利用代谢工程大肠杆菌从葡萄糖中重新生产1,6-己二醇和1,6-己二胺。

IF 3.9 2区 生物学 Q1 BIOCHEMICAL RESEARCH METHODS
ACS Synthetic Biology Pub Date : 2025-02-21 Epub Date: 2025-02-12 DOI:10.1021/acssynbio.4c00881
Nan Qin, Fanghuan Zhu, Youmeng Liu, Dehua Liu, Zhen Chen
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引用次数: 0

摘要

1,6-己二胺(HMD)和1,6-己二醇(HDO)是关键的C6平台化学品,作为合成尼龙,聚氨酯和聚酯的关键单体,具有广泛的应用。从廉价和可再生的生物资源中生产HMD和HDO是可持续化学工业的一种无害环境的战略。本文报道了在大肠杆菌中直接将d-葡萄糖转化为HMD和HDO的一种新的生物催化途径的发展。这是通过集成己二酸合成模块和为HMD和HDO生产量身定制的转换模块来实现的。该研究需要对途径酶、蛋白表达和前体供应进行全面优化。此外,为了提高分工效率,采用共培养发酵策略,以葡萄糖为唯一碳源,两菌株共培养的HMD产量为16.62 mg/L, HDO产量为214.93 mg/L。本研究为利用可再生资源推进HMD和HDO的可持续生物生产工艺建立了基础框架。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
De Novo Production of 1,6-Hexanediol and 1,6-Hexamethylenediamine from Glucose by Metabolic Engineered Escherichia coli.

1,6-Hexamethylenediamine (HMD) and 1,6-hexanediol (HDO) are pivotal C6 platform chemicals with extensive applications as key monomers in the synthesis of nylons, polyurethanes, and polyesters. The biological production of HMD and HDO from cheap and renewable bioresources represents an environmentally benign strategy for the sustainable chemical industry. Herein, we report the development of a novel biocatalytic route for the direct conversion of d-glucose to HMD and HDO in Escherichia coli. This was achieved through the integration of an adipic acid synthesis module with conversion modules tailored for HMD and HDO production. The study entailed a comprehensive optimization of pathway enzymes, protein expression, and precursor supply. Furthermore, a co-culture fermentation strategy was employed to enhance the efficiency of labor division, resulting in a two-strain cocultivation process that yielded 16.62 mg/L of HMD and 214.93 mg/L of HDO using glucose as the sole carbon source. This study establishes a foundational framework for the advancement of sustainable biological production processes for HMD and HDO from renewable resources.

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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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