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Characterization of Hydrocortisone Biometabolites and 18S rRNA Gene in Chlamydomonas reinhardtii Cultures
A unicellular microalga, Chlamydomonas reinhardtii, was isolated from rice paddy-field soil and water samples and used in the biotransformation of hydrocortisone (1). This strain has not been previously tested for steroid bioconversion. Fermentation was carried out in BG-11 medium supplemented with...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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MDPI
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6245355/ https://www.ncbi.nlm.nih.gov/pubmed/18830164 http://dx.doi.org/10.3390/molecules13102416 |
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author | Ghasemi, Younes Rasoul-Amini, Sara Morowvat, Mohammad Hossein Raee, Mohammad Javad Ghoshoon, Mohammad Bagher Nouri, Fatemeh Negintaji, Narges Parvizi, Rezvan Mosavi-Azam, Seyed Bagher |
author_facet | Ghasemi, Younes Rasoul-Amini, Sara Morowvat, Mohammad Hossein Raee, Mohammad Javad Ghoshoon, Mohammad Bagher Nouri, Fatemeh Negintaji, Narges Parvizi, Rezvan Mosavi-Azam, Seyed Bagher |
author_sort | Ghasemi, Younes |
collection | PubMed |
description | A unicellular microalga, Chlamydomonas reinhardtii, was isolated from rice paddy-field soil and water samples and used in the biotransformation of hydrocortisone (1). This strain has not been previously tested for steroid bioconversion. Fermentation was carried out in BG-11 medium supplemented with 0.05% substrate at 25°C for 14 days of incubation. The products obtained were chromatographically purified and characterized using spectroscopic methods. 11β,17β-Dihydroxyandrost-4-en-3-one (2), 11β- hydroxyandrost-4-en-3,17-dione (3), 11β,17α,20β,21-tetrahydroxypregn-4-en-3-one (4) and prednisolone (5) were the main products of the bioconversion. The observed bioreaction features were the side chain degradation of the substrate to give compounds 2 and 3 and the 20-ketone reduction and 1,2-dehydrogenation affording compounds 4 and 5, respectively. A time course study showed the accumulation of product 2 from the second day of the fermentation and of compounds 3, 4 and 5 from the third day. All the metabolites reached their maximum concentration in seven days. Microalgal 18S rRNA gene was also amplified by PCR. PCR products were sequenced to confirm their authenticity as 18S rRNA gene of microalgae. The result of PCR blasted with other sequenced microalgae in NCBI showed 100% homology to the 18S small subunit rRNA of two Chlamydomonas reinhardtii spp. |
format | Online Article Text |
id | pubmed-6245355 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-62453552018-11-30 Characterization of Hydrocortisone Biometabolites and 18S rRNA Gene in Chlamydomonas reinhardtii Cultures Ghasemi, Younes Rasoul-Amini, Sara Morowvat, Mohammad Hossein Raee, Mohammad Javad Ghoshoon, Mohammad Bagher Nouri, Fatemeh Negintaji, Narges Parvizi, Rezvan Mosavi-Azam, Seyed Bagher Molecules Article A unicellular microalga, Chlamydomonas reinhardtii, was isolated from rice paddy-field soil and water samples and used in the biotransformation of hydrocortisone (1). This strain has not been previously tested for steroid bioconversion. Fermentation was carried out in BG-11 medium supplemented with 0.05% substrate at 25°C for 14 days of incubation. The products obtained were chromatographically purified and characterized using spectroscopic methods. 11β,17β-Dihydroxyandrost-4-en-3-one (2), 11β- hydroxyandrost-4-en-3,17-dione (3), 11β,17α,20β,21-tetrahydroxypregn-4-en-3-one (4) and prednisolone (5) were the main products of the bioconversion. The observed bioreaction features were the side chain degradation of the substrate to give compounds 2 and 3 and the 20-ketone reduction and 1,2-dehydrogenation affording compounds 4 and 5, respectively. A time course study showed the accumulation of product 2 from the second day of the fermentation and of compounds 3, 4 and 5 from the third day. All the metabolites reached their maximum concentration in seven days. Microalgal 18S rRNA gene was also amplified by PCR. PCR products were sequenced to confirm their authenticity as 18S rRNA gene of microalgae. The result of PCR blasted with other sequenced microalgae in NCBI showed 100% homology to the 18S small subunit rRNA of two Chlamydomonas reinhardtii spp. MDPI 2008-10-01 /pmc/articles/PMC6245355/ /pubmed/18830164 http://dx.doi.org/10.3390/molecules13102416 Text en © 2008 by the authors. Licensee Molecular Diversity Preservation International, Basel, Switzerland. This article is an open-access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/). |
spellingShingle | Article Ghasemi, Younes Rasoul-Amini, Sara Morowvat, Mohammad Hossein Raee, Mohammad Javad Ghoshoon, Mohammad Bagher Nouri, Fatemeh Negintaji, Narges Parvizi, Rezvan Mosavi-Azam, Seyed Bagher Characterization of Hydrocortisone Biometabolites and 18S rRNA Gene in Chlamydomonas reinhardtii Cultures |
title | Characterization of Hydrocortisone Biometabolites and 18S rRNA Gene in Chlamydomonas reinhardtii Cultures |
title_full | Characterization of Hydrocortisone Biometabolites and 18S rRNA Gene in Chlamydomonas reinhardtii Cultures |
title_fullStr | Characterization of Hydrocortisone Biometabolites and 18S rRNA Gene in Chlamydomonas reinhardtii Cultures |
title_full_unstemmed | Characterization of Hydrocortisone Biometabolites and 18S rRNA Gene in Chlamydomonas reinhardtii Cultures |
title_short | Characterization of Hydrocortisone Biometabolites and 18S rRNA Gene in Chlamydomonas reinhardtii Cultures |
title_sort | characterization of hydrocortisone biometabolites and 18s rrna gene in chlamydomonas reinhardtii cultures |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6245355/ https://www.ncbi.nlm.nih.gov/pubmed/18830164 http://dx.doi.org/10.3390/molecules13102416 |
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