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Expression strategies for the efficient synthesis of antimicrobial peptides in plastids

Author

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  • Matthijs P. Hoelscher

    (Max-Planck-Institut für Molekulare Pflanzenphysiologie
    Utrecht University, Pharmaceutical sciences, Pharmaceutics)

  • Joachim Forner

    (Max-Planck-Institut für Molekulare Pflanzenphysiologie)

  • Silvia Calderone

    (Max-Planck-Institut für Molekulare Pflanzenphysiologie
    CSIC-IRTA-UAB-UB, Campus UAB, Bellaterra)

  • Carolin Krämer

    (Max-Planck-Institut für Molekulare Pflanzenphysiologie)

  • Zachary Taylor

    (Max-Planck-Institut für Molekulare Pflanzenphysiologie)

  • F. Vanessa Loiacono

    (Max-Planck-Institut für Molekulare Pflanzenphysiologie)

  • Shreya Agrawal

    (Max-Planck-Institut für Molekulare Pflanzenphysiologie
    Neoplants, 630 Rue Noetzlin Bâtiment)

  • Daniel Karcher

    (Max-Planck-Institut für Molekulare Pflanzenphysiologie)

  • Fabio Moratti

    (Max-Planck-Institut für Molekulare Pflanzenphysiologie)

  • Xenia Kroop

    (Max-Planck-Institut für Molekulare Pflanzenphysiologie)

  • Ralph Bock

    (Max-Planck-Institut für Molekulare Pflanzenphysiologie)

Abstract

Antimicrobial peptides (AMPs) kill microbes or inhibit their growth and are promising next-generation antibiotics. Harnessing their full potential as antimicrobial agents will require methods for cost-effective large-scale production and purification. Here, we explore the possibility to exploit the high protein synthesis capacity of the chloroplast to produce AMPs in plants. Generating a large series of 29 sets of transplastomic tobacco plants expressing nine different AMPs as fusion proteins, we show that high-level constitutive AMP expression results in deleterious plant phenotypes. However, by utilizing inducible expression and fusions to the cleavable carrier protein SUMO, the cytotoxic effects of AMPs and fused AMPs are alleviated and plants with wild-type-like phenotypes are obtained. Importantly, purified AMP fusion proteins display antimicrobial activity independently of proteolytic removal of the carrier. Our work provides expression strategies for the synthesis of toxic polypeptides in chloroplasts, and establishes transplastomic plants as efficient production platform for antimicrobial peptides.

Suggested Citation

  • Matthijs P. Hoelscher & Joachim Forner & Silvia Calderone & Carolin Krämer & Zachary Taylor & F. Vanessa Loiacono & Shreya Agrawal & Daniel Karcher & Fabio Moratti & Xenia Kroop & Ralph Bock, 2022. "Expression strategies for the efficient synthesis of antimicrobial peptides in plastids," Nature Communications, Nature, vol. 13(1), pages 1-17, December.
  • Handle: RePEc:nat:natcom:v:13:y:2022:i:1:d:10.1038_s41467-022-33516-1
    DOI: 10.1038/s41467-022-33516-1
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    References listed on IDEAS

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    1. Shyr-Jiann Li & Mark Hochstrasser, 1999. "A new protease required for cell-cycle progression in yeast," Nature, Nature, vol. 398(6724), pages 246-251, March.
    2. Michael Zasloff, 2002. "Antimicrobial peptides of multicellular organisms," Nature, Nature, vol. 415(6870), pages 389-395, January.
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    1. Shahid Chaudhary & Zahir Ali & Muhammad Tehseen & Evan F. Haney & Aarón Pantoja-Angles & Salwa Alshehri & Tiannyu Wang & Gerard J. Clancy & Maya Ayach & Charlotte Hauser & Pei-Ying Hong & Samir M. Ham, 2023. "Efficient in planta production of amidated antimicrobial peptides that are active against drug-resistant ESKAPE pathogens," Nature Communications, Nature, vol. 14(1), pages 1-16, December.

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