Sha Yuanyuan, Ge Mianshen, Lu Minrui, Xu Zhaoxian, Zhai Rui, Jin Mingjie
School of Environmental and Biological Engineering, Nanjing University of Science and Technology, Nanjing, China.
Biorefinery Research Institution, Nanjing University of Science and Technology, Nanjing, China.
Crit Rev Biotechnol. 2025 Jun;45(4):904-922. doi: 10.1080/07388551.2024.2399542. Epub 2024 Sep 12.
Acetyl-CoA is an intermediate metabolite in cellular central metabolism. It's a precursor for various valuable commercial products, including: terpenoids, fatty acids, and polyketides. With the advancement of metabolic and synthetic biology tools, microbial cell factories have been constructed for the efficient synthesis of acetyl-CoA and derivatives, with the and as two prominent chassis. This review summarized the recent developments in the biosynthetic pathways and metabolic engineering approaches for acetyl-CoA and its derivatives synthesis in these two yeasts. First, the metabolic routes involved in the biosynthesis of acetyl-CoA and derived products were outlined. Then, the advancements in metabolic engineering strategies for channeling acetyl-CoA toward the desired products were summarized, with particular emphasis on: enhancing metabolic flux in different organelles, refining precursor CoA synthesis, optimizing substrate utilization, and modifying protein acetylation level. Finally, future developments in advancing the metabolic engineering strategies for acetyl-CoA and related derivatives synthesis, including: reducing CO emissions, dynamically regulating metabolic pathways, and exploring the regulatory functions between acetyl-CoA levels and protein acetylation, are highlighted. This review provided new insights into regulating acetyl-CoA synthesis to create more effective microbial cell factories for bio-manufacturing.
乙酰辅酶A是细胞中心代谢中的一种中间代谢产物。它是多种有价值商业产品的前体,包括萜类化合物、脂肪酸和聚酮化合物。随着代谢和合成生物学工具的发展,已经构建了微生物细胞工厂用于高效合成乙酰辅酶A及其衍生物,酿酒酵母和毕赤酵母是两种突出的底盘细胞。本综述总结了这两种酵母中乙酰辅酶A及其衍生物合成的生物合成途径和代谢工程方法的最新进展。首先,概述了乙酰辅酶A及其衍生产品生物合成所涉及的代谢途径。然后,总结了将乙酰辅酶A导向所需产品的代谢工程策略的进展,特别强调了:增强不同细胞器中的代谢通量、优化前体辅酶A的合成、优化底物利用以及调节蛋白质乙酰化水平。最后,强调了推进乙酰辅酶A及相关衍生物合成代谢工程策略的未来发展,包括:减少二氧化碳排放、动态调节代谢途径以及探索乙酰辅酶A水平与蛋白质乙酰化之间的调控功能。本综述为调节乙酰辅酶A合成以创建更有效的生物制造微生物细胞工厂提供了新的见解。