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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.

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

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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