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Monitoring the Metabolic Status of Geobacter Species in Contaminated Groundwater by Quantifying Key Metabolic Proteins with Geobacter-Specific Antibodies

机译:通过使用特定于土壤细菌的抗体定量关键代谢蛋白来监测受污染的地下水中土壤细菌物种的代谢状况

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Simple and inexpensive methods for assessing the metabolic status and bioremediation activities of subsurface microorganisms are required before bioremediation practitioners will adopt molecular diagnosis of the bioremediation community as a routine practice for guiding the development of bioremediation strategies. Quantifying gene transcripts can diagnose important aspects of microbial physiology during bioremediation but is technically challenging and does not account for the impact of translational modifications on protein abundance. An alternative strategy is to directly quantify the abundance of key proteins that might be diagnostic of physiological state. To evaluate this strategy, an antibody-based quantification approach was developed to investigate subsurface Geobacter communities. The abundance of citrate synthase corresponded with rates of metabolism of Geobacter bemidjiensis in chemostat cultures. During in situ bioremediation of uranium-contaminated groundwater the quantity of Geobacter citrate synthase increased with the addition of acetate to the groundwater and decreased when acetate amendments stopped. The abundance of the nitrogen-fixation protein, NifD, increased as ammonium became less available in the groundwater and then declined when ammonium concentrations increased. In a petroleum-contaminated aquifer, the abundance of BamB, an enzyme subunit involved in the anaerobic degradation of mono-aromatic compounds by Geobacter species, increased in zones in which Geobacter were expected to play an important role in aromatic hydrocarbon degradation. These results suggest that antibody-based detection of key metabolic proteins, which should be readily adaptable to standardized kits, may be a feasible method for diagnosing the metabolic state of microbial communities responsible for bioremediation, aiding in the rational design of bioremediation strategies.
机译:在生物修复从业人员将生物修复群落的分子诊断作为指导生物修复策略发展的常规方法之前,需要一种简单且廉价的方法来评估地下微生物的代谢状态和生物修复活性。量化基因转录本可以诊断生物修复过程中微生物生理学的重要方面,但是在技术上具有挑战性,并且不能解释翻译修饰对蛋白质丰度的影响。一种替代策略是直接量化可能诊断生理状态的关键蛋白质的含量。为了评估该策略,开发了一种基于抗体的定量方法来研究地下地下细菌群落。柠檬酸盐合酶的丰度与化学恒温器培养物中的贝米吉球菌的代谢速率相对应。在铀污染的地下水的原位生物修复过程中,柠檬酸盐合成酶的数量随向水中添加乙酸盐而增加,而当乙酸盐修正剂停止时,其数量减少。氮固定蛋白NifD的丰度随着地下水中铵态氮含量的增加而增加,然后随着铵盐浓度的增加而下降。在受石油污染的含水层中,BamB(一种参与土壤杆菌物种对单芳族化合物的厌氧降解的酶亚基)的丰度在预计土壤杆菌在芳烃降解中起重要作用的区域中会增加。这些结果表明,关键代谢蛋白的基于抗体的检测应易于适应标准化试剂盒,可能是诊断负责生物修复的微生物群落代谢状态的可行方法,有助于合理设计生物修复策略。

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