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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.

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

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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