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A twofold retrosynthetic implementation of a novel biochemical pathway (RETROBIO)

A twofold retrosynthetic implementation of a novel biochemical pathway (RETROBIO)

Rolf Breinbauer (ORCID: 0000-0001-6009-7359)
  • Grant DOI 10.55776/I1722
  • Funding program International - Multilateral Initiatives
  • Status ended
  • Start October 1, 2014
  • End September 30, 2018
  • Funding amount € 155,085

Disciplines

Biology (25%); Chemistry (50%); Industrial Biotechnology (25%)

Keywords

    Synthetic Biology, Pathway Engineering, Protein Engineering, Chemical Biology, Biosynthesis

Abstract Final report

We retrosynthetically designed a pathway along a completely novel set of new-to-nature metabolites for the synthesis of biotin, a high-value-added commercially relevant product currently manufactured by a chemical synthesis. The pathway will be implemented using rational design approaches complemented by advanced high throughput screening methods for the reprogramming of the substrate specificities of known enzymes. The project aims to demonstrate that multi-step biopathway design largely outside of the scope of reactions already known in nature is possible and provides attractive solutions to some of synthetic biology`s currently most intractable synthetic problems. Furthermore, we will demonstrate experimentally that retrosynthetic design is an excellent basis for rational biopathway design. We expect the results to be a milestone in the demonstration of the potential of synthetic biology for the development of chemical syntheses, which hopefully encourages the more frequent application of biosynthesis as an alternative to chemical methods.

In this project it was attempted to develop a new biotechnological access to a vitamin. New enzymes should be discovered through the use of methods of directed evolution, which would allow the production of the vitamin via a synthetic route not yet used by nature. It was necessary to produce the appropriate intermediates for the evolutionary selection process via chemical synthesis. While for the last step of the new biosynthetic route an appropriate enzyme has been identified, this development is still pending for the earlier steps of the biosynthesis.

Research institution(s)
  • Technische Universität Graz - 100%
International project participants
  • Rolf Daniel, Georg-August-Universität Göttingen - Germany
  • Sven Panke, Eidgenössische Technische Hochschule Zürich - Switzerland
  • Florian Seebeck, Universität Basel - Switzerland

Research Output

  • 7 Citations
  • 1 Publications
Publications
  • 2020
    Title Stereoselective synthesis of chiral thiol-containing 1,2-aminoalcohols via SmI2-mediated coupling
    DOI 10.1016/j.tet.2020.131249
    Type Journal Article
    Author Doler C
    Journal Tetrahedron
    Pages 131249
    Link Publication

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