Biodegradation and Identification of Transformation Products of Fluorene by Ascomycete Fungi

Fluorene belongs to the polycyclic aromatic hydrocarbons (PAHs) which are potentially carcinogenic or mutagenic. However, very few studies on biodegradation of three-ring fluorene were investigated as compared to other three-ring PAHs such as phenanthrene and anthracene. The aim of this work is to e...

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Main Authors: Risky Ayu, Kristanti, Hadibarata, Tony
Format: Article
Language:English
Published: Springer 2015
Subjects:
Online Access:http://umpir.ump.edu.my/id/eprint/11254/
http://umpir.ump.edu.my/id/eprint/11254/
http://umpir.ump.edu.my/id/eprint/11254/
http://umpir.ump.edu.my/id/eprint/11254/1/Biodegradation%20and%20Identification%20of%20Transformation%20Products%20of%20Fluorene%20by%20Ascomycete%20Fungi.pdf
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spelling ump-112542018-02-01T04:21:04Z http://umpir.ump.edu.my/id/eprint/11254/ Biodegradation and Identification of Transformation Products of Fluorene by Ascomycete Fungi Risky Ayu, Kristanti Hadibarata, Tony T Technology (General) Fluorene belongs to the polycyclic aromatic hydrocarbons (PAHs) which are potentially carcinogenic or mutagenic. However, very few studies on biodegradation of three-ring fluorene were investigated as compared to other three-ring PAHs such as phenanthrene and anthracene. The aim of this work is to evaluate fluorene degradation by fungal strain isolated from the decayed wood in tropical rain forest, Malaysia, and examine the effectiveness of the strain for degrading fluorene in liquid culture supplemented with the nonionic surfactants. Detailed taxonomic studies identified the organisms as Pestalotiopsis species and designated as strain Pestalotiopsis sp. W15. In this study, fluorene was totally degraded by Pestalotiopsis sp. W15 after incubation for 23 days. Various analytical studies confirmed the biotransformation of fluorene by detection of two metabolites in the treated medium: indanone (R f 0.45; λ max 240 and 290 nm; t R 7.1 min and m/z 132) and salicylic acid (λ max 205, 235, 290 nm; t R 9.4 min and m/z 382). Based on these products, a probable pathway has been proposed for the degradation of fluorene by Pestalotiopsis sp. W15. None of the intermediates were identified as dead-end metabolites. Springer 2015 Article PeerReviewed application/pdf en http://umpir.ump.edu.my/id/eprint/11254/1/Biodegradation%20and%20Identification%20of%20Transformation%20Products%20of%20Fluorene%20by%20Ascomycete%20Fungi.pdf Risky Ayu, Kristanti and Hadibarata, Tony (2015) Biodegradation and Identification of Transformation Products of Fluorene by Ascomycete Fungi. Water, Air and Soil Pollution , 226 (12). p. 406. ISSN 0049-6979 (print); 1573-2932 (online) http://dx.doi.org/10.1007/s11270-015-2674-1 DOI: 10.1007/s11270-015-2674-1
repository_type Digital Repository
institution_category Local University
institution Universiti Malaysia Pahang
building UMP Institutional Repository
collection Online Access
language English
topic T Technology (General)
spellingShingle T Technology (General)
Risky Ayu, Kristanti
Hadibarata, Tony
Biodegradation and Identification of Transformation Products of Fluorene by Ascomycete Fungi
description Fluorene belongs to the polycyclic aromatic hydrocarbons (PAHs) which are potentially carcinogenic or mutagenic. However, very few studies on biodegradation of three-ring fluorene were investigated as compared to other three-ring PAHs such as phenanthrene and anthracene. The aim of this work is to evaluate fluorene degradation by fungal strain isolated from the decayed wood in tropical rain forest, Malaysia, and examine the effectiveness of the strain for degrading fluorene in liquid culture supplemented with the nonionic surfactants. Detailed taxonomic studies identified the organisms as Pestalotiopsis species and designated as strain Pestalotiopsis sp. W15. In this study, fluorene was totally degraded by Pestalotiopsis sp. W15 after incubation for 23 days. Various analytical studies confirmed the biotransformation of fluorene by detection of two metabolites in the treated medium: indanone (R f 0.45; λ max 240 and 290 nm; t R 7.1 min and m/z 132) and salicylic acid (λ max 205, 235, 290 nm; t R 9.4 min and m/z 382). Based on these products, a probable pathway has been proposed for the degradation of fluorene by Pestalotiopsis sp. W15. None of the intermediates were identified as dead-end metabolites.
format Article
author Risky Ayu, Kristanti
Hadibarata, Tony
author_facet Risky Ayu, Kristanti
Hadibarata, Tony
author_sort Risky Ayu, Kristanti
title Biodegradation and Identification of Transformation Products of Fluorene by Ascomycete Fungi
title_short Biodegradation and Identification of Transformation Products of Fluorene by Ascomycete Fungi
title_full Biodegradation and Identification of Transformation Products of Fluorene by Ascomycete Fungi
title_fullStr Biodegradation and Identification of Transformation Products of Fluorene by Ascomycete Fungi
title_full_unstemmed Biodegradation and Identification of Transformation Products of Fluorene by Ascomycete Fungi
title_sort biodegradation and identification of transformation products of fluorene by ascomycete fungi
publisher Springer
publishDate 2015
url http://umpir.ump.edu.my/id/eprint/11254/
http://umpir.ump.edu.my/id/eprint/11254/
http://umpir.ump.edu.my/id/eprint/11254/
http://umpir.ump.edu.my/id/eprint/11254/1/Biodegradation%20and%20Identification%20of%20Transformation%20Products%20of%20Fluorene%20by%20Ascomycete%20Fungi.pdf
first_indexed 2023-09-18T22:11:47Z
last_indexed 2023-09-18T22:11:47Z
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