量、滴度或生产率。为了克服这一挑战,碳代谢通量分析(C-MFA)不断发展并被广泛应用,以严格研究细胞代谢并量化中心代谢途径中的碳通量分布。在过去十年中,许多碳代谢通量分析研究在学术实验室和生物技术行业开展,以查明与基于微生物的化学品生产相关的关键问题。已提供了有关代谢重排的深刻信息,以指导制定适当的代谢工程策略来提高生化产品产量。在本综述中,我们将介绍碳代谢通量分析的基础知识,并说明碳代谢通量分析如何通过与代谢工程相结合来应用,以识别和解决各种宿主微生物在生化生产中的限速步骤。