Abstract
Summary
Over 90% of C14 fixed by HeLa or conjunctival cells growing in a trisbuffered nutrient medium containing 5 micro-curies of NaHC14O3 per 10 ml was recovered in the acid soluble and nucleic acid fractions. Most of this activity was found associated with the purines and the pyrimidines of such cells. The ribonucleosides were partially effective as a substitute for CO2 in supporting cell multiplication. A combination of ribosides and oxaloacetate provided conditions as good as or better than CO2 for multiplication of CO2-depleted conjunctival cells. It may be concluded that, under the described experimental conditions, the chief functions of CO2 in human cells are to provide specific precursors for syntheses of the purines, the pyrimidines and oxaloacetate.
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