White-Pettigrew Matthew, Shaw Samuel, Hughes Lewis, Boothman Christopher, Graham James, Abrahamsen-Mills Liam, Morris Katherine, Lloyd Jonathan R
Research Centre for Radwaste Disposal and Williamson Research Centre for Molecular Environmental Science, Department of Earth and Environmental Sciences, The University of Manchester, Manchester M13 9PL, United Kingdom.
National Nuclear Laboratory, Warrington, Cheshire WA3 6AE, United Kingdom.
ACS Earth Space Chem. 2024 Feb 26;8(3):483-498. doi: 10.1021/acsearthspacechem.3c00252. eCollection 2024 Mar 21.
Microbial ureolysis offers the potential to remove metals including Sr as carbonate minerals via the generation of alkalinity coupled to NH and HCO production. Here, we investigated the potential for bacteria, indigenous to sediments representative of the U.K. Sellafield nuclear site where Sr is present as a groundwater contaminant, to utilize urea in order to target Sr-associated (Ca)CO formation in sediment microcosm studies. Strontium removal was enhanced in most sediments in the presence of urea only, coinciding with a significant pH increase. Adding the biostimulation agents acetate/lactate, Fe(III), and yeast extract to further enhance microbial metabolism, including ureolysis, enhanced ureolysis and increased Sr and Ca removal. Environmental scanning electron microscopy analyses suggested that coprecipitation of Ca and Sr occurred, with evidence of Sr associated with calcium carbonate polymorphs. Sr -edge X-ray absorption spectroscopy analysis was conducted on authentic Sellafield sediments stimulated with Fe(III) and quarry outcrop sediments amended with yeast extract. Spectra from the treated Sellafield and quarry sediments showed Sr local coordination environments indicative of incorporation into calcite and vaterite crystal structures, respectively. 16S rRNA gene analysis identified ureolytic bacteria of the genus in these incubations, suggesting they have a key role in enhancing strontium removal. The onset of ureolysis also appeared to enhance the microbial reduction of Fe(III), potentially via a tight coupling between Fe(III) and NH as an electron donor for metal reduction. This suggests ureolysis may support the immobilization of Sr via coprecipitation with insoluble calcium carbonate and cofacilitate reductive precipitation of certain redox active radionuclides, e.g., uranium.
微生物尿素分解作用具有通过产生与铵和碳酸氢根生成相关的碱度来去除包括锶在内的金属并形成碳酸盐矿物的潜力。在此,我们研究了来自英国塞拉菲尔德核场地代表性沉积物中的细菌利用尿素的潜力,在该场地锶作为地下水污染物存在,我们在沉积物微观研究中以形成与锶相关的(碳酸钙)碳酸盐为目标。仅在存在尿素的情况下,大多数沉积物中的锶去除率有所提高,同时pH值显著升高。添加生物刺激剂乙酸盐/乳酸盐、铁(III)和酵母提取物以进一步增强微生物代谢,包括尿素分解作用,增强了尿素分解并增加了锶和钙的去除率。环境扫描电子显微镜分析表明钙和锶发生了共沉淀,有证据表明锶与碳酸钙多晶型物相关。对用铁(III)刺激的真实塞拉菲尔德沉积物和用酵母提取物改良的采石场露头沉积物进行了锶边缘X射线吸收光谱分析。处理后的塞拉菲尔德沉积物和采石场沉积物的光谱显示,锶的局部配位环境分别表明其掺入了方解石和球霰石晶体结构中。16S rRNA基因分析确定了这些培养物中脲酶细菌的属,表明它们在增强锶去除方面具有关键作用。尿素分解作用的开始似乎也增强了铁(III)的微生物还原作用,这可能是通过铁(III)与作为金属还原电子供体的铵之间的紧密耦合实现的。这表明尿素分解作用可能通过与不溶性碳酸钙共沉淀来支持锶的固定,并共同促进某些氧化还原活性放射性核素(如铀)的还原沉淀。