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Substrate-inducible and antibiotic-free high-level 4-hydroxyvaleric acid production in engineered Escherichia coli.


ABSTRACT: In this study, we developed a levulinic acid (LA)-inducible and antibiotic-free plasmid system mediated by HpdR/P hpdH and infA-complementation to produce 4-hydroxyvaleric acid (4-HV) from LA in an engineered Escherichia coli strain. The system was efficiently induced by the addition of the LA substrate and resulted in tight dose-dependent control and fine-tuning of gene expression. By engineering the 5' untranslated region (UTR) of hpdR mRNA, the gene expression of green fluorescent protein (GFP) increased by at least two-fold under the hpdH promoter. Furthermore, by evaluating the robustness and plasmid stability of the proposed system, the engineered strain, IRV750f, expressing the engineered 3-hydroxybutyrate dehydrogenase (3HBDH) and formate dehydrogenase (CbFDH), produced 82 g/L of 4-HV from LA, with a productivity of 3.4 g/L/h and molar conversion of 92% in the fed-batch cultivation (5 L fermenter) without the addition of antibiotics or external inducers. Overall, the reported system was highly beneficial for the large-scale and cost-effective microbial production of value-added products and bulk chemicals from the renewable substrate, LA.

SUBMITTER: Sathesh-Prabu C 

PROVIDER: S-EPMC9398171 | biostudies-literature | 2022

REPOSITORIES: biostudies-literature

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Substrate-inducible and antibiotic-free high-level 4-hydroxyvaleric acid production in engineered <i>Escherichia coli</i>.

Sathesh-Prabu Chandran C   Tiwari Rameshwar R   Lee Sung Kuk SK  

Frontiers in bioengineering and biotechnology 20220809


In this study, we developed a levulinic acid (LA)-inducible and antibiotic-free plasmid system mediated by HpdR/P <sub><i>hpdH</i></sub> and <i>infA</i>-complementation to produce 4-hydroxyvaleric acid (4-HV) from LA in an engineered <i>Escherichia coli</i> strain. The system was efficiently induced by the addition of the LA substrate and resulted in tight dose-dependent control and fine-tuning of gene expression. By engineering the 5' untranslated region (UTR) of <i>hpdR</i> mRNA, the gene expr  ...[more]

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