Navone Laura, McCubbin Tim, Gonzalez-Garcia Ricardo A, Nielsen Lars K, Marcellin Esteban
Australian Institute for Bioengineering and Nanotechnology, The University of Queensland, Australia.
Queensland Node of Metabolomics Australia, The University of Queensland, Australia.
Metab Eng Commun. 2017 Nov 24;6:1-12. doi: 10.1016/j.meteno.2017.11.001. eCollection 2018 Jun.
Production of propionic acid by fermentation of propionibacteria has gained increasing attention in the past few years. However, biomanufacturing of propionic acid cannot compete with the current oxo-petrochemical synthesis process due to its well-established infrastructure, low oil prices and the high downstream purification costs of microbial production. Strain improvement to increase propionic acid yield is the best alternative to reduce downstream purification costs. The recent generation of genome-scale models for a number of species facilitates the rational design of metabolic engineering strategies and provides a new opportunity to explore the metabolic potential of the Wood-Werkman cycle. Previous strategies for strain improvement have individually targeted acid tolerance, rate of propionate production or minimisation of by-products. Here we used the subsp and the pan- genome-scale metabolic models (GEMs) to simultaneously target these combined issues. This was achieved by focussing on strategies which yield higher energies and directly suppress acetate formation. Using subsp, two strategies were assessed. The first tested the ability to manipulate the redox balance to favour propionate production by over-expressing the first two enzymes of the pentose-phosphate pathway (PPP), Zwf (glucose-6-phosphate 1-dehydrogenase) and Pgl (6-phosphogluconolactonase). Results showed a 4-fold increase in propionate to acetate ratio during the exponential growth phase. Secondly, the ability to enhance the energy yield from propionate production by over-expressing an ATP-dependent phosphoenolpyruvate carboxykinase (PEPCK) and sodium-pumping methylmalonyl-CoA decarboxylase (MMD) was tested, which extended the exponential growth phase. Together, these strategies demonstrate that design strategies are predictive and can be used to reduce by-product formation in . We also describe the benefit of carbon dioxide to propionibacteria growth, substrate conversion and propionate yield.
在过去几年中,丙酸杆菌发酵生产丙酸受到了越来越多的关注。然而,由于其成熟的基础设施、低廉的油价以及微生物生产中高昂的下游纯化成本,丙酸的生物制造无法与当前的羰基石油化学合成工艺竞争。提高丙酸产量的菌株改良是降低下游纯化成本的最佳选择。最近为多个物种构建的基因组规模模型有助于合理设计代谢工程策略,并为探索伍德-韦克曼循环的代谢潜力提供了新机会。以前的菌株改良策略分别针对耐酸性、丙酸盐生产速率或副产物最小化。在这里,我们使用亚种和泛基因组规模代谢模型(GEMs)同时解决这些综合问题。这是通过专注于产生更高能量并直接抑制乙酸盐形成的策略来实现的。使用亚种,评估了两种策略。第一种策略测试了通过过表达戊糖磷酸途径(PPP)的前两种酶Zwf(葡萄糖-6-磷酸1-脱氢酶)和Pgl(6-磷酸葡萄糖酸内酯酶)来操纵氧化还原平衡以促进丙酸盐生产的能力。结果表明,在指数生长期,丙酸盐与乙酸盐的比例增加了4倍。其次,测试了通过过表达ATP依赖性磷酸烯醇丙酮酸羧激酶(PEPCK)和钠泵甲基丙二酰辅酶A脱羧酶(MMD)来提高丙酸盐生产能量产量的能力,这延长了指数生长期。总之,这些策略表明设计策略具有预测性,可用于减少亚种中的副产物形成。我们还描述了二氧化碳对丙酸杆菌生长、底物转化和丙酸盐产量的益处。