Environmental Engineering and Earth Sciences, Clemson University, 168 Rich Laboratory, Anderson, South Carolina 29625, United States.
Environ Sci Technol. 2011 Apr 1;45(7):3012-8. doi: 10.1021/es103362k. Epub 2011 Mar 8.
Anaerobic mineralization of tert-butyl alcohol (TBA) and methyl tert-butyl ether (MTBE) were studied in sediment incubations prepared with fuel-contaminated aquifer material. Microbial community compositions in all incubations were characterized by amplified ribosomal DNA restriction analysis (ARDRA). The aquifer material mineralized 42.3±9.9% of [U-(14)C]-TBA to 14CO2 without electron acceptor amendment. Fe(III), sulfate, and Fe(III) plus anthraquinone-2,6-disulfonate addition also promoted U-[14C]-TBA mineralization at levels similar to those of the unamended controls. Nitrate actually inhibited TBA mineralization relative to unamended controls. In contrast to TBA, [U-(14)C]-MTBE was not significantly mineralized in 400 days regardless of electron acceptor amendment. Microbial community analysis indicated that the abundance of one dominant clone group correlated closely with anaerobic TBA mineralization. The clone was phylogenetically distinct from known aerobic TBA-degrading microorganisms, Fe(III)- or sulfate-reducing bacteria. It was most closely associated with organisms belonging to the alphaproteobacteria. Microbial communities were different in MTBE and TBA amended incubations. Shannon indices and Simpson indices (statistical community comparison tools) both demonstrated that microbial community diversity decreased in incubations actively mineralizing TBA, with distinct "dominant" clones developing. These data contribute to our understanding of anaerobic microbial transformation of fuel oxygenates in contaminated aquifer material and the organisms that may catalyze the reactions.
采用受燃料污染的含水层物质制备沉积物培养物,研究了叔丁醇(TBA)和甲基叔丁基醚(MTBE)的厌氧矿化作用。所有培养物中的微生物群落组成均通过扩增核糖体 DNA 限制分析(ARDRA)进行了表征。含水层物质在未添加电子受体的情况下,将 42.3±9.9%的 [U-(14)C]-TBA 矿化为 14CO2。Fe(III)、硫酸盐和 Fe(III)加蒽醌-2,6-二磺酸钠的添加也促进了 U-[14C]-TBA 的矿化,其水平与未添加的对照相似。与未添加的对照相比,硝酸盐实际上抑制了 TBA 的矿化。与 TBA 相反,[U-(14)C]-MTBE 无论是否添加电子受体,在 400 天内均未被显著矿化。微生物群落分析表明,一个优势克隆群的丰度与厌氧 TBA 矿化密切相关。该克隆与已知的好氧 TBA 降解微生物、Fe(III)或硫酸盐还原菌在系统发育上不同。它与属于α变形菌的生物最为密切相关。在 MTBE 和 TBA 加标培养物中,微生物群落不同。Shannon 指数和 Simpson 指数(统计群落比较工具)均表明,在积极矿化 TBA 的培养物中,微生物群落的多样性降低,形成了独特的“优势”克隆。这些数据有助于我们了解受污染含水层物质中燃料含氧物的厌氧微生物转化以及可能催化反应的生物。