Demonstrates enhanced 3-hydroxypropionic acid production in Escherichia coli, indicating effective metabolic regulation.
High Resolution Image Download MS PowerPoint Slide Efficient microbial production of platform chemicals requires precise regulation of metabolic fluxes. However, static control strategies─including constitutive overexpression and multi-inducer systems requiring manual optimization─cannot adapt in real time to changing intracellular states and therefore hinder fine-tuning of cofactor and precursor pools. Here, we constructed a product-responsive regulatory circuit in Escherichia coli that coordinates two key biosynthetic determinants─NADPH regeneration and malonyl-CoA allocation─in response to intracellular 3-hydroxypropionic acid (3-HP) accumulation. Following initial IPTG induction of the 3-HP biosynthesis module, intracellular 3-HP accumulation activates the downstream product-responsive regulatory circuit, enabling coordinated modulation of NADPH regeneration and malonyl-CoA allocation without additional external intervention. The final engineered strain, SBH40, achieved a 3-HP titer of 3.0 g/L and a yield of 0.19 g/g glucose, representing an approximately 5-fold improvement in both metrics relative to a nonregulated control strain (0.64 g/L; 0.04 g/g glucose). These results demonstrate that a single-input product-responsive circuit can autonomously coordinate multiple metabolic nodes after pathway initiation, offering a practical and modular framework for dynamic regulation of cofactor- and precursor-intensive biosynthesis.
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Kim et al. (2026) studied this question.
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