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五价镎在希瓦氏菌属海藻的完整细胞和细胞组分上的表面络合:模型与实验研究。

Surface complexation of Neptunium(V) onto whole cells and cell components of Shewanella alga: modeling and experimental study.

机构信息

Center for Environmental Biotechnology, Biodesign Institute, Arizona State University, Tempe, Arizona 85287-5701, USA.

出版信息

Environ Sci Technol. 2010 Jul 1;44(13):4930-5. doi: 10.1021/es9035336.

Abstract

We systematically quantified surface complexation of Np(V) onto whole cells, cell wall, and extracellular polymeric substances (EPS) of Shewanella alga strain BrY. We first performed acid and base titrations and used the mathematical model FITEQL to estimate the concentrations and deprotonation constants of specific surface functional groups. Deprotonation constants most likely corresponded to a carboxyl group not associated with amino acids (pK(a) approximately 5), a phosphoryl site (pK(a) approximately 7.2), and an amine site (pK(a) > 10). We then carried out batch sorption experiments with Np(V) and each of the S. alga components as a function of pH. Since significant Np(V) sorption was observed on S. alga whole cells and its components in the pH range 2-5, we assumed the existence of a fourth site: a low-pK(a) carboxyl site (pK(a) approximately 2.4) that is associated with amino acids. We used the SPECIATE submodel of the biogeochemical model CCBATCH to compute the stability constants for Np(V) complexation to each surface functional group. The stability constants were similar for each functional group on S. alga bacterial whole cells, cell walls, and EPS, and they explain the complicated sorption patterns when they are combined with the aqueous-phase speciation of Np(V). For pH < 8, the aquo NpO(2)(+) species was the dominant form of Np(V), and its log K values for the low-pK(a) carboxyl, mid-pK(a) carboxyl, and phosphoryl groups were 1.8, 1.8, and 2.5-3.1, respectively. For pH greater than 8, the key surface ligand was amine >XNH(3)(+), which complexed with NpO(2)(CO(3))(3)(5-). The log K for NpO(2)(CO(3))(3)(5-) complexed onto the amine groups was 3.1-3.9. All of the log K values are similar to those of Np(V) complexes with aqueous carboxyl and N-containing carboxyl ligands. These results help quantify the role of surface complexation in defining actinide-microbiological interactions in the subsurface.

摘要

我们系统地量化了 Np(V) 在整条 Shewanella alga 菌 BrY 细胞、细胞壁和胞外聚合物 (EPS) 上的表面络合作用。我们首先进行了酸堿滴定,并使用数学模型 FITEQL 来估计特定表面官能团的浓度和去质子化常数。去质子化常数最有可能对应于非氨基酸相关的羧基(pK(a)约为 5)、磷酸基位点(pK(a)约为 7.2)和胺基位点(pK(a) > 10)。然后,我们进行了一系列 Np(V)与 S. alga 各成分在 pH 值下的分批吸附实验。由于在 pH 值为 2-5 的范围内观察到 S. alga 整细胞及其成分对 Np(V)有明显的吸附,因此我们假设存在第四个位点:与氨基酸相关的低 pK(a)羧基位点(pK(a)约为 2.4)。我们使用生物地球化学模型 CCBATCH 的 SPECIATE 子模型来计算 Np(V)与每个表面官能团络合的稳定常数。S. alga 细菌整细胞、细胞壁和 EPS 上的每个官能团的稳定常数相似,当与 Np(V)的水相形态结合时,它们可以解释复杂的吸附模式。对于 pH < 8,水合 NpO(2)(+)物种是 Np(V)的主要形式,其低 pK(a)羧基、中 pK(a)羧基和磷酸基的 log K 值分别为 1.8、1.8 和 2.5-3.1。对于 pH 值大于 8,关键的表面配体是胺基>XNH(3)(+),它与 NpO(2)(CO(3))(3)(5-)络合。与胺基络合的 NpO(2)(CO(3))(3)(5-)的 log K 值为 3.1-3.9。所有的 log K 值都与水合羧基和含 N 羧基配体的 Np(V)络合物相似。这些结果有助于量化表面络合作用在定义地下环境中锕系元素-微生物相互作用中的作用。

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