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Plutonium(IV) Reduction by the Metal-Reducing Bacteria Geobacter metallireducens GS15 and Shewanella oneidensis MR1▿

机译:还原金属细菌Geobacter metallireducens GS15和Shewanella oneidensisMR1▿还原(

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摘要

The bacterial reduction of actinides has been suggested as a possible remedial strategy for actinide-contaminated environments, and the bacterial reduction of Pu(VI/V) has the potential to produce highly insoluble Pu(IV) solid phases. However, the behavior of plutonium with regard to bacterial reduction is more complex than for other actinides because it is possible for Pu(IV) to be further reduced to Pu(III), which is relatively more soluble than Pu(IV). This work investigates the ability of the metal-reducing bacteria Geobacter metallireducens GS15 and Shewanella oneidensis MR1 to enzymatically reduce freshly precipitated amorphous Pu(IV) (OH)4 [Pu(IV)(OH)4(am)] and soluble Pu(IV)(EDTA). In cell suspensions without added complexing ligands, minor Pu(III) production was observed in cultures containing S. oneidensis, but little or no Pu(III) production was observed in cultures containing G. metallireducens. In the presence of EDTA, most of the Pu(IV)(OH)4(am) present was reduced to Pu(III) and remained soluble in cell suspensions of both S. oneidensis and G. metallireducens. When soluble Pu(IV)(EDTA) was provided as the terminal electron acceptor, cell suspensions of both S. oneidensis and G. metallireducens rapidly reduced Pu(IV)(EDTA) to Pu(III)(EDTA) with nearly complete reduction within 20 to 40 min, depending on the initial concentration. Neither bacterium was able to use Pu(IV) (in any of the forms used) as a terminal electron acceptor to support growth. These results have significant implications for the potential remediation of plutonium and suggest that strongly reducing environments where complexing ligands are present may produce soluble forms of reduced Pu species.
机译:act系元素的细菌还原已被建议作为act系元素污染环境的一种可能的补救策略,Pu(VI / V)的细菌还原具有产生高度不溶性Pu(IV)固相的潜力。但是,bacterial在细菌还原方面的行为比其他act系元素更为复杂,因为Pu(IV)可能会进一步还原为Pu(III),而Pu(III)比Pu(IV)相对易溶。这项工作研究金属还原细菌金属还原细菌GS15和Shewanella oneidensis MR1​​酶促还原新鲜沉淀的非晶态Pu(IV)(OH)4 [Pu(IV)(OH)4(am)]和可溶性Pu(IV)的能力。 )(EDTA)。在没有添加络合配体的细胞悬浮液中,在含有拟南芥的培养物中观察到少量的Pu(III)产生,但是在含有金属假单胞菌的培养物中观察到极少或没有Pu(III)产生。在EDTA存在下,存在的大多数Pu(IV)(OH)4(am)被还原为Pu(III),并仍可溶于拟南芥和金属假单胞菌的细胞悬浮液中。当提供可溶性Pu(IV)(EDTA)作为末端电子受体时,S。oneidensis和G.metallireducens的细胞悬液迅速将Pu(IV)(EDTA)还原为Pu(III)(EDTA),并且在20至40分钟,具体取决于初始浓度。两种细菌都不能使用Pu(IV)(以任何形式使用)作为末端电子受体来支持生长。这些结果对for的潜在修复具有重大意义,并表明存在络合配体的强还原性环境可能会产生可溶形式的还原型Pu物种。

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