Affiliation:
1. School of Chemistry The University of Manchester, Manchester Institute of Biotechnology (MIB) 131 Princess Street Manchester M1 7DN UK
2. School of Chemistry and Molecular Biosciences The University of Queensland St. Lucia Brisbane 4072 Australia
3. Compound Synthesis and Management Discovery Sciences R&D AstraZeneca Gothenburg SE
Abstract
AbstractSelective, one‐step C−H activation of fatty acids from biomass is an attractive concept in sustainable chemistry. Biocatalysis has shown promise for generating high‐value hydroxy acids, but to date enzyme discovery has relied on laborious screening and produced limited hits, which predominantly oxidise the subterminal positions of fatty acids. Herein we show that ancestral sequence reconstruction (ASR) is an effective tool to explore the sequence‐activity landscape of a family of multidomain, self‐sufficient P450 monooxygenases. We resurrected 11 catalytically active CYP116B ancestors, each with a unique regioselectivity fingerprint that varied from subterminal in the older ancestors to mid‐chain in the lineage leading to the extant, P450‐TT. In lineages leading to extant enzymes in thermophiles, thermostability increased from ancestral to extant forms, as expected if thermophily had arisen de novo. Our studies show that ASR can be applied to multidomain enzymes to develop active, self‐sufficient monooxygenases as regioselective biocatalysts for fatty acid hydroxylation.
Funder
FP7 Ideas: European Research Council
Cited by
1 articles.
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