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Diamondoids are not forever: microbial biotransformation of diamondoid carboxylic acids
Oil sands process‐affected waters (OSPW) contain persistent, toxic naphthenic acids (NAs), including the abundant yet little‐studied diamondoid carboxylic acids. Therefore, we investigated the aerobic microbial biotransformation of two of the most abundant, chronically toxic and environmentally rele...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2019
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7017837/ https://www.ncbi.nlm.nih.gov/pubmed/31714688 http://dx.doi.org/10.1111/1751-7915.13500 |
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author | Folwell, Benjamin D. McGenity, Terry J. Whitby, Corinne |
author_facet | Folwell, Benjamin D. McGenity, Terry J. Whitby, Corinne |
author_sort | Folwell, Benjamin D. |
collection | PubMed |
description | Oil sands process‐affected waters (OSPW) contain persistent, toxic naphthenic acids (NAs), including the abundant yet little‐studied diamondoid carboxylic acids. Therefore, we investigated the aerobic microbial biotransformation of two of the most abundant, chronically toxic and environmentally relevant diamondoid carboxylic acids: adamantane‐1‐carboxylic acid (A1CA) and 3‐ethyl adamantane carboxylic acid (3EA). We inoculated into minimal salts media with diamondoid carboxylic acids as sole carbon and energy source two samples: (i) a surface water sample (designated TPW) collected from a test pit from the Mildred Lake Settling Basin and (ii) a water sample (designated 2 m) collected at a water depth of 2 m from a tailings pond. By day 33, in TPW enrichments, 71% of A1CA and 50% of 3EA was transformed, with 50% reduction in EC(20) toxicity. Similar results were found for 2 m enrichments. Biotransformation of A1CA and 3EA resulted in the production of two metabolites, tentatively identified as 2‐hydroxyadamantane‐1‐carboxylic acid and 3‐ethyladamantane‐2‐ol respectively. Accumulation of both metabolites was less than the loss of the parent compound, indicating that they would have continued to be transformed beyond 33 days and not accumulate as dead‐end metabolites. There were shifts in bacterial community composition during biotransformation, with Pseudomonas species, especially P. stutzeri, dominating enrichments irrespective of the diamondoid carboxylic acid. In conclusion, we demonstrated the microbial biotransformation of two diamondoid carboxylic acids, which has potential application for their removal and detoxification from vast OSPW that are a major environmental threat. |
format | Online Article Text |
id | pubmed-7017837 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-70178372020-03-06 Diamondoids are not forever: microbial biotransformation of diamondoid carboxylic acids Folwell, Benjamin D. McGenity, Terry J. Whitby, Corinne Microb Biotechnol Research Articles Oil sands process‐affected waters (OSPW) contain persistent, toxic naphthenic acids (NAs), including the abundant yet little‐studied diamondoid carboxylic acids. Therefore, we investigated the aerobic microbial biotransformation of two of the most abundant, chronically toxic and environmentally relevant diamondoid carboxylic acids: adamantane‐1‐carboxylic acid (A1CA) and 3‐ethyl adamantane carboxylic acid (3EA). We inoculated into minimal salts media with diamondoid carboxylic acids as sole carbon and energy source two samples: (i) a surface water sample (designated TPW) collected from a test pit from the Mildred Lake Settling Basin and (ii) a water sample (designated 2 m) collected at a water depth of 2 m from a tailings pond. By day 33, in TPW enrichments, 71% of A1CA and 50% of 3EA was transformed, with 50% reduction in EC(20) toxicity. Similar results were found for 2 m enrichments. Biotransformation of A1CA and 3EA resulted in the production of two metabolites, tentatively identified as 2‐hydroxyadamantane‐1‐carboxylic acid and 3‐ethyladamantane‐2‐ol respectively. Accumulation of both metabolites was less than the loss of the parent compound, indicating that they would have continued to be transformed beyond 33 days and not accumulate as dead‐end metabolites. There were shifts in bacterial community composition during biotransformation, with Pseudomonas species, especially P. stutzeri, dominating enrichments irrespective of the diamondoid carboxylic acid. In conclusion, we demonstrated the microbial biotransformation of two diamondoid carboxylic acids, which has potential application for their removal and detoxification from vast OSPW that are a major environmental threat. John Wiley and Sons Inc. 2019-11-12 /pmc/articles/PMC7017837/ /pubmed/31714688 http://dx.doi.org/10.1111/1751-7915.13500 Text en © 2019 The Authors. Microbial Biotechnology published by John Wiley & Sons Ltd and Society for Applied Microbiology. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles Folwell, Benjamin D. McGenity, Terry J. Whitby, Corinne Diamondoids are not forever: microbial biotransformation of diamondoid carboxylic acids |
title | Diamondoids are not forever: microbial biotransformation of diamondoid carboxylic acids |
title_full | Diamondoids are not forever: microbial biotransformation of diamondoid carboxylic acids |
title_fullStr | Diamondoids are not forever: microbial biotransformation of diamondoid carboxylic acids |
title_full_unstemmed | Diamondoids are not forever: microbial biotransformation of diamondoid carboxylic acids |
title_short | Diamondoids are not forever: microbial biotransformation of diamondoid carboxylic acids |
title_sort | diamondoids are not forever: microbial biotransformation of diamondoid carboxylic acids |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7017837/ https://www.ncbi.nlm.nih.gov/pubmed/31714688 http://dx.doi.org/10.1111/1751-7915.13500 |
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