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Plant cell packs: a scalable platform for recombinant protein production and metabolic engineering

Industrial plant biotechnology applications include the production of sustainable fuels, complex metabolites and recombinant proteins, but process development can be impaired by a lack of reliable and scalable screening methods. Here, we describe a rapid and versatile expression system which involve...

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Autores principales: Rademacher, Thomas, Sack, Markus, Blessing, Daniel, Fischer, Rainer, Holland, Tanja, Buyel, Johannes
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6662111/
https://www.ncbi.nlm.nih.gov/pubmed/30672078
http://dx.doi.org/10.1111/pbi.13081
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author Rademacher, Thomas
Sack, Markus
Blessing, Daniel
Fischer, Rainer
Holland, Tanja
Buyel, Johannes
author_facet Rademacher, Thomas
Sack, Markus
Blessing, Daniel
Fischer, Rainer
Holland, Tanja
Buyel, Johannes
author_sort Rademacher, Thomas
collection PubMed
description Industrial plant biotechnology applications include the production of sustainable fuels, complex metabolites and recombinant proteins, but process development can be impaired by a lack of reliable and scalable screening methods. Here, we describe a rapid and versatile expression system which involves the infusion of Agrobacterium tumefaciens into three‐dimensional, porous plant cell aggregates deprived of cultivation medium, which we have termed plant cell packs (PCPs). This approach is compatible with different plant species such as Nicotiana tabacum BY2, Nicotiana benthamiana or Daucus carota and 10‐times more effective than transient expression in liquid plant cell culture. We found that the expression of several proteins was similar in PCPs and intact plants, for example, 47 and 55 mg/kg for antibody 2G12 expressed in BY2 PCPs and N. tabacum plants respectively. Additionally, the expression of specific enzymes can either increase the content of natural plant metabolites or be used to synthesize novel small molecules in the PCPs. The PCP method is currently scalable from a microtiter plate format suitable for high‐throughput screening to 150‐mL columns suitable for initial product preparation. It therefore combined the speed of transient expression in plants with the throughput of microbial screening systems. Plant cell packs therefore provide a convenient new platform for synthetic biology approaches, metabolic engineering and conventional recombinant protein expression techniques that require the multiplex analysis of several dozen up to hundreds of constructs for efficient product and process development.
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spelling pubmed-66621112019-08-05 Plant cell packs: a scalable platform for recombinant protein production and metabolic engineering Rademacher, Thomas Sack, Markus Blessing, Daniel Fischer, Rainer Holland, Tanja Buyel, Johannes Plant Biotechnol J Research Articles Industrial plant biotechnology applications include the production of sustainable fuels, complex metabolites and recombinant proteins, but process development can be impaired by a lack of reliable and scalable screening methods. Here, we describe a rapid and versatile expression system which involves the infusion of Agrobacterium tumefaciens into three‐dimensional, porous plant cell aggregates deprived of cultivation medium, which we have termed plant cell packs (PCPs). This approach is compatible with different plant species such as Nicotiana tabacum BY2, Nicotiana benthamiana or Daucus carota and 10‐times more effective than transient expression in liquid plant cell culture. We found that the expression of several proteins was similar in PCPs and intact plants, for example, 47 and 55 mg/kg for antibody 2G12 expressed in BY2 PCPs and N. tabacum plants respectively. Additionally, the expression of specific enzymes can either increase the content of natural plant metabolites or be used to synthesize novel small molecules in the PCPs. The PCP method is currently scalable from a microtiter plate format suitable for high‐throughput screening to 150‐mL columns suitable for initial product preparation. It therefore combined the speed of transient expression in plants with the throughput of microbial screening systems. Plant cell packs therefore provide a convenient new platform for synthetic biology approaches, metabolic engineering and conventional recombinant protein expression techniques that require the multiplex analysis of several dozen up to hundreds of constructs for efficient product and process development. John Wiley and Sons Inc. 2019-02-14 2019-08 /pmc/articles/PMC6662111/ /pubmed/30672078 http://dx.doi.org/10.1111/pbi.13081 Text en © 2019 The Authors. Plant Biotechnology Journal published by Society for Experimental Biology and The Association of Applied Biologists and John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Rademacher, Thomas
Sack, Markus
Blessing, Daniel
Fischer, Rainer
Holland, Tanja
Buyel, Johannes
Plant cell packs: a scalable platform for recombinant protein production and metabolic engineering
title Plant cell packs: a scalable platform for recombinant protein production and metabolic engineering
title_full Plant cell packs: a scalable platform for recombinant protein production and metabolic engineering
title_fullStr Plant cell packs: a scalable platform for recombinant protein production and metabolic engineering
title_full_unstemmed Plant cell packs: a scalable platform for recombinant protein production and metabolic engineering
title_short Plant cell packs: a scalable platform for recombinant protein production and metabolic engineering
title_sort plant cell packs: a scalable platform for recombinant protein production and metabolic engineering
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6662111/
https://www.ncbi.nlm.nih.gov/pubmed/30672078
http://dx.doi.org/10.1111/pbi.13081
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