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Structure and Regulation of Bacterial Biofilm-Promoting Exopolysaccharide Secretion Systems

The project aims to decode the assembly and function of exopolysaccharide secretion systems in bacteria to develop novel anti-infectives and enhance beneficial EPS production.

Subsidie
€ 1.950.000
2024

Projectdetails

Introduction

Bacteria are commonly defined as unicellular organisms; however, they constantly exchange substances and information with their confrères and the environment. They can efficiently shelter themselves and achieve homeostasis by building multicellular collaborative macrocolonies called biofilms.

Biofilm Characteristics

Members of these sessile communities can undergo significant functional differentiation and are typically embedded in a complex extracellular matrix that secures both mechanical protection and a medium for intercellular exchange. Importantly, the switch between sessile and motile lifestyles in pathogenic bacteria can correlate directly with the development of chronic vs. acute infections.

Biotechnological Applications

Extracted bacterial matrix components can find a variety of beneficial biotechnological applications. Exopolysaccharides (EPS) are a major biofilm matrix component and are typically produced by trans-envelope secretion nanomachines, many of which are controlled at multiple levels by the intracellular second messenger c-di-GMP.

Research Objectives

Here, we will consolidate our expertise in biofilm formation, cyclic dinucleotide signaling, bacterial secretion, and integrative structural biology to decipher EPS secretion system assembly and function in several medically and industrially relevant species.

Methodology

We will use complementary recombinant and in situ structural biology approaches together with established genetic and imaging techniques to decipher the molecular events controlling EPS biogenesis, including:

  1. Transcription initiation
  2. Interdependent protein folding
  3. Cooperative subunit interactions
  4. Secretion system assembly
  5. Formation of supramolecular secretory nanoarrays
  6. EPS modifications

Goals

Our aim is to harness the biosynthetic processes for the engineering of novel anti-infectives or beneficial EPS superproducers. Over the last years, we have spearheaded these studies by providing unprecedented mechanistic insights into several secretion systems and have demonstrated the feasibility of such an ambitious project.

Financiële details & Tijdlijn

Financiële details

Subsidiebedrag€ 1.950.000
Totale projectbegroting€ 1.950.000

Tijdlijn

Startdatum1-12-2024
Einddatum30-11-2029
Subsidiejaar2024

Partners & Locaties

Projectpartners

  • CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE CNRSpenvoerder

Land(en)

France

Inhoudsopgave

European Research Council

Financiering tot €10 miljoen voor baanbrekend frontier-onderzoek via ERC-grants (Starting, Consolidator, Advanced, Synergy, Proof of Concept).

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