Cargando…
Destruction of Cell Topography, Morphology, Membrane, Inhibition of Respiration, Biofilm Formation, and Bioactive Molecule Production by Nanoparticles of Ag, ZnO, CuO, TiO(2), and Al(2)O(3) toward Beneficial Soil Bacteria
[Image: see text] The unregulated discharge of nanoparticles (NPs) from various nanotechnology industries into the environment is expected to alter the composition and physiological functions of soil microbiota. Considering this knowledge gap, the impact of five NPs (Ag, ZnO, CuO, Al(2)O(3), and TiO...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2020
|
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7160826/ https://www.ncbi.nlm.nih.gov/pubmed/32309695 http://dx.doi.org/10.1021/acsomega.9b04084 |
_version_ | 1783522828501385216 |
---|---|
author | Ahmed, Bilal Ameen, Fuad Rizvi, Asfa Ali, Khursheed Sonbol, Hana Zaidi, Almas Khan, Mohammad Saghir Musarrat, Javed |
author_facet | Ahmed, Bilal Ameen, Fuad Rizvi, Asfa Ali, Khursheed Sonbol, Hana Zaidi, Almas Khan, Mohammad Saghir Musarrat, Javed |
author_sort | Ahmed, Bilal |
collection | PubMed |
description | [Image: see text] The unregulated discharge of nanoparticles (NPs) from various nanotechnology industries into the environment is expected to alter the composition and physiological functions of soil microbiota. Considering this knowledge gap, the impact of five NPs (Ag, ZnO, CuO, Al(2)O(3), and TiO(2)) differing in size and morphology on growth behavior and physiological activity of Azotobacter chroococcum, Bacillus thuringiensis, Pseudomonas mosselii, and Sinorhizobium meliloti were investigated. Various biochemical and microscopic approaches were adopted. Interestingly, all bacterial strains were found sensitive to Ag-NPs and ZnO-NPs but showed tolerance toward CuO, Al(2)O(3), and TiO(2)-NPs. The loss of cellular respiration due to NPs was coupled with a reduction in population size. ZnO-NPs at 387.5 μg mL(–1) had a maximum inhibitory impact on A. chroococcum and reduced its population by 72%. Under Ag-NP stress, the reduction in IAA secretion by bacterial strains followed the order S. meliloti (74%) > P. mosselii (63%) > A. chroococcum (49%). The surface of bacterial cells had small- or large-sized aggregates of NPs. Also, numerous gaps, pits, fragmented, and disorganized cell envelopes were visible. Additionally, a treated cell surface appeared corrugated with depressions and alteration in cell length and a strong heterogeneity was noticed under atomic force microscopy (AFM). For instance, NPs induced cell roughness for P. mosselii followed the order 12.6 nm (control) > 58 nm (Ag-NPs) > 41 nm (ZnO-NPs). TEM analysis showed aberrant morphology, cracking, and disruption of the cell envelope with extracellular electron-dense materials. Increased permeability of the inner cell membrane caused cell death and lowered EPS production. Ag-NPs and ZnO-NPs also disrupted the surface adhering ability of bacteria, which varied with time and concentration of NPs. Conclusively, a plausible mechanism of NP toxicity to bacteria has been proposed to understand the mechanistic basis of ecological interaction between NPs and resourceful bacteria. These results also emphasize to develop strategies for the safe disposal of NPs. |
format | Online Article Text |
id | pubmed-7160826 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-71608262020-04-17 Destruction of Cell Topography, Morphology, Membrane, Inhibition of Respiration, Biofilm Formation, and Bioactive Molecule Production by Nanoparticles of Ag, ZnO, CuO, TiO(2), and Al(2)O(3) toward Beneficial Soil Bacteria Ahmed, Bilal Ameen, Fuad Rizvi, Asfa Ali, Khursheed Sonbol, Hana Zaidi, Almas Khan, Mohammad Saghir Musarrat, Javed ACS Omega [Image: see text] The unregulated discharge of nanoparticles (NPs) from various nanotechnology industries into the environment is expected to alter the composition and physiological functions of soil microbiota. Considering this knowledge gap, the impact of five NPs (Ag, ZnO, CuO, Al(2)O(3), and TiO(2)) differing in size and morphology on growth behavior and physiological activity of Azotobacter chroococcum, Bacillus thuringiensis, Pseudomonas mosselii, and Sinorhizobium meliloti were investigated. Various biochemical and microscopic approaches were adopted. Interestingly, all bacterial strains were found sensitive to Ag-NPs and ZnO-NPs but showed tolerance toward CuO, Al(2)O(3), and TiO(2)-NPs. The loss of cellular respiration due to NPs was coupled with a reduction in population size. ZnO-NPs at 387.5 μg mL(–1) had a maximum inhibitory impact on A. chroococcum and reduced its population by 72%. Under Ag-NP stress, the reduction in IAA secretion by bacterial strains followed the order S. meliloti (74%) > P. mosselii (63%) > A. chroococcum (49%). The surface of bacterial cells had small- or large-sized aggregates of NPs. Also, numerous gaps, pits, fragmented, and disorganized cell envelopes were visible. Additionally, a treated cell surface appeared corrugated with depressions and alteration in cell length and a strong heterogeneity was noticed under atomic force microscopy (AFM). For instance, NPs induced cell roughness for P. mosselii followed the order 12.6 nm (control) > 58 nm (Ag-NPs) > 41 nm (ZnO-NPs). TEM analysis showed aberrant morphology, cracking, and disruption of the cell envelope with extracellular electron-dense materials. Increased permeability of the inner cell membrane caused cell death and lowered EPS production. Ag-NPs and ZnO-NPs also disrupted the surface adhering ability of bacteria, which varied with time and concentration of NPs. Conclusively, a plausible mechanism of NP toxicity to bacteria has been proposed to understand the mechanistic basis of ecological interaction between NPs and resourceful bacteria. These results also emphasize to develop strategies for the safe disposal of NPs. American Chemical Society 2020-04-01 /pmc/articles/PMC7160826/ /pubmed/32309695 http://dx.doi.org/10.1021/acsomega.9b04084 Text en Copyright © 2020 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes. |
spellingShingle | Ahmed, Bilal Ameen, Fuad Rizvi, Asfa Ali, Khursheed Sonbol, Hana Zaidi, Almas Khan, Mohammad Saghir Musarrat, Javed Destruction of Cell Topography, Morphology, Membrane, Inhibition of Respiration, Biofilm Formation, and Bioactive Molecule Production by Nanoparticles of Ag, ZnO, CuO, TiO(2), and Al(2)O(3) toward Beneficial Soil Bacteria |
title | Destruction of Cell Topography, Morphology, Membrane,
Inhibition of Respiration, Biofilm Formation, and Bioactive Molecule
Production by Nanoparticles of Ag, ZnO, CuO, TiO(2), and
Al(2)O(3) toward Beneficial Soil Bacteria |
title_full | Destruction of Cell Topography, Morphology, Membrane,
Inhibition of Respiration, Biofilm Formation, and Bioactive Molecule
Production by Nanoparticles of Ag, ZnO, CuO, TiO(2), and
Al(2)O(3) toward Beneficial Soil Bacteria |
title_fullStr | Destruction of Cell Topography, Morphology, Membrane,
Inhibition of Respiration, Biofilm Formation, and Bioactive Molecule
Production by Nanoparticles of Ag, ZnO, CuO, TiO(2), and
Al(2)O(3) toward Beneficial Soil Bacteria |
title_full_unstemmed | Destruction of Cell Topography, Morphology, Membrane,
Inhibition of Respiration, Biofilm Formation, and Bioactive Molecule
Production by Nanoparticles of Ag, ZnO, CuO, TiO(2), and
Al(2)O(3) toward Beneficial Soil Bacteria |
title_short | Destruction of Cell Topography, Morphology, Membrane,
Inhibition of Respiration, Biofilm Formation, and Bioactive Molecule
Production by Nanoparticles of Ag, ZnO, CuO, TiO(2), and
Al(2)O(3) toward Beneficial Soil Bacteria |
title_sort | destruction of cell topography, morphology, membrane,
inhibition of respiration, biofilm formation, and bioactive molecule
production by nanoparticles of ag, zno, cuo, tio(2), and
al(2)o(3) toward beneficial soil bacteria |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7160826/ https://www.ncbi.nlm.nih.gov/pubmed/32309695 http://dx.doi.org/10.1021/acsomega.9b04084 |
work_keys_str_mv | AT ahmedbilal destructionofcelltopographymorphologymembraneinhibitionofrespirationbiofilmformationandbioactivemoleculeproductionbynanoparticlesofagznocuotio2andal2o3towardbeneficialsoilbacteria AT ameenfuad destructionofcelltopographymorphologymembraneinhibitionofrespirationbiofilmformationandbioactivemoleculeproductionbynanoparticlesofagznocuotio2andal2o3towardbeneficialsoilbacteria AT rizviasfa destructionofcelltopographymorphologymembraneinhibitionofrespirationbiofilmformationandbioactivemoleculeproductionbynanoparticlesofagznocuotio2andal2o3towardbeneficialsoilbacteria AT alikhursheed destructionofcelltopographymorphologymembraneinhibitionofrespirationbiofilmformationandbioactivemoleculeproductionbynanoparticlesofagznocuotio2andal2o3towardbeneficialsoilbacteria AT sonbolhana destructionofcelltopographymorphologymembraneinhibitionofrespirationbiofilmformationandbioactivemoleculeproductionbynanoparticlesofagznocuotio2andal2o3towardbeneficialsoilbacteria AT zaidialmas destructionofcelltopographymorphologymembraneinhibitionofrespirationbiofilmformationandbioactivemoleculeproductionbynanoparticlesofagznocuotio2andal2o3towardbeneficialsoilbacteria AT khanmohammadsaghir destructionofcelltopographymorphologymembraneinhibitionofrespirationbiofilmformationandbioactivemoleculeproductionbynanoparticlesofagznocuotio2andal2o3towardbeneficialsoilbacteria AT musarratjaved destructionofcelltopographymorphologymembraneinhibitionofrespirationbiofilmformationandbioactivemoleculeproductionbynanoparticlesofagznocuotio2andal2o3towardbeneficialsoilbacteria |