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dc.contributor.advisorSuflita, Joseph M.,en_US
dc.contributor.authorLondry, Kathleen Louise.en_US
dc.date.accessioned2013-08-16T12:29:32Z
dc.date.available2013-08-16T12:29:32Z
dc.date.issued1997en_US
dc.identifier.urihttps://hdl.handle.net/11244/5435
dc.description.abstractThe toxicity and biodegradation of mixtures of thiols, thiophenes, thiophenic acids and aromatic sulfides were determined under anaerobic conditions. Toxicity effects were dependent on the structure of the organosulfur compounds, the amounts added to cultures, and the available electron acceptor. The anaerobic biodegradation of eight different organothiols was observed under nitrate-reducing conditions but not methanogenic or sulfate-reducing conditions. Degradation of hexanethiol was linked to nitrate reduction and nitrite production.en_US
dc.description.abstractFor biodegradation studies, enrichment cultures were established with target compounds added singly or as mixtures, often in a hydrophobic carrier. The degradation of compounds such as n-alkanes, n-alkanols, and n-alkcanoic acids depended on chemical structure as well as redox potential. n-alkanoic acids were degraded faster than n-alkanols, whereas n-alkanes were not metabolized. The susceptibility of n-alkanols and n-alkanoic acids to degradation was chain-length dependent. Alkanols were transformed to the corresponding alkanoic acids, and the formation of esters as a minor fate process was also noted.en_US
dc.description.abstractThe anaerobic degradation of a variety of aromatic compounds was investigated with the sulfate-reducing bacterium Desulfotomaculum strain Groll. Initial steps of metabolic pathways for the degradation of m- and p-cresol were proposed. Degradation of both isomers proceeded by hydroxylation of the methyl groups to yield hydroxybenzyl alcohols which were further oxidized to hydroxybenzoic acids then metabolized as benzoyl-coenzyme A thioesters. These proposed pathways were supported by substrate degradation profiles, detection of metabolites, and biochemical studies. Although strain Groll degraded these cresol isomers by similar reactions, the enzymes catalyzing the oxidation of the meta and para isomers were biochemically distinct.en_US
dc.description.abstractA variety of compounds associated with petroleum and petroleum-derived wastes were examined for their susceptibility to biodegradation under methanogenic, sulfate-reducing, and nitrate-reducing conditions. Inocula from chronically contaminated environments were used to explore the limits of anaerobic degradation potential. In addition, an ecological approach to the prevention of sulfide emissions was evaluated. Nitrate was added to oily sludge incubations to test its efficacy in preventing sulfidogenesis by sulfate-reducing bacteria. Nitrate inhibited sulfate reduction in a concentration-dependent manner, and reduced sulfide concentrations under a variety of salinity conditions.en_US
dc.format.extentxviii, 174 leaves :en_US
dc.subjectAnaerobic bacteria.en_US
dc.subjectEnvironmental Sciences.en_US
dc.subjectAromatic compounds Biodegradation.en_US
dc.subjectBiology, Microbiology.en_US
dc.titleThe anaerobic biodegradation of petroleum-related compounds.en_US
dc.typeThesisen_US
dc.thesis.degreePh.D.en_US
dc.thesis.degreeDisciplineDepartment of Microbiology and Plant Biologyen_US
dc.noteAdviser: Joseph M. Suflita.en_US
dc.noteSource: Dissertation Abstracts International, Volume: 58-02, Section: B, page: 0526.en_US
ou.identifier(UMI)AAI9721055en_US
ou.groupCollege of Arts and Sciences::Department of Microbiology and Plant Biology


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