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Polyketide and Nonribosomal Peptide Antibiotics: Modularity and Versatility
Christopher T. Walsh
Polyketide (PK) and nonribosomal peptides (NRP), constructedon multimodular enzymatic assembly lines, often attain the conformationsthat establish biological activity by cyclization constraintsintroduced by tailoring enzymes. The dedicated tailoring enzymesare encoded by genes clustered with the assembly line genesfor coordinated regulation. NRP heterocyclizations to thiazolesand oxazoles can occur on the elongating framework of acyl-Senzyme intermediates, whereas tandem cyclic PK polyether formationof furans and pyrans can be initiated by postassemblyline epoxidases. Macrocyclizations of NRP, PK, and hybrid NRP-PKscaffolds occur in assembly line chain termination steps. Postassemblyline cascades of enzymatic oxidations also create cross-linkedand cyclized architectures that generate the mature scaffoldsof natural product antibiotics. The modularity of the naturalproduct assembly lines and permissivity of tailoring enzymesoffer prospects for reprogramming to create novel antibioticswith optimized properties.
Department of Biological Chemistry and Molecular Pharmacology, Harvard Medical School, Boston, MA 02115, USA.
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