» Articles » PMID: 37462214

Impact of Biogenic and Chemogenic Selenium Nanoparticles on Model Eukaryotic Lipid Membranes

Overview
Journal Langmuir
Specialty Chemistry
Date 2023 Jul 18
PMID 37462214
Authors
Affiliations
Soon will be listed here.
Abstract

Microbial nanotechnology is an expanding research area devoted to producing biogenic metal and metalloid nanomaterials (NMs) using microorganisms. Often, biogenic NMs are explored as antimicrobial, anticancer, or antioxidant agents. Yet, most studies focus on their applications rather than the underlying mechanism of action or toxicity. Here, we evaluate the toxicity of our well-characterized biogenic selenium nanoparticles (bSeNPs) produced by the strain SeITE02 against the model yeast comparing it with chemogenic SeNPs (cSeNPs). Knowing from previous studies that the biogenic extract contained bSeNPs in an organic material (OM) and supported here by Fourier transform infrared spectroscopy, we removed and incubated it with cSeNPs (cSeNPs_OM) to assess its influence on the toxicity of these formulations. Specifically, we focused on the first stages of the eukaryotic cell exposure to these samples─i.e., their interaction with the cell lipid membrane, which was mimicked by preparing vesicles from yeast polar lipid extract or phosphatidylcholine lipids. Fluidity changes derived from biogenic and chemogenic samples revealed that the bSeNP extract mediated the overall rigidification of lipid vesicles, while cSeNPs showed negligible effects. The OM and cSeNPs_OM induced similar modifications to the bSeNP extract, reiterating the need to consider the OM influence on the physical-chemical and biological properties of bSeNP extracts.

Citing Articles

Characterization and biological activity of selenium nanoparticles biosynthesized by Yarrowia lipolytica.

Lashani E, Moghimi H, Turner R, Amoozegar M Microb Biotechnol. 2024; 17(10):e70013.

PMID: 39364622 PMC: 11450378. DOI: 10.1111/1751-7915.70013.


Unveiling the vital role of soil microorganisms in selenium cycling: a review.

Jiang Z, Wang Z, Zhao Y, Peng M Front Microbiol. 2024; 15:1448539.

PMID: 39323878 PMC: 11422209. DOI: 10.3389/fmicb.2024.1448539.


Bacterial synthesis of metal nanoparticles as antimicrobials.

Arora A, Lashani E, Turner R Microb Biotechnol. 2024; 17(8):e14549.

PMID: 39150434 PMC: 11328525. DOI: 10.1111/1751-7915.14549.

References
1.
Chen X, Tieleman D, Liang Q . Modulating interactions between ligand-coated nanoparticles and phase-separated lipid bilayers by varying the ligand density and the surface charge. Nanoscale. 2018; 10(5):2481-2491. DOI: 10.1039/c7nr06494b. View

2.
Wang X, Wang X, Bai X, Yan L, Liu T, Wang M . Nanoparticle Ligand Exchange and Its Effects at the Nanoparticle-Cell Membrane Interface. Nano Lett. 2018; 19(1):8-18. DOI: 10.1021/acs.nanolett.8b02638. View

3.
de Jonge M, Pehau-Arnaudet G, Fretz M, Romain F, Bottai D, Brodin P . ESAT-6 from Mycobacterium tuberculosis dissociates from its putative chaperone CFP-10 under acidic conditions and exhibits membrane-lysing activity. J Bacteriol. 2007; 189(16):6028-34. PMC: 1952024. DOI: 10.1128/JB.00469-07. View

4.
Daear W, Mundle R, Sule K, Prenner E . The degree and position of phosphorylation determine the impact of toxic and trace metals on phosphoinositide containing model membranes. BBA Adv. 2023; 1:100021. PMC: 10074965. DOI: 10.1016/j.bbadva.2021.100021. View

5.
Corbo C, Molinaro R, Taraballi F, Toledano Furman N, Sherman M, Parodi A . Effects of the protein corona on liposome-liposome and liposome-cell interactions. Int J Nanomedicine. 2016; 11:3049-63. PMC: 4938145. DOI: 10.2147/IJN.S109059. View