Dietz Katharina, Sagstetter Carina, Speck Melanie, Roth Arne, Klamt Steffen, Fabarius Jonathan Thomas
Fraunhofer Institute for Interfacial Engineering and Biotechnology, Straubing Branch BioCat, Schulgasse 11a, Straubing, Germany.
Max Planck Institute for Dynamics of Complex Technical Systems, Sandtorstr. 1, Magdeburg, Germany.
Microb Cell Fact. 2024 Dec 23;23(1):344. doi: 10.1186/s12934-024-02583-y.
The conversion of CO into methanol depicts one of the most promising emerging renewable routes for the chemical and biotech industry. Under this regard, native methylotrophs have a large potential for converting methanol into value-added products but require targeted engineering approaches to enhance their performances and to widen their product spectrum. Here we use a systems-based approach to analyze and engineer M. extorquens TK 0001 for production of glycolic acid. Application of constraint-based metabolic modeling reveals the great potential of M. extorquens for that purpose, which is not yet described in literature. In particular, a superior theoretical product yield of 1.0 C-mol C-mol is predicted by our model, surpassing theoretical yields of sugar fermentation. Following this approach, we show here that strain engineering is viable and present 1st generation strains producing glycolic acid via a heterologous NADPH-dependent glyoxylate reductase. It was found that lactic acid is a surprising by-product of glycolic acid formation in M. extorquens, most likely due to a surplus of available NADH upon glycolic acid synthesis. Finally, the best performing strain was tested in a fed-batch fermentation producing a mixture of up to total 1.2 g L glycolic acid and lactic acid. Several key performance indicators of our glycolic acid producer strain are superior to state-of-the-art synthetic methylotrophs. The presented results open the door for further strain engineering of the native methylotroph M. extorquens and pave the way to produce two promising biopolymer building blocks from green methanol, i.e., glycolic acid and lactic acid.
将一氧化碳转化为甲醇是化学和生物技术行业最有前景的新兴可再生途径之一。在这方面,天然甲基营养菌具有将甲醇转化为增值产品的巨大潜力,但需要有针对性的工程方法来提高其性能并拓宽其产品谱。在这里,我们采用基于系统的方法来分析和改造嗜甲基菌TK 0001以生产乙醇酸。基于约束的代谢建模应用揭示了嗜甲基菌在此方面的巨大潜力,这在文献中尚未有描述。特别是,我们的模型预测其理论产品产率高达1.0 C-摩尔/碳摩尔,超过了糖发酵的理论产率。按照这种方法,我们在此表明菌株工程是可行的,并展示了通过异源NADPH依赖性乙醛酸还原酶生产乙醇酸的第一代菌株。研究发现,乳酸是嗜甲基菌中乙醇酸形成过程中令人惊讶的副产物,这很可能是由于乙醇酸合成时可用NADH过剩所致。最后,在补料分批发酵中对性能最佳的菌株进行了测试,其可产生总量高达1.2 g/L的乙醇酸和乳酸混合物。我们的乙醇酸生产菌株的几个关键性能指标优于现有最先进的合成甲基营养菌。所呈现的结果为天然甲基营养菌嗜甲基菌的进一步菌株工程打开了大门,并为从绿色甲醇生产两种有前景的生物聚合物构建模块,即乙醇酸和乳酸铺平了道路。