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Development of a method to assay the microbial population in heap bioleaching operations

机译:堆生物浸提操作中微生物种群分析方法的开发

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Heap bioleaohing is an economically viable approach to the mining of low-grade ores. Oxidation is microbially assisted, involving a consortium of microorganisms that together span the mesophilic to extreme thetmophilic range of temperatures (25-80 deg C). Temperatures inside the heap are not externally regulated, making the microbial interactions difficult to predict. In order to gain insight into these interactions, a qualitative and quantitative assay of the microorganisms that colonise the ore surface or are present in the liquid phase between the ore clusters at different levels within a heap has been developed. This method was developed using crude ore and liquid samples obtained from the GeoBiotics temperature controlled mesophilic heap operation at the Agnes Gold Mine in Barberton, South Africa, and the high temperature test columns at SGS Lakefield Research, Johannesburg, South Africa. This method of sample analysis may be applied to bioheap leach operations with and without temperature control. Ease of application, reproducibility and turn around time influenced technique design in order to provide a useful assay for commercial bioleaching operations. Following microbial removal from the solid phase using successive washes with detergent and acidified water, the cells were enumerated and genetic DNA was isolated. Microbial identification was achieved via restriction endonudease analysis of the 16S rRNA genes, as well as 16S rRNA gene sequencing where necessaiy. Quantification was achieved using species-and genus-specific probes through fluorescent in situ hybridisation (FISH).
机译:堆生物浸出法是开采低品位矿石的一种经济可行的方法。氧化是由微生物协助的,涉及一群微生物,它们共同跨越了中温至极端嗜温范围的温度(25-80摄氏度)。堆内的温度不受外部调节,因此很难预测微生物之间的相互作用。为了深入了解这些相互作用,已经开发了定性和定量测定微生物的方法,这些微生物定居在矿石表面或存在于堆中不同水平的矿石簇之间的液相中。该方法是使用从南非Barberton的Agnes金矿的GeoBiotics温控中温堆操作以及南非Johannesburg的SGS Lakefield Research的高温测试柱获得的粗矿石和液体样品开发的。这种样品分析方法可以应用于有和没有温度控制的生物堆浸操作。易于应用,可重复性和周转时间影响了技术设计,以便为商业生物浸出操作提供有用的检测方法。通过使用去污剂和酸化水连续洗涤从固相中去除微生物后,对细胞进行计数并分离出遗传DNA。通过对16S rRNA基因进行限制性内切酶分析以及必要时进行16S rRNA基因测序来实现微生物鉴定。使用物种和属特异性探针通过荧光原位杂交(FISH)进行定量。

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