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Title

Selective Synthesis of the Human Drug Metabolite 5′-Hydroxypropranolol by an Evolved Self-Sufficient Peroxygenase

AuthorsGómez de Santos, Patricia ; Cañelas, Marina; Tieves, Florian; Younes, Sabry H. H.; Molina-Espeja, Patricia CSIC ORCID ; Hofrichter, Martin; Hollmann, Frank; Guallar, Victor; Alcalde Galeote, Miguel CSIC ORCID
Keywords5′-hydroxypropranolol
Directed evolution
Human drug metabolites
In situ H2O2 generation system
Peroxidative activity
Peroxygenative activity
Unspecific peroxygenase
Issue Date19-Apr-2018
PublisherAmerican Chemical Society
CitationACS Catalysis 8(6): 4789-4799 (2018)
AbstractPropranolol is a widely used beta-blocker that is metabolized by human liver P450 monooxygenases into equipotent hydroxylated human drug metabolites (HDMs). It is paramount for the pharmaceutical industry to evaluate the toxicity and activity of these metabolites, but unfortunately, their synthesis has hitherto involved the use of severe conditions, with poor reaction yields and unwanted byproducts. Unspecific peroxygenases (UPOs) catalyze the selective oxyfunctionalization of C–H bonds, and they are of particular interest in synthetic organic chemistry. Here, we describe the engineering of UPO from Agrocybe aegerita for the efficient synthesis of 5′-hydroxypropranolol (5′-OHP). We employed a structure-guided evolution approach combined with computational analysis, with the aim of avoiding unwanted phenoxyl radical coupling without having to dope the reaction with radical scavengers. The evolved biocatalyst showed a catalytic efficiency enhanced by 2 orders of magnitude and 99% regioselectivity for the synthesis of 5′-OHP. When the UPO mutant was combined with an H2O2 in situ generation system using methanol as sacrificial electron donor, total turnover numbers of up to 264 000 were achieved, offering a cost-effective and readily scalable method to rapidly prepare 5′-OHP.
Publisher version (URL)http://dx.doi.org/10.1021/acscatal.8b01004
URIhttp://hdl.handle.net/10261/165825
DOI10.1021/acscatal.8b01004
E-ISSN2155-5435
Appears in Collections:(ICP) Artículos

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