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Homebrewed psilocybin: can new routes for pharmaceutical psilocybin production enable recreational use?

William E. Gibbons, Madeline G. Mckinney, Philip J. O’dell, Brooke A. Bollinger, J. Andrew Jones

Bioengineered 2021 DOI: 10.1080/21655979.2021.1987090 (opens in new tab)

Study at a glance

AI-extracted from the abstract
Characteristics Experimental study Peer reviewed
Duration Less than 2 days
Topics Psilocybin
Keywords Hallucinogen Pharmacology
Citations 8
Key findings Psilocybin can be produced in biologically relevant quantities (approximately 300 mg/L) using a recombinant E. coli strain in a homebrew-style environment in less than 2 days.

Abstract

Psilocybin, a drug most commonly recognized as a recreational psychedelic, is quickly gaining attention as a promising therapy for an expanding range of neurological conditions, including depression, anxiety, and addiction. This growing interest has led to many recent advancements in psilocybin synthesis strategies, including multiple in vivo fermentation-based approaches catalyzed by recombinant microorganisms. In this work, we show that psilocybin can be produced in biologically relevant quantities using a recombinant E. coli strain in a homebrew style environment. In less than 2 days, we successfully produced approximately 300 mg/L of psilocybin under simple conditions with easily sourced equipment and supplies. This finding raises the question of how this new technology should be regulated as to not facilitate clandestine biosynthesis efforts, while still enabling advancements in psilocybin synthesis technology for pharmaceutical applications. Here, we present our homebrew results, and suggestions on how to address the regulatory concerns accompanying this new technology.

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