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Stable Production of the Antimalarial Drug Artemisinin in the Moss Physcomitrella patens
Malaria is a real and constant danger to nearly half of the world’s population of 7.4 billion people. In 2015, 212 million cases were reported along with 429,000 estimated deaths. The World Health Organization recommends artemisinin-based combinatorial therapies, and the artemisinin for this purpose...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5559433/ https://www.ncbi.nlm.nih.gov/pubmed/28861412 http://dx.doi.org/10.3389/fbioe.2017.00047 |
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author | Khairul Ikram, Nur Kusaira Binti Beyraghdar Kashkooli, Arman Peramuna, Anantha Vithakshana van der Krol, Alexander R. Bouwmeester, Harro Simonsen, Henrik Toft |
author_facet | Khairul Ikram, Nur Kusaira Binti Beyraghdar Kashkooli, Arman Peramuna, Anantha Vithakshana van der Krol, Alexander R. Bouwmeester, Harro Simonsen, Henrik Toft |
author_sort | Khairul Ikram, Nur Kusaira Binti |
collection | PubMed |
description | Malaria is a real and constant danger to nearly half of the world’s population of 7.4 billion people. In 2015, 212 million cases were reported along with 429,000 estimated deaths. The World Health Organization recommends artemisinin-based combinatorial therapies, and the artemisinin for this purpose is mainly isolated from the plant Artemisia annua. However, the plant supply of artemisinin is irregular, leading to fluctuation in prices. Here, we report the development of a simple, sustainable, and scalable production platform of artemisinin. The five genes involved in artemisinin biosynthesis were engineered into the moss Physcomitrella patens via direct in vivo assembly of multiple DNA fragments. In vivo biosynthesis of artemisinin was obtained without further modifications. A high initial production of 0.21 mg/g dry weight artemisinin was observed after only 3 days of cultivation. Our study shows that P. patens can be a sustainable and efficient production platform of artemisinin that without further modifications allow for industrial-scale production. A stable supply of artemisinin will lower the price of artemisinin-based treatments, hence become more affordable to the lower income communities most affected by malaria; an important step toward containment of this deadly disease threatening millions every year. |
format | Online Article Text |
id | pubmed-5559433 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-55594332017-08-31 Stable Production of the Antimalarial Drug Artemisinin in the Moss Physcomitrella patens Khairul Ikram, Nur Kusaira Binti Beyraghdar Kashkooli, Arman Peramuna, Anantha Vithakshana van der Krol, Alexander R. Bouwmeester, Harro Simonsen, Henrik Toft Front Bioeng Biotechnol Bioengineering and Biotechnology Malaria is a real and constant danger to nearly half of the world’s population of 7.4 billion people. In 2015, 212 million cases were reported along with 429,000 estimated deaths. The World Health Organization recommends artemisinin-based combinatorial therapies, and the artemisinin for this purpose is mainly isolated from the plant Artemisia annua. However, the plant supply of artemisinin is irregular, leading to fluctuation in prices. Here, we report the development of a simple, sustainable, and scalable production platform of artemisinin. The five genes involved in artemisinin biosynthesis were engineered into the moss Physcomitrella patens via direct in vivo assembly of multiple DNA fragments. In vivo biosynthesis of artemisinin was obtained without further modifications. A high initial production of 0.21 mg/g dry weight artemisinin was observed after only 3 days of cultivation. Our study shows that P. patens can be a sustainable and efficient production platform of artemisinin that without further modifications allow for industrial-scale production. A stable supply of artemisinin will lower the price of artemisinin-based treatments, hence become more affordable to the lower income communities most affected by malaria; an important step toward containment of this deadly disease threatening millions every year. Frontiers Media S.A. 2017-08-15 /pmc/articles/PMC5559433/ /pubmed/28861412 http://dx.doi.org/10.3389/fbioe.2017.00047 Text en Copyright © 2017 Khairul Ikram, Beyraghdar Kashkooli, Peramuna, van der Krol, Bouwmeester and Simonsen. 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) or licensor 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 Khairul Ikram, Nur Kusaira Binti Beyraghdar Kashkooli, Arman Peramuna, Anantha Vithakshana van der Krol, Alexander R. Bouwmeester, Harro Simonsen, Henrik Toft Stable Production of the Antimalarial Drug Artemisinin in the Moss Physcomitrella patens |
title | Stable Production of the Antimalarial Drug Artemisinin in the Moss Physcomitrella patens |
title_full | Stable Production of the Antimalarial Drug Artemisinin in the Moss Physcomitrella patens |
title_fullStr | Stable Production of the Antimalarial Drug Artemisinin in the Moss Physcomitrella patens |
title_full_unstemmed | Stable Production of the Antimalarial Drug Artemisinin in the Moss Physcomitrella patens |
title_short | Stable Production of the Antimalarial Drug Artemisinin in the Moss Physcomitrella patens |
title_sort | stable production of the antimalarial drug artemisinin in the moss physcomitrella patens |
topic | Bioengineering and Biotechnology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5559433/ https://www.ncbi.nlm.nih.gov/pubmed/28861412 http://dx.doi.org/10.3389/fbioe.2017.00047 |
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