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一种基于系统的方法用于通过促进金生物浸出来实现氰化物过量产生 。

A Systems-Based Approach for Cyanide Overproduction by for Gold Bioleaching Enhancement.

作者信息

Aminian-Dehkordi Javad, Mousavi Seyyed Mohammad, Marashi Sayed-Amir, Jafari Arezou, Mijakovic Ivan

机构信息

Biotechnology Group, Department of Chemical Engineering, Tarbiat Modares University, Tehran, Iran.

Department of Biotechnology, College of Science, University of Tehran, Tehran, Iran.

出版信息

Front Bioeng Biotechnol. 2020 Jun 3;8:528. doi: 10.3389/fbioe.2020.00528. eCollection 2020.

Abstract

With the constant accumulation of electronic waste, extracting precious metals contained therein is becoming a major challenge for sustainable development. is currently one of the microbes used for the production of cyanide, which is the main leaching agent for gold recovery. The present study aimed to propose a strategy for metabolic engineering of to overproduce cyanide, and thus ameliorate the bioleaching process. For this, we employed constraint-based modeling, running simulations on JA1121, the genome-scale metabolic model of DSM319. Flux balance analysis (FBA) was initially used to identify amino acids to be added to the culture medium. Considering cyanide as the desired product, we used growth-coupled methods, constrained minimal cut sets (cMCSs) and OptKnock to identify gene inactivation targets. To identify gene overexpression targets, flux scanning based on enforced objective flux (FSEOF) was performed. Further analysis was carried out on the identified targets to determine compounds with beneficial regulatory effects. We have proposed a chemical-defined medium for accelerating cyanide production on the basis of microplate assays to evaluate the components with the greatest improving effects. Accordingly, the cultivation of DSM319 in a chemically-defined medium with 5.56 mM glucose as the carbon source, and supplemented with 413 μM cysteine, led to the production of considerably increased amounts of cyanide. Bioleaching experiments were successfully performed in this medium to recover gold and copper from telecommunication printed circuit boards. The results of inductively coupled plasma (ICP) analysis confirmed that gold recovery peaked out at around 55% after 4 days, whereas copper recovery continued to increase for several more days, peaking out at around 85%. To further validate the bioleaching results, FESEM, XRD, FTIR, and EDAX mapping analyses were performed. We concluded that the proposed strategy represents a viable route for improving the performance of the bioleaching processes.

摘要

随着电子废弃物的不断积累,提取其中所含的贵金属正成为可持续发展面临的一项重大挑战。目前是用于生产氰化物的微生物之一,氰化物是黄金回收的主要浸出剂。本研究旨在提出一种对进行代谢工程改造以过量生产氰化物的策略,从而改善生物浸出过程。为此,我们采用基于约束的建模方法,在DSM319的基因组规模代谢模型JA1121上进行模拟。通量平衡分析(FBA)最初用于确定添加到培养基中的氨基酸。将氰化物视为目标产物,我们使用生长偶联方法、约束最小割集(cMCSs)和OptKnock来确定基因失活靶点。为了确定基因过表达靶点,进行了基于强制目标通量的通量扫描(FSEOF)。对确定的靶点进行进一步分析,以确定具有有益调节作用的化合物。我们基于微孔板试验提出了一种化学限定培养基,以评估具有最大改善效果的成分,从而加速氰化物的生产。因此,在以5.56 mM葡萄糖作为碳源并补充413 μM半胱氨酸的化学限定培养基中培养DSM319,导致氰化物产量大幅增加。在该培养基中成功进行了生物浸出实验,以从电信印刷电路板中回收金和铜。电感耦合等离子体(ICP)分析结果证实,4天后金回收率在55%左右达到峰值,而铜回收率在接下来的几天里持续增加,在85%左右达到峰值。为了进一步验证生物浸出结果,进行了场发射扫描电子显微镜(FESEM)、X射线衍射(XRD)、傅里叶变换红外光谱(FTIR)和能谱分析(EDAX)映射分析。我们得出结论,所提出的策略是提高生物浸出过程性能的可行途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/172a/7283520/fa4b8bd79665/fbioe-08-00528-g0001.jpg

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