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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.

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

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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