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Synergy between Sunlight, Titanium Dioxide, and Microbes Enhances Cellulose Diacetate Degradation in the Ocean
[Image: see text] Sunlight chemically transforms marine plastics into a suite of products, with formulation—the specific mixture of polymers and additives—driving rates and products. However, the effect of light-driven transformations on subsequent microbial lability is poorly understood. Here, we e...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9535896/ https://www.ncbi.nlm.nih.gov/pubmed/36103552 http://dx.doi.org/10.1021/acs.est.2c04348 |
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author | Walsh, Anna N. Mazzotta, Michael G. Nelson, Taylor F. Reddy, Christopher M. Ward, Collin P. |
author_facet | Walsh, Anna N. Mazzotta, Michael G. Nelson, Taylor F. Reddy, Christopher M. Ward, Collin P. |
author_sort | Walsh, Anna N. |
collection | PubMed |
description | [Image: see text] Sunlight chemically transforms marine plastics into a suite of products, with formulation—the specific mixture of polymers and additives—driving rates and products. However, the effect of light-driven transformations on subsequent microbial lability is poorly understood. Here, we examined the interplay between photochemical and biological degradation of fabrics made from cellulose diacetate (CDA), a biobased polymer used commonly in consumer products. We also examined the influence of ∼1% titanium dioxide (TiO(2)), a common pigment and photocatalyst. We sequentially exposed CDA to simulated sunlight and native marine microbes to understand how photodegradation influences metabolic rates and pathways. Nuclear magnetic resonance spectroscopy revealed that sunlight initiated chain scission reactions, reducing CDA’s average molecular weight. Natural abundance carbon isotope measurements demonstrated that chain scission ultimately yields CO(2), a newly identified abiotic loss term of CDA in the environment. Measurements of fabric mass loss and enzymatic activities in seawater implied that photodegradation enhanced biodegradation by performing steps typically facilitated by cellulase. TiO(2) accelerated CDA photodegradation, expediting biodegradation. Collectively, these findings (i) underline the importance of formulation in plastic’s environmental fate and (ii) suggest that overlooking synergy between photochemical and biological degradation may lead to overestimates of marine plastic persistence. |
format | Online Article Text |
id | pubmed-9535896 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-95358962022-10-07 Synergy between Sunlight, Titanium Dioxide, and Microbes Enhances Cellulose Diacetate Degradation in the Ocean Walsh, Anna N. Mazzotta, Michael G. Nelson, Taylor F. Reddy, Christopher M. Ward, Collin P. Environ Sci Technol [Image: see text] Sunlight chemically transforms marine plastics into a suite of products, with formulation—the specific mixture of polymers and additives—driving rates and products. However, the effect of light-driven transformations on subsequent microbial lability is poorly understood. Here, we examined the interplay between photochemical and biological degradation of fabrics made from cellulose diacetate (CDA), a biobased polymer used commonly in consumer products. We also examined the influence of ∼1% titanium dioxide (TiO(2)), a common pigment and photocatalyst. We sequentially exposed CDA to simulated sunlight and native marine microbes to understand how photodegradation influences metabolic rates and pathways. Nuclear magnetic resonance spectroscopy revealed that sunlight initiated chain scission reactions, reducing CDA’s average molecular weight. Natural abundance carbon isotope measurements demonstrated that chain scission ultimately yields CO(2), a newly identified abiotic loss term of CDA in the environment. Measurements of fabric mass loss and enzymatic activities in seawater implied that photodegradation enhanced biodegradation by performing steps typically facilitated by cellulase. TiO(2) accelerated CDA photodegradation, expediting biodegradation. Collectively, these findings (i) underline the importance of formulation in plastic’s environmental fate and (ii) suggest that overlooking synergy between photochemical and biological degradation may lead to overestimates of marine plastic persistence. American Chemical Society 2022-09-14 2022-10-04 /pmc/articles/PMC9535896/ /pubmed/36103552 http://dx.doi.org/10.1021/acs.est.2c04348 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Walsh, Anna N. Mazzotta, Michael G. Nelson, Taylor F. Reddy, Christopher M. Ward, Collin P. Synergy between Sunlight, Titanium Dioxide, and Microbes Enhances Cellulose Diacetate Degradation in the Ocean |
title | Synergy
between
Sunlight, Titanium Dioxide, and Microbes
Enhances Cellulose Diacetate Degradation in the Ocean |
title_full | Synergy
between
Sunlight, Titanium Dioxide, and Microbes
Enhances Cellulose Diacetate Degradation in the Ocean |
title_fullStr | Synergy
between
Sunlight, Titanium Dioxide, and Microbes
Enhances Cellulose Diacetate Degradation in the Ocean |
title_full_unstemmed | Synergy
between
Sunlight, Titanium Dioxide, and Microbes
Enhances Cellulose Diacetate Degradation in the Ocean |
title_short | Synergy
between
Sunlight, Titanium Dioxide, and Microbes
Enhances Cellulose Diacetate Degradation in the Ocean |
title_sort | synergy
between
sunlight, titanium dioxide, and microbes
enhances cellulose diacetate degradation in the ocean |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9535896/ https://www.ncbi.nlm.nih.gov/pubmed/36103552 http://dx.doi.org/10.1021/acs.est.2c04348 |
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