Abstract
Mass analysis was used to determine the amount of acetate which is totally synthesized from (13)CO(2) during fermentations by Clostridium formicoaceticum, C. acidiurici, C. cylindrosporum, Butyribacterium rettgeri, and Diplococcus glycinophilus. In the fermentation of fructose by C. formicoaceticum, 27% of the acetate was found to be totally synthesized from CO(2), and the remaining acetate was unlabeled, having been formed from fructose. Evidence is presented that the purine-fermenting organisms, C. acidiurici and C. cylindrosporum, totally synthesized about 9% of the acetate from CO(2), and that the methyl group of an additional 9% was formed from CO(2). The remaining acetate was formed from the carbons of the purine and not via CO(2). It has been postulated that the fermentation of the purines and synthesis of acetate from CO(2) both occur via derivatives of tetrahydrofolate. Evidence is presented that a compartmentalization of these folate intermediates is required if both the purine degradation and the CO(2) utilization involve identical intermediates. Neither B. rettgeri nor D. glycinophilus incorporated sufficient (13)CO(2) into acetate to allow determination of the types of acetate by mass analysis, although they did incorporate labeled (14)CO(2) in both positions of acetate.
MeSH Terms
Acetates/analysis,biosynthesis,isolation & purification
Anaerobiosis
Butyrates/biosynthesis
Carbon Dioxide/metabolism
Carbon Isotopes
Chemical Phenomena
Chemistry
Chromatography
Clostridium/growth & development,metabolism
Culture Media
Eubacterium/growth & development,metabolism
Fermentation
Formates/biosynthesis
Fructose/metabolism
Glucose/metabolism
Glycine/metabolism
Hypoxanthines/metabolism
Lactates/biosynthesis
Mass Spectrometry
Peptococcus/growth & development,metabolism
Phenolphthaleins
Species Specificity
Spectrophotometry
Chemicals
Acetates
Butyrates
Carbon Isotopes
Culture Media
Formates
Hypoxanthines
Lactates
Phenolphthaleins
Carbon Dioxide
Fructose
Glucose
Glycine
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Schulman M
Parker D
Ljungdahl L G
Wood H G
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