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Scalable Microbial Metabolite Discovery Through Synthetic Biology

Project description

Harnessing microbial secondary metabolites for novel drug discovery

Microorganisms such as bacteria and fungi produce organic compounds known as secondary metabolites (SMs) with various ecological functions, including defence, competition, and communication. These metabolites are produced through biosynthetic pathways encoded in microbial genomes, but their expression remains dormant under laboratory conditions, limiting the discovery of new compounds such as antibiotics. Funded by the European Research Council, the MeDiSyn project proposes to explore untapped biosynthetic genes in soil bacteria through heterologous expression in other hosts. Researchers will optimise activation of these biosynthetic genes, paving the way towards a novel drug discovery platform.

Objective

The discoveries of microbial secondary metabolites (SM) led to an incalculable impact on human health and lifespan. A large share of the antibiotics, anticancers and immunosuppressants in use today originate from microorganisms. However, discoveries of SMs of microbial origin through traditional approaches have declined in the past decades, depriving drug pipelines from a key source of bioactive molecules. The consequences are dire, in particular in the case of antibiotics. Encouragingly, the study of the biosynthetic genes responsible for the synthesis of SMs indicates that the natural repertoire remains vastly underexplored, and new ways to access it are enabled by DNA technologies.
In particular, untapped biosynthetic genes can be interrogated by transferring them into heterologous hosts. I am developing a method for transfer which fulfils the conditions to unleash theoretically massive economies of scale. Here I propose to multiply the scalability of the current heterologous expression framework and effectively overcome the diminishing returns faced by traditional approaches.
In the first axis, I will implement a full-fledged discovery platform, optimized to systematically interrogate novel biosynthetic gene clusters identified bioinformatically from a large collection of soil bacteria. Second, the scale and parallel nature of the heterologous expression setup will be used to better understand the logic of activation of biosynthetic genes, and identify optimal ways to increase activation rates among the large reservoir of conditionally silent biosynthetic genes. Finally, the general strategy will be extended to new fungal and bacterial clades to enable interrogation of their vast potential through scalable heterologous expression.
Overall, this proposal aims at developing heterologous expression into a major way to discover microbial secondary metabolites and drug leads.

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Programme(s)

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Topic(s)

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Funding Scheme

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HORIZON-ERC - HORIZON ERC Grants

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Call for proposal

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(opens in new window) ERC-2023-STG

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Host institution

INSTITUT NATIONAL DE LA SANTE ET DE LA RECHERCHE MEDICALE
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.

€ 1 490 250,00
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.

€ 1 490 250,00

Beneficiaries (1)

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