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InVivoRuBisCO SIGNED

In vivo Directed Evolution of Ribulose-1,5-Bisphosphate Carboxylase/Oxygenase in Saccharomyces cerevisiae Using an Orthogonal DNA Replication System

Total Cost €

0

EC-Contrib. €

0

Partnership

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 InVivoRuBisCO project word cloud

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

conduit    prokaryotic    energy    fuels    evolution    laboratory    biofuels    designing    fuel    parts    isolate    transportation    techniques    propagate    reactivity    solar    participatory    cell    organism    additions    yields    overcome    catalytic    limiting    25    inefficacies    eukaryotic    re    hindered    2030    warming    vivo    suffers    poor    atmospheric    ant    fixation    yielded    co2    dramatically    selectivity    regard    enzyme    date    bisphosphate    water    efficient    rate    host    practical    fidelity    sufficiently    gene    improvements    hosts    consuming    clean    serve    create    oxygenase    substantial    divided    primary    substrate    photosynthesis    directed    continuous    dependent    assay    arbiter    breakthrough    fellowship    slowness    bacteria    replacing    carboxylase    splitting    fixed    marginal    carbon    biosphere    deletions    linking    match    mitigated    selective    turnover    usher    experiment    input    rubisco    enhanced    slow    enzymes    pressures    renewable    ribulose    combined    mutants    hydrogen    evolutionary    fossil    bioethanol    cerevisiae    global    synthesis    rates   

Project "InVivoRuBisCO" data sheet

The following table provides information about the project.

Coordinator
VIB 

Organization address
address: RIJVISSCHESTRAAT 120
city: ZWIJNAARDE - GENT
postcode: 9052
website: www.vib.be

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 Belgium [BE]
 Total cost 178˙320 €
 EC max contribution 178˙320 € (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 2020
 Duration (year-month-day) from 2020-12-01   to  2022-11-30

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    VIB BE (ZWIJNAARDE - GENT) coordinator 178˙320.00

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 Project objective

Global warming can be greatly mitigated by replacing fossil fuels with renewable solar energy. In one approach, researchers have combined solar water splitting with bacteria capable of consuming atmospheric CO2 and solar derived hydrogen to produce solar fuels. All CO2 fixed by these bacteria must go through the enzyme Ribulose 1,5-Bisphosphate Carboxylase/Oxygenase (RuBisCO). RuBisCO is the arbiter of photosynthesis and is the primary conduit linking carbon into the biosphere. However, the enzyme suffers from slow reactivity and poor selectivity for its primary substrate (CO2), making it the rate-limiting step for solar fuel synthesis and cell growth. To create an efficient and effective solar fuels process, any participatory enzymes need to have sufficiently high turnover rates to match the input of solar energy. A substantial breakthrough in this regard would be to develop an improved RuBisCO with enhanced turnover rate and selectivity. To date, directed evolution of RuBisCO has been hindered by traditional laboratory evolution techniques with prokaryotic hosts and yielded only marginal improvements in enzyme activity. To overcome evolutionary slowness and host inefficacies, I propose the in vivo directed evolution of RuBisCO in eukaryotic S. cerevisiae. This work will be divided into three parts: 1.) Designing a host organism that is dependent on RuBisCO activity through specific gene additions and deletions 2.) Develop a continuous directed evolution experiment to increase CO2 fixation, fidelity, and catalytic rate by applying selective pressures; and 3.) Isolate, propagate, and assay the resultant mutants, and test practical applications. The results of this work will serve to dramatically increase bioethanol yields through CO2 re-uptake and help achieve the European Commission's goal of using 25% biofuels in the transportation sector by 2030. This fellowship will enable the necessary research to usher in a clean and renewable future.

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