Background: To address the severe health risks posed by aflatoxin B (AFB) in grain, this study employed polydopamine-based atom transfer radical polymerization (p-ATRP) and cytochrome C-catalyzed atom transfer radical polymerization (c-ATRP) as cytocompatible modification techniques to coat the surface of living Lactobacillus plantarum (LAB) cells with the temperature-sensitive polymer poly(N-isopropylacrylamide) (PNIPAAm).
Results: Two novel bioadsorbents were synthesized. The incorporation of PNIPAAm as an 'AFB vacuum cleaner' layer significantly enhances LAB's adsorption efficiency and enables temperature-controlled desorption. Compared with p-ATRP, c-ATRP uses cytochrome C (from LAB's membrane protein) as a biocatalyst to replace the necessary copper catalyst in p-ATRP, eliminating the risk of copper toxicity and pollution. The exceptional AFB adsorption capabilities of LAB@PNIPAAm can be precisely modeled using the Lagergren pseudo-second-order and Freundlich frameworks, with an adsorption capacity attaining 74.88 ng mL. Furthermore, LAB@PNIPAAm displays unique temperature-responsive properties, achieving an adsorption efficiency of 78% at 22 °C and a temperature-controlled desorption rate of 69% upon temperature elevation to 37 °C. It is noteworthy that the c-ATRP technology also enhances the stress resistance of LAB.
Conclusion: These findings offer novel insights into the surface engineering of viable bacterial cells and the efficient bioremediation of multiple pollutants in complex environments. © 2025 Society of Chemical Industry.
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http://dx.doi.org/10.1002/jsfa.14216 | DOI Listing |
ChemSusChem
March 2025
UOW: University of Wollongong, Australian Institute of Innovative Materials, Innovation Campus, University of Wollongong, Squires Way, 2500, North Wollongong, AUSTRALIA.
Visible-light-driven CO2 reduction presents a long-term answer to environmental challenges. The limited effective optical carriers generated by the limited response dynamics of the existing photocatalyst have severely hindered the development of high efficiency photocatalysts. Here, we report a method of cobalt atoms intercalation in ultrathin BiOBr nanosheets for boosted photocatalytic CO2 reduction.
View Article and Find Full Text PDFChempluschem
March 2025
CIMAP: Centre de recherche sur les ions les materiaux et la photonique, UMR 6252 CEA/CNRS/Unicaen/Ensicaen, GANIL, Bd Becquerel, 14070, CAEN, FRANCE.
The direct effects of ionizing radiation on antibiotics are largely unknown. Here, we report mass spectra of the cationic products of the irradiation of three antibiotics by carbon ions at 10.4 MeV kinetic energy.
View Article and Find Full Text PDFJ Sci Food Agric
March 2025
Hebei Key Laboratory of Quality & Safety Analysis-Testing for Agro-products and Food, Hebei North University, Zhangjiakou, China.
Background: To address the severe health risks posed by aflatoxin B (AFB) in grain, this study employed polydopamine-based atom transfer radical polymerization (p-ATRP) and cytochrome C-catalyzed atom transfer radical polymerization (c-ATRP) as cytocompatible modification techniques to coat the surface of living Lactobacillus plantarum (LAB) cells with the temperature-sensitive polymer poly(N-isopropylacrylamide) (PNIPAAm).
Results: Two novel bioadsorbents were synthesized. The incorporation of PNIPAAm as an 'AFB vacuum cleaner' layer significantly enhances LAB's adsorption efficiency and enables temperature-controlled desorption.
Acta Crystallogr E Crystallogr Commun
March 2025
Instituto de Física de São Carlos (IFSC) Universidade de São Paulo (USP) 13566-590 São Carlos SP Brazil.
A new mebendazolium di-hydrogen phosphate phospho-ric acid solid material was obtained and characterized by single-crystal X-ray diffraction and complementary solid-state techniques {systematic name: 5-benzoyl-2-[(meth-oxy-carbon-yl)amino]-1-1,3-benzo-diazol-3-ium di-hydrogen phosphate-phos-pho-ric acid (1/1), CHNO ·HPO ·HPO}. Structure solution confirmed proton transfer from phospho-ric acid towards the basic imidazole ring of mebendazole. The mebendazolium cation and the di-hydrogen phosphate anion assemble in the solid state in a cyclic hydrogen-bond-driven supra-molecular motif, as observed in all mebendazolium/oxyanions structures reported in the literature.
View Article and Find Full Text PDFPhys Chem Chem Phys
March 2025
Voevodsky Institute of Chemical Kinetics and Combustion, SB RAS, 3, Institutskaya str., Novosibirsk, 630090, Russia.
This study focuses on primary radical ionic species created in liquid carbonates upon high-energy radiation. We studied the radiation-induced fluorescence intensity decays observed from solutions of luminophores in dimethyl, diethyl, ethylene, and propylene carbonates. Based on the effects of external magnetic and electric fields on the fluorescence decays on a timescale of 1-60 ns and quantum chemical calculations, we found that in all studied carbonates, solvent ionization was rapidly followed by the formation of comparatively long-lived positive charge and unpaired electron spin carriers.
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