利用混合途径和辅助因子再生技术加强前体供应,实现 3-羟基丙酸的生物生产

IF 3.7 2区 生物学 Q1 BIOCHEMICAL RESEARCH METHODS
ACS Synthetic Biology Pub Date : 2024-10-18 Epub Date: 2024-09-25 DOI:10.1021/acssynbio.4c00427
Tingting Chen, Yufei Zhang, Junhua Yun, Mei Zhao, Cunsheng Zhang, Ziwei Chen, Hossain M Zabed, Wenjing Sun, Xianghui Qi
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引用次数: 0

摘要

3-羟基丙酸(3-HP)是 12 种有价值的平台化学品之一,可广泛应用于化工、食品和化妆品行业。然而,由于缺乏稳健的底盘和发酵过程的高成本,3-HP 的生物合成面临着挑战。为了应对这些挑战,我们努力通过利用代谢调节、控制碳通量、平衡辅因子生成和优化发酵条件来增强 3-HP 生产底盘的稳健性。首先,在大肠杆菌中招募并重新平衡丙二酰-CoA(MCA)途径。随后,系统地调节了恩伯登-梅耶霍夫-帕尔纳斯(Embden-Meyerhof-Parnas)途径与非氧化性糖酵解途径的混合途径,以提高 MCA 途径的碳通量,并对 NADPH 的再生进行了微调。然后,通过优化发酵条件,3-HP 的产量显著提高,达到 6.8 克/升。最后,在喂料批次实验中,最终底盘产生了 42.8 克/升的 3-HP,相当于 0.4 摩尔/摩尔的产量和 0.6 克/(升-小时)的生产率。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Bioproduction of 3-Hydroxypropionic Acid by Enhancing the Precursor Supply with a Hybrid Pathway and Cofactor Regeneration.

3-Hydroxypropionic acid (3-HP) is one of the 12 valuable platform chemicals with versatile applications in the chemical, food, and cosmetic industries. However, the biosynthesis of 3-HP faces challenges due to the lack of robust chassis and the high costs associated with the fermentation process. To address these challenges, we made efforts to augment the robustness of 3-HP-producing chassis by exploiting metabolic regulation, controlling carbon flux, balancing cofactor generation, and optimizing fermentation conditions. First, the malonyl-CoA (MCA) pathway was recruited and rebalanced in Escherichia coli. Subsequently, a hybrid pathway integrating the Embden-Meyerhof-Parnas pathway with the nonoxidative glycolysis pathway was systematically modulated to enhance carbon flux to the MCA pathway, followed by fine-tuning NADPH regeneration. Then, by optimizing the fermentation conditions, 3-HP production was significantly improved, reaching 6.8 g/L. Finally, in a fed-batch experiment, the final chassis produced 42.8 g/L 3-HP, corresponding to a 0.4 mol/mol yield and 0.6 g/(L·h) productivity.

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来源期刊
CiteScore
8.00
自引率
10.60%
发文量
380
审稿时长
6-12 weeks
期刊介绍: The journal is particularly interested in studies on the design and synthesis of new genetic circuits and gene products; computational methods in the design of systems; and integrative applied approaches to understanding disease and metabolism. Topics may include, but are not limited to: Design and optimization of genetic systems Genetic circuit design and their principles for their organization into programs Computational methods to aid the design of genetic systems Experimental methods to quantify genetic parts, circuits, and metabolic fluxes Genetic parts libraries: their creation, analysis, and ontological representation Protein engineering including computational design Metabolic engineering and cellular manufacturing, including biomass conversion Natural product access, engineering, and production Creative and innovative applications of cellular programming Medical applications, tissue engineering, and the programming of therapeutic cells Minimal cell design and construction Genomics and genome replacement strategies Viral engineering Automated and robotic assembly platforms for synthetic biology DNA synthesis methodologies Metagenomics and synthetic metagenomic analysis Bioinformatics applied to gene discovery, chemoinformatics, and pathway construction Gene optimization Methods for genome-scale measurements of transcription and metabolomics Systems biology and methods to integrate multiple data sources in vitro and cell-free synthetic biology and molecular programming Nucleic acid engineering.
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