Biochemical characterization of a non-canonical branching module of the rhizoxin polyketide synthase

Sundaram, Srividhya GND

The biosynthesis of the -lactone moiety of the macrolide rhizoxin affords the incorporation of a rare β-branch by Michael addition of a C2 unit to the α,β-unsaturated polyketide intermediate in the branching module (KS-B-ACP). The branching module accepts amine- and carboxamide-substituted substrates to yield -lactam and glutarimide rings respectively. This result is relevant to the biosynthesis of glutarimide in cycloheximide-type of antibiotics. In the presence of methylmalonyl-CoA extender unit, the branching module forms a dual branched product. In a single step, two (α and β) branches are produced in a vinylogous stereoselective branching event. In addition to the formation of 6-membered rings, the branching module could also form an array of 5- to 10-membered lactones. The branching module is therefore an excellent candidate to generate non-natural and potentially bioactive compounds. The glutarimide moiety of the cycloheximide-type of antibiotics is also biosynthesized by a similar branching module (KS-X-ACP). However, the roles of the cryptic B and X domains remained unclear. By constructing chimeras of the B domain with the X domain and a homologous DH domain, this thesis reveals that the B/X domains do not play any catalytic role but are critical for maintaining the structural integrity of the KS-B didomain. Therefore, the KS domain is solely capable of the branching and cyclization reactions. Site-directed mutagenesis of the conserved amino acids of the branching-KS identified key residues for catalysis and sets the stage to probe further into the mechanistic details of the complex branching reaction. Taken together, the results from this thesis validate that the branching module exhibits tolerance towards a non-natural substrates to produce novel ring systems. It further provides a detailed functional analysis of its key components (KS and B).



Sundaram, Srividhya: Biochemical characterization of a non-canonical branching module of the rhizoxin polyketide synthase. Jena 2018.


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