| Literature DB >> 31806816 |
Mark A Huffman1, Anna Fryszkowska1, Oscar Alvizo2, Margie Borra-Garske2, Kevin R Campos3, Keith A Canada3, Paul N Devine3, Da Duan2, Jacob H Forstater3, Shane T Grosser3, Holst M Halsey3, Gregory J Hughes3, Junyong Jo3, Leo A Joyce3, Joshua N Kolev3, Jack Liang2, Kevin M Maloney3, Benjamin F Mann3, Nicholas M Marshall3, Mark McLaughlin3, Jeffrey C Moore3, Grant S Murphy3, Christopher C Nawrat3, Jovana Nazor2, Scott Novick2, Niki R Patel3, Agustina Rodriguez-Granillo4, Sandra A Robaire3, Edward C Sherer4, Matthew D Truppo3, Aaron M Whittaker3, Deeptak Verma4, Li Xiao4, Yingju Xu3, Hao Yang3.
Abstract
Enzyme-catalyzed reactions have begun to transform pharmaceutical manufacturing, offering levels of selectivity and tunability that can dramatically improve chemical synthesis. Combining enzymatic reactions into multistep biocatalytic cascades brings additional benefits. Cascades avoid the waste generated by purification of intermediates. They also allow reactions to be linked together to overcome an unfavorable equilibrium or avoid the accumulation of unstable or inhibitory intermediates. We report an in vitro biocatalytic cascade synthesis of the investigational HIV treatment islatravir. Five enzymes were engineered through directed evolution to act on non-natural substrates. These were combined with four auxiliary enzymes to construct islatravir from simple building blocks in a three-step biocatalytic cascade. The overall synthesis requires fewer than half the number of steps of the previously reported routes.Entities:
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Year: 2019 PMID: 31806816 DOI: 10.1126/science.aay8484
Source DB: PubMed Journal: Science ISSN: 0036-8075 Impact factor: 47.728