XPS and XANES Studies of Uranium Reduction by Clostridium spArokiasamy J. Francis, Cleveland J. Dodge, Fulong Lu et al.|Environmental Science & Technology|1994 ADVERTISEMENT RETURN TO ISSUEPREVArticleNEXTXPS and XANES Studies of Uranium Reduction by Clostridium spArokiasamy J. Francis, Cleveland J. Dodge, Fulong. Lu, Gary P. Halada, and Clive R. ClaytonCite this: Environ. Sci. Technol. 1994, 28, 4, 636–639Publication Date (Print):April 1, 1994Publication History Published online1 May 2002Published inissue 1 April 1994https://pubs.acs.org/doi/10.1021/es00053a016https://doi.org/10.1021/es00053a016research-articleACS PublicationsRequest reuse permissionsArticle Views1164Altmetric-Citations195LEARN ABOUT THESE METRICSArticle Views are the COUNTER-compliant sum of full text article downloads since November 2008 (both PDF and HTML) across all institutions and individuals. These metrics are regularly updated to reflect usage leading up to the last few days.Citations are the number of other articles citing this article, calculated by Crossref and updated daily. Find more information about Crossref citation counts.The Altmetric Attention Score is a quantitative measure of the attention that a research article has received online. Clicking on the donut icon will load a page at altmetric.com with additional details about the score and the social media presence for the given article. Find more information on the Altmetric Attention Score and how the score is calculated. Share Add toView InAdd Full Text with ReferenceAdd Description ExportRISCitationCitation and abstractCitation and referencesMore Options Share onFacebookTwitterWechatLinked InRedditEmail Other access optionsGet e-Alertsclose Get e-Alerts
Anaerobic microbial remobilization of toxic metals coprecipitated with iron oxideArokiasamy J. Francis, Cleveland J. Dodge|Environmental Science & Technology|1990 ADVERTISEMENT RETURN TO ISSUEPREVArticleNEXTAnaerobic microbial remobilization of toxic metals coprecipitated with iron oxideArokiasamy J. Francis and Cleveland J. DodgeCite this: Environ. Sci. Technol. 1990, 24, 3, 373–378Publication Date (Print):March 1, 1990Publication History Published online1 May 2002Published inissue 1 March 1990https://pubs.acs.org/doi/10.1021/es00073a013https://doi.org/10.1021/es00073a013research-articleACS PublicationsRequest reuse permissionsArticle Views383Altmetric-Citations94LEARN ABOUT THESE METRICSArticle Views are the COUNTER-compliant sum of full text article downloads since November 2008 (both PDF and HTML) across all institutions and individuals. These metrics are regularly updated to reflect usage leading up to the last few days.Citations are the number of other articles citing this article, calculated by Crossref and updated daily. Find more information about Crossref citation counts.The Altmetric Attention Score is a quantitative measure of the attention that a research article has received online. Clicking on the donut icon will load a page at altmetric.com with additional details about the score and the social media presence for the given article. Find more information on the Altmetric Attention Score and how the score is calculated. Share Add toView InAdd Full Text with ReferenceAdd Description ExportRISCitationCitation and abstractCitation and referencesMore Options Share onFacebookTwitterWechatLinked InRedditEmail Other access optionsGet e-Alertsclose Get e-Alerts
Uranium association with halophilic and non-halophilic bacteria and archaeaSummary We determined the association of uranium with bacteria isolated from the Waste Isolation Pilot Plant (WIPP), Carlsbad, New Mexico, and compared this with known strains of halophilic and non-halophilic bacteria and archaea. Examination of the cultures by transmission electron microscopy (TEM) and energy dispersive X-ray spectroscopy (EDS) showed uranium accumulation extracellularly and/or intracellularly to a varying degree. In Pseudomonas fluorescens and Bacillus subtilis uranium was associated with the cell surface and in the latter it was present as irregularly shaped grains. In Halobacterium halobium , the only archeon studied here, uranium was present as dense deposits and with Haloanaerobium praevalens as spikey deposits. Halomonas sp . isolated from the WIPP site accumulated uranium both extracellularly on the cell surface and intracellularly as electron-dense discrete granules. Extended X-ray absorption fine structure (EXAFS) analysis of uranium with the halophilic and non-halophilic bacteria and archaea showed that the uranium present in whole cells was bonded to an average of 2.4±0.7 phosphoryl groups at a distance of 3.65±0.03 Å. Comparison of whole cells of Halomonas sp . with the cell wall fragments of lysed cells showed the presence of a uranium bidentate complex at 2.91±0.03 Å with the carboxylate group on the cell wall, and uranyl hydroxide with U-U interaction at 3.71±0.03 Å due to adsorption or precipitation reactions; no U-P interaction was observed. Addition of uranium to the cell lysate of Halomonas sp . resulted in the precipitation of uranium due to the inorganic phosphate produced by the cells. These results show that the phosphates released from bacteria bind a significant amount of uranium. However, the bacterially immobilized uranium was readily solubilized by bicarbonate with concurrent release of phosphate into solution.
Reduction of Uranium(VI) to Uranium(IV) by ClostridiaWeimin Gao, Arokiasamy J. Francis|Applied and Environmental Microbiology|2008 Several different species of clostridia reduced U(VI) to U(IV) to various degrees. The optimal pH for U(VI) reduction is 5 to 6 in most cases; a Clostridium sp. showed the highest rate at pH 4. Nitrate did not affect U(VI) reduction, indicating that this process in clostridia is nitrate independent.
Nano/bio treatment of polychlorinated biphenyls with evaluation of comparative toxicityThao Thanh Le, Khanh Hoang Nguyen, Jong‐Rok Jeon et al.|Journal of Hazardous Materials|2015