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首页> 外文期刊>Hydrometallurgy >Extracellular DNA enhances the adsorption of Sulfobacillus thermosulfidooxidans strain ST on chalcopyrite surface
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Extracellular DNA enhances the adsorption of Sulfobacillus thermosulfidooxidans strain ST on chalcopyrite surface

机译:细胞外DNA增强了磺基霉氟苯脱氧氧磷脂菌株ST在黄铜矿表面上的吸附

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摘要

Extracellular polymeric substances (EPS) and their key components play an important role in bioleaching. Herein, the amount of extracellular DNA (eDNA) secreted by Sulfobacillus thermosulfidooxidans strain ST during bioleaching of chalcopyrite concentrate was investigated through traditional extraction method and confocal laser scanning microscope (CLSM) analysis. DNase I was added into the bioleaching system to degrade eDNA, and then the effects of eDNA deficiency on bacterial adsorption, copper extraction and the synthesis of other key components of EPS were evaluated. The results of adsorption experiment indicated that the adsorption time was prolonged and the equilibrium adsorption quantity was decreased when the eDNA was absent. The bioleaching experiment showed that eDNA in the EPS was favorable to the copper extraction, which increased by 18.5% compared with that of the eDNA-deficient group. Furthermore, it was found that the removal of eDNA decreased the formation of other key EPS components like polysaccharides and proteins. 1n situ observation and monitoring of eDNA on the chalcopyrite surface by CLSM were carried out. The results showed that the loss of eDNA attenuated the fluorescence intensity of each component of EPS, which was consistent with the above results. These studies suggested that eDNA in the EPS could enhance the adsorption of bacteria on the surface of chalcopyrite and further increase the copper extraction.
机译:细胞外聚合物物质(EPS)及其关键组分在生物浸出中起重要作用。这里,通过传统的提取方法和共聚焦激光扫描显微镜(CLSM)分析,研究了通过传统的提取方法和共聚焦激光扫描显微镜(CLSM)分析在石铜矿浓缩物生物酰化期间分泌的细胞外DNA(EDNA)的量。将DNase I加入到生物浸入系统中以降解EDNA,然后评估EDNA缺乏对细菌吸附,铜提取和EPS其他关键组分的合成的影响。吸附实验结果表明,当eDNA不存在时,延长吸附时间延长,降低平衡吸附量。生物浸入实验表明EPS中的EDNA有利于铜萃取,与EDNA缺陷组相比增加了18.5%。此外,发现去除EDNA降低了多糖和蛋白质等其他关键EPS组分的形成。通过CLSM进行1N原位观察和监测CHALCYRITE表面的edna。结果表明,EDNA的丧失抑制了EPS各组分的荧光强度,这与上述结果一致。这些研究表明,EDNA中的EDNA可以增强细菌在核黄素表面上的吸附,进一步增加铜提取。

著录项

  • 来源
    《Hydrometallurgy 》 |2018年第2018期| 共7页
  • 作者单位

    Cent S Univ Sch Minerals Proc &

    Bioengn Changsha 410083 Hunan Peoples R China;

    Cent S Univ Sch Minerals Proc &

    Bioengn Changsha 410083 Hunan Peoples R China;

    Cent S Univ Sch Minerals Proc &

    Bioengn Changsha 410083 Hunan Peoples R China;

    Cent S Univ Sch Minerals Proc &

    Bioengn Changsha 410083 Hunan Peoples R China;

    Cent S Univ Sch Minerals Proc &

    Bioengn Changsha 410083 Hunan Peoples R China;

    Cent S Univ Sch Minerals Proc &

    Bioengn Changsha 410083 Hunan Peoples R China;

    Cent S Univ Sch Minerals Proc &

    Bioengn Changsha 410083 Hunan Peoples R China;

    Cent S Univ Sch Minerals Proc &

    Bioengn Changsha 410083 Hunan Peoples R China;

    Cent S Univ Sch Minerals Proc &

    Bioengn Changsha 410083 Hunan Peoples R China;

    Cent S Univ Sch Publ Hlth Management Changsha Hunan Peoples R China;

    Cent S Univ Sch Minerals Proc &

    Bioengn Changsha 410083 Hunan Peoples R China;

    CSIRO Mineral Resources Clayton Vic Australia;

    Cent S Univ Sch Minerals Proc &

    Bioengn Changsha 410083 Hunan Peoples R China;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 冶金技术 ;
  • 关键词

    Adsorption; Sulfobacillus thermosulfidooxidans strain ST; Extracellular DNA; Chalcopyrite; In situ observation and monitoring;

    机译:吸附;磺嘧虫热氟苯脱毒素菌株ST;细胞外DNA;核黄素;原位观察和监测;

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