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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...

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Autores principales: Ghasemi, Younes, Rasoul-Amini, Sara, Morowvat, Mohammad Hossein, Raee, Mohammad Javad, Ghoshoon, Mohammad Bagher, Nouri, Fatemeh, Negintaji, Narges, Parvizi, Rezvan, Mosavi-Azam, Seyed Bagher
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2008
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.
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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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