ja8b10521_si_001.pdf (4.2 MB)
Engineering the Substrate Specificity of a Modular Polyketide Synthase for Installation of Consecutive Non-Natural Extender Units
journal contributionposted on 2019-01-24, 19:39 authored by Edward Kalkreuter, Jared M. CroweTipton, Andrew N. Lowell, David H. Sherman, Gavin J. Williams
There is significant interest in diversifying the structures of polyketides to create new analogues of these bioactive molecules. This has traditionally been done by focusing on engineering the acyltransferase (AT) domains of polyketide synthases (PKSs) responsible for the incorporation of malonyl-CoA extender units. Non-natural extender units have been utilized by engineered PKSs previously; however, most of the work to date has been accomplished with ATs that are either naturally promiscuous and/or located in terminal modules lacking downstream bottlenecks. These limitations have prevented the engineering of ATs with low native promiscuity and the study of any potential gatekeeping effects by domains downstream of an engineered AT. In an effort to address this gap in PKS engineering knowledge, the substrate preferences of the final two modules of the pikromycin PKS were compared for several non-natural extender units and through active site mutagenesis. This led to engineering of the methylmalonyl-CoA specificity of both modules and inversion of their selectivity to prefer consecutive non-natural derivatives. Analysis of the product distributions of these bimodular reactions revealed unexpected metabolites resulting from gatekeeping by the downstream ketoreductase and ketosynthase domains. Despite these new bottlenecks, AT engineering provided the first full-length polyketide products incorporating two non-natural extender units. Together, this combination of tandem AT engineering and the identification of previously poorly characterized bottlenecks provides a platform for future advancements in the field.
bioactive moleculesPKS engineering knowledgeNon-natural extender unitsbottlenecksite mutagenesisgatekeeping effectsketosynthase domainsnon-natural derivativesterminal modulesproduct distributionsnon-natural extender unitsModular Polyketide Synthasefuture advancementsATpikromycin PKSpolyketide productsmalonyl-CoA extender unitssubstrate preferencespolyketide synthasesbimodular reactionsmethylmalonyl-CoA specificityConsecutive Non-Natural Extender UnitsSubstrate Specificity