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Modeling of Contaminant Biodegradation and Compound-Specific Isotope Fractionation in Chemostats at Low Dilution Rates
[Image: see text] We present a framework to model microbial transformations in chemostats and retentostats under transient or quasi-steady state conditions. The model accounts for transformation-induced isotope fractionation and mass-transfer across the cell membrane. It also verifies that the isoto...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American
Chemical Society
2018
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6986770/ https://www.ncbi.nlm.nih.gov/pubmed/30339002 http://dx.doi.org/10.1021/acs.est.8b02498 |
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author | Gharasoo, Mehdi Ehrl, Benno N. Cirpka, Olaf A. Elsner, Martin |
author_facet | Gharasoo, Mehdi Ehrl, Benno N. Cirpka, Olaf A. Elsner, Martin |
author_sort | Gharasoo, Mehdi |
collection | PubMed |
description | [Image: see text] We present a framework to model microbial transformations in chemostats and retentostats under transient or quasi-steady state conditions. The model accounts for transformation-induced isotope fractionation and mass-transfer across the cell membrane. It also verifies that the isotope fractionation ϵ can be evaluated as the difference of substrate-specific isotope ratios between inflow and outflow. We explicitly considered that the dropwise feeding of substrate into the reactor at very low dilution rates leads to transient behavior of concentrations and transformation rates and use this information to validate conditions under which a quasi-steady state treatment is justified. We demonstrate the practicality of the code by modeling a chemostat experiment of atrazine degradation at low dilution/growth rates by the strain Arthrobacter aurescens TC1. Our results shed light on the interplay of processes that control biodegradation and isotope fractionation of contaminants at low (μg/L) concentration levels. With the help of the model, an estimate of the mass-transfer coefficient of atrazine through the cell membrane was achieved (0.0025s(–1)). |
format | Online Article Text |
id | pubmed-6986770 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | American
Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-69867702020-01-29 Modeling of Contaminant Biodegradation and Compound-Specific Isotope Fractionation in Chemostats at Low Dilution Rates Gharasoo, Mehdi Ehrl, Benno N. Cirpka, Olaf A. Elsner, Martin Environ Sci Technol [Image: see text] We present a framework to model microbial transformations in chemostats and retentostats under transient or quasi-steady state conditions. The model accounts for transformation-induced isotope fractionation and mass-transfer across the cell membrane. It also verifies that the isotope fractionation ϵ can be evaluated as the difference of substrate-specific isotope ratios between inflow and outflow. We explicitly considered that the dropwise feeding of substrate into the reactor at very low dilution rates leads to transient behavior of concentrations and transformation rates and use this information to validate conditions under which a quasi-steady state treatment is justified. We demonstrate the practicality of the code by modeling a chemostat experiment of atrazine degradation at low dilution/growth rates by the strain Arthrobacter aurescens TC1. Our results shed light on the interplay of processes that control biodegradation and isotope fractionation of contaminants at low (μg/L) concentration levels. With the help of the model, an estimate of the mass-transfer coefficient of atrazine through the cell membrane was achieved (0.0025s(–1)). American Chemical Society 2018-10-19 2019-02-05 /pmc/articles/PMC6986770/ /pubmed/30339002 http://dx.doi.org/10.1021/acs.est.8b02498 Text en Copyright © 2018 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes. |
spellingShingle | Gharasoo, Mehdi Ehrl, Benno N. Cirpka, Olaf A. Elsner, Martin Modeling of Contaminant Biodegradation and Compound-Specific Isotope Fractionation in Chemostats at Low Dilution Rates |
title | Modeling
of Contaminant Biodegradation and Compound-Specific
Isotope Fractionation in Chemostats at Low Dilution Rates |
title_full | Modeling
of Contaminant Biodegradation and Compound-Specific
Isotope Fractionation in Chemostats at Low Dilution Rates |
title_fullStr | Modeling
of Contaminant Biodegradation and Compound-Specific
Isotope Fractionation in Chemostats at Low Dilution Rates |
title_full_unstemmed | Modeling
of Contaminant Biodegradation and Compound-Specific
Isotope Fractionation in Chemostats at Low Dilution Rates |
title_short | Modeling
of Contaminant Biodegradation and Compound-Specific
Isotope Fractionation in Chemostats at Low Dilution Rates |
title_sort | modeling
of contaminant biodegradation and compound-specific
isotope fractionation in chemostats at low dilution rates |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6986770/ https://www.ncbi.nlm.nih.gov/pubmed/30339002 http://dx.doi.org/10.1021/acs.est.8b02498 |
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