Heterotrophic Carbon Metabolism by Beggiatoa alba

The assimilation and metabolism of CO2 and acetate byBeggiatoa alba strain B18LD was investigated. AlthoughB. alba was shown to require CO2 for growth, the addition of excess CO2 (as NaHCO3 ) to the medium in a closed system did not stimulate growth. Approximately 24 to 31% of the methyl-labeled acetate and 38 to 46% of the carboxyl-labeled acetate were oxidized to14 CO2 byB. alba . The apparentV max values for combined assimilation and oxidation of [2-14 C]acetate byB. alba were 126 to 202 nmol min−1 mg of protein−1 under differing growth conditions. TheV max values for CO2 assimilation by heterotrophic and mixotrophic cells were 106 and 131 pmol min−1 mg of protein−1 , respectively. The lowV max values for CO2 assimilation, coupled with the highV max values for acetate oxidation, suggested that the required CO2 was endogenously produced from acetate. Moreover, exogenously supplied acetate was required byB. alba for the fixation of CO2 . From 61 to 73% of the [14 C]acetate assimilated by washed trichomes was incorporated into lipid. Fifty-five percent of the assimilated [2-14 C]acetate was incorporated into poly-β-hydroxybutyric acid. This was consistent with chemical data showing that 56% of the heterotrophic cell dry weight was poly-β-hydroxybutyric acid. Succinate and CO2 were incorporated into cell wall material, proteins, lipids, nucleic acids, and amino and organic acids, but not into poly-β-hydroxybutyric acid. Glutamate and succinate were the major stable products after short-term [1-14 C]acetate assimilation. Glutamate and aspartate were the first stable14 CO2 fixation products, whereas glutamate, a phosphorylated compound, succinate, and aspartate were the major stable14 CO2 fixation products over a 30-min period. The CO2 fixation enzymes isocitrate dehydrogenase (nicotinamide adenine dinucleotide phosphate; reversed) and malate dehydrogenase (nicotinamide adenine dinucleotide phosphate; decarboxylating) were found in cell-free extracts of both mixotrophically grown and heterotrophically grown cells. The data indicate that the typical autotrophic CO2 fixation mechanisms are absent fromB. alba B18LD and that the CO2 and acetate metabolism pathways are probably linked.