Glutamine replenishment and ammonia removal in hybridoma cell cultures via immobilized glutamine synthetase
| dc.contributor.author | Okeson, Carl D. | |
| dc.creator | Okeson, Carl D. | en_US |
| dc.date.accessioned | 2013-04-03T13:34:03Z | |
| dc.date.available | 2013-04-03T13:34:03Z | |
| dc.date.issued | 1999 | en_US |
| dc.identifier.uri | http://hdl.handle.net/10150/278706 | |
| dc.description.abstract | Hybridoma cells utilize glutamine as their primary nitrogen source and excrete ammonia as a metabolic waste product. This ammonia can quickly accumulate to toxic levels in hybridoma culture media, and can severely reduce monoclonal antibody production (Ozturk et al., 1991). The enzyme glutamine synthetase (E.C. 6.3.1.2), which catalyzes the reaction UNFORMATTED EQUATION FOLLOWS: NH₄⁺ + L-glutamate + ATP Mg²⁺ → L-glutamine + ADP +Pᵢ +H⁺, UNFORMATTED EQUATION ENDS was evaluated as a means of reducing ammonia and replenishing glutamine in hybridoma culture medium. The effect of each enzyme reactant on soluble glutamine synthetase activity was quantified, and enzymatic reaction equilibrium evaluated. Enzyme reaction rates in two culture media, both with and without serum, were compared. Glutamine synthetase was immobilized via three different methods, and their effects compared. Cell sensitivity to each enzymatic reactant was studied. Finally, immobilized glutamine synthetase was incorporated in a hybridoma cultivation, and its effect on culture characteristics evaluated. | |
| dc.language.iso | en_US | en_US |
| dc.publisher | The University of Arizona. | en_US |
| dc.rights | Copyright © is held by the author. Digital access to this material is made possible by the University Libraries, University of Arizona. Further transmission, reproduction or presentation (such as public display or performance) of protected items is prohibited except with permission of the author. | en_US |
| dc.subject | Chemistry, Biochemistry. | en_US |
| dc.subject | Chemistry, Biochemistry. | en_US |
| dc.title | Glutamine replenishment and ammonia removal in hybridoma cell cultures via immobilized glutamine synthetase | en_US |
| dc.type | text | en_US |
| dc.type | Thesis-Reproduction (electronic) | en_US |
| thesis.degree.grantor | University of Arizona | en_US |
| thesis.degree.level | masters | en_US |
| dc.identifier.proquest | 1396517 | en_US |
| thesis.degree.discipline | Graduate College | en_US |
| thesis.degree.discipline | Agricultural & Biosystems Engineering | en_US |
| thesis.degree.name | M.S. | en_US |
| dc.identifier.bibrecord | .b39916881 | en_US |
| refterms.dateFOA | 2018-08-27T16:05:54Z | |
| html.description.abstract | Hybridoma cells utilize glutamine as their primary nitrogen source and excrete ammonia as a metabolic waste product. This ammonia can quickly accumulate to toxic levels in hybridoma culture media, and can severely reduce monoclonal antibody production (Ozturk et al., 1991). The enzyme glutamine synthetase (E.C. 6.3.1.2), which catalyzes the reaction UNFORMATTED EQUATION FOLLOWS: NH₄⁺ + L-glutamate + ATP Mg²⁺ → L-glutamine + ADP +Pᵢ +H⁺, UNFORMATTED EQUATION ENDS was evaluated as a means of reducing ammonia and replenishing glutamine in hybridoma culture medium. The effect of each enzyme reactant on soluble glutamine synthetase activity was quantified, and enzymatic reaction equilibrium evaluated. Enzyme reaction rates in two culture media, both with and without serum, were compared. Glutamine synthetase was immobilized via three different methods, and their effects compared. Cell sensitivity to each enzymatic reactant was studied. Finally, immobilized glutamine synthetase was incorporated in a hybridoma cultivation, and its effect on culture characteristics evaluated. |
