Monooxygenase and kynurenine 3-monooxygenase showed increasing intensities during growth. Moreover, other sets of spots that corresponded to the same protein were notably different (Figure 3B), suggesting that the isoforms are regulated in different ways or are involved in different physiological processes. This form of regulation has been previously reported for some proteins involved in carbohydrate metabolism [16, 31]. Unfortunately, no data could be extracted from our MALDI-TOF analyses to identify differences between the probable isoforms identified. Figure 3 Relative intensities of multiple

spots for X. dendrorhous proteins in MM-glucose. The growth phases are represented by different colors. A. Multi-spot proteins that exhibited essentially the same SCH772984 ic50 general pattern of variation. B. Multi-spot proteins that were regulated in different ABT-263 research buy ways. The axis numbers correspond to the SSP spot identifications generated by PDQuest software. The y axis scale (× 103) corresponds to the normalized spot intensity. To normalize, the spot intensities were divided

by the total density of valid spots and then multiplied by 106. Finally, the normalized values from replicates of 24-h, 70-h and 96-h were averaged. Asterisks represent p < 0.01 and circles represent p < 0.05. Regarding the migration of proteins, for which full X. dendrorhous sequences were available, the experimental Mr and pI values corresponded closely to the theoretical values, except for acetyl-CoA carboxylase (N°84). For this protein, the experimental Mr was markedly lower than the Dimethyl sulfoxide theoretical Mr. This discrepancy in Mr could be linked to either in vivo or in vitro protein degradation. In fact, this protein was identified with peptides that spanned the middle and carboxy terminal regions of the reported amino acid sequence. However, for the orthologous proteins identified, we found reasonable correlations between the experimental

and theoretical migrations (see additional file 2 Table S1). Most discrepancies corresponded to a lower Mr value and more acidic pI value for the gel-estimated value compared to the theoretical value. For instance, phosphatidylserine decarboxylase (protein N°85) was detected in the acidic range (pI 6.24), but this protein has a basic theoretical pI of 9.45. This unusual migration has been observed in ribosomal proteins in previous BIRB 796 datasheet studies [30]; while this behavior still has no explanation, it is probably related to the presence of posttranslational modifications. Protein identification and classification into functional groups We employed the approach of cross-species protein identification for X. dendrorhous because this yeast is poorly characterized at the gene and protein levels. The conserved nature of many biosynthetic and metabolic pathways in different organisms has been the basis for several studies of species that lack genome sequence data [18, 20, 21].