Biodegradation of Naphthalene and Anthracene by Aspergillus glaucus Strain Isolated from Antarctic Soil
Biotechnologies based on microbial species capable of destroying harmful pollutants are a successful way to solve some of the most important problems associated with a clean environment. The subject of investigation is the Antarctic fungal strain Aspergillus glaucus AL1. The culturing of the examine...
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ftmdpi:oai:mdpi.com:/2227-9717/10/5/873/ 2023-08-20T04:00:43+02:00 Biodegradation of Naphthalene and Anthracene by Aspergillus glaucus Strain Isolated from Antarctic Soil Katya Stoyanova Maria Gerginova Ivayla Dincheva Nadejda Peneva Zlatka Alexieva agris 2022-04-28 application/pdf https://doi.org/10.3390/pr10050873 EN eng Multidisciplinary Digital Publishing Institute Environmental and Green Processes https://dx.doi.org/10.3390/pr10050873 https://creativecommons.org/licenses/by/4.0/ Processes; Volume 10; Issue 5; Pages: 873 biodegradation PAH Aspergillus glaucus phenol 2-monooxygenase catechol 1,2-dioxygenase Text 2022 ftmdpi https://doi.org/10.3390/pr10050873 2023-08-01T04:54:15Z Biotechnologies based on microbial species capable of destroying harmful pollutants are a successful way to solve some of the most important problems associated with a clean environment. The subject of investigation is the Antarctic fungal strain Aspergillus glaucus AL1. The culturing of the examined strain was performed with 70 mg of wet mycelium being inoculated in a Czapek Dox liquid medium containing naphthalene, anthracene, or phenanthrene (0.3 g/L) as the sole carbon source. Progressively decreasing naphthalene and anthracene concentrations were monitored in the culture medium until the 15th day of the cultivation of A. glaucus AL1. The degradation was determined through gas chromatography–mass spectrometry. Both decreased by 66% and 44%, respectively, for this period. The GC-MS analyses were applied to identify salicylic acid, catechol, and ketoadipic acid as intermediates in the naphthalene degradation. The intermediates identified in anthracene catabolism are 2-hydroxy-1-naphthoic acid, o-phthalic acid, and protocatechuic acid. The enzyme activities for phenol 2-monooxygenase (1.14.13.7) and catechol 1,2-dioxygenase (1.13.11.1) were established. A gene encoding an enzyme with catechol 1,2-dioxygenase activity was identified and sequenced (GeneBank Ac. No KM360483). The recent study provides original data on the potential of an ascomycete’s fungal strain A. glaucus strain AL 1 to degrade naphthalene and anthracene. Text Antarc* Antarctic MDPI Open Access Publishing Antarctic The Antarctic Processes 10 5 873 |
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Open Polar |
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MDPI Open Access Publishing |
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ftmdpi |
language |
English |
topic |
biodegradation PAH Aspergillus glaucus phenol 2-monooxygenase catechol 1,2-dioxygenase |
spellingShingle |
biodegradation PAH Aspergillus glaucus phenol 2-monooxygenase catechol 1,2-dioxygenase Katya Stoyanova Maria Gerginova Ivayla Dincheva Nadejda Peneva Zlatka Alexieva Biodegradation of Naphthalene and Anthracene by Aspergillus glaucus Strain Isolated from Antarctic Soil |
topic_facet |
biodegradation PAH Aspergillus glaucus phenol 2-monooxygenase catechol 1,2-dioxygenase |
description |
Biotechnologies based on microbial species capable of destroying harmful pollutants are a successful way to solve some of the most important problems associated with a clean environment. The subject of investigation is the Antarctic fungal strain Aspergillus glaucus AL1. The culturing of the examined strain was performed with 70 mg of wet mycelium being inoculated in a Czapek Dox liquid medium containing naphthalene, anthracene, or phenanthrene (0.3 g/L) as the sole carbon source. Progressively decreasing naphthalene and anthracene concentrations were monitored in the culture medium until the 15th day of the cultivation of A. glaucus AL1. The degradation was determined through gas chromatography–mass spectrometry. Both decreased by 66% and 44%, respectively, for this period. The GC-MS analyses were applied to identify salicylic acid, catechol, and ketoadipic acid as intermediates in the naphthalene degradation. The intermediates identified in anthracene catabolism are 2-hydroxy-1-naphthoic acid, o-phthalic acid, and protocatechuic acid. The enzyme activities for phenol 2-monooxygenase (1.14.13.7) and catechol 1,2-dioxygenase (1.13.11.1) were established. A gene encoding an enzyme with catechol 1,2-dioxygenase activity was identified and sequenced (GeneBank Ac. No KM360483). The recent study provides original data on the potential of an ascomycete’s fungal strain A. glaucus strain AL 1 to degrade naphthalene and anthracene. |
format |
Text |
author |
Katya Stoyanova Maria Gerginova Ivayla Dincheva Nadejda Peneva Zlatka Alexieva |
author_facet |
Katya Stoyanova Maria Gerginova Ivayla Dincheva Nadejda Peneva Zlatka Alexieva |
author_sort |
Katya Stoyanova |
title |
Biodegradation of Naphthalene and Anthracene by Aspergillus glaucus Strain Isolated from Antarctic Soil |
title_short |
Biodegradation of Naphthalene and Anthracene by Aspergillus glaucus Strain Isolated from Antarctic Soil |
title_full |
Biodegradation of Naphthalene and Anthracene by Aspergillus glaucus Strain Isolated from Antarctic Soil |
title_fullStr |
Biodegradation of Naphthalene and Anthracene by Aspergillus glaucus Strain Isolated from Antarctic Soil |
title_full_unstemmed |
Biodegradation of Naphthalene and Anthracene by Aspergillus glaucus Strain Isolated from Antarctic Soil |
title_sort |
biodegradation of naphthalene and anthracene by aspergillus glaucus strain isolated from antarctic soil |
publisher |
Multidisciplinary Digital Publishing Institute |
publishDate |
2022 |
url |
https://doi.org/10.3390/pr10050873 |
op_coverage |
agris |
geographic |
Antarctic The Antarctic |
geographic_facet |
Antarctic The Antarctic |
genre |
Antarc* Antarctic |
genre_facet |
Antarc* Antarctic |
op_source |
Processes; Volume 10; Issue 5; Pages: 873 |
op_relation |
Environmental and Green Processes https://dx.doi.org/10.3390/pr10050873 |
op_rights |
https://creativecommons.org/licenses/by/4.0/ |
op_doi |
https://doi.org/10.3390/pr10050873 |
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Processes |
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10 |
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5 |
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873 |
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1774719885680574464 |