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An Engineered Cytidine Deaminase for Biocatalytic Production of a Key Intermediate of the Covid-19 Antiviral Molnupiravir.

Ashleigh J BurkeWilliam R BirminghamYing ZhuoThomas W ThorpeBruna Zucoloto da CostaRebecca CrawshawIan RowlesJames D FinniganCarl YoungGregory M HolgateMark P MuldowneySimon J CharnockSarah L LovelockNicholas J TurnerAnthony P Green
Published in: Journal of the American Chemical Society (2022)
The Covid-19 pandemic highlights the urgent need for cost-effective processes to rapidly manufacture antiviral drugs at scale. Here we report a concise biocatalytic process for Molnupiravir, a nucleoside analogue recently approved as an orally available treatment for SARS-CoV-2. Key to the success of this process was the development of an efficient biocatalyst for the production of N -hydroxy-cytidine through evolutionary adaption of the hydrolytic enzyme cytidine deaminase. This engineered biocatalyst performs >85 000 turnovers in less than 3 h, operates at 180 g/L substrate loading, and benefits from in situ crystallization of the N -hydroxy-cytidine product (85% yield), which can be converted to Molnupiravir by a selective 5'-acylation using Novozym 435.
Keyphrases
  • sars cov
  • coronavirus disease
  • respiratory syndrome coronavirus
  • gene expression
  • replacement therapy