Establishing an Autonomous Cascaded Artificial Dynamic (AutoCAD) regulation system for improved pathway performance

Endogenous metabolic pathways in microbial cells are usually precisely controlled by sophisticated regulation networks. However, the lack of such regulations when introducing heterologous pathways in microbial hosts often causes unbalanced enzyme expression and carbon flux distribution, hindering th...

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Veröffentlicht in:Metabolic engineering 2022-11, Vol.74, p.1-10
Hauptverfasser: Jiang, Tian, Li, Chenyi, Zou, Yusong, Zhang, Jianli, Gan, Qi, Yan, Yajun
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Sprache:eng
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Zusammenfassung:Endogenous metabolic pathways in microbial cells are usually precisely controlled by sophisticated regulation networks. However, the lack of such regulations when introducing heterologous pathways in microbial hosts often causes unbalanced enzyme expression and carbon flux distribution, hindering the construction of highly efficient microbial biosynthesis systems. Here, using naringenin as the target compound, we developed an Autonomous Cascaded Artificial Dynamic (AutoCAD) regulation system to automatically coordinate the pathway expression and redirect carbon fluxes for enhanced naringenin production. The AutoCAD regulation system, consisting of both intermediate-based feedforward and product-based feedback control genetic circuits, resulted in a 16.5-fold increase in naringenin titer compared with the static control. Fed-batch fermentation using the strain with AutoCAD regulation further enhanced the naringenin titer to 277.2 mg/L. The AutoCAD regulation system, with intermediate-based feedforward control and product-triggered feedback control, provides a new paradigm of developing complicated cascade dynamic control to engineer heterologous pathways. •An Autonomous Cascaded Artificial Dynamic (AutoCAD) regulation system was developed.•AutoCAD system included both intermediate-based feedforward and product-based feedback control circuits.•The application of AutoCAD system resulted in a 16.5-fold increase in naringenin titer.
ISSN:1096-7176
1096-7184
DOI:10.1016/j.ymben.2022.08.009