1.中国科学院天津工业生物技术研究所,天津 300308
2.中国农业科学院饲料研究所,北京 100081
任玉文(1994—),女,博士研究生。研究方向为乙醇梭菌细胞工厂固碳途径改造机制研究。
王杰(1989—),男,副研究员,硕士生导师,研究方向为一碳菌体蛋白创制与饲料应用。
李德茂(1978—),男,研究员,博士生导师,研究方向为一碳化合物生物转化微生物蛋白/油脂研究。
收稿:2026-07-24,
修回:2026-10-27,
网络首发:2026-10-30,
移动端阅览
任玉文, 隆柳成, 陈利梅, 薛敏, 王杰, 李德茂. 面向工业尾气利用的产乙酸菌底盘细胞设计构建与应用进展[J]. 合成生物学, 2026, 7. DOI: 10.12211/2096-8280.2026-065
REN Yuwen, LONG Liucheng, CHEN Limei, XUE Min, WANG Jie, LI Demao. Advances in the design, construction, and application of acetogenic chassis cells for industrial off-gas utilization[J]. Synthetic Biology Journal, 2026, 7. DOI: 10.12211/2096-8280.2026-065
任玉文, 隆柳成, 陈利梅, 薛敏, 王杰, 李德茂. 面向工业尾气利用的产乙酸菌底盘细胞设计构建与应用进展[J]. 合成生物学, 2026, 7. DOI: 10.12211/2096-8280.2026-065 DOI:
REN Yuwen, LONG Liucheng, CHEN Limei, XUE Min, WANG Jie, LI Demao. Advances in the design, construction, and application of acetogenic chassis cells for industrial off-gas utilization[J]. Synthetic Biology Journal, 2026, 7. DOI: 10.12211/2096-8280.2026-065 DOI:
钢铁冶炼、铁合金、炼油裂解和煤化工等重工业每年排放大量含CO、CO₂和H₂的工业尾气,既是温室气体来源,也是可观的碳资源。产乙酸菌依靠Wood-Ljungdahl途径高效固定一碳气体,是尾气生物转化最具潜力的底盘。本文系统综述了产乙酸菌底盘构建与应用进展,一是生物学基础,包括产物途径的代谢机制、热力学约束、能量守恒机制及核心菌株的选择;二是遗传工具,涵盖基因转移、CRISPR-Cas9/Cas12a、内源I-B型系统和RecT重组工程;三是代谢工程策略,包括提高天然产物产量、构建非天然产物异源合成途径、改造中心碳代谢,以及适应性实验室进化与理性设计的协同;四是气-液传质与过程工程,涉及反应器构型、连续及两阶段发酵、在线监控与过程控制;五是结合不同产业化阶段的案例,分析关键瓶颈并探讨以工艺协同优化为主的突破路径。本文旨在为产乙酸菌底盘的理性设计与工程化推广,以及一碳气体生物转化的产业化提供系统参考。
Heavy industries such as steelmaking
ferroalloy production
petroleum refining and cracking
and coal chemical processing release large volumes of industrial off-gases containing CO
CO₂
and H₂ every year. These gases are not only a major source of greenhouse gas emissions but also a substantial reservoir of carbon and chemical energy. Acetogens
which fix one-carbon gases efficiently through the Wood-Ljungdahl pathway
have emerged as the most promising chassis organisms for the bioconversion of industrial off-gases. This review summarizes advances in the design
construction
and application of acetogenic chassis cells for industrial off-gas utilization. First
the biological basis of acetogens is outlined
including the biochemistry and thermodynamic constraints of the pathway and the Rnf- and Ech-type energy conservation mechanisms. Chassis selection is discussed in relation to variations in gas composition and impurity profiles. Second
genetic tools are reviewed: DNA transfer
CRISPR-Cas9/Cas12a
endogenous type I-B systems
and RecT-mediated recombineering. Their industrial suitability is assessed by transformation efficiency
design-build cycle time
iterative editing capacity
marker dependence
and transferability across strains. Third
metabolic engineering strategies are discussed. They cover native product enhancement
heterologous pathways
central carbon and energy metabolism engineering
genome-scale metabolic modeling
and the combination of adaptive laboratory evolution with rational design. Energy supply
reducing power
and product toxicity emerge as shared bottlenecks. In addition
process engineering is addressed: gas–liquid mass transfer
reactor configuration
continuous and two-stage fermentation
and scale-down simulations
with particular emphasis on their integration with chassis design. Based on cases at different industrialization stages (commercial operation
trial production
under construction
demonstration
and pilot)
the review identifies the thermodynamic limit of energy metabolism
strain-specific tool adaptation
stability at scale
and downstream separation as core challenges. It outlines future directions: strengthening energy-conservation modules
co-optimizing strains and processes
and diversifying products and carbon conversion routes. This review aims to provide a reference for the rational design of acetogenic chassis and the industrial deployment of one-carbon gas bioconversion.
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