Department of Earth Resource Engineering, Faculty of Engineering, Kyushu University, 744 Motooka, Nishi-ku, Fukuoka, 819-0395, Japan.
Extremophiles. 2019 Sep;23(5):549-556. doi: 10.1007/s00792-019-01106-7. Epub 2019 Jun 19.
The thermo-acidophilic archaeon, Sulfolobus tokodaii, was utilized for the production of Pd(0) bionanoparticles from acidic Pd(II) solution. Use of active cells was essential to form well-dispersed Pd(0) nanoparticles located on the cell surface. The particle size could be manipulated by modifying the concentration of formate (as electron donor; e-donor) and by addition of enzymatic inhibitor (Cu) in the range of 14-63 nm mean size. Since robust Pd(II) reduction progressed in pre-grown S. tokodaii cells even in the presence of up to 500 mM Cl, it was possible to conversely utilize the effect of Cl to produce even finer and denser particles in the range of 8.7-15 nm mean size. This effect likely resulted from the increasing stability of anionic Pd(II)-chloride complex at elevated Cl concentrations, eventually allowing involvement of greater number of initial Pd(0) crystal nucleation sites (enzymatic sites). The catalytic activity [evaluated based on Cr(VI) reduction reaction] of Pd(0) bionanoparticles of varying particle size formed under different conditions were compared. The finest Pd(0) bionanoparticles obtained at 50 mM Cl (mean 8.7 nm; median 5.6 nm) exhibited the greatest specific Cr(VI) reduction rate, with four times higher catalytic activity compared to commercial Pd/C. The potential applicability of S. tokodaii cells in the recovery of highly catalytic Pd(0) nanoparticles from actual acidic chloride leachate was, thus, suggested.
嗜热嗜酸古菌(Sulfolobus tokodaii)可用于从酸性 Pd(II) 溶液中生产 Pd(0) 生物纳米粒子。使用活性细胞对于形成位于细胞表面的分散良好的 Pd(0) 纳米粒子至关重要。通过改变甲酸盐(作为电子供体)的浓度,并在 14-63nm 的平均粒径范围内添加酶抑制剂(Cu),可以控制颗粒尺寸。由于在预生长的 S. tokodaii 细胞中,即使存在高达 500mM 的 Cl,也能有效地进行稳健的 Pd(II) 还原,因此有可能反过来利用 Cl 的作用,在 8.7-15nm 的平均粒径范围内产生更细和更密集的颗粒。这种效果可能是由于在高 Cl 浓度下,阴离子 Pd(II)-氯化物络合物的稳定性增加,最终允许更多初始 Pd(0) 晶核形成点(酶活性点)参与。比较了在不同条件下形成的不同粒径的 Pd(0) 生物纳米粒子的催化活性(基于 Cr(VI) 还原反应评估)。在 50mM Cl 下获得的最细的 Pd(0) 生物纳米粒子(平均 8.7nm;中位数 5.6nm)表现出最大的 Cr(VI) 还原速率,与商业 Pd/C 相比,催化活性提高了四倍。因此,建议将 S. tokodaii 细胞应用于从实际酸性氯化浸出液中回收高催化活性的 Pd(0) 纳米粒子。