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Biomethylation and Volatilization of Arsenic by Model Protozoan Tetrahymena pyriformis under Different Phosphate Regimes

Tetrahymena pyriformis, a freshwater protozoan, is common in aquatic systems. Arsenic detoxification through biotransformation by T. pyriformis is important but poorly understood. Arsenic metabolic pathways (including cellular accumulation, effluxion, biomethylation, and volatilization) of T. pyrifo...

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Autores principales: Yin, Xixiang, Wang, Lihong, Zhang, Zhanchao, Fan, Guolan, Liu, Jianjun, Sun, Kaizhen, Sun, Guo-Xin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5334742/
https://www.ncbi.nlm.nih.gov/pubmed/28216593
http://dx.doi.org/10.3390/ijerph14020188
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author Yin, Xixiang
Wang, Lihong
Zhang, Zhanchao
Fan, Guolan
Liu, Jianjun
Sun, Kaizhen
Sun, Guo-Xin
author_facet Yin, Xixiang
Wang, Lihong
Zhang, Zhanchao
Fan, Guolan
Liu, Jianjun
Sun, Kaizhen
Sun, Guo-Xin
author_sort Yin, Xixiang
collection PubMed
description Tetrahymena pyriformis, a freshwater protozoan, is common in aquatic systems. Arsenic detoxification through biotransformation by T. pyriformis is important but poorly understood. Arsenic metabolic pathways (including cellular accumulation, effluxion, biomethylation, and volatilization) of T. pyriformis were investigated at various phosphate concentrations. The total intracellular As concentration increased markedly as the external phosphate concentration decreased. The highest concentration was 168.8 mg·kg(−1) dry weight, after exposure to As(V) for 20 h. Inorganic As was dominant at low phosphate concentrations (3, 6, and 15 mg·L(−1)), but the concentration was much lower at 30 mg·L(−1) phosphate, and As(V) contributed only ~7% of total cellular As. Methylated As contributed 84% of total As at 30 mg·L(−1) phosphate, and dimethylarsenate (DMAs(V)) was dominant, contributing up to 48% of total As. Cellular As effluxion was detected, including inorganic As(III), methylarsenate (MAs(V)) and DMAs(V). Volatile As was determined at various phosphate concentrations in the medium. All methylated As concentrations (intracellular, extracellular, and volatilized) had significant linear positive relationships with the initial phosphate concentration. To the best of our knowledge, this is the first study of As biotransformation by protozoa at different phosphate concentrations.
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spelling pubmed-53347422017-03-16 Biomethylation and Volatilization of Arsenic by Model Protozoan Tetrahymena pyriformis under Different Phosphate Regimes Yin, Xixiang Wang, Lihong Zhang, Zhanchao Fan, Guolan Liu, Jianjun Sun, Kaizhen Sun, Guo-Xin Int J Environ Res Public Health Article Tetrahymena pyriformis, a freshwater protozoan, is common in aquatic systems. Arsenic detoxification through biotransformation by T. pyriformis is important but poorly understood. Arsenic metabolic pathways (including cellular accumulation, effluxion, biomethylation, and volatilization) of T. pyriformis were investigated at various phosphate concentrations. The total intracellular As concentration increased markedly as the external phosphate concentration decreased. The highest concentration was 168.8 mg·kg(−1) dry weight, after exposure to As(V) for 20 h. Inorganic As was dominant at low phosphate concentrations (3, 6, and 15 mg·L(−1)), but the concentration was much lower at 30 mg·L(−1) phosphate, and As(V) contributed only ~7% of total cellular As. Methylated As contributed 84% of total As at 30 mg·L(−1) phosphate, and dimethylarsenate (DMAs(V)) was dominant, contributing up to 48% of total As. Cellular As effluxion was detected, including inorganic As(III), methylarsenate (MAs(V)) and DMAs(V). Volatile As was determined at various phosphate concentrations in the medium. All methylated As concentrations (intracellular, extracellular, and volatilized) had significant linear positive relationships with the initial phosphate concentration. To the best of our knowledge, this is the first study of As biotransformation by protozoa at different phosphate concentrations. MDPI 2017-02-14 2017-02 /pmc/articles/PMC5334742/ /pubmed/28216593 http://dx.doi.org/10.3390/ijerph14020188 Text en © 2017 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Yin, Xixiang
Wang, Lihong
Zhang, Zhanchao
Fan, Guolan
Liu, Jianjun
Sun, Kaizhen
Sun, Guo-Xin
Biomethylation and Volatilization of Arsenic by Model Protozoan Tetrahymena pyriformis under Different Phosphate Regimes
title Biomethylation and Volatilization of Arsenic by Model Protozoan Tetrahymena pyriformis under Different Phosphate Regimes
title_full Biomethylation and Volatilization of Arsenic by Model Protozoan Tetrahymena pyriformis under Different Phosphate Regimes
title_fullStr Biomethylation and Volatilization of Arsenic by Model Protozoan Tetrahymena pyriformis under Different Phosphate Regimes
title_full_unstemmed Biomethylation and Volatilization of Arsenic by Model Protozoan Tetrahymena pyriformis under Different Phosphate Regimes
title_short Biomethylation and Volatilization of Arsenic by Model Protozoan Tetrahymena pyriformis under Different Phosphate Regimes
title_sort biomethylation and volatilization of arsenic by model protozoan tetrahymena pyriformis under different phosphate regimes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5334742/
https://www.ncbi.nlm.nih.gov/pubmed/28216593
http://dx.doi.org/10.3390/ijerph14020188
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