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PROTOBAC SIGNED

Engineering of complex protocells by micro-compartmentalization of living bacteria

Total Cost €

0

EC-Contrib. €

0

Partnership

0

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 PROTOBAC project word cloud

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

sequestration    physical    replication    life    mitochondria    last    segregation    construction    functions    genetic    compartmentalized    structural    minimal    organization    university    living    inanimate    biotechnology    pioneering    lack    cellular    suitable    gene    perform    introducing    endomembrane    membrane    protocell    internally    artificial    transition    group    bacterial    first    efforts    expression    combined    assemblage    capacity    bristol    complexity    nuclear    sensing    colonies    compartmentalization    manifestations    components    synthesis    biology    starting    metabolism    hosting    bound    frs    plasmids    material    proto    disruption    organisational    functionally    microbiology    protoeukaryote    bacteria    transduction    answer    loaded    synthetic    engineering    exhibiting    energy    behaviours    spatial    instead    biological    multidisciplinary    question    protocells    mann    functional    designs    active    precisely    outcome    lipids    professor    organelles    metabolic    rudimentary    forms    materials    expertise    stephen    few   

Project "PROTOBAC" data sheet

The following table provides information about the project.

Coordinator
UNIVERSITY OF BRISTOL 

Organization address
address: BEACON HOUSE QUEENS ROAD
city: BRISTOL
postcode: BS8 1QU
website: www.bristol.ac.uk

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 United Kingdom [UK]
 Total cost 212˙933 €
 EC max contribution 212˙933 € (100%)
 Programme 1. H2020-EU.1.3.2. (Nurturing excellence by means of cross-border and cross-sector mobility)
 Code Call H2020-MSCA-IF-2018
 Funding Scheme MSCA-IF-EF-ST
 Starting year 2019
 Duration (year-month-day) from 2019-12-01   to  2021-11-30

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    UNIVERSITY OF BRISTOL UK (BRISTOL) coordinator 212˙933.00

Map

 Project objective

The engineering of artificial cellular systems (i.e. protocells) exhibiting rudimentary life-like properties, such as minimal metabolism, sensing or replication, gene expression and compartmentalization, represents the most suitable path to undertake to answer the important question on how inanimate systems can transition into proto-living manifestations of physical matter. However, most of the current protocell designs still lack the structural and organisational complexity required for them to perform advanced functions and behaviours. Instead of starting from non-living materials, the aim of this proposal is precisely to design and construction of complex multi-component protocells based on the controlled sequestration and disruption of compartmentalized living bacterial colonies. The result protocells will bound by an assemblage of bacterial membrane lipids and internally loaded with a large number of functionally active metabolic and genetic components. Furthermore, the structural and functional complexity of the bacteria-derived protocells will be increased by introducing several important biological organelles such as proto-nuclear, proto-mitochondria components and endomembrane system, which is expected to produce the first example of protoeukaryote. The previous expertise of the applicant in the field of biotechnology, synthetic biology and microbiology will be applied to the multidisciplinary and emerging field of protocells in which the hosting group of Professor Stephen Mann FRS at the University of Bristol has been pioneering over the last few years. The key outcome of the combined research efforts of the applicant and the Mann group will lead to the synthesis of bacteria derived protocells and develop their advanced forms capable of increased energy (metabolic) capacity and transduction, spatial segregation of genetic material (plasmids etc), and higher-order organization and processing.

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The information about "PROTOBAC" are provided by the European Opendata Portal: CORDIS opendata.

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