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A modular and synthetic biosynthesis platform for de novo production of diverse halogenated tryptophan-derived molecules

Author

Listed:
  • Kevin B. Reed

    (The University of Texas at Austin)

  • Sierra M. Brooks

    (The University of Texas at Austin)

  • Jordan Wells

    (The University of Texas at Austin)

  • Kristin J. Blake

    (The University of Texas at Austin)

  • Minye Zhao

    (The University of Texas at Austin)

  • Kira Placido

    (The University of Texas at Austin)

  • Simon d’Oelsnitz

    (The University of Texas at Austin)

  • Adit Trivedi

    (The University of Texas at Austin)

  • Shruti Gadhiyar

    (The University of Texas at Austin)

  • Hal S. Alper

    (The University of Texas at Austin
    The University of Texas at Austin)

Abstract

Halogen-containing molecules are ubiquitous in modern society and present unique chemical possibilities. As a whole, de novo fermentation and synthetic pathway construction for these molecules remain relatively underexplored and could unlock molecules with exciting new applications in industries ranging from textiles to agrochemicals to pharmaceuticals. Here, we report a mix-and-match co-culture platform to de novo generate a large array of halogenated tryptophan derivatives in Escherichia coli from glucose. First, we engineer E. coli to produce between 300 and 700 mg/L of six different halogenated tryptophan precursors. Second, we harness the native promiscuity of multiple downstream enzymes to access unexplored regions of metabolism. Finally, through modular co-culture fermentations, we demonstrate a plug-and-play bioproduction platform, culminating in the generation of 26 distinct halogenated molecules produced de novo including precursors to prodrugs 4-chloro- and 4-bromo-kynurenine and new-to-nature halogenated beta carbolines.

Suggested Citation

  • Kevin B. Reed & Sierra M. Brooks & Jordan Wells & Kristin J. Blake & Minye Zhao & Kira Placido & Simon d’Oelsnitz & Adit Trivedi & Shruti Gadhiyar & Hal S. Alper, 2024. "A modular and synthetic biosynthesis platform for de novo production of diverse halogenated tryptophan-derived molecules," Nature Communications, Nature, vol. 15(1), pages 1-13, December.
  • Handle: RePEc:nat:natcom:v:15:y:2024:i:1:d:10.1038_s41467-024-47387-1
    DOI: 10.1038/s41467-024-47387-1
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    References listed on IDEAS

    as
    1. Alhosna Benjdia & Stéphane Pierre & Carmen Gherasim & Alain Guillot & Manon Carmona & Patricia Amara & Ruma Banerjee & Olivier Berteau, 2015. "The thiostrepton A tryptophan methyltransferase TsrM catalyses a cob(II)alamin-dependent methyl transfer reaction," Nature Communications, Nature, vol. 6(1), pages 1-10, December.
    2. Weerawat Runguphan & Xudong Qu & Sarah E. O’Connor, 2010. "Integrating carbon–halogen bond formation into medicinal plant metabolism," Nature, Nature, vol. 468(7322), pages 461-464, November.
    3. Sunil V. Sharma & Xiaoxue Tong & Cristina Pubill-Ulldemolins & Christopher Cartmell & Emma J. A. Bogosyan & Emma J. Rackham & Enrico Marelli & Refaat B. Hamed & Rebecca J. M. Goss, 2017. "Living GenoChemetics by hyphenating synthetic biology and synthetic chemistry in vivo," Nature Communications, Nature, vol. 8(1), pages 1-10, December.
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