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Physiological and transcriptomic analyses reveal mechanistic insight into the adaption of marine Bacillus subtilis C01 to alumina nanoparticles
An increasing number of studies have investigated the effects of nanoparticles (NPs) on microbial systems; however, few existing reports have focused on the defense mechanisms of bacteria against NPs. Whether secondary metabolism biosynthesis is a response to NP stress and contributes to the adaptio...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4954987/ https://www.ncbi.nlm.nih.gov/pubmed/27440502 http://dx.doi.org/10.1038/srep29953 |
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author | Mu, Dashuai Yu, Xiuxia Xu, Zhenxing Du, Zongjun Chen, Guanjun |
author_facet | Mu, Dashuai Yu, Xiuxia Xu, Zhenxing Du, Zongjun Chen, Guanjun |
author_sort | Mu, Dashuai |
collection | PubMed |
description | An increasing number of studies have investigated the effects of nanoparticles (NPs) on microbial systems; however, few existing reports have focused on the defense mechanisms of bacteria against NPs. Whether secondary metabolism biosynthesis is a response to NP stress and contributes to the adaption of bacteria to NPs is unclear. Here, a significant induction in the surfactin production and biofilm formation were detected by adding Al(2)O(3) NPs to the B. subtilis fermentation broth. Physiological analysis showed that Al(2)O(3) NP stress could also affect the cell and colony morphogenesis and inhibit the motility and sporulation. Exogenously adding commercial surfactin restored the swarming motility. Additionally, a suite of toxicity assays analyzing membrane damage, cellular ROS generation, electron transport activity and membrane potential was used to determine the molecular mechanisms of toxicity of Al(2)O(3) NPs. Furthermore, whole transcriptomic analysis was used to elucidate the mechanisms of B. subtilis adaption to Al(2)O(3) NPs. These results revealed several mechanisms by which marine B. subtilis C01 adapt to Al(2)O(3) NPs. Additionally, this study broadens the applications of nanomaterials and describes the important effects on secondary metabolism and multicellularity regulation by using Al(2)O(3) NPs or other nano-products. |
format | Online Article Text |
id | pubmed-4954987 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-49549872016-07-26 Physiological and transcriptomic analyses reveal mechanistic insight into the adaption of marine Bacillus subtilis C01 to alumina nanoparticles Mu, Dashuai Yu, Xiuxia Xu, Zhenxing Du, Zongjun Chen, Guanjun Sci Rep Article An increasing number of studies have investigated the effects of nanoparticles (NPs) on microbial systems; however, few existing reports have focused on the defense mechanisms of bacteria against NPs. Whether secondary metabolism biosynthesis is a response to NP stress and contributes to the adaption of bacteria to NPs is unclear. Here, a significant induction in the surfactin production and biofilm formation were detected by adding Al(2)O(3) NPs to the B. subtilis fermentation broth. Physiological analysis showed that Al(2)O(3) NP stress could also affect the cell and colony morphogenesis and inhibit the motility and sporulation. Exogenously adding commercial surfactin restored the swarming motility. Additionally, a suite of toxicity assays analyzing membrane damage, cellular ROS generation, electron transport activity and membrane potential was used to determine the molecular mechanisms of toxicity of Al(2)O(3) NPs. Furthermore, whole transcriptomic analysis was used to elucidate the mechanisms of B. subtilis adaption to Al(2)O(3) NPs. These results revealed several mechanisms by which marine B. subtilis C01 adapt to Al(2)O(3) NPs. Additionally, this study broadens the applications of nanomaterials and describes the important effects on secondary metabolism and multicellularity regulation by using Al(2)O(3) NPs or other nano-products. Nature Publishing Group 2016-07-21 /pmc/articles/PMC4954987/ /pubmed/27440502 http://dx.doi.org/10.1038/srep29953 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 Mu, Dashuai Yu, Xiuxia Xu, Zhenxing Du, Zongjun Chen, Guanjun Physiological and transcriptomic analyses reveal mechanistic insight into the adaption of marine Bacillus subtilis C01 to alumina nanoparticles |
title | Physiological and transcriptomic analyses reveal mechanistic insight into the adaption of marine Bacillus subtilis C01 to alumina nanoparticles |
title_full | Physiological and transcriptomic analyses reveal mechanistic insight into the adaption of marine Bacillus subtilis C01 to alumina nanoparticles |
title_fullStr | Physiological and transcriptomic analyses reveal mechanistic insight into the adaption of marine Bacillus subtilis C01 to alumina nanoparticles |
title_full_unstemmed | Physiological and transcriptomic analyses reveal mechanistic insight into the adaption of marine Bacillus subtilis C01 to alumina nanoparticles |
title_short | Physiological and transcriptomic analyses reveal mechanistic insight into the adaption of marine Bacillus subtilis C01 to alumina nanoparticles |
title_sort | physiological and transcriptomic analyses reveal mechanistic insight into the adaption of marine bacillus subtilis c01 to alumina nanoparticles |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4954987/ https://www.ncbi.nlm.nih.gov/pubmed/27440502 http://dx.doi.org/10.1038/srep29953 |
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