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PRO_PHAGE SIGNED

Impact and interaction of prophage elements in bacterial host strains of biotechnological relevance

Total Cost €

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EC-Contrib. €

0

Partnership

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 PRO_PHAGE project word cloud

Explore the words cloud of the PRO_PHAGE project. It provides you a very rough idea of what is the project "PRO_PHAGE" about.

compounds    pursuing    shaped    pro    bacteria    ht    unprecedented    proteins    workflow    flexible    abundant    generate    xenogeneic    improvement    hosts    inhabitants    insights    encoded    genetic    spontaneous    significantly    reveal    unexplored    purpose    fitness    bioeconomy    integration    prophages    molecular    genome    microbial    industrial    chassis    activated    explorative    combining    host    dynamics    phage    traits    genomic    applicable    genomes    dna    generation    bacterial    bioinformatic    resource    association    bacteriophages    sorting    ngs    earth    evolution    decipher    benchmarked    diverse    beneficial    silencing    viruses    triggers    risks    engineering    added    foreign    illustrated    sustainable    immense    subsequent    single    gene    broadly    microbes    sequencing    integrate    phages    transition    analysed    metabolic    temperate    resolution    strains    mutually    regulatory    throughput    almost    fluorescence    will    product    phenotyping    virus    population    prey    interaction    close    activation    expression    cell   

Project "PRO_PHAGE" data sheet

The following table provides information about the project.

Coordinator
FORSCHUNGSZENTRUM JULICH GMBH 

Organization address
address: WILHELM JOHNEN STRASSE
city: JULICH
postcode: 52428
website: www.fz-juelich.de

contact info
title: n.a.
name: n.a.
surname: n.a.
function: n.a.
email: n.a.
telephone: n.a.
fax: n.a.

 Coordinator Country Germany [DE]
 Total cost 1˙482˙672 €
 EC max contribution 1˙482˙672 € (100%)
 Programme 1. H2020-EU.1.1. (EXCELLENT SCIENCE - European Research Council (ERC))
 Code Call ERC-2017-STG
 Funding Scheme ERC-STG
 Starting year 2018
 Duration (year-month-day) from 2018-01-01   to  2022-12-31

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    FORSCHUNGSZENTRUM JULICH GMBH DE (JULICH) coordinator 1˙482˙672.00

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 Project objective

Phages, viruses that prey on bacteria, are the most abundant and diverse inhabitants of the Earth. Temperate bacteriophages are able to integrate into the host genome and maintain as prophages a long-term association with their host. Illustrated by the development of mutually beneficial traits, this close interaction between host and virus has significantly shaped bacterial evolution. However, the immense genetic resources of phage genomes still remain almost unexplored. For the transition to a sustainable bioeconomy, we strongly depend on microbes as hosts for the production of value-added compounds. PRO_PHAGE will exploit recent advances in next-generation sequencing (NGS), single-cell analysis, and high-throughput (HT) phenotyping to evaluate the impact of phage elements on host fitness and to use this knowledge for the improvement of future metabolic engineering approaches. By combining an explorative approach with subsequent molecular analysis of selected targets, PRO_PHAGE will deliver novel insights into this genetic resource and will reveal the risks and potential for metabolic engineering by pursuing four major objectives. 1) Based on a comprehensive bioinformatic analysis, the impact of phage elements will be studied by HT phenotyping of selected strains. 2) The regulatory interaction of phage and host will be analysed by focusing on host-encoded xenogeneic silencing proteins and their role in the integration of foreign DNA. 3) The spontaneous activation of phage elements will be studied at the genomic scale to decipher molecular triggers and their impact on host gene expression. For this purpose, a novel workflow combining fluorescence-activated cell sorting and NGS will be developed, which will be broadly applicable for studying microbial population dynamics at unprecedented resolution. 4) Finally, the insights obtained will be benchmarked for metabolic engineering approaches in order to generate robust and flexible chassis strains for industrial product

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