SAT-1806 NMR Metabolite Profiling of Acidobacterium capsulatum Grown in Minimal Media with Glucose as the Sole Carbon Source

Saturday, October 13, 2012: 8:20 AM
Hall 4E/F (WSCC)
Pariss Trujillo , Chemistry, Fort Lewis College, Durango, CO
Sunny Ketchum , Chemistry, Fort Lewis College, Durango, CO
Katherine McLain , Chemistry, Fort Lewis College, Durango
Leslie Sommerville, Ph.D. , Chemistry, Fort Lewis College, Durango
Acidobacterium capsulatum is an acidophilic chemotrophic organism first cultured in 1991 and its genome was reported in 2009. Organisms in this phylum are ubiquitous in the environment. Genomic information suggests that A. capsulatum may be a key decomposer in soil and aquatic environments because of the number of potentially encoded polysaccharide-degrading enzymes capable of providing simple sugars. However, A. capsulatum potentially cannot metabolize glucose and other sugars directly through the glycolytic or Entner-Doudoroff pathways because no F1,6BP aldolase or KDPG dehydratase genes were identified in the genome. A. capsulatum does have a transaldolase and most of the genes for the Pentose Phosphate Shunt (PPS) suggesting that these organisms use PPS to distribute carbon between biomass production, energy generation and polysaccharide synthesis. To test this hypothesis A. capsulatum growth under aerobic conditions in a minimal media with glucose as the sole carbon source was characterized. Free glucose was found to be completely consumed after about 90 hours at ambient temperature and distributed about 40% in biomass, 40% consumed for energy and 20% used for polysaccharide synthesis. Aqueous cell lysates of A. capsulatum quenched with perchloric acid at the top of exponential were shown by 1H-NMR to be rich in ribonucleotides, sugars, alcohols and precursors to membrane components. However, from these results we could not conclude that the PPS is the central metabolic pathway for the catabolism of glucose. Future studies will use 13C-labeled glucose, 13C-NMR and LC-MS to better determine the glucose metabolites under these conditions.