The biotransformation of didecyldimethylammonium chloride by the hyphomycetes gliocladium roseum and verticillium bulbillosum

Two mould fungi, Gliocladium roseum and Verticillium bulbillosum, that had demonstrated an inherent ability to degrade didecyldimethylammonium chloride (DDAC), were used in the biodegradation experiments. DDAC was a) added to liquid media or b) used to treat wood pieces that were then subjected t...

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Main Author: Dubois, Jason
Format: Others
Language:English
Published: 2009
Online Access:http://hdl.handle.net/2429/9366
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spelling ndltd-UBC-oai-circle.library.ubc.ca-2429-93662018-01-05T17:34:45Z The biotransformation of didecyldimethylammonium chloride by the hyphomycetes gliocladium roseum and verticillium bulbillosum Dubois, Jason Two mould fungi, Gliocladium roseum and Verticillium bulbillosum, that had demonstrated an inherent ability to degrade didecyldimethylammonium chloride (DDAC), were used in the biodegradation experiments. DDAC was a) added to liquid media or b) used to treat wood pieces that were then subjected to fungal biodegradation. A metabolite from the degradation of DDAC in the treated wood was discovered from the HPLC chromatogram, where the peak due to DDAC decreased and was replaced by a new peak at a longer retention time. It was isolated by preparative HPLC and further purified. Proton nuclear magnetic resonance (NMR) and Fourier transformed infrared spectroscopy (FTIR) were used to identify the metabolite. From the spectra the compound was determined to be a quaternary ammonium compound (QAC) that differed only slightly from DDAC. The metabolite had two methyl groups and two decyl groups attached to the central nitrogen, with a hydroxyl group attached to one of the decyl chains. The hydroxyl group was not at the terminal carbon of the chain, suggesting that it was not the initiation of P-oxidation of the alkyl chain. The structure of this metabolite suggested that it was not an intermediate in the breakdown and possible mineralization of DDAC, but rather it appeared to be a biotransformation. It was hypothesised that this biotransformation reduced the toxicity of the DDAC to fungi. This is supported in the literature, which cites many cases of moulds employing hydroxylating enzymes to detoxify compounds. The two mould fungi and the basidiomycetes, Postia placenta and Trametes versicolor were used to screen various QACs with oxidized alkyl chains to determine their toxicity. It was found that a QAC that was heavily oxidized along its long alkyl chains (QAC-OXID) was significantly less toxic to both the mould fungi and the basidiomycetes than DDAC. Forestry, Faculty of Graduate 2009-06-16T23:57:11Z 2009-06-16T23:57:11Z 1999 1999-05 Text Thesis/Dissertation http://hdl.handle.net/2429/9366 eng For non-commercial purposes only, such as research, private study and education. Additional conditions apply, see Terms of Use https://open.library.ubc.ca/terms_of_use. 18235478 bytes application/pdf
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language English
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description Two mould fungi, Gliocladium roseum and Verticillium bulbillosum, that had demonstrated an inherent ability to degrade didecyldimethylammonium chloride (DDAC), were used in the biodegradation experiments. DDAC was a) added to liquid media or b) used to treat wood pieces that were then subjected to fungal biodegradation. A metabolite from the degradation of DDAC in the treated wood was discovered from the HPLC chromatogram, where the peak due to DDAC decreased and was replaced by a new peak at a longer retention time. It was isolated by preparative HPLC and further purified. Proton nuclear magnetic resonance (NMR) and Fourier transformed infrared spectroscopy (FTIR) were used to identify the metabolite. From the spectra the compound was determined to be a quaternary ammonium compound (QAC) that differed only slightly from DDAC. The metabolite had two methyl groups and two decyl groups attached to the central nitrogen, with a hydroxyl group attached to one of the decyl chains. The hydroxyl group was not at the terminal carbon of the chain, suggesting that it was not the initiation of P-oxidation of the alkyl chain. The structure of this metabolite suggested that it was not an intermediate in the breakdown and possible mineralization of DDAC, but rather it appeared to be a biotransformation. It was hypothesised that this biotransformation reduced the toxicity of the DDAC to fungi. This is supported in the literature, which cites many cases of moulds employing hydroxylating enzymes to detoxify compounds. The two mould fungi and the basidiomycetes, Postia placenta and Trametes versicolor were used to screen various QACs with oxidized alkyl chains to determine their toxicity. It was found that a QAC that was heavily oxidized along its long alkyl chains (QAC-OXID) was significantly less toxic to both the mould fungi and the basidiomycetes than DDAC. === Forestry, Faculty of === Graduate
author Dubois, Jason
spellingShingle Dubois, Jason
The biotransformation of didecyldimethylammonium chloride by the hyphomycetes gliocladium roseum and verticillium bulbillosum
author_facet Dubois, Jason
author_sort Dubois, Jason
title The biotransformation of didecyldimethylammonium chloride by the hyphomycetes gliocladium roseum and verticillium bulbillosum
title_short The biotransformation of didecyldimethylammonium chloride by the hyphomycetes gliocladium roseum and verticillium bulbillosum
title_full The biotransformation of didecyldimethylammonium chloride by the hyphomycetes gliocladium roseum and verticillium bulbillosum
title_fullStr The biotransformation of didecyldimethylammonium chloride by the hyphomycetes gliocladium roseum and verticillium bulbillosum
title_full_unstemmed The biotransformation of didecyldimethylammonium chloride by the hyphomycetes gliocladium roseum and verticillium bulbillosum
title_sort biotransformation of didecyldimethylammonium chloride by the hyphomycetes gliocladium roseum and verticillium bulbillosum
publishDate 2009
url http://hdl.handle.net/2429/9366
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