微调大肠杆菌中的 5'-磷酸吡哆醛合成,以便在最小培养基中生产尸胺。

IF 3.7 2区 生物学 Q1 BIOCHEMICAL RESEARCH METHODS ACS Synthetic Biology Pub Date : 2024-05-20 DOI:10.1021/acssynbio.4c00102
Cunping Liu, Cong Gao, Longfei Song, Xiaomin Li, Xiulai Chen, Jing Wu, Wei Song, Wanqing Wei and Liming Liu*, 
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引用次数: 0

摘要

尸胺是生产聚酰胺的重要 C5 单体。5'- 磷酸吡哆醛(PLP)是尸胺生物合成途径中关键酶赖氨酸脱羧酶的重要辅助因子,但它一直短缺,导致尸胺生产受到限制。为解决这一问题,我们实施了双途径策略,协同增强内源和异源 PLP 合成模块,从而提高了 PLP 的合成。随后,引入了生长阶段依赖性分子开关,以平衡 PLP 合成与细胞生长之间的前体竞争。此外,通过整合新发现的 PLP 响应启动子 PygjH 和阿拉伯糖调控系统,构建了基于 PLP 传感器的负反馈电路,动态调节 PLP 合成基因的表达,防止细胞内 PLP 过度积累。在最小培养基 AM1 中培养出的最佳菌株 L18 能生产尸胺,其滴度、产量和生产率分别为 64.03 克/升、0.23 克/克葡萄糖和 1.33 克/升/小时。这是迄今为止所报道的工程大肠杆菌在最小培养基中通过饲料批量发酵产生的最高滴度。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Fine-Tuning Pyridoxal 5′-Phosphate Synthesis in Escherichia coli for Cadaverine Production in Minimal Culture Media

Cadaverine is a critical C5 monomer for the production of polyamides. Pyridoxal 5′-phosphate (PLP), as a crucial cofactor for the key enzyme lysine decarboxylase in the cadaverine biosynthesis pathway, has seen a persistent shortage, leading to limitations in cadaverine production. To address this issue, a dual-pathway strategy was implemented, synergistically enhancing both endogenous and heterologous PLP synthesis modules and resulting in improved PLP synthesis. Subsequently, a growth-stage-dependent molecular switch was introduced to balance the precursor competition between PLP synthesis and cell growth. Additionally, a PLP sensor-based negative feedback circuit was constructed by integrating a newly identified PLP-responsive promoter PygjH and an arabinose-regulated system, dynamically regulating the expression of the PLP synthetic genes and preventing excessive intracellular PLP accumulation. The optimal strain, L18, cultivated in the minimal medium AM1, demonstrated cadaverine production with a titer, yield, and productivity of 64.03 g/L, 0.23 g/g glucose, and 1.33 g/L/h, respectively. This represents the highest titer reported to date in engineered Escherichia coli by fed-batch fermentation in a minimal medium.

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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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