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Diazaquinomycin Biosynthetic Gene Clusters from Marine and Freshwater Actinomycetes

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posted on 24.05.2019 by Jana Braesel, Jung-Ho Lee, Benoit Arnould, Brian T. Murphy, Alessandra S. Eustáquio
Tuberculosis is an infectious disease of global concern. Members of the diazaquinomycin (DAQ) class of natural products have shown potent and selective activity against drug-resistant Mycobacterium tuberculosis. However, poor solubility has prevented further development of this compound class. Understanding DAQ biosynthesis may provide a viable route for the generation of derivatives with improved properties. We have sequenced the genomes of two actinomycete bacteria that produce distinct DAQ derivatives. While software tools for automated biosynthetic gene cluster (BGC) prediction failed to detect DAQ BGCs, comparative genomics using MAUVE alignment led to the identification of putative BGCs in the marine Streptomyces sp. F001 and in the freshwater Micromonospora sp. B006. Deletion of the identified daq BGC in strain B006 using CRISPR-Cas9 genome editing abolished DAQ production, providing experimental evidence for BGC assignment. A complete model for DAQ biosynthesis is proposed based on the genes identified. Insufficient knowledge of natural product biosynthesis is one of the major challenges of productive, genome mining approaches. The results reported here fill a gap in knowledge regarding the genetic basis for the biosynthesis of DAQ antibiotics. Moreover, identification of the daq BGC shall enable future generations of improved derivatives using biosynthetic methods.

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We thank G. Pauli (University of Illinois at Chicago) and N. Ziemert (University of Tübingen) for access to LC/MS instrumentation, and suggestions regarding MAUVE alignments, respectively. We also thank H. Zhao (University of Illinois at Urbana-Champaign) for pCRISPomyces-2 (via Addgene, plasmid #61737). Financial support for this work was provided by the National Center for Advancing Translational Sciences, National Institutes of Health (NIH), under grant KL2TR002002 (to ASE), and by startup funds from the Department of Medicinal Chemistry and Pharmacognosy and the Center for Biomolecular Sciences, University of Illinois at Chicago (to ASE). The content is solely the responsibility of the authors and does not necessarily represent the official views of the NIH.

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Citation

Braesel, J., Lee, J. H., Arnould, B., Murphy, B. T., & Eustáquio, A. S. (2019). Diazaquinomycin Biosynthetic Gene Clusters from Marine and Freshwater Actinomycetes. Journal of Natural Products. doi:10.1021/acs.jnatprod.8b01028

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American Chemical Society

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en

issn

0163-3864

Issue date

21/03/2019

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