Premium
Metabolic flux analysis of hybridoma cells in different culture media using mass balances
Author(s) -
Bonarius Hendrik P. J.,
Hatzimanikatis Vassily,
Meesters Koen P. H.,
de Gooijer Cornelis D.,
Schmid Georg,
Tramper Johannes
Publication year - 1996
Publication title -
biotechnology and bioengineering
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.136
H-Index - 189
eISSN - 1097-0290
pISSN - 0006-3592
DOI - 10.1002/(sici)1097-0290(19960505)50:3<299::aid-bit9>3.0.co;2-b
Subject(s) - metabolic flux analysis , amino acid , intracellular , biochemistry , flux (metallurgy) , chemistry , metabolism , hydrolysate , metabolic pathway , hydrolysis , organic chemistry
Abstract The estimation of the intracellular fluxes of mammalian cells using only the mass balances of the relevant metabolites is not possible because the set of linear equations defined by these mass balances is underdetermined. Either additional experimental flux data or additional theoretical constraints are required to find one unique flux distribution out of the solution space that is bound by the mass balances. Here, a method is developed using the latter approach. The uptake and production rates of amino acids, glucose, lactate, O 2 , CO 2 , NH 4 , MAB, and the intracellular amino acid pools have been determined for two different steady‐states. The cellular composition {total protein and protein composition, total lipids and fatty acid distribution, total carbohydrates, DNA and RNA} has been measured to calculate the requirements for biosynthesis. It is shown to be essential to determine the uptake/production rates of ammonia and either carbon dioxide or oxygen. In mammalian cells these are cometabolites of cyclic metabolic pathways. The flux distribution that is found using the Euclidean minimum norm as the additional theoretical constraint and taking either the CO 2 or the NAD(P)H mass balance into account is shown to be in agreement with the measured O 2 and CO 2 metabolic rates. The metabolic fluxes in hybridoma cells in continuous culture at a specific growth rate of 0.83 day −1 are estimated for a medium with (optimal medium) and without (suboptimal medium) Primatone RL, an enzymatic hydrolysate of animal tissue that causes a more than twofold increase in cell density. It is concluded that (i) The majority of the consumed glucose (>90%) is channeled through the pentose‐phosphate pathway in rapidly proliferating cells. (ii) Pyruvate oxidation and tricarboxylic acid (TCA) cycle activity are relatively low, i.e., 8% of the glucose uptake in suboptimal and 14% in optimal medium, respectively. Under both conditions, only a small fraction of pyruvate is further oxidized to CO 2 . (iii) The flux from glutamate to α‐ketoglutarate (catalyzed by glutamate dehydrogenase) is almost zero in medium with and even slightly reversed in medium without Primatone RL. Almost all glutamate enters the TCA cycle due to the action of transaminases. (iv) Transhydrogenation plays a significant role in hybridoma cells under our experimental conditions. NADPH is produced at relatively high rates (11 × 10 −12 to 13 × 10 −12 mol · cell −1 · day −1 ) compared to other fluxes in both culture media. © 1996 John Wiley & Sons, Inc.