Rewiring Escherichia coli to transform formate into methyl groups.

IF 4.9 2区 生物学 Q1 BIOTECHNOLOGY & APPLIED MICROBIOLOGY Microbial Cell Factories Pub Date : 2025-03-07 DOI:10.1186/s12934-025-02674-4
Michael K F Mohr, Ari Satanowski, Steffen N Lindner, Tobias J Erb, Jennifer N Andexer
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Abstract

Background: Biotechnological applications are steadily growing and have become an important tool to reinvent the synthesis of chemicals and pharmaceuticals for lower dependence on fossil resources. In order to sustain this progression, new feedstocks for biotechnological hosts have to be explored. One-carbon (C1-)compounds, including formate, derived from CO2 or organic waste are accessible in large quantities with renewable energy, making them promising candidates. Previous studies showed that introducing the formate assimilation machinery from Methylorubrum extorquens into Escherichia coli allows assimilation of formate through the C1-tetrahydrofolate (C1-H4F) metabolism. Applying this route for formate assimilation, we here investigated utilisation of formate for the synthesis of value-added building blocks in E. coli using S-adenosylmethionine (SAM)-dependent methyltransferases (MT).

Results: We first used a two-vector system to link formate assimilation and SAM-dependent methylation with three different MTs in E. coli BL21. By feeding isotopically labelled formate, methylated products with 51-81% 13C-labelling could be obtained without substantial changes in conversion rates. Focussing on improvement of product formation with one MT, we analysed the engineered C1-auxotrophic E. coli strain C1S. Screening of different formate concentrations allowed doubling of the conversion rate in comparison to the not formate-supplemented BL21 strain with a share of more than 70% formate-derived methyl groups.

Conclusions: Within this study transformation of formate into methyl groups is demonstrated in E. coli. Our findings support that feeding formate can improve the availability of usable C1-compounds and, as a result, increase whole-cell methylation with engineered E. coli. Using this as a starting point, the introduction of additional auxiliary enzymes and ideas to make the system more energy-efficient are discussed for future applications.

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重组大肠杆菌将甲酸转化为甲基。
背景:生物技术的应用正在稳步增长,并已成为重塑化学品和药物合成的重要工具,以降低对化石资源的依赖。为了维持这一进展,必须探索用于生物技术宿主的新原料。从二氧化碳或有机废物中提取的一碳(C1-)化合物,包括甲酸酯,可以通过可再生能源大量获取,使其成为有希望的候选者。先前的研究表明,将来自Methylorubrum exexquens的甲酸同化机制引入大肠杆菌,可以通过c1 -四氢叶酸(C1-H4F)代谢对甲酸进行同化。在此,我们利用s -腺苷甲硫氨酸(SAM)依赖的甲基转移酶(MT)研究了在大肠杆菌中利用甲酸酯合成增值构建块的途径。结果:我们首先使用双载体系统将大肠杆菌BL21中甲酸盐同化和sam依赖的甲基化与三种不同的mt联系起来。通过添加同位素标记的甲酸盐,可以获得具有51-81% 13c标记的甲基化产物,而转化率没有实质性变化。我们对改良的c1 -营养不良大肠杆菌菌株C1S进行了分析,重点研究了单MT对产物形成的改善作用。与未添加甲酸的BL21菌株相比,不同甲酸浓度的筛选使转化率增加了一倍,其中甲酸衍生甲基的份额超过70%。结论:在本研究中,证明了甲酸酯在大肠杆菌中转化为甲基。我们的研究结果支持,饲喂甲酸盐可以提高可用c1化合物的可用性,从而增加工程大肠杆菌的全细胞甲基化。以此为出发点,介绍了其他辅助酶的引入以及使系统更节能的想法,以供将来的应用。
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来源期刊
Microbial Cell Factories
Microbial Cell Factories 工程技术-生物工程与应用微生物
CiteScore
9.30
自引率
4.70%
发文量
235
审稿时长
2.3 months
期刊介绍: Microbial Cell Factories is an open access peer-reviewed journal that covers any topic related to the development, use and investigation of microbial cells as producers of recombinant proteins and natural products, or as catalyzers of biological transformations of industrial interest. Microbial Cell Factories is the world leading, primary research journal fully focusing on Applied Microbiology. The journal is divided into the following editorial sections: -Metabolic engineering -Synthetic biology -Whole-cell biocatalysis -Microbial regulations -Recombinant protein production/bioprocessing -Production of natural compounds -Systems biology of cell factories -Microbial production processes -Cell-free systems
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