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Investigation of the removal mechanism of antibiotic ceftazidime by green algae and subsequent microbic impact assessment

The present study provides an integrated view of algal removal of the antibiotic ceftazidime and its basic parent structure 7-aminocephalosporanic acid (7-ACA), including contribution analysis, bacteriostatic and aquatic toxic assessment and metabolite verification. 92.70% and 96.07% of the two targ...

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Autores principales: Yu, Ying, Zhou, Yangyang, Wang, Zhiliang, Torres, Oscar Lopez, Guo, Ruixin, Chen, Jianqiu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5482816/
https://www.ncbi.nlm.nih.gov/pubmed/28646154
http://dx.doi.org/10.1038/s41598-017-04128-3
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author Yu, Ying
Zhou, Yangyang
Wang, Zhiliang
Torres, Oscar Lopez
Guo, Ruixin
Chen, Jianqiu
author_facet Yu, Ying
Zhou, Yangyang
Wang, Zhiliang
Torres, Oscar Lopez
Guo, Ruixin
Chen, Jianqiu
author_sort Yu, Ying
collection PubMed
description The present study provides an integrated view of algal removal of the antibiotic ceftazidime and its basic parent structure 7-aminocephalosporanic acid (7-ACA), including contribution analysis, bacteriostatic and aquatic toxic assessment and metabolite verification. 92.70% and 96.07% of the two target compounds was removed after the algal treatment, respectively. The algal removal can be separated into three steps: a rapid adsorption, a slow cell wall-transmission and the final biodegradation. Additionally, while ceftazidime demonstrated an excellent inhibitory effect on Escherichia coli, there was no bacteriostasis introduced after the algal treatment, which could avoid favoring the harmful selective pressure. On the other hand, no significant aquatic impact of the two target compounds on rotifers was observed and it was not enhanced after the algal treatment. To better reveal the mechanism involved, metabolite analyses were performed. Δ-3 ceftazidime and trans-ceftazidime were regarded as the metabolites of ceftazidime and the metabolite of 7-ACA was regarded as a compound which shared the similar structure with 4-chlorocinnamic acid. Our study indicated that the green algae performed a satisfactory growth capacity and played a dominant role for the biodegradation of the target antibiotics, which achieved high removal efficiency and low environmental impact.
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spelling pubmed-54828162017-06-26 Investigation of the removal mechanism of antibiotic ceftazidime by green algae and subsequent microbic impact assessment Yu, Ying Zhou, Yangyang Wang, Zhiliang Torres, Oscar Lopez Guo, Ruixin Chen, Jianqiu Sci Rep Article The present study provides an integrated view of algal removal of the antibiotic ceftazidime and its basic parent structure 7-aminocephalosporanic acid (7-ACA), including contribution analysis, bacteriostatic and aquatic toxic assessment and metabolite verification. 92.70% and 96.07% of the two target compounds was removed after the algal treatment, respectively. The algal removal can be separated into three steps: a rapid adsorption, a slow cell wall-transmission and the final biodegradation. Additionally, while ceftazidime demonstrated an excellent inhibitory effect on Escherichia coli, there was no bacteriostasis introduced after the algal treatment, which could avoid favoring the harmful selective pressure. On the other hand, no significant aquatic impact of the two target compounds on rotifers was observed and it was not enhanced after the algal treatment. To better reveal the mechanism involved, metabolite analyses were performed. Δ-3 ceftazidime and trans-ceftazidime were regarded as the metabolites of ceftazidime and the metabolite of 7-ACA was regarded as a compound which shared the similar structure with 4-chlorocinnamic acid. Our study indicated that the green algae performed a satisfactory growth capacity and played a dominant role for the biodegradation of the target antibiotics, which achieved high removal efficiency and low environmental impact. Nature Publishing Group UK 2017-06-23 /pmc/articles/PMC5482816/ /pubmed/28646154 http://dx.doi.org/10.1038/s41598-017-04128-3 Text en © The Author(s) 2017 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
Yu, Ying
Zhou, Yangyang
Wang, Zhiliang
Torres, Oscar Lopez
Guo, Ruixin
Chen, Jianqiu
Investigation of the removal mechanism of antibiotic ceftazidime by green algae and subsequent microbic impact assessment
title Investigation of the removal mechanism of antibiotic ceftazidime by green algae and subsequent microbic impact assessment
title_full Investigation of the removal mechanism of antibiotic ceftazidime by green algae and subsequent microbic impact assessment
title_fullStr Investigation of the removal mechanism of antibiotic ceftazidime by green algae and subsequent microbic impact assessment
title_full_unstemmed Investigation of the removal mechanism of antibiotic ceftazidime by green algae and subsequent microbic impact assessment
title_short Investigation of the removal mechanism of antibiotic ceftazidime by green algae and subsequent microbic impact assessment
title_sort investigation of the removal mechanism of antibiotic ceftazidime by green algae and subsequent microbic impact assessment
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5482816/
https://www.ncbi.nlm.nih.gov/pubmed/28646154
http://dx.doi.org/10.1038/s41598-017-04128-3
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