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Influence of Uranium Concentration and pH on U-Phosphate Biomineralization by Caulobacter OR37

磷酸盐 环境化学 环境修复 化学 磷酸盐矿物 生物矿化 生物修复 铁酸盐 溶解度 污染 矿化(土壤科学) 生态学 地质学 生物化学 生物 材料科学 冶金 古生物学 有机化学 吸附 氮气
作者
Keith D. Morrison,Mavrik Zavarin,Annie B. Kersting,James D. Begg,Harris E. Mason,Enrica Balboni,Yongqin Jiao
出处
期刊:Environmental Science & Technology [American Chemical Society]
卷期号:55 (3): 1626-1636 被引量:42
标识
DOI:10.1021/acs.est.0c05437
摘要

Uranium contamination of soils and groundwater in the United States represents a significant health risk and will require multiple remediation approaches. Microbial phosphatase activity coupled to the addition of an organic P source has recently been studied as a remediation strategy that provides an extended release of inorganic P (Pi) into U-contaminated sites, resulting in the precipitation of meta-autunite minerals. Previous laboratory- and field-based biomineralization studies have investigated environments with relatively high U concentrations (>20 μM). However, most contaminated sites have much lower U concentrations (<2 μM). The Environmental Protection Agency (EPA) limit for U in drinking water is 0.126 μM. Reaching this regulatory limit becomes challenging as U concentrations approach autunite solubility. We studied the precipitation of U(VI)-phosphate minerals by an environmental isolate of Caulobacter sp. (strain OR37) from an Oak Ridge, Tennessee, U-contaminated site. Abiotic U(VI) solubility experiments reveal that U(VI)-phosphate minerals do not form in the presence of excess Pi (500 μM) when U(VI) concentrations are <1 μM and pH is <5. When OR37 cells are reacted under the same conditions with Pi or glycerol-2-phosphate, U(VI)-phosphate mineral formation was observed, along with the formation of intracellular polyphosphate granules. These results show that bacteria provide supersaturated microenvironments needed for U(VI)-phosphate mineralization while hydrolyzing organic P sources. This provides a pathway to lower U concentrations to below EPA limits for drinking water.
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