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Directed evolution for improved total secretory protein production in Escherichia coli

David Gonzalez-Perez, James Ratcliffe, Shu Khan Tan, Mary Chen May Wong, Yi Pei Yee, Natsai Nyabadza, Jian-He Xu, View ORCID ProfileTuck Seng Wong, View ORCID ProfileKang Lan Tee
doi: https://doi.org/10.1101/2020.11.03.366773
David Gonzalez-Perez
1Department of Chemical & Biological Engineering, The University of Sheffield, Sir Robert Hadfield Building, Mappin Street, Sheffield S1 3JD, UK
2Moffitt Cancer Center & Research Institute, Department of Drug Discovery, Stabile Research Building, 12902 Magnolia Dr, Tampa, FL 33612, USA
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James Ratcliffe
1Department of Chemical & Biological Engineering, The University of Sheffield, Sir Robert Hadfield Building, Mappin Street, Sheffield S1 3JD, UK
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Shu Khan Tan
1Department of Chemical & Biological Engineering, The University of Sheffield, Sir Robert Hadfield Building, Mappin Street, Sheffield S1 3JD, UK
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Mary Chen May Wong
1Department of Chemical & Biological Engineering, The University of Sheffield, Sir Robert Hadfield Building, Mappin Street, Sheffield S1 3JD, UK
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Yi Pei Yee
1Department of Chemical & Biological Engineering, The University of Sheffield, Sir Robert Hadfield Building, Mappin Street, Sheffield S1 3JD, UK
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Natsai Nyabadza
1Department of Chemical & Biological Engineering, The University of Sheffield, Sir Robert Hadfield Building, Mappin Street, Sheffield S1 3JD, UK
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Jian-He Xu
3Laboratory of Biocatalysis and Bioprocessing, State Key Laboratory of Bioreactor Engineering, East China University of Science and Technology, 130 Meilong Road, Shanghai 200237, People’s Republic of China
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Tuck Seng Wong
1Department of Chemical & Biological Engineering, The University of Sheffield, Sir Robert Hadfield Building, Mappin Street, Sheffield S1 3JD, UK
4National Center for Genetic Engineering and Biotechnology, 113 Thailand Science Park, Phahonyothin Road, Khlong Luang, Pathum Thani 12120, Thailand
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  • ORCID record for Tuck Seng Wong
  • For correspondence: k.tee@sheffield.ac.uk t.wong@sheffield.ac.uk
Kang Lan Tee
1Department of Chemical & Biological Engineering, The University of Sheffield, Sir Robert Hadfield Building, Mappin Street, Sheffield S1 3JD, UK
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  • ORCID record for Kang Lan Tee
  • For correspondence: k.tee@sheffield.ac.uk t.wong@sheffield.ac.uk
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ABSTRACT

Production of secretory protein in Gram-negative bacteria simplifies downstream processing in recombinant protein production, accelerates protein engineering, and advances synthetic biology. Signal peptides and secretory carrier proteins are commonly used to effect the secretion of heterologous recombinant protein in Gram-negative bacteria. The Escherichia coli osmotically-inducible protein Y (OsmY) is a carrier protein that secretes a target protein extracellularly, and we have successfully applied it in the Bacterial Extracellular Protein Secretion System (BENNY) to accelerate the directed evolution workflow. In this study, we applied directed evolution on OsmY to enhance its total secretory protein production.

After just one round of directed evolution followed by combining the mutations found, OsmY(M3) (L6P, V43A, S154R, V191E) was identified as the best carrier protein. OsmY(M3) produced 3.1 ± 0.3 fold and 2.9 ± 0.8 fold more secretory Tfu0937 β-glucosidase than its wildtype counterpart in E. coli strains BL21(DE3) and C41(DE3), respectively. OsmY(M3) also produced more secretory Tfu0937 at different cultivation temperatures (37 °C, 30 °C and 25 °C). Subcellular fractionation of the expressed protein confirmed the essential role of OsmY in protein secretion. Up to 80.8 ± 12.2% of total soluble protein was secreted after 15 h of cultivation. When fused to a red fluorescent protein or a lipase from Bacillus subtillis, OsmY(M3) also produced more secretory protein compared to the wildtype.

This is the first report of applying directed evolution on a carrier protein to enhance total secretory protein production. The methodology can be further extended to evolve other signal peptides or carrier proteins for secretory protein production in E. coli and other bacteria. In this study, OsmY(M3) improved the production of three proteins, originating from diverse organisms and with diverse properties, in secreted form, clearly demonstrating its wide-ranging applications.

Competing Interest Statement

The authors have declared no competing interest.

  • LIST OF ABBREVIATIONS

    dATP
    deoxyadenosine triphosphate
    dCTP
    deoxycytidine triphosphate
    dGTP
    deoxyguanosine triphosphate
    dNTP
    deoxynucleotide
    dTTP
    deoxythymidine triphosphate
    DyP4
    dye-decolorizing peroxidase 4 from Pleurotus ostreatus strain PC15
    Em
    emission wavelength
    E. coli
    Escherichia coli
    Ex
    excitation wavelength
    epPCR
    error-prone polymerase chain reaction
    HTS
    high-throughput screening
    Mw
    molecular weight
    pNPA
    p-nitrophenyl acetate
    pNPG
    p-nitrophenyl-β-D-glucopyranoside
    OD600
    optical density at 600 nm
    OsmY
    osmotically-inducible protein Y
    PCR
    polymerase chain reaction
    RFP
    red fluorescent protein
    WT
    wildtype
  • Copyright 
    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-NC-ND 4.0 International license.
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    Posted November 03, 2020.
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    Directed evolution for improved total secretory protein production in Escherichia coli
    David Gonzalez-Perez, James Ratcliffe, Shu Khan Tan, Mary Chen May Wong, Yi Pei Yee, Natsai Nyabadza, Jian-He Xu, Tuck Seng Wong, Kang Lan Tee
    bioRxiv 2020.11.03.366773; doi: https://doi.org/10.1101/2020.11.03.366773
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    Directed evolution for improved total secretory protein production in Escherichia coli
    David Gonzalez-Perez, James Ratcliffe, Shu Khan Tan, Mary Chen May Wong, Yi Pei Yee, Natsai Nyabadza, Jian-He Xu, Tuck Seng Wong, Kang Lan Tee
    bioRxiv 2020.11.03.366773; doi: https://doi.org/10.1101/2020.11.03.366773

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