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Rapidly Probing Antibacterial Activity of Graphene Oxide by Mass Spectrometry-based Metabolite Fingerprinting

Application of nanomaterials as anti-bacteria agents has aroused great attention. To investigate the antibacterial activity and antibacterial mechanism of nanomaterials from a molecular perspective is important for efficient developing of nanomaterial antibiotics. In the current work, a new mass spe...

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Autores principales: Zhang, Ning, Hou, Jian, Chen, Suming, Xiong, Caiqiao, Liu, Huihui, Jin, Yulong, Wang, Jianing, He, Qing, Zhao, Rui, Nie, Zongxiu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4910068/
https://www.ncbi.nlm.nih.gov/pubmed/27306507
http://dx.doi.org/10.1038/srep28045
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author Zhang, Ning
Hou, Jian
Chen, Suming
Xiong, Caiqiao
Liu, Huihui
Jin, Yulong
Wang, Jianing
He, Qing
Zhao, Rui
Nie, Zongxiu
author_facet Zhang, Ning
Hou, Jian
Chen, Suming
Xiong, Caiqiao
Liu, Huihui
Jin, Yulong
Wang, Jianing
He, Qing
Zhao, Rui
Nie, Zongxiu
author_sort Zhang, Ning
collection PubMed
description Application of nanomaterials as anti-bacteria agents has aroused great attention. To investigate the antibacterial activity and antibacterial mechanism of nanomaterials from a molecular perspective is important for efficient developing of nanomaterial antibiotics. In the current work, a new mass spectrometry-based method was established to investigate the bacterial cytotoxicity of graphene oxide (GO) by the metabolite fingerprinting of microbes. The mass spectra of extracted metabolites from two strains DH5α and ATCC25922 were obtained before and after the incubation with nanomaterials respectively. Then principal component analysis (PCA) of these spectra was performed to reveal the relationship between the metabolism disorder of microbes and bactericidal activity of GO. A parameter “D” obtained from PCA scores was proposed that is capable to quantitatively evaluate the antibacterial activity of GO in concentration and time-dependent experiments. Further annotation of the fingerprinting spectra shows the variabilities of important metabolites such as phosphatidylethanolamine, phosphatidylglycerol and glutathione. This metabolic perturbation of E. coli indicates cell membrane destruction and oxidative stress mechanisms for anti-bacteria activity of graphene oxide. It is anticipated that this mass spectrometry-based metabolite fingerprinting method will be applicable to other antibacterial nanomaterials and provide more clues as to their antibacterial mechanism at molecular level.
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spelling pubmed-49100682016-06-16 Rapidly Probing Antibacterial Activity of Graphene Oxide by Mass Spectrometry-based Metabolite Fingerprinting Zhang, Ning Hou, Jian Chen, Suming Xiong, Caiqiao Liu, Huihui Jin, Yulong Wang, Jianing He, Qing Zhao, Rui Nie, Zongxiu Sci Rep Article Application of nanomaterials as anti-bacteria agents has aroused great attention. To investigate the antibacterial activity and antibacterial mechanism of nanomaterials from a molecular perspective is important for efficient developing of nanomaterial antibiotics. In the current work, a new mass spectrometry-based method was established to investigate the bacterial cytotoxicity of graphene oxide (GO) by the metabolite fingerprinting of microbes. The mass spectra of extracted metabolites from two strains DH5α and ATCC25922 were obtained before and after the incubation with nanomaterials respectively. Then principal component analysis (PCA) of these spectra was performed to reveal the relationship between the metabolism disorder of microbes and bactericidal activity of GO. A parameter “D” obtained from PCA scores was proposed that is capable to quantitatively evaluate the antibacterial activity of GO in concentration and time-dependent experiments. Further annotation of the fingerprinting spectra shows the variabilities of important metabolites such as phosphatidylethanolamine, phosphatidylglycerol and glutathione. This metabolic perturbation of E. coli indicates cell membrane destruction and oxidative stress mechanisms for anti-bacteria activity of graphene oxide. It is anticipated that this mass spectrometry-based metabolite fingerprinting method will be applicable to other antibacterial nanomaterials and provide more clues as to their antibacterial mechanism at molecular level. Nature Publishing Group 2016-06-16 /pmc/articles/PMC4910068/ /pubmed/27306507 http://dx.doi.org/10.1038/srep28045 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Zhang, Ning
Hou, Jian
Chen, Suming
Xiong, Caiqiao
Liu, Huihui
Jin, Yulong
Wang, Jianing
He, Qing
Zhao, Rui
Nie, Zongxiu
Rapidly Probing Antibacterial Activity of Graphene Oxide by Mass Spectrometry-based Metabolite Fingerprinting
title Rapidly Probing Antibacterial Activity of Graphene Oxide by Mass Spectrometry-based Metabolite Fingerprinting
title_full Rapidly Probing Antibacterial Activity of Graphene Oxide by Mass Spectrometry-based Metabolite Fingerprinting
title_fullStr Rapidly Probing Antibacterial Activity of Graphene Oxide by Mass Spectrometry-based Metabolite Fingerprinting
title_full_unstemmed Rapidly Probing Antibacterial Activity of Graphene Oxide by Mass Spectrometry-based Metabolite Fingerprinting
title_short Rapidly Probing Antibacterial Activity of Graphene Oxide by Mass Spectrometry-based Metabolite Fingerprinting
title_sort rapidly probing antibacterial activity of graphene oxide by mass spectrometry-based metabolite fingerprinting
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4910068/
https://www.ncbi.nlm.nih.gov/pubmed/27306507
http://dx.doi.org/10.1038/srep28045
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