Institute of Intelligent Machines, Hefei Institutes of Physical Science, Chinese Academy of Sciences, Hefei , 230031, China.
University of Science and Technology of China, Hefei, 230026, China.
Microb Cell Fact. 2022 May 28;21(1):101. doi: 10.1186/s12934-022-01823-3.
Menaquinone-7 (MK-7), which is associated with complex and tightly regulated pathways and redox imbalances, is produced at low titres in Bacillus subtilis. Synthetic biology provides a rational engineering principle for the transcriptional optimisation of key enzymes and the artificial creation of cofactor regeneration systems without regulatory interference. This holds great promise for alleviating pathway bottlenecks and improving the efficiency of carbon and energy utilisation.
We used a bottom-up synthetic biology approach for the synthetic redesign of central carbon and to improve the adaptability between material and energy metabolism in MK-7 synthesis pathways. First, the rate-limiting enzymes, 1-deoxyxylulose-5-phosphate synthase (DXS), isopentenyl-diphosphate delta-isomerase (Fni), 1-deoxyxylulose-5-phosphate reductase (DXR), isochorismate synthase (MenF), and 3-deoxy-7-phosphoheptulonate synthase (AroA) in the MK-7 pathway were sequentially overexpressed. Promoter engineering and fusion tags were used to overexpress the key enzyme MenA, and the titre of MK-7 was 39.01 mg/L. Finally, after stoichiometric calculation and optimisation of the cofactor regeneration pathway, we constructed two NADPH regeneration systems, enhanced the endogenous cofactor regeneration pathway, and introduced a heterologous NADH kinase (Pos5P) to increase the availability of NADPH for MK-7 biosynthesis. The strain expressing pos5P was more efficient in converting NADH to NADPH and had excellent MK-7 synthesis ability. Following three Design-Build-Test-Learn cycles, the titre of MK-7 after flask fermentation reached 53.07 mg/L, which was 4.52 times that of B. subtilis 168. Additionally, the artificially constructed cofactor regeneration system reduced the amount of NADH-dependent by-product lactate in the fermentation broth by 9.15%. This resulted in decreased energy loss and improved carbon conversion.
In summary, a "high-efficiency, low-carbon, cofactor-recycling" MK-7 synthetic strain was constructed, and the strategy used in this study can be generally applied for constructing high-efficiency synthesis platforms for other terpenoids, laying the foundation for the large-scale production of high-value MK-7 as well as terpenoids.
menaquinone-7(MK-7)与复杂且受严格调控的途径和氧化还原失衡有关,在枯草芽孢杆菌中产量较低。合成生物学为关键酶的转录优化和人工创建辅酶再生系统提供了合理的工程原理,而不会受到调控干扰。这为缓解途径瓶颈和提高碳和能源利用效率带来了巨大的希望。
我们使用自下而上的合成生物学方法对中心碳的合成进行了重新设计,并改进了 MK-7 合成途径中物质和能量代谢之间的适应性。首先,逐步过表达 MK-7 途径中的限速酶 1-脱氧木酮糖-5-磷酸合酶(DXS)、异戊烯二磷酸 delta-异构酶(Fni)、1-脱氧木酮糖-5-磷酸还原酶(DXR)、异戊烯焦磷酸合酶(MenF)和 3-脱氧-7-磷酸庚酮糖合酶(AroA)。利用启动子工程和融合标签过表达关键酶 MenA,MK-7 的产量为 39.01mg/L。最后,经过辅酶再生途径的化学计量计算和优化,我们构建了两个 NADPH 再生系统,增强了内源性辅酶再生途径,并引入了一种异源 NADH 激酶(Pos5P),以增加 NADPH 用于 MK-7 生物合成的可用性。表达 pos5P 的菌株在将 NADH 转化为 NADPH 方面更有效,并且具有出色的 MK-7 合成能力。经过三个设计-构建-测试-学习循环,摇瓶发酵后 MK-7 的产量达到 53.07mg/L,是枯草芽孢杆菌 168 的 4.52 倍。此外,人工构建的辅酶再生系统使发酵液中依赖 NADH 的副产物乳酸的量减少了 9.15%。这导致能量损失减少,碳转化率提高。
总之,构建了“高效、低碳、辅酶循环”的 MK-7 合成菌株,本研究中使用的策略可广泛应用于构建其他萜类化合物的高效合成平台,为大规模生产高价值的 MK-7 和萜类化合物奠定了基础。