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Downstream Processing of Chlamydomonas reinhardtii TN72 for Recombinant Protein Recovery

The green microalga Chlamydomonas reinhardtii is under development as a production host for recombinant proteins and whole-cell therapeutics. In particular, the cell wall-reduced strain TN72 is used as a model organism for protein expression and algal synthetic biology. However, the bioprocessing ch...

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Autores principales: Stoffels, Laura, Finlan, Arran, Mannall, Gareth, Purton, Saul, Parker, Brenda
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6908742/
https://www.ncbi.nlm.nih.gov/pubmed/31867315
http://dx.doi.org/10.3389/fbioe.2019.00383
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author Stoffels, Laura
Finlan, Arran
Mannall, Gareth
Purton, Saul
Parker, Brenda
author_facet Stoffels, Laura
Finlan, Arran
Mannall, Gareth
Purton, Saul
Parker, Brenda
author_sort Stoffels, Laura
collection PubMed
description The green microalga Chlamydomonas reinhardtii is under development as a production host for recombinant proteins and whole-cell therapeutics. In particular, the cell wall-reduced strain TN72 is used as a model organism for protein expression and algal synthetic biology. However, the bioprocessing characteristics of TN72 and other C. reinhardtii strains have yet to be examined. Here we use a TN72 strain expressing a protein-based antibiotic (Pal) to study the scale-up of cell harvest and product recovery. Cell harvest was examined with 100L cultures in two intermittent-discharge continuous-flow disc-stack centrifuges at flow rates of 150–250 L.h(−1), as well as with an ultra scale-down (USD) mimic of the centrifuges. Solids recovery exceeded 99.5% and the loss of product to the supernatant was below 2–3%. TN72 is intact following the high shear conditions of the feed zone, however discharge from both disc-stack centrifuges resulted in full cell breakage and in the case of Pal, partial degradation in the subsequent hours. We demonstrated that shake flask cultivation and the USD centrifuge technique can be used to predict the pilot-scale clarification efficiency and product release at the centrifuge inlet for TN72, but not the cell breakage on discharge. This study outlines a number of challenges for scale-up of recombinant protein production in the microalgal host in particular for whole cell therapeutics, but also opportunities for the bioprocessing of intracellular products from TN72.
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spelling pubmed-69087422019-12-20 Downstream Processing of Chlamydomonas reinhardtii TN72 for Recombinant Protein Recovery Stoffels, Laura Finlan, Arran Mannall, Gareth Purton, Saul Parker, Brenda Front Bioeng Biotechnol Bioengineering and Biotechnology The green microalga Chlamydomonas reinhardtii is under development as a production host for recombinant proteins and whole-cell therapeutics. In particular, the cell wall-reduced strain TN72 is used as a model organism for protein expression and algal synthetic biology. However, the bioprocessing characteristics of TN72 and other C. reinhardtii strains have yet to be examined. Here we use a TN72 strain expressing a protein-based antibiotic (Pal) to study the scale-up of cell harvest and product recovery. Cell harvest was examined with 100L cultures in two intermittent-discharge continuous-flow disc-stack centrifuges at flow rates of 150–250 L.h(−1), as well as with an ultra scale-down (USD) mimic of the centrifuges. Solids recovery exceeded 99.5% and the loss of product to the supernatant was below 2–3%. TN72 is intact following the high shear conditions of the feed zone, however discharge from both disc-stack centrifuges resulted in full cell breakage and in the case of Pal, partial degradation in the subsequent hours. We demonstrated that shake flask cultivation and the USD centrifuge technique can be used to predict the pilot-scale clarification efficiency and product release at the centrifuge inlet for TN72, but not the cell breakage on discharge. This study outlines a number of challenges for scale-up of recombinant protein production in the microalgal host in particular for whole cell therapeutics, but also opportunities for the bioprocessing of intracellular products from TN72. Frontiers Media S.A. 2019-12-06 /pmc/articles/PMC6908742/ /pubmed/31867315 http://dx.doi.org/10.3389/fbioe.2019.00383 Text en Copyright © 2019 Stoffels, Finlan, Mannall, Purton and Parker. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Bioengineering and Biotechnology
Stoffels, Laura
Finlan, Arran
Mannall, Gareth
Purton, Saul
Parker, Brenda
Downstream Processing of Chlamydomonas reinhardtii TN72 for Recombinant Protein Recovery
title Downstream Processing of Chlamydomonas reinhardtii TN72 for Recombinant Protein Recovery
title_full Downstream Processing of Chlamydomonas reinhardtii TN72 for Recombinant Protein Recovery
title_fullStr Downstream Processing of Chlamydomonas reinhardtii TN72 for Recombinant Protein Recovery
title_full_unstemmed Downstream Processing of Chlamydomonas reinhardtii TN72 for Recombinant Protein Recovery
title_short Downstream Processing of Chlamydomonas reinhardtii TN72 for Recombinant Protein Recovery
title_sort downstream processing of chlamydomonas reinhardtii tn72 for recombinant protein recovery
topic Bioengineering and Biotechnology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6908742/
https://www.ncbi.nlm.nih.gov/pubmed/31867315
http://dx.doi.org/10.3389/fbioe.2019.00383
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