cDehalococcoides species are key players in the anaerobic transformation of halogenated solvents at contaminated sites. Here, we analyze isotopologue distributions in amino acid pools from peptides of Dehalococcoides strain CBDB1 after incubation with 13 C-labeled acetate or bicarbonate as a carbon source. The resulting data were interpreted with regard to genome annotations to identify amino acid biosynthesis pathways. In addition to using gas chromatography-mass spectrometry (GC-MS) for analyzing derivatized amino acids after protein hydrolysis, we introduce a second, much milder method, in which we directly analyze peptide masses after tryptic digest and peptide fragments by nano-liquid chromatography-electrospray ionization-tandem mass spectrometry (nano-LC-ESI-MS/MS). With this method, we identify isotope incorporation patterns for 17 proteinaceous amino acids, including proline, cysteine, lysine, and arginine, which escaped previous analyses in Dehalococcoides. Our results confirmed lysine biosynthesis via the ␣-aminoadipate pathway, precluding lysine formation from aspartate. Similarly, the isotopologue pattern obtained for arginine provided biochemical evidence of its synthesis from glutamate. Direct peptide MS/MS analysis of the labeling patterns of glutamine and asparagine, which were converted to glutamate and aspartate during protein hydrolysis, gave biochemical evidence of their precursors and confirmed glutamate biosynthesis via a Re-specific citrate synthase. By addition of unlabeled free amino acids to labeled cells, we show that in strain CBDB1 none of the 17 tested amino acids was incorporated into cell mass, indicating that they are all synthesized de novo. Our approach is widely applicable and provides a means to analyze amino acid metabolism by studying specific proteins even in mixed consortia.
Dehalococcoides species are strictly anaerobic bacteria known for the ability to use a variety of halogenated aliphatic and aromatic compounds as respiratory electron acceptors. Many of these organohalides are persistent and toxic groundwater pollutants. Dehalococcoides isolates use hydrogen as the sole electron donor and acetate plus bicarbonate as carbon sources. While some biochemical details of the respiratory electron chain have been studied, knowledge of the carbon metabolism of Dehalococcoides spp. is scarce. Sequenced and annotated genomes of several Dehalococcoides strains provide a basis for the generation of hypotheses for carbon metabolism but also highlight gaps in our understanding (12,15,21). For instance, the genome annotations lack key genes for the biosynthesis of methionine, alanine, serine, glycine, and threonine. In addition, genes may be annotated incorrectly as evidenced by the recent identification of a gene encoding a Recitrate synthase previously annotated as homocitrate synthase (14). A modeling approach has used a pan-genome of all available Dehalococcoides sequences to develop a model for the central metabolism and growth of Dehalococcoides species (2). This study emphasi...