Willrodt Christian, Hoschek Anna, Bühler Bruno, Schmid Andreas, Julsing Mattijs K
Department Solar Materials, Helmholtz Centre for Environmental Research (UFZ), Leipzig, Germany.
Department of Biochemical and Chemical Engineering, Laboratory of Chemical Biotechnology, TU Dortmund University, Dortmund, Germany.
Biotechnol Bioeng. 2016 Jun;113(6):1305-14. doi: 10.1002/bit.25883. Epub 2015 Dec 17.
The microbial production of isoprenoids has recently developed into a prime example for successful bottom-up synthetic biology or top-down systems biology strategies. Respective fermentation processes typically rely on growing recombinant microorganisms. However, the fermentative production of isoprenoids has to compete with cellular maintenance and growth for carbon and energy. Non-growing but metabolically active E. coli cells were evaluated in this study as alternative biocatalyst configurations to reduce energy and carbon loss towards biomass formation. The use of non-growing cells in an optimized fermentation medium resulted in more than fivefold increased specific limonene yields on cell dry weight and glucose, as compared to the traditional growing-cell-approach. Initially, the stability of the resting-cell activity was limited. This instability was overcome via the optimization of the minimal fermentation medium enabling high and stable limonene production rates for up to 8 h and a high specific yield of ≥50 mg limonene per gram cell dry weight. Omitting MgSO4 from the fermentation medium was very promising to prohibit growth and allow high productivities. Applying a MgSO4 -limitation also improved limonene formation by growing cells during non-exponential growth involving a reduced biomass yield on glucose and a fourfold increase in specific limonene yields on biomass as compared to non-limited cultures. The control of microbial growth via the medium composition was identified as a key but yet underrated strategy for efficient isoprenoid production. Biotechnol. Bioeng. 2016;113: 1305-1314. © 2015 Wiley Periodicals, Inc.
类异戊二烯的微生物生产最近已发展成为自下而上的合成生物学或自上而下的系统生物学策略成功应用的一个典型例子。相应的发酵过程通常依赖于培养重组微生物。然而,类异戊二烯的发酵生产必须与细胞维持和生长竞争碳源和能源。在本研究中,对非生长但代谢活跃的大肠杆菌细胞作为替代生物催化剂配置进行了评估,以减少生物质形成过程中的能量和碳损失。与传统的生长细胞方法相比,在优化的发酵培养基中使用非生长细胞使基于细胞干重和葡萄糖的柠檬烯比产量提高了五倍以上。最初,静息细胞活性的稳定性有限。通过优化基本发酵培养基克服了这种不稳定性,从而实现了长达8小时的高且稳定的柠檬烯生产率以及≥50mg柠檬烯/克细胞干重的高比产量。从发酵培养基中省略硫酸镁对于抑制生长和实现高生产率非常有前景。在非指数生长期间,对生长细胞应用硫酸镁限制也改善了柠檬烯的形成,与非限制培养相比,葡萄糖上的生物质产量降低,生物质上的柠檬烯比产量提高了四倍。通过培养基组成控制微生物生长被确定为高效生产类异戊二烯的关键但尚未得到充分重视的策略。《生物技术与生物工程》2016年;113:1305 - 1314。©2015威利期刊公司