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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.

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

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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