In any case, the results of the current study show that effects of H2-limitation occur widely for proteins of methanogenesis. The overall increase in methanogenic proteins with H2 limitation likely reflects a regulatory response that maintains flux through the methanogenic pathway when the electron donating substrate is limiting. One protein decreased strikingly with

H2-limitation, the H2-dependent methylenetetrahydromethanopterin dehydrogenase, Hmd (Table 1). The previous study of the transcriptome [5] indicated an increase in hmd mRNA with faster growth, but no change with H2-limitation. The discrepancy could be explained by any of the factors discussed above. In any case, the results indicate that NVP-BGJ398 in vivo Hmd has a decreased role under H2-limitation. In hydrogenotrophic methanogens, Hmd catalyses the reduction of methenyltetrahydromethanopterin to methylenetetrahydromethanopterin, LY2874455 datasheet using H2 directly as electron donor. As such, Hmd provides an alternative to F420-reducing hydrogenase (Fru or Frc in M. maripaludis) and F420-dependent methylenetetrahydromethanopterin dehydrogenase (Mtd) working together: Fru or Frc reduces F420 using H2, and Mtd reduces methenyltetrahydromethanopterin to methylenetetrahydromethanopterin using reduced F420. Hmd is an unusual [Fe] hydrogenase that

has a lower affinity for H2 than the F420-reducing hydrogenases [12, 13], and could be preferred when H2 is in excess, while Fru or Frc with Mtd could be preferred when H2 is limiting. Other proteins that decreased were a hypothetical protein (encoded in a putative

operon with Hmd), a putative iron transporter subunit, glutamine synthetase, and an S-layer protein (MMP0875). Aurora Kinase An additional S-layer protein (MMP0383) was not significantly affected by any nutrient limitation. Nitrogen limitation The abundance of 106 proteins was significantly affected by nitrogen limitation; 79 had increased abundance and 27 decreased. N/H and N/P ratios and their averages are shown in Additional file 3. Of the 79 proteins with increased abundance, 13 have known functions in nitrogen assimilation (Table 2). These are the nitrogen fixation (Nif) proteins, glutamine synthetase (GlnA) which Quisinostat supplier assimilates ammonia, ammonia transporters (Amt), and nitrogen sensor/regulators (GlnK). Since the Nif proteins showed a consistent and relatively marked increase in abundance, the mRNA encoding one (nifK) was selected for qRT-PCR to determine whether the effect occurred with similar magnitude at the transcriptome level. The magnitude was much greater, with an average log2 ratio of 7.09 (136-fold) for the mRNA compared to 2.03 (4.1-fold) for the protein. Previous measurements of nif transcription using lacZ fusions also showed a greater magnitude of regulation (5–100 fold, [14, 15]). The results suggest that for proteins that are present at high levels under derepressed conditions, the proteomic ratios may be compressed as noted above.