Department of Chemical and Biomolecular Engineering, Metabolic Engineering and Systems Biology Laboratory, University of Delaware, 150 Academy St., Newark, DE 19716, USA.
Department of Chemical and Biomolecular Engineering, Metabolic Engineering and Systems Biology Laboratory, University of Delaware, 150 Academy St., Newark, DE 19716, USA.
Metab Eng. 2017 Nov;44:191-197. doi: 10.1016/j.ymben.2017.10.008. Epub 2017 Oct 16.
Vibrio natriegens is a fast-growing, non-pathogenic bacterium that is being considered as the next-generation workhorse for the biotechnology industry. However, little is known about the metabolism of this organism which is limiting our ability to apply rational metabolic engineering strategies. To address this critical gap in current knowledge, here we have performed a comprehensive analysis of V. natriegens metabolism. We constructed a detailed model of V. natriegens core metabolism, measured the biomass composition, and performed high-resolution C metabolic flux analysis (C-MFA) to estimate intracellular fluxes using parallel labeling experiments with the optimal tracers [1,2-C]glucose and [1,6-C]glucose. During exponential growth in glucose minimal medium, V. natriegens had a growth rate of 1.70 1/h (doubling time of 24min) and a glucose uptake rate of 3.90g/g/h, which is more than two 2-fold faster than E. coli, although slower than the fast-growing thermophile Geobacillus LC300. C-MFA revealed that the core metabolism of V. natriegens is similar to that of E. coli, with the main difference being a 33% lower normalized flux through the oxidative pentose phosphate pathway. Quantitative analysis of co-factor balances provided additional insights into the energy and redox metabolism of V. natriegens. Taken together, the results presented in this study provide valuable new information about the physiology of V. natriegens and establish a solid foundation for future metabolic engineering efforts with this promising microorganism.
嗜盐菌是一种快速生长的、非致病性细菌,被认为是下一代生物技术产业的主力军。然而,我们对这种生物的代谢知之甚少,这限制了我们应用合理的代谢工程策略的能力。为了解决当前知识中的这一关键差距,我们在这里对嗜盐菌的代谢进行了全面分析。我们构建了嗜盐菌核心代谢的详细模型,测量了生物量组成,并通过使用最优示踪剂[1,2-C]葡萄糖和[1,6-C]葡萄糖进行平行标记实验,进行了高分辨率 C 代谢通量分析(C-MFA)来估计细胞内通量。在葡萄糖最小培养基中进行指数生长时,嗜盐菌的生长速率为 1.70 1/h(倍增时间为 24 分钟),葡萄糖摄取速率为 3.90g/g/h,这比大肠杆菌快两倍多,尽管比快速生长的嗜热菌 Geobacillus LC300 慢。C-MFA 表明,嗜盐菌的核心代谢与大肠杆菌相似,主要区别在于氧化戊糖磷酸途径的归一化通量低 33%。辅酶平衡的定量分析为嗜盐菌的能量和氧化还原代谢提供了更多的见解。总之,本研究的结果提供了有关嗜盐菌生理学的有价值的新信息,并为未来对这种有前途的微生物进行代谢工程提供了坚实的基础。