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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.

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

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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