C. hydrogenoformans were grown in triplicate on either 55% CO and or syngas. Harvested cells were disrupted by a French pressure cell. Proteins were digested with trypsin and the resulting peptides from the paired samples were isobarically labeled, separated by liquid chromatography, and spotted directly onto MALDI plates. Samples were analyzed by quadrupole time-of-flight mass spectrometry. The data generated was analyzed using Mascot™ and protein assignments were statistically validated using PeptideProphet™ and ProteinProphet™.
Initial results showed relatively few proteins up regulated in the presence of syngas and while several of these are proteins of unknown function, others may be related to sporulation, iron chelation, and sulfur metabolism. A total of 37 proteins were down regulated by 2-fold or more in the presence of syngas. General classes of proteins down regulated included those related to amino acid and protein synthesis, anabolic activities, chemotaxis, and cell division.