Anti-Pdc1p Nanobodyas a Genetically Encoded Inhibitorof Ethanol Production Enables Dual Transcriptional and Post-translationalControls of Yeast Fermentations

Microbial fermentation provides a sustainable method of producing valuable chemicals. Adding dynamic control to fermentations can significantly improve titers, but most systems rely on transcriptional controls of metabolic enzymes, leaving existing intracellular enzymes unregulated. This limits the ability of transcriptional controls to switch off metabolic pathways, especially when metabolic enzymes have long half-lives. We developed a two-layer transcriptional/post-translational control system for yeast fermentations. Specifically, the system uses blue light to transcriptionally activate the major pyruvate decarboxylase <i>PDC1</i>, required for cell growth and concomitant ethanol production. Switching to darkness transcriptionally inactivates <i>PDC1</i> and instead activates the anti-Pdc1p nanobody, NbJRI, to act as a genetically encoded inhibitor of Pdc1p accumulated during the growth phase. This dual transcriptional/post-translational control improves the production of 2,3-BDO and citramalate by up to 100 and 92% compared to using transcriptional controls alone in dynamic two-phase fermentations. This study establishes the NbJRI nanobody as an effective genetically encoded inhibitor of Pdc1p that can enhance the production of pyruvate-derived chemicals.

Publication Details

Journal
Figshare
Published
2025-03-17
DOI
https://doi.org/10.1021/acssynbio.4c00617.s001
Primary Topic
Microbial Metabolic Engineering and Bioproduction
Type
article
Field-Weighted Citation Impact
0.00
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article

Anti-Pdc1p Nanobodyas a Genetically Encoded Inhibitorof Ethanol Production Enables Dual Transcriptional and Post-translationalControls of Yeast Fermentations

Figshare
Microbial Metabolic Engineering and Bioproduction
article

Anti-Pdc1p Nanobodyas a Genetically Encoded Inhibitorof Ethanol Production Enables Dual Transcriptional and Post-translationalControls of Yeast Fermentations

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Abstract

Microbial fermentation provides a sustainable method of producing valuable chemicals. Adding dynamic control to fermentations can significantly improve titers, but most systems rely on transcriptional controls of metabolic enzymes, leaving existing intracellular enzymes unregulated. This limits the ability of transcriptional controls to switch off metabolic pathways, especially when metabolic enzymes have long half-lives. We developed a two-layer transcriptional/post-translational control system for yeast fermentations. Specifically, the system uses blue light to transcriptionally activate the major pyruvate decarboxylase <i>PDC1</i>, required for cell growth and concomitant ethanol production. Switching to darkness transcriptionally inactivates <i>PDC1</i> and instead activates the anti-Pdc1p nanobody, NbJRI, to act as a genetically encoded inhibitor of Pdc1p accumulated during the growth phase. This dual transcriptional/post-translational control improves the production of 2,3-BDO and citramalate by up to 100 and 92% compared to using transcriptional controls alone in dynamic two-phase fermentations. This study establishes the NbJRI nanobody as an effective genetically encoded inhibitor of Pdc1p that can enhance the production of pyruvate-derived chemicals.

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