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Induction of secondary metabolism of Aspergillus terreus ATCC 20542 in the batch bioreactor cultures
Cultivation of Aspergillus terreus ATCC 20542 in a stirred tank bioreactor was performed to induce the biosynthesis of secondary metabolites and provide the bioprocess-related insights into the metabolic capabilities of the investigated strain. The activation of biosynthetic routes was attempted by...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Springer Berlin Heidelberg
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4786612/ https://www.ncbi.nlm.nih.gov/pubmed/26603760 http://dx.doi.org/10.1007/s00253-015-7157-1 |
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author | Boruta, Tomasz Bizukojc, Marcin |
author_facet | Boruta, Tomasz Bizukojc, Marcin |
author_sort | Boruta, Tomasz |
collection | PubMed |
description | Cultivation of Aspergillus terreus ATCC 20542 in a stirred tank bioreactor was performed to induce the biosynthesis of secondary metabolites and provide the bioprocess-related insights into the metabolic capabilities of the investigated strain. The activation of biosynthetic routes was attempted by the diversification of process conditions and growth media. Several strategies were tested, including the addition of rapeseed oil or inulin, changing the concentration of nitrogen source, reduction of chlorine supply, cultivation under saline conditions, and using various aeration schemes. Fifteen secondary metabolites were identified in the course of the study by using ultra-high performance liquid chromatography coupled with mass spectrometry, namely mevinolinic acid, 4a,5-dihydromevinolinic acid, 3α-hydroxy-3,5-dihydromonacolin L acid, terrein, aspulvinone E, dihydroisoflavipucine, (+)-geodin, (+)-bisdechlorogeodin, (+)-erdin, asterric acid, butyrolactone I, desmethylsulochrin, questin, sulochrin, and demethylasterric acid. The study also presents the collection of mass spectra that can serve as a resource for future experiments. The growth in a salt-rich environment turned out to be strongly inhibitory for secondary metabolism and the formation of dense and compact pellets was observed. Generally, the addition of inulin, reducing the oxygen supply, and increasing the content of nitrogen source did not enhance the production of examined molecules. The most successful strategy involved the addition of rapeseed oil to the chlorine-deficient medium. Under these conditions, the highest levels of butyrolactone I, asterric acid, and mevinolinic acid were achieved and the presence of desmethylsulochrin and (+)-bisdechlorogeodin was detected in the broth. The constant and relatively high aeration rate in the idiophase was shown to be beneficial for terrein and (+)-geodin biosynthesis. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00253-015-7157-1) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4786612 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-47866122016-04-09 Induction of secondary metabolism of Aspergillus terreus ATCC 20542 in the batch bioreactor cultures Boruta, Tomasz Bizukojc, Marcin Appl Microbiol Biotechnol Biotechnological Products and Process Engineering Cultivation of Aspergillus terreus ATCC 20542 in a stirred tank bioreactor was performed to induce the biosynthesis of secondary metabolites and provide the bioprocess-related insights into the metabolic capabilities of the investigated strain. The activation of biosynthetic routes was attempted by the diversification of process conditions and growth media. Several strategies were tested, including the addition of rapeseed oil or inulin, changing the concentration of nitrogen source, reduction of chlorine supply, cultivation under saline conditions, and using various aeration schemes. Fifteen secondary metabolites were identified in the course of the study by using ultra-high performance liquid chromatography coupled with mass spectrometry, namely mevinolinic acid, 4a,5-dihydromevinolinic acid, 3α-hydroxy-3,5-dihydromonacolin L acid, terrein, aspulvinone E, dihydroisoflavipucine, (+)-geodin, (+)-bisdechlorogeodin, (+)-erdin, asterric acid, butyrolactone I, desmethylsulochrin, questin, sulochrin, and demethylasterric acid. The study also presents the collection of mass spectra that can serve as a resource for future experiments. The growth in a salt-rich environment turned out to be strongly inhibitory for secondary metabolism and the formation of dense and compact pellets was observed. Generally, the addition of inulin, reducing the oxygen supply, and increasing the content of nitrogen source did not enhance the production of examined molecules. The most successful strategy involved the addition of rapeseed oil to the chlorine-deficient medium. Under these conditions, the highest levels of butyrolactone I, asterric acid, and mevinolinic acid were achieved and the presence of desmethylsulochrin and (+)-bisdechlorogeodin was detected in the broth. The constant and relatively high aeration rate in the idiophase was shown to be beneficial for terrein and (+)-geodin biosynthesis. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00253-015-7157-1) contains supplementary material, which is available to authorized users. Springer Berlin Heidelberg 2015-11-25 2016 /pmc/articles/PMC4786612/ /pubmed/26603760 http://dx.doi.org/10.1007/s00253-015-7157-1 Text en © The Author(s) 2015 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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. |
spellingShingle | Biotechnological Products and Process Engineering Boruta, Tomasz Bizukojc, Marcin Induction of secondary metabolism of Aspergillus terreus ATCC 20542 in the batch bioreactor cultures |
title | Induction of secondary metabolism of Aspergillus terreus ATCC 20542 in the batch bioreactor cultures |
title_full | Induction of secondary metabolism of Aspergillus terreus ATCC 20542 in the batch bioreactor cultures |
title_fullStr | Induction of secondary metabolism of Aspergillus terreus ATCC 20542 in the batch bioreactor cultures |
title_full_unstemmed | Induction of secondary metabolism of Aspergillus terreus ATCC 20542 in the batch bioreactor cultures |
title_short | Induction of secondary metabolism of Aspergillus terreus ATCC 20542 in the batch bioreactor cultures |
title_sort | induction of secondary metabolism of aspergillus terreus atcc 20542 in the batch bioreactor cultures |
topic | Biotechnological Products and Process Engineering |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4786612/ https://www.ncbi.nlm.nih.gov/pubmed/26603760 http://dx.doi.org/10.1007/s00253-015-7157-1 |
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