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Improvement of the transient expression system for production of recombinant proteins in plants
An efficient and high yielding expression system is required to produce recombinant proteins. Furthermore, the transient expression system can be used to identify the localization of proteins in plant cells. In this study, we demonstrated that combination of a geminiviral replication and a double te...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5859073/ https://www.ncbi.nlm.nih.gov/pubmed/29555968 http://dx.doi.org/10.1038/s41598-018-23024-y |
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author | Yamamoto, Tsuyoshi Hoshikawa, Ken Ezura, Kentaro Okazawa, Risa Fujita, Satoshi Takaoka, Miyo Mason, Hugh S. Ezura, Hiroshi Miura, Kenji |
author_facet | Yamamoto, Tsuyoshi Hoshikawa, Ken Ezura, Kentaro Okazawa, Risa Fujita, Satoshi Takaoka, Miyo Mason, Hugh S. Ezura, Hiroshi Miura, Kenji |
author_sort | Yamamoto, Tsuyoshi |
collection | PubMed |
description | An efficient and high yielding expression system is required to produce recombinant proteins. Furthermore, the transient expression system can be used to identify the localization of proteins in plant cells. In this study, we demonstrated that combination of a geminiviral replication and a double terminator dramatically enhanced the transient protein expression level in plants. The GFP protein was expressed transiently in lettuce, Nicotiana benthamiana, tomatoes, eggplants, hot peppers, melons, and orchids with agroinfiltration. Compared to a single terminator, a double terminator enhanced the expression level. A heat shock protein terminator combined with an extensin terminator resulted in the highest protein expression. Transiently expressed GFP was confirmed by immunoblot analysis with anti-GFP antibodies. Quantitative analysis revealed that the geminiviral vector with a double terminator resulted in the expression of at least 3.7 mg/g fresh weight of GFP in Nicotiana benthamiana, approximately 2-fold that of the geminiviral vector with a single terminator. These results indicated that combination of the geminiviral replication and a double terminator is a useful tool for transient expression of the gene of interest in plant cells. |
format | Online Article Text |
id | pubmed-5859073 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-58590732018-03-20 Improvement of the transient expression system for production of recombinant proteins in plants Yamamoto, Tsuyoshi Hoshikawa, Ken Ezura, Kentaro Okazawa, Risa Fujita, Satoshi Takaoka, Miyo Mason, Hugh S. Ezura, Hiroshi Miura, Kenji Sci Rep Article An efficient and high yielding expression system is required to produce recombinant proteins. Furthermore, the transient expression system can be used to identify the localization of proteins in plant cells. In this study, we demonstrated that combination of a geminiviral replication and a double terminator dramatically enhanced the transient protein expression level in plants. The GFP protein was expressed transiently in lettuce, Nicotiana benthamiana, tomatoes, eggplants, hot peppers, melons, and orchids with agroinfiltration. Compared to a single terminator, a double terminator enhanced the expression level. A heat shock protein terminator combined with an extensin terminator resulted in the highest protein expression. Transiently expressed GFP was confirmed by immunoblot analysis with anti-GFP antibodies. Quantitative analysis revealed that the geminiviral vector with a double terminator resulted in the expression of at least 3.7 mg/g fresh weight of GFP in Nicotiana benthamiana, approximately 2-fold that of the geminiviral vector with a single terminator. These results indicated that combination of the geminiviral replication and a double terminator is a useful tool for transient expression of the gene of interest in plant cells. Nature Publishing Group UK 2018-03-19 /pmc/articles/PMC5859073/ /pubmed/29555968 http://dx.doi.org/10.1038/s41598-018-23024-y Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Yamamoto, Tsuyoshi Hoshikawa, Ken Ezura, Kentaro Okazawa, Risa Fujita, Satoshi Takaoka, Miyo Mason, Hugh S. Ezura, Hiroshi Miura, Kenji Improvement of the transient expression system for production of recombinant proteins in plants |
title | Improvement of the transient expression system for production of recombinant proteins in plants |
title_full | Improvement of the transient expression system for production of recombinant proteins in plants |
title_fullStr | Improvement of the transient expression system for production of recombinant proteins in plants |
title_full_unstemmed | Improvement of the transient expression system for production of recombinant proteins in plants |
title_short | Improvement of the transient expression system for production of recombinant proteins in plants |
title_sort | improvement of the transient expression system for production of recombinant proteins in plants |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5859073/ https://www.ncbi.nlm.nih.gov/pubmed/29555968 http://dx.doi.org/10.1038/s41598-018-23024-y |
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