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Mechanistic studies on enzymatic nitroarene reduction and implications for the fate of nitroarene mixtures in redox-stratified biofilm.

机译:酶催化硝基芳烃还原的机理研究及其对氧化还原分层生物膜中硝基芳烃混合物的结局的影响。

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摘要

At military bases and munitions factories, 2,A,6-trinitrotoluene (TNT), 2,4-dinitrotoluene (24DNT), and 2,6-dinitrotoluene (26DNT) are persistent soil and groundwater contaminants. Although the reduction of nitro groups in these compounds has been extensively investigated, few researchers have studied the link between the reduction rates and the electrochemical properties of these compounds. In this work, the standard one-electron redox potentials at pH 7 (E1°') for TNT and related nitroorenes were measured for the first time by pulse rodiolysis. The reduction kinetics were investigated using a bacterial nitroreduclase. Contrary to most whole cell studies wherein amino group formation has been observed, nitro group reduction halted at the level of the hydroxylamino group. A linear free energy relationship was observed between the enzymatic reduction rates and the E1°' values. Enzymatic TNT reduction did not obey simple Michoelis-Menten kinetics, and clear evidence of enzyme inactivation during TNT transformation was obtained.; Batch experiments were conducted to test whether 2-amino-4,6-dinitrotoluene, 4-amino-2,6-dinitrotoluene, and 2,4-diamino-6-nitrotoluene, potential TNT degradation products, were aerobically transformed by a mixed culture that mineralizes DNTs. None of the compounds were degraded to any extent when provided as sole carbon and nitrogen sources or when DNTs were provided as primary substrate. 26DNT degradation was inhibited in the presence of 4-amino-2,6-dinitrotoluene.; As a first step in testing the feasibility of using a redox-stratified biofilm for simultaneous DNT and TNT mineralization, a comprehensive biofilm model was developed. A novel model form was derived to depict nitroarene reduction as a function of the compound E1°' and the intracellular NADH concentration, an indicator for solution redox potential. Using the comprehensive biofilm model, several reactor types (fluidized bed, hollow fiber membrane, and extractive membrane) were investigated. Model results suggested that membrane biofilm reactors are most effective because they promote thicker biofilm growth and redox stratification. A sensitivity analysis demonstrated that additional investigation of aminodinitrotoluene mineralization, oxygen limitation, and ozoxy dimer production ore necessary to better predict this technology. This model will guide application of this treatment process, as more mechanistic detail becomes available. However, these model results are preliminary due to several assumptions that require more stringent validation.
机译:在军事基地和军需品工厂,2,A,6-三硝基甲苯(TNT),2,4-二硝基甲苯(24DNT)和2,6-二硝基甲苯(26DNT)是持久的土壤和地下水污染物。尽管已经广泛研究了这些化合物中硝基的还原,但是很少有研究者研究这些化合物的还原速率和电化学性质之间的联系。在这项工作中,首次通过脉冲热解法测量了TNT和相关硝基酮在pH 7(E1°')下的标准单电子氧化还原电势。使用细菌硝基还原酶研究还原动力学。与大多数已观察到氨基形成的全细胞研究相反,硝基还原在羟氨基水平停止。在酶促还原速率和E1°'值之间观察到线性自由能关系。酶促TNT的降低没有遵循简单的Michoelis-Menten动力学,并且获得了在TNT转化过程中酶失活的明确证据。进行分批实验以测试通过混合培养是否有氧转化了2-氨基-4,6-二硝基甲苯,4-氨基-2,6-二硝基甲苯和2,4-二氨基-6-硝基甲苯(可能的TNT降解产物)使DNT矿化。当作为唯一的碳和氮源提供或当DNT作为主要底物提供时,没有一种化合物在任何程度上降解。在4-氨基-2,6-二硝基甲苯的存在下抑制了26DNT的降解。作为测试使用氧化还原分层生物膜同时进行DNT和TNT矿化的可行性的第一步,开发了一个全面的生物膜模型。得出了新的模型形式来描述硝基芳烃的还原与化合物E1''和细胞内NADH浓度(溶液氧化还原电势指标)的关系。使用综合的生物膜模型,研究了几种反应器类型(流化床,中空纤维膜和萃取膜)。模型结果表明,膜生物膜反应器最有效,因为它们可促进较厚的生物膜生长和氧化还原分层。敏感性分析表明,对氨基二硝基甲苯矿化,氧限制和盎司氧化二聚体生产矿石的进一步研究是更好地预测该技术所必需的。随着更多机械细节的出现,该模型将指导该处理过程的应用。但是,由于一些需要更严格验证的假设,这些模型结果是初步的。

著录项

  • 作者

    Riefler, Roger Guy.;

  • 作者单位

    University of Connecticut.;

  • 授予单位 University of Connecticut.;
  • 学科 Engineering Environmental.
  • 学位 Ph.D.
  • 年度 1999
  • 页码 257 p.
  • 总页数 257
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 环境污染及其防治;
  • 关键词

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