Thesis (Ph.D.) OGI School of Science & Engineering at OHSU, January 2007. / Abstract: leaf x. Includes bibliographical references (leaves 124-138).

Thesis (Ph. D.)--Virginia Polytechnic Institute and State University, 1992. / Vita. Abstract. Includes bibliographical references (leaves 165-177). Also available via the Internet.

Mycobacterium vaccae JOB5 and Graphium sp. were studied to evaluate their ability to cometabolize methyl tert-butyl ether (MTBE) and its metabolites after growth on two different alkanes, propane and iso-pentane. Both cultures were capable of cometabolizing MTBE and the metabolites, tert-butyl formate (TBF) and tert-butyl alcohol (TBA). MTBE, TBF, and TBA did not support growth of either microbe. Higher degradation rates were obtained in the bacterial system when the cultures were grown on iso-pentane. Nonlinear least squares regression and direct linear plot methods were used to estimate kinetic coefficients and provided comparable results. The enzymes from Mycobacterium vaccae JOB5 and Graphium sp. that promote the cometabolism of MTBE and its metabolites exhibited similar kinetics and substrate inhibition. The presence of the substrate decreased the degradation rate of MTBE and TBA suggesting competitive inhibition and preference for the substrate. Blockage experiment with acetylene suggested the presence of an alkane monooxygenase for the metabolism of MTBE and TBA, and a hydrolytic enzyme for the degradation of TBF. The presence of a hydrolase enzyme was supported by the fact that TBF was degraded to TBA under either aerobic or anaerobic conditions and was not inhibited by the presence of acetylene, propane, or isopentane. Measured rates of abiotic hydrolysis of TBF were significantly less than biodegradation rates. Acetylene acted as a reversible inhibitor for both cultures when tested in the presence of the growth media and as an inactivator when tested in the presence of a phosphate solution for the bacterial system. Growth-batch reactor experiments were conducted to compare the degradation of iso-pentane and MTBE with the predicted degradation rates based upon kinetic constants determined from single and dual-compound experiments. Experimental data was modeled with Monod kinetics and STELLA�� software. Reasonable predictions of reactor performance were achieved when Monod maximum utilization rates were increased compared to single and dual-compound experiments. / Graduation date: 2002

Thesis (Ph. D.)--University of Hong Kong, 2005. / Title proper from title frame. Also available in printed format.

published_or_final_version / abstract / Ecology and Biodiversity / Doctoral / Doctor of Philosophy

Thesis (Ph. D.)--Rutgers University, 2009. / "Graduate Program in Microbiology and Molecular Genetics." Includes bibliographical references (p. 112-131).

Thesis (Ph. D.)--Michigan State University. Dept. of Sociology, 2008. / Title from PDF t.p. (viewed on Apr. 16, 2009) Includes bibliographical references (p. 173-198). Also issued in print.

No description available.

Thesis (Ph. D.)--Rutgers University, 2010. / "Graduate Program in Environmental Sciences." Includes bibliographical references (p. 141-155).

Tertiary butyl alcohol (TBA), methyl tertiary butyl ether (MTBE) and ethyl tertiary butyl ether (ETBE) are compounds with the potential for use as oxygenates in reformulated gasolines. Being relatively soluble in water, these organics, if accidentally discharged into the subsurface, may rapidly spread and pose threats to groundwater. The purpose of this work was to evaluate the biodegradation potential of these oxygenates in soils and to determine the influence of subsurface environments on their degradation. Biodegradation was evaluated in static soil/water microcosms. Aquifer material was collected from various depths at three sites with different soil characteristics. Potential electron acceptors including O₂ in the form of H₂O₂, nitrate or sulfate were added to induce the desired metabolism (aerobic respiration, denitrification, sulfate reduction, or methanogenesis). In each metabolic process, the influence of several subsurface environmental factors on biodegradation was investigated. The data show that biodegradation potential of MTBE, ETBE and TBA varied substantially with site and depth. TBA was the easiest compound to biodegrade, whereas MTBE was the most recalcitrant. Cleavage of the ether bond is the first and rate-limiting step in the degradation of ETBE and possibly MTBE. Addition of H₂O₂, caused chemical oxidation of MTBE and ETBE. The chemical oxidation was faster in the organically rich soils, but slower in the organic-poor soils. Soil microorganisms were able to catalyze the cleavage of the ether bond in ETBE but not MTBE. This biological reaction was not significant when chemical oxidation occurred. TBA, on the other hand, was aerobically biodegraded in all soils. Under denitrifying and anaerobic conditions TBA degradation occurred in all soils but the degradation of ETBE and MTBE was only observed at one of three sites. TBA degradation was enhanced by nutrient addition in the nutrient-poor soil but hindered by the presence of other easily-degraded organic compounds. Degradation of MTBE and ETBE occurred only in soils containing low organic matter with a pH around 5.5. No degradation of MTBE and ETBE was observed in the organic-rich soils and in the organically poor soils, the addition of ethanol inhibited MTBE and ETBE degradation. / Ph. D.