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Engineered bidirectional promoters enable rapid multi-gene co-expression optimization

Author

Listed:
  • Thomas Vogl

    (Graz University of Technology
    Weizmann Institute of Science)

  • Thomas Kickenweiz

    (Graz University of Technology)

  • Julia Pitzer

    (Austrian Centre of Industrial Biotechnology (ACIB GmbH))

  • Lukas Sturmberger

    (Austrian Centre of Industrial Biotechnology (ACIB GmbH))

  • Astrid Weninger

    (Graz University of Technology)

  • Bradley W. Biggs

    (Manus Biosynthesis
    Northwestern University)

  • Eva-Maria Köhler

    (Graz University of Technology)

  • Armin Baumschlager

    (Graz University of Technology
    ETH Zürich)

  • Jasmin Elgin Fischer

    (Graz University of Technology)

  • Patrick Hyden

    (Graz University of Technology)

  • Marlies Wagner

    (Graz University of Technology)

  • Martina Baumann

    (Austrian Centre of Industrial Biotechnology (ACIB GmbH)
    University of Natural Resources and Life Sciences)

  • Nicole Borth

    (Austrian Centre of Industrial Biotechnology (ACIB GmbH)
    University of Natural Resources and Life Sciences)

  • Martina Geier

    (Austrian Centre of Industrial Biotechnology (ACIB GmbH))

  • Parayil Kumaran Ajikumar

    (Manus Biosynthesis)

  • Anton Glieder

    (Graz University of Technology)

Abstract

Numerous synthetic biology endeavors require well-tuned co-expression of functional components for success. Classically, monodirectional promoters (MDPs) have been used for such applications, but MDPs are limited in terms of multi-gene co-expression capabilities. Consequently, there is a pressing need for new tools with improved flexibility in terms of genetic circuit design, metabolic pathway assembly, and optimization. Here, motivated by nature’s use of bidirectional promoters (BDPs) as a solution for efficient gene co-expression, we generate a library of 168 synthetic BDPs in the yeast Komagataella phaffii (syn. Pichia pastoris), leveraging naturally occurring BDPs as a parts repository. This library of synthetic BDPs allows for rapid screening of diverse expression profiles and ratios to optimize gene co-expression, including for metabolic pathways (taxadiene, β-carotene). The modular design strategies applied for creating the BDP library could be relevant in other eukaryotic hosts, enabling a myriad of metabolic engineering and synthetic biology applications.

Suggested Citation

  • Thomas Vogl & Thomas Kickenweiz & Julia Pitzer & Lukas Sturmberger & Astrid Weninger & Bradley W. Biggs & Eva-Maria Köhler & Armin Baumschlager & Jasmin Elgin Fischer & Patrick Hyden & Marlies Wagner , 2018. "Engineered bidirectional promoters enable rapid multi-gene co-expression optimization," Nature Communications, Nature, vol. 9(1), pages 1-13, December.
  • Handle: RePEc:nat:natcom:v:9:y:2018:i:1:d:10.1038_s41467-018-05915-w
    DOI: 10.1038/s41467-018-05915-w
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    Cited by:

    1. Charlotte Cautereels & Jolien Smets & Peter Bircham & Dries De Ruysscher & Anna Zimmermann & Peter De Rijk & Jan Steensels & Anton Gorkovskiy & Joleen Masschelein & Kevin J. Verstrepen, 2024. "Combinatorial optimization of gene expression through recombinase-mediated promoter and terminator shuffling in yeast," Nature Communications, Nature, vol. 15(1), pages 1-17, December.

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