| Literature DB >> 32357274 |
Aaron A Koch1, Jennifer J Schmidt1, Andrew N Lowell1,2, Douglas A Hansen1, Katherine M Coburn1, Joseph A Chemler1, David H Sherman1,3.
Abstract
Engineering polyketide synthases (PKS) to produce new metabolites requires an understanding of catalytic points of failure during substrate processing. Growing evidence indicates the thioesterase (TE) domain as a significant bottleneck within engineered PKS systems. We created a series of hybrid PKS modules bearing exchanged TE domains from heterologous pathways and challenged them with both native and non-native polyketide substrates. Reactions pairing wildtype PKS modules with non-native substrates primarily resulted in poor conversions to anticipated macrolactones. Likewise, product formation with native substrates and hybrid PKS modules bearing non-cognate TE domains was severely reduced. In contrast, non-native substrates were converted by most hybrid modules containing a substrate compatible TE, directly implicating this domain as the major catalytic gatekeeper and highlighting its value as a target for protein engineering to improve analog production in PKS pathways.Entities:
Keywords: PKS engineering; biocatalysis; biosynthesis; natural products; polyketides
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Year: 2020 PMID: 32357274 PMCID: PMC7395861 DOI: 10.1002/anie.202004991
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336