Mathematical models for biodegradation of chlorinated solvents. 1: Model framework
X. Zhang, Samir K. Banerji, R. Bajpai
Abstract
X. Zhang, Samir K. Banerji, R. Bajpai
Abstract
Complete mineralization of chlorinated solvents by microbial action has been demonstrated under aerobic as well as anaerobic conditions. In most of the cases, it is believed that the biodegradation is initiated by broad-specificity enzymes involved in metabolism of a primary substrate. Under aerobic conditions, some of the primary carbon and energy substrates are methane, propane, toluene, phenol, and ammonia; under anaerobic conditions, glucose, sucrose, acetate, propionate, isopropanol, methanol, and even natural organics act as the carbon source. Published biochemical studies suggest that the limiting step is often the initial part of the biodegradation pathway within the microbial system. For aerobic systems, the limiting step is thought to be the reaction catalyzed by mono- and dioxygenases which are induced by most primary substrates, although some constitutive strains have been reported. Other critical features of the biodegradative pathway include: (1) activity losses of critical enzyme(s) through the action of metabolic byproducts, (2) energetic needs of contaminant biodegradation which must be met by catabolism of the primary substrates, (3) changes in metabolic patterns in mixed cultures found in nature depending on the availability of electron acceptors, and (4) the associated accumulation and disappearance of metabolic intermediates. Often, the contaminant pool itself consists ofmore » several chlorinated solvents with separate and interactive biochemical needs. The existing models address some of the issues mentioned above. However, their ability to successfully predict biological fate of chlorinated solvents in nature is severely limited due to the existing mathematical models. Limiting step(s), inactivation of critical enzymes, recovery action, energetics, and a framework for multiple degradative pathways will be presented as a comprehensive model. 91 refs.« less
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Complete mineralization of chlorinated solvents by microbial action has been demonstrated under aerobic as well as anaerobic conditions. In most of the cases, it is believed that the biodegradation is initiated by broad-specificity enzymes involved in metabolism of a primary substrate. Under aerobic conditions, some of the primary carbon and energy substrates are methane, propane, toluene, phenol, and ammonia; under anaerobic conditions, glucose, sucrose, acetate, propionate, isopropanol, methanol, and even natural organics act as the carbon source. Published biochemical studies suggest that the limiting step is often the initial part of the biodegradation pathway within the microbial system. For aerobic systems, the limiting step is thought to be the reaction catalyzed by mono- and dioxygenases which are induced by most primary substrates, although some constitutive strains have been reported. Other critical features of the biodegradative pathway include: (1) activity losses of critical enzyme(s) through the action of metabolic byproducts, (2) energetic needs of contaminant biodegradation which must be met by catabolism of the primary substrates, (3) changes in metabolic patterns in mixed cultures found in nature depending on the availability of electron acceptors, and (4) the associated accumulation and disappearance of metabolic intermediates. Often, the contaminant pool itself consists ofmore » several chlorinated solvents with separate and interactive biochemical needs. The existing models address some of the issues mentioned above. However, their ability to successfully predict biological fate of chlorinated solvents in nature is severely limited due to the existing mathematical models. Limiting step(s), inactivation of critical enzymes, recovery action, energetics, and a framework for multiple degradative pathways will be presented as a comprehensive model. 91 refs.« less
Key concepts: Biodegradation, Chemistry, Primary (astronomy), Anaerobic exercise, Metabolic pathway, Organic chemistry, Environmental chemistry, Enzyme