Zero-valent sulfur, commonly utilized as a fertilizer or fungicide, is prevalent in various environmental contexts. Its most stable and predominant form, octasulfur (S), plays a crucial role in microbial sulfur metabolism, either through oxidation or reduction. However, the mechanism underlying its cellular uptake remains elusive. We presented evidence that zero-valent sulfur was adsorbed to the cell surface and then dissolved into the membrane lipid layer as lipid-soluble S molecules, which reacted with cellular low-molecular thiols to form persulfide, e.g., glutathione persulfide (GSSH), in the cytoplasm. The process brought extracellular zero-valent sulfur into the cells. When persulfide dioxygenase is present in the cells, GSSH will be oxidized. Otherwise, GSSH will react with another glutathione (GSH) to produce glutathione disulfide (GSSG) and hydrogen sulfide (HS). The mechanism is different from simple diffusion, as insoluble S becomes soluble GSSH after crossing the cytoplasmic membrane. The uptake process is limited by physical contact of insoluble zero-valent sulfur with microbial cells and the regeneration of cellular thiols. Our findings elucidate the cellular uptake mechanism of zero-valent sulfur, which provides critical information for its application in agricultural practices and the bioremediation of sulfur contaminants and heavy metals.
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http://dx.doi.org/10.1016/j.scitotenv.2024.170504 | DOI Listing |
Environ Res
December 2024
School of Environmental and Chemical Engineering, Shanghai University, Shanghai, 200444, PR China. Electronic address:
The lipophilic, bioaccumulative, persistent nature of Tetrabromobisphenol A (TBBPA) contributes to its widespread detection in various environmental media, posing significant negative implications for the living environment and human health. In this study, a reduction system and a reduction-oxidation sequential reaction system were developed using a magnetic core-shell bimetallic amendment (S-Fe/Co@GC) to investigate the degradation and mineralization properties of TBBPA. Additionally, the degradation mechanism and degradation pathway of TBBPA in various systems were analyzed.
View Article and Find Full Text PDFChemosphere
October 2024
Department of Civil and Environmental Engineering, Pusan National University, 2, Busandaehak-ro 63beon-gil, Geumjeong-gu, Busan, 46241, Republic of Korea. Electronic address:
Soil contamination with hazardous substances like phenol poses significant environmental and health risks. In situ soil mixing can be a promising technological solution to this challenge. A persulfate and sulfidated zero-valent iron (S-ZVI) system for remediating contaminated soil was developed and tested to be suited to in situ soil mixing.
View Article and Find Full Text PDFJ Hazard Mater
December 2024
Shandong Key Laboratory of Water Pollution Control and Resource Reuse, School of Environmental Science and Engineering, Shandong University, Qingdao 266237, China; College of Chemistry, Chemical Engineering and Materials Science, Shandong Normal University, Jinan, Shandong 250014, China.
J Contam Hydrol
November 2024
Sealaska, 3200 George Washington Way, Richland, WA 99364, United States of America.
Spectral induced polarization (SIP) responses are not well understood within the context of remediation applications at contaminated sites. Systematic SIP studies are needed to gain further insights into the complex electrical response of dynamic, biogeochemical states to enable the use of SIP for subsurface site characterization and remediation monitoring. Although SIP measurements on zero valent iron have been previously published, the SIP response for sulfur modified iron (SMI), a similar potential subsurface reductive amendment, has not yet been reported.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
September 2024
Key Laboratory of Pesticide & Chemical Biology of Ministry of Education, Institute of Applied & Environmental Chemistry, College of Chemistry, Central China Normal University, Wuhan, 430079, P. R. China.
Microscale zero-valent iron (mZVI) is widely used for water pollutant control and environmental remediation, yet its reactivity is still constrained by the inert oxide shell. Herein, we demonstrate that mechanochemical thioglycolate (TG) modification can dramatically enhance heavy metal (Ni, Cr, Cd, Pb, Hg, and Sb) removal rates of mZVI by times of 16.7 to 88.
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