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HEx: a heterologous expression platform for the discovery of fungal natural products

View ORCID ProfileColin JB Harvey, Mancheng Tang, Ulrich Schlecht, Joe Horecka, Curt R Fischer, Hsiao-ching Lin, Jian Li, Brian Naughton, James Cherry, Molly Miranda, Yong Fuga Li, Angela M Chu, James R Hennessy, Gergana A Vandova, Diane Inglis, Raeka Aiyar, Lars M. Steinmetz, Ronald W. Davis, Marnix H. Medema, Elizabeth Sattely, Chaitan Khosla, Robert P St.Onge, Yi Tang, Maureen E. Hillenmeyer
doi: https://doi.org/10.1101/247940
Colin JB Harvey
1Stanford Genome Technology Center, Stanford University, Palo Alto, CA, 94304, United States
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  • ORCID record for Colin JB Harvey
  • For correspondence: maureenh@stanford.edu cjharvey@stanford.edu
Mancheng Tang
6Department of Chemical and Biomolecular Engineering, University of California, Los Angeles, CA 90095, United States
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Ulrich Schlecht
1Stanford Genome Technology Center, Stanford University, Palo Alto, CA, 94304, United States
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Joe Horecka
1Stanford Genome Technology Center, Stanford University, Palo Alto, CA, 94304, United States
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Curt R Fischer
1Stanford Genome Technology Center, Stanford University, Palo Alto, CA, 94304, United States
2Stanford ChEM-H, Stanford University, Palo Alto, CA, 94304, United States
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Hsiao-ching Lin
6Department of Chemical and Biomolecular Engineering, University of California, Los Angeles, CA 90095, United States
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Jian Li
1Stanford Genome Technology Center, Stanford University, Palo Alto, CA, 94304, United States
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Brian Naughton
1Stanford Genome Technology Center, Stanford University, Palo Alto, CA, 94304, United States
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James Cherry
1Stanford Genome Technology Center, Stanford University, Palo Alto, CA, 94304, United States
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Molly Miranda
1Stanford Genome Technology Center, Stanford University, Palo Alto, CA, 94304, United States
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Yong Fuga Li
1Stanford Genome Technology Center, Stanford University, Palo Alto, CA, 94304, United States
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Angela M Chu
1Stanford Genome Technology Center, Stanford University, Palo Alto, CA, 94304, United States
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James R Hennessy
1Stanford Genome Technology Center, Stanford University, Palo Alto, CA, 94304, United States
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Gergana A Vandova
1Stanford Genome Technology Center, Stanford University, Palo Alto, CA, 94304, United States
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Diane Inglis
2Stanford ChEM-H, Stanford University, Palo Alto, CA, 94304, United States
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Raeka Aiyar
1Stanford Genome Technology Center, Stanford University, Palo Alto, CA, 94304, United States
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Lars M. Steinmetz
1Stanford Genome Technology Center, Stanford University, Palo Alto, CA, 94304, United States
8The European Molecular Biology Laboratory Heidelberg, 69117 Heidelberg, Germany
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Ronald W. Davis
1Stanford Genome Technology Center, Stanford University, Palo Alto, CA, 94304, United States
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Marnix H. Medema
9Bioinformatics Group, Wageningen University, Wageningen, The Netherlands
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Elizabeth Sattely
4Department of Chemical Engineering, Stanford University, Palo Alto, CA, 94304, United States
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Chaitan Khosla
2Stanford ChEM-H, Stanford University, Palo Alto, CA, 94304, United States
4Department of Chemical Engineering, Stanford University, Palo Alto, CA, 94304, United States
5Department of Chemistry, Stanford University, Palo Alto, CA, 94304, United States
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Robert P St.Onge
1Stanford Genome Technology Center, Stanford University, Palo Alto, CA, 94304, United States
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Yi Tang
6Department of Chemical and Biomolecular Engineering, University of California, Los Angeles, CA 90095, United States
7Department of Chemistry and Biochemistry, University of California, Los Angeles, CA 90095, United States
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Maureen E. Hillenmeyer
1Stanford Genome Technology Center, Stanford University, Palo Alto, CA, 94304, United States
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  • For correspondence: maureenh@stanford.edu cjharvey@stanford.edu
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Abstract

For decades, fungi have been a source of FDA-approved natural products such as penicillin, cyclosporine, and the statins. Recent breakthroughs in DNA sequencing suggest that millions of fungal species exist on Earth with each genome encoding pathways capable of generating as many as dozens of natural products. However, the majority of encoded molecules are difficult or impossible to access because the organisms are uncultivable or the genes are transcriptionally silent. To overcome this bottleneck in natural product discovery, we developed the HEx (Heterologous EXpression) synthetic biology platform for rapid, scalable expression of fungal biosynthetic genes and their encoded metabolites in Saccharomyces cerevisiae. We applied this platform to 41 fungal biosynthetic gene clusters from diverse fungal species from around the world, 22 of which produced detectable compounds. These included novel compounds with unexpected biosynthetic origins, particularly from poorly studied species. This result establishes the HEx platform for rapid discovery of natural products from any fungal species, even those that are uncultivable, and opens the door to discovery of the next generation of natural products.

Summary Here we present the largest scale effort reported to date toward the complete refactoring and heterologous expression of fungal biosynthetic gene clusters utilizing HEx, a novel synthetic biology platform.

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The copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under a CC-BY 4.0 International license.
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Posted January 15, 2018.
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HEx: a heterologous expression platform for the discovery of fungal natural products
Colin JB Harvey, Mancheng Tang, Ulrich Schlecht, Joe Horecka, Curt R Fischer, Hsiao-ching Lin, Jian Li, Brian Naughton, James Cherry, Molly Miranda, Yong Fuga Li, Angela M Chu, James R Hennessy, Gergana A Vandova, Diane Inglis, Raeka Aiyar, Lars M. Steinmetz, Ronald W. Davis, Marnix H. Medema, Elizabeth Sattely, Chaitan Khosla, Robert P St.Onge, Yi Tang, Maureen E. Hillenmeyer
bioRxiv 247940; doi: https://doi.org/10.1101/247940
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HEx: a heterologous expression platform for the discovery of fungal natural products
Colin JB Harvey, Mancheng Tang, Ulrich Schlecht, Joe Horecka, Curt R Fischer, Hsiao-ching Lin, Jian Li, Brian Naughton, James Cherry, Molly Miranda, Yong Fuga Li, Angela M Chu, James R Hennessy, Gergana A Vandova, Diane Inglis, Raeka Aiyar, Lars M. Steinmetz, Ronald W. Davis, Marnix H. Medema, Elizabeth Sattely, Chaitan Khosla, Robert P St.Onge, Yi Tang, Maureen E. Hillenmeyer
bioRxiv 247940; doi: https://doi.org/10.1101/247940

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