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. 1967 Mar;93(3):879–885. doi: 10.1128/jb.93.3.879-885.1967

14CO2 Fixation, Glutamate Labeling, and the Krebs Cycle in Ribose-grown Hydrogenomonas facilis

Bruce A McFadden a,1, Glenn D Kuehn a,2, H Robert Homann a,3
PMCID: PMC276531  PMID: 16562153

Abstract

Exposure of ribose-grown Hydrogenomonas facilis to 14CO2 for 6 to 12 sec during ribose oxidation resulted in labeling of a number of compounds, three of which were glutamate, phosphoglycerate, and pyruvate. Phosphoglycerate and pyruvate were labeled almost exclusively in C1, suggesting operation of the reductive pentose phosphate cycle. Glutamate was labeled initially to the extent of 90% in C1 and 10% in C5, and this was followed by a concentration of radioisotope in C5. All of the enzymes of the tricarboxylic acid cycle were detectable in ribose-grown cells, and, in general, specific activities were similar to those found in yeast extract-grown cells. Reduced nicotinamide adenine dinucleotide oxidase, aconitase, and the dehydrogenases for pyruvate, α-ketoglutarate, and succinate appeared to be of particulate origin. In addition to enzymes of the tricarboxylic acid cycle, an acetyl coenzyme A-stimulated phosphoenolpyruvate carboxylase was found, as was isocitrate lyase. Possible participation of these catalysts in glutamate synthesis is discussed.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

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