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LightZymes SIGNED

Evolution of artificial enzymes for light-driven reactions by implementing unnatural cofactors in protein scaffolds

Total Cost €

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EC-Contrib. €

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Partnership

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 LightZymes project word cloud

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

conversions    source    combine    code    atp    small    acyl    proteins    biocatalysis    preferentially    differs    chemists    light    catalyzing    natural    enzymatic    variants    purifications    drive    opens    redox    chemical    photoredox    photo    reaction    paves    asymmetric    mass    inside    cytoplasm    efficient    huge    form    time    pcs    employing    substantially    spectrometry    stereoselectivities    first    reactivities    naturally    door    render    cofactors    create    strength    generate    sustainable    radical    nature    cell    evolution    engineering    enzymes    regio    photosynthesis    assembly    catalysts    ribosomal    diversity    industrial    throughput    bio    lightzymes    converting    acids    expand    pc    trna    economy    directed    bridging    organo    intermediates    perform    enzyme    catalyst    screening    biocatalytic    instead    needing    photocatalysis    energy    molecules    ncaa    genetic    engineered    reactions    canonical    catalysis    difficult    synthesis    envision    photoorganocatalysis    hybrid    synthetases    modifications    repertoire    supply    nadph    facs    organic    incorporate    selective    expanding    amino    artificial   

Project "LightZymes" data sheet

The following table provides information about the project.

Coordinator
UNIVERSITAET GREIFSWALD 

Organization address
address: DOMSTRASSE 11
city: GREIFSWALD
postcode: 17489
website: www.uni-greifswald.de

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 Germany [DE]
 Total cost 1˙498˙749 €
 EC max contribution 1˙498˙749 € (100%)
 Programme 1. H2020-EU.1.1. (EXCELLENT SCIENCE - European Research Council (ERC))
 Code Call ERC-2017-STG
 Funding Scheme ERC-STG
 Starting year 2018
 Duration (year-month-day) from 2018-02-01   to  2023-01-31

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    UNIVERSITAET GREIFSWALD DE (GREIFSWALD) coordinator 1˙498˙749.00

Map

 Project objective

The LightZymes project aims to create artificial enzymes (LightZymes) catalyzing selective light-driven conversions of small organic molecules. Enzyme catalysis has a large potential in the development of a sustainable, bio-based economy and is increasingly applied on industrial scale. Nature’s repertoire of enzymatic reactions is huge, but for many reactions developed by chemists, no natural enzyme is available. I envision expanding the chemical diversity of enzymes to photoredox catalysis. Chemists perform this type of reactions by employing photo(organo) redox catalysts (PC). However, achieving regio- and stereoselectivities is challenging, because radical intermediates generated during the reaction are difficult to control. To solve this problem, I will combine the strength of bio- and photocatalysis: organic PCs as artificial cofactors provide new reactivities, and the proteins will be evolved to render the reactions highly selective. This approach differs from artificial photosynthesis: instead converting light energy in high-energy cofactors (NADPH, ATP), light will directly enable selective synthesis reactions. Efficient directed evolution requires an easy assembly of the catalyst, preferentially inside the cell. I propose to apply genetic code engineering and to supply the PC in the form of non-canonical amino acids (ncAA). Engineered amino acyl tRNA synthetases will incorporate the PC directly during ribosomal synthesis. This will facilitate–for the first time–the assembly of hybrid catalysts in the cytoplasm without needing further modifications or purifications. This opens the door for applying high-throughput screening based on mass spectrometry and FACS to generate highly selective variants. By bridging the concepts of photoorganocatalysis and biocatalysis, LightZymes will substantially expand the chemical repertoire of naturally evolved enzymes. This paves the way to directly using light as energy source to drive biocatalytic asymmetric reactions.

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The information about "LIGHTZYMES" are provided by the European Opendata Portal: CORDIS opendata.

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