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耐酸真菌康氏木霉的铀结合机制。

Uranium Binding Mechanisms of the Acid-Tolerant Fungus Coniochaeta fodinicola.

机构信息

∥Nuclear Science and Engineering Center, Japan Atomic Energy Agency, Ibaraki 319-1184, Japan.

出版信息

Environ Sci Technol. 2015 Jul 21;49(14):8487-96. doi: 10.1021/acs.est.5b01342. Epub 2015 Jul 9.

Abstract

The uptake and binding of uranium [as (UO2)(2+)] by a moderately acidophilic fungus, Coniochaeta fodinicola, recently isolated from a uranium mine site, is examined in this work in order to better understand the potential impact of organisms such as this on uranium sequestration in hydrometallurgical systems. Our results show that the viability of the fungal biomass is critical to their capacity to remove uranium from solution. Indeed, live biomass (viable cells based on vital staining) were capable of removing ∼16 mg U/g dry weight in contrast with dead biomass (autoclaved) which removed ∼45 mg U/g dry weight after 2 h. Furthermore, the uranium binds with different strength, with a fraction ranging from ∼20-50% being easily leached from the exposed biomass by a 10 min acid wash. Results from X-ray absorption spectroscopy measurements show that the strength of uranium binding is strongly influenced by cell viability, with live cells showing a more well-ordered uranium bonding environment, while the distance to carbon or phosphorus second neighbors is similar in all samples. When coupled with time-resolved laser fluorescence and Fourier transformed infrared measurements, the importance of organic acids, phosphates, and polysaccharides, likely released with fungal cell death, appear to be the primary determinants of uranium binding in this system. These results provide an important progression to our understanding with regard to uranium sequestration in hydrometallurgical applications with implications to the unwanted retention of uranium in biofilms and/or its mobility in a remediation context.

摘要

本文研究了一种从铀矿现场分离出的中度嗜酸真菌——康氏曲霉(Coniochaeta fodinicola)对铀(UO2)的摄取和结合作用,以便更好地理解此类生物对水冶系统中铀固定的潜在影响。我们的研究结果表明,真菌生物量的存活能力对其从溶液中去除铀的能力至关重要。事实上,活生物质(基于活细胞染色的有活力的细胞)能够去除约 16 mg U/g 干重的铀,而死生物质(高压灭菌)在 2 小时后能够去除约 45 mg U/g 干重的铀。此外,铀的结合强度不同,暴露的生物质经 10 分钟酸洗后,约 20-50%的铀可轻易从生物质中浸出。X 射线吸收光谱测量结果表明,铀结合强度受细胞存活能力的强烈影响,活细胞显示出更有序的铀键合环境,而与碳或磷第二近邻的距离在所有样品中相似。当与时间分辨激光荧光和傅里叶变换红外测量相结合时,有机酸、磷酸盐和多糖(可能随着真菌细胞死亡而释放)的重要性似乎是该体系中铀结合的主要决定因素。这些结果为我们在水冶应用中对铀固定的理解提供了重要进展,对生物膜中铀的不必要滞留及其在修复环境中的迁移性具有重要意义。

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