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Advanced Butanol and Hexanol Production from CO2: Integrating Genetically Modified Clostridium strains in Bioelectrochemical Systems

Project description

Optimising syngas fermentation to butanol and hexanol in bioelectrochemical systems

Syngas is a synthetic gas mixture of CO and hydrogen (H2) and often CO2. It is a key product of high-temperature pyrolysis of carbon-rich materials including coal, biomass and waste, and of steam reforming of natural gas. Syngas fermentation can produce butanol and hexanol – valuable compounds used in many sectors – increasing the sustainability of chemical manufacturing. With the support of the Marie Skłodowska-Curie Actions programme, the Bioelectrochemistry project aims to increase the efficiency with which the bacterium Clostridium ljungdahlii ferments syngas. To do so, the team will leverage genetic engineering, metabolic engineering, improved fermentation conditions, and revolutionary bioelectrochemical systems that harness the metabolisms of microorganisms to avoid using precious metal catalysts.

Objective

The production of butanol and hexanol from syngas (CO and CO2) fermentation represents a significant advancement in sustainable chemical manufacturing. This project aims to enhance the efficiency of this process by leveraging the capabilities of Clostridium ljungdahlii, a bacterium known for its robust syngas fermentation capabilities. C. ljungdahlii can convert CO2 into valuable products like butanol and hexanol, but current production levels are limited. Existing research shows that engineered strains of Clostridium can produce butanol at levels of 6–8 g/L from syngas. With ongoing advancements in genetic engineering, these yields are expected to rise to 10 g/L, and potentially up to 20 g/L with further metabolic engineering and optimized fermentation conditions. Similarly, while current hexanol production stands at 1–2 g/L, genetic engineering holds the potential to increase this to 2–3 g/L by enhancing chain elongation and managing acetate accumulation.
The project here focuses on two main objectives: a) optimizing genetic modifications in Clostridium strains and integrating bioelectrochemical systems (BES) to address the current limitations. Genetic engineering efforts will target the Wood-Ljungdahl pathway (WLP), a crucial metabolic route for converting CO2 and CO into acetate. By knocking out the acoA gene (acetyl-CoA synthetase) and upregulating adhE (alcohol dehydrogenase), we aim to redirect carbon flux from acetate production to alcohol synthesis. Additionally, utilizing BES will help mitigate acetate toxicity and enhance product yields through electrochemical stimulation, which improves cellular redox metabolism and supports the conversion of excess acetate into butanol (C4) and hexanol (C6). In effect, this combined approach will increase the production of multi-carbon chemicals in the system, which will provide new insights and improved efficiency in BES for increased CO2 fixation and bioconversion.

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Topic(s)

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Funding Scheme

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HORIZON-TMA-MSCA-PF-EF - HORIZON TMA MSCA Postdoctoral Fellowships - European Fellowships

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Call for proposal

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(opens in new window) HORIZON-MSCA-2024-PF-01

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Coordinator

CHALMERS TEKNISKA HOGSKOLA AB
Net EU contribution

Net EU financial contribution. The sum of money that the participant receives, deducted by the EU contribution to its linked third party. It considers the distribution of the EU financial contribution between direct beneficiaries of the project and other types of participants, like third-party participants.

€ 252 180,00
Address
-
412 96 GOTEBORG
Sweden

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Region
Södra Sverige Västsverige Västra Götalands län
Activity type
Higher or Secondary Education Establishments
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Total cost

The total costs incurred by this organisation to participate in the project, including direct and indirect costs. This amount is a subset of the overall project budget.

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