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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.

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

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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