Lapcin, a potent dual topoisomerase I/II inhibitor discovered by soil metagenome guided total chemical synthesis

Zongqiang Wang, Nicholas Forelli, Yozen Hernandez, Melinda Ternei and Sean F. Brady ()
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Zongqiang Wang: Laboratory of Genetically Encoded Small Molecules, The Rockefeller University
Nicholas Forelli: Laboratory of Genetically Encoded Small Molecules, The Rockefeller University
Yozen Hernandez: Laboratory of Genetically Encoded Small Molecules, The Rockefeller University
Melinda Ternei: Laboratory of Genetically Encoded Small Molecules, The Rockefeller University
Sean F. Brady: Laboratory of Genetically Encoded Small Molecules, The Rockefeller University

Nature Communications, 2022, vol. 13, issue 1, 1-9

Abstract: Abstract In natural product discovery programs, the power of synthetic chemistry is often leveraged for the total synthesis and diversification of characterized metabolites. The synthesis of structures that are bioinformatically predicted to arise from uncharacterized biosynthetic gene clusters (BGCs) provides a means for synthetic chemistry to enter this process at an early stage. The recent identification of non-ribosomal peptides (NRPs) containing multiple ρ-aminobenzoic acids (PABAs) led us to search soil metagenomes for BGCs that polymerize PABA. Here, we use PABA-specific adenylation-domain sequences to guide the cloning of the lap BGC directly from soil. This BGC was predicted to encode a unique N-acylated PABA and thiazole containing structure. Chemical synthesis of this structure gave lapcin, a dual topoisomerase I/II inhibitor with nM to pM IC50s against diverse cancer cell lines. The discovery of lapcin highlights the power of coupling metagenomics, bioinformatics and total chemical synthesis to unlock the biosynthetic potential contained in even complex uncharacterized BGCs.

Date: 2022
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DOI: 10.1038/s41467-022-28292-x

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