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Increased CO2 fixation enables high carbon-yield production of 3-hydroxypropionic acid in yeast

Author

Listed:
  • Ning Qin

    (Beijing University of Chemical Technology)

  • Lingyun Li

    (Beijing University of Chemical Technology
    Chalmers University of Technology)

  • Xiaozhen Wan

    (Beijing University of Chemical Technology)

  • Xu Ji

    (Beijing University of Chemical Technology)

  • Yu Chen

    (Chinese Academy of Sciences)

  • Chaokun Li

    (University of Helsinki)

  • Ping Liu

    (Beijing University of Chemical Technology)

  • Yijie Zhang

    (Beijing University of Chemical Technology)

  • Weijie Yang

    (Beijing University of Chemical Technology)

  • Junfeng Jiang

    (Chinese Academy of Sciences)

  • Jianye Xia

    (Chinese Academy of Sciences)

  • Shuobo Shi

    (Beijing University of Chemical Technology)

  • Tianwei Tan

    (Beijing University of Chemical Technology)

  • Jens Nielsen

    (Beijing University of Chemical Technology
    Chalmers University of Technology
    BioInnovation Institute)

  • Yun Chen

    (Chalmers University of Technology
    Technical University of Denmark)

  • Zihe Liu

    (Beijing University of Chemical Technology)

Abstract

CO2 fixation plays a key role to make biobased production cost competitive. Here, we use 3-hydroxypropionic acid (3-HP) to showcase how CO2 fixation enables approaching theoretical-yield production. Using genome-scale metabolic models to calculate the production envelope, we demonstrate that the provision of bicarbonate, formed from CO2, restricts previous attempts for high yield production of 3-HP. We thus develop multiple strategies for bicarbonate uptake, including the identification of Sul1 as a potential bicarbonate transporter, domain swapping of malonyl-CoA reductase, identification of Esbp6 as a potential 3-HP exporter, and deletion of Uga1 to prevent 3-HP degradation. The combined rational engineering increases 3-HP production from 0.14 g/L to 11.25 g/L in shake flask using 20 g/L glucose, approaching the maximum theoretical yield with concurrent biomass formation. The engineered yeast forms the basis for commercialization of bio-acrylic acid, while our CO2 fixation strategies pave the way for CO2 being used as the sole carbon source.

Suggested Citation

  • Ning Qin & Lingyun Li & Xiaozhen Wan & Xu Ji & Yu Chen & Chaokun Li & Ping Liu & Yijie Zhang & Weijie Yang & Junfeng Jiang & Jianye Xia & Shuobo Shi & Tianwei Tan & Jens Nielsen & Yun Chen & Zihe Liu, 2024. "Increased CO2 fixation enables high carbon-yield production of 3-hydroxypropionic acid in yeast," Nature Communications, Nature, vol. 15(1), pages 1-15, December.
  • Handle: RePEc:nat:natcom:v:15:y:2024:i:1:d:10.1038_s41467-024-45557-9
    DOI: 10.1038/s41467-024-45557-9
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    References listed on IDEAS

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    1. Kathleen A. Curran & Nathan C. Crook & Ashty S. Karim & Akash Gupta & Allison M. Wagman & Hal S. Alper, 2014. "Design of synthetic yeast promoters via tuning of nucleosome architecture," Nature Communications, Nature, vol. 5(1), pages 1-8, September.
    2. Kathryn Tunyasuvunakool & Jonas Adler & Zachary Wu & Tim Green & Michal Zielinski & Augustin Žídek & Alex Bridgland & Andrew Cowie & Clemens Meyer & Agata Laydon & Sameer Velankar & Gerard J. Kleywegt, 2021. "Highly accurate protein structure prediction for the human proteome," Nature, Nature, vol. 596(7873), pages 590-596, August.
    3. Quanli Liu & Tao Yu & Xiaowei Li & Yu Chen & Kate Campbell & Jens Nielsen & Yun Chen, 2019. "Rewiring carbon metabolism in yeast for high level production of aromatic chemicals," Nature Communications, Nature, vol. 10(1), pages 1-13, December.
    4. John Jumper & Richard Evans & Alexander Pritzel & Tim Green & Michael Figurnov & Olaf Ronneberger & Kathryn Tunyasuvunakool & Russ Bates & Augustin Žídek & Anna Potapenko & Alex Bridgland & Clemens Me, 2021. "Highly accurate protein structure prediction with AlphaFold," Nature, Nature, vol. 596(7873), pages 583-589, August.
    5. Rosemary Yu & Kate Campbell & Rui Pereira & Johan Björkeroth & Qi Qi & Egor Vorontsov & Carina Sihlbom & Jens Nielsen, 2020. "Nitrogen limitation reveals large reserves in metabolic and translational capacities of yeast," Nature Communications, Nature, vol. 11(1), pages 1-12, December.
    6. John M. DeCicco & Danielle Yuqiao Liu & Joonghyeok Heo & Rashmi Krishnan & Angelika Kurthen & Louise Wang, 2016. "Carbon balance effects of U.S. biofuel production and use," Climatic Change, Springer, vol. 138(3), pages 667-680, October.
    7. Hongzhong Lu & Feiran Li & Benjamín J. Sánchez & Zhengming Zhu & Gang Li & Iván Domenzain & Simonas Marcišauskas & Petre Mihail Anton & Dimitra Lappa & Christian Lieven & Moritz Emanuel Beber & Nikola, 2019. "A consensus S. cerevisiae metabolic model Yeast8 and its ecosystem for comprehensively probing cellular metabolism," Nature Communications, Nature, vol. 10(1), pages 1-13, December.
    8. Zongjie Dai & Mingtao Huang & Yun Chen & Verena Siewers & Jens Nielsen, 2018. "Global rewiring of cellular metabolism renders Saccharomyces cerevisiae Crabtree negative," Nature Communications, Nature, vol. 9(1), pages 1-8, December.
    9. André B. Canelas & Nicola Harrison & Alessandro Fazio & Jie Zhang & Juha-Pekka Pitkänen & Joost van den Brink & Barbara M. Bakker & Lara Bogner & Jildau Bouwman & Juan I. Castrillo & Ayca Cankorur & P, 2010. "Integrated multilaboratory systems biology reveals differences in protein metabolism between two reference yeast strains," Nature Communications, Nature, vol. 1(1), pages 1-8, December.
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