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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...

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Autores principales: Mu, Dashuai, Yu, Xiuxia, Xu, Zhenxing, Du, Zongjun, Chen, Guanjun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
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.
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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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