In Vitro Psilocybin Synthesis by Co‐Immobilized Enzymes

GND
1299220282
Zugehörigkeit
Pharmaceutical Microbiology Friedrich Schiller University Beutenbergstrasse 11a Jena Germany
Schäfer, Tim;
Zugehörigkeit
The Usona Institute 2780 Woods Hollow Road Madison WI USA
Sherwood, Alexander;
Zugehörigkeit
Research & Development Promega Corporation 2800 Woods Hollow Road Madison WI USA
Kirkland, Thomas;
GND
142208159
Zugehörigkeit
Molecular and Applied Microbiology Leibniz Institute for Natural Product Research and Infection Biology – Hans Knöll Institute Beutenbergstrasse 11a Jena Germany
Krüger, Thomas;
Zugehörigkeit
Pharmaceutical Microbiology Friedrich Schiller University Beutenbergstrasse 11a Jena Germany
Worbs, Jakob;
GND
1146436270
Zugehörigkeit
Molecular and Applied Microbiology Leibniz Institute for Natural Product Research and Infection Biology – Hans Knöll Institute Beutenbergstrasse 11a Jena Germany
Kniemeyer, Olaf;
GND
1072725606
Zugehörigkeit
Pharmaceutical Microbiology Friedrich Schiller University Beutenbergstrasse 11a Jena Germany
Gressler, Markus;
GND
124018092
Zugehörigkeit
Pharmaceutical Microbiology Friedrich Schiller University Beutenbergstrasse 11a Jena Germany
Hoffmeister, Dirk

Advanced clinical trials investigate the Psilocybe magic mushroom natural product psilocybin as a treatment against major depressive disorder. Currently, synthetic material is used to meet the demand for legitimate pharmaceutical purposes. Here, we report an in vitro approach to biocatalytically produce psilocybin on a solid‐phase matrix charged with five covalently bound biosynthetic enzymes. These enzymes include three Psilocybe enzymes: IasA*, an engineered l ‐tryptophan decarboxylase/aromatic aldehyde synthase, the 4‐hydroxytryptamine kinase PsiK and the norbaeocystin methyltransferase PsiM, along with Escherichia coli nucleosidase MtnN and adenine deaminase Ade. In a proof‐of‐principle experiment, this enzyme‐charged resin allowed for quantitative turnover of 4‐hydroxy‐ l ‐tryptophan into psilocybin. This facile process i) represents a sustainable approach with reusable enzymes, ii) circumvents the drawbacks of in vivo processes while harnessing the selectivity of enzymatic catalysis and iii) helps access an urgently needed drug candidate.

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