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The influence of four pharmaceuticals on Chlorellapyrenoidosa culture
There has been a developing technology in algae with pharmaceuticals wastewater. However, the effect and the underlying mechanism of pharmaceuticals on algae are not well understood. To investigate the effect and mechanism of pharmaceuticalson microalgae, four pharmaceuticals of clofibric acid (CLF)...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6367373/ https://www.ncbi.nlm.nih.gov/pubmed/30733460 http://dx.doi.org/10.1038/s41598-018-36609-4 |
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author | Zhang, Yonggang Guo, Jun Yao, Tianming Zhang, Yalei Zhou, Xuefei Chu, Huaqiang |
author_facet | Zhang, Yonggang Guo, Jun Yao, Tianming Zhang, Yalei Zhou, Xuefei Chu, Huaqiang |
author_sort | Zhang, Yonggang |
collection | PubMed |
description | There has been a developing technology in algae with pharmaceuticals wastewater. However, the effect and the underlying mechanism of pharmaceuticals on algae are not well understood. To investigate the effect and mechanism of pharmaceuticalson microalgae, four pharmaceuticals of clofibric acid (CLF), ciprofloxacin (CIP), diclofenac (DCF) and carbamazepine (CBZ) on C. pyrenoidosa culture were analyzed. At low concentrations (<10 mg/L), the pharmaceuticals, especially the DCF, exhibited positive effects on both the structure and function of algal cultures; algal growth (i.e., chlorophyll a accumulation, lipid accumulation) and activities of antioxidant enzymes were stimulated. The algal metabolite differences of various DCF concentrations were investigated and a total of 91 substances were identified, whose samples were clustered and clearly separated. The key metabolomics pathway analysis found that the DCF promoted the carbohydrate and fatty acid metabolic pathway in C. pyrenoidosa under relatively low concentrations (<10 mg/L). However, the algae metabolomics pathway was disturbed significantly under the action of a high concentration of DCF (>100 mg/L). The study detected the effects of four pharmaceuticals on C. pyrenoidosa and demonstrated that the usage of metabolomics analysis complemented with DCF could be an effective approach to understand the mechanism of molecular evolution in C. pyrenoidosa for microalgal biomass and bioenergy from wastewater in researches of biological resources. |
format | Online Article Text |
id | pubmed-6367373 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-63673732019-02-11 The influence of four pharmaceuticals on Chlorellapyrenoidosa culture Zhang, Yonggang Guo, Jun Yao, Tianming Zhang, Yalei Zhou, Xuefei Chu, Huaqiang Sci Rep Article There has been a developing technology in algae with pharmaceuticals wastewater. However, the effect and the underlying mechanism of pharmaceuticals on algae are not well understood. To investigate the effect and mechanism of pharmaceuticalson microalgae, four pharmaceuticals of clofibric acid (CLF), ciprofloxacin (CIP), diclofenac (DCF) and carbamazepine (CBZ) on C. pyrenoidosa culture were analyzed. At low concentrations (<10 mg/L), the pharmaceuticals, especially the DCF, exhibited positive effects on both the structure and function of algal cultures; algal growth (i.e., chlorophyll a accumulation, lipid accumulation) and activities of antioxidant enzymes were stimulated. The algal metabolite differences of various DCF concentrations were investigated and a total of 91 substances were identified, whose samples were clustered and clearly separated. The key metabolomics pathway analysis found that the DCF promoted the carbohydrate and fatty acid metabolic pathway in C. pyrenoidosa under relatively low concentrations (<10 mg/L). However, the algae metabolomics pathway was disturbed significantly under the action of a high concentration of DCF (>100 mg/L). The study detected the effects of four pharmaceuticals on C. pyrenoidosa and demonstrated that the usage of metabolomics analysis complemented with DCF could be an effective approach to understand the mechanism of molecular evolution in C. pyrenoidosa for microalgal biomass and bioenergy from wastewater in researches of biological resources. Nature Publishing Group UK 2019-02-07 /pmc/articles/PMC6367373/ /pubmed/30733460 http://dx.doi.org/10.1038/s41598-018-36609-4 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Zhang, Yonggang Guo, Jun Yao, Tianming Zhang, Yalei Zhou, Xuefei Chu, Huaqiang The influence of four pharmaceuticals on Chlorellapyrenoidosa culture |
title | The influence of four pharmaceuticals on Chlorellapyrenoidosa culture |
title_full | The influence of four pharmaceuticals on Chlorellapyrenoidosa culture |
title_fullStr | The influence of four pharmaceuticals on Chlorellapyrenoidosa culture |
title_full_unstemmed | The influence of four pharmaceuticals on Chlorellapyrenoidosa culture |
title_short | The influence of four pharmaceuticals on Chlorellapyrenoidosa culture |
title_sort | influence of four pharmaceuticals on chlorellapyrenoidosa culture |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6367373/ https://www.ncbi.nlm.nih.gov/pubmed/30733460 http://dx.doi.org/10.1038/s41598-018-36609-4 |
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