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Systems-level organization of yeast methylotrophic lifestyle
VerfasserRußmayer, Hannes ; Buchetics, Markus ; Gruber, Clemens ; Valli, Minoska ; Grillitsch, Karlheinz ; Modarres, Gerda ; Guerrasio, Raffaele ; Klavins, Kristaps ; Neubauer, Stefan ; Drexler, Hedda ; Steiger, Matthias ; Troyer, Christina ; Al Chalabi, Ali ; Krebiehl, Guido ; Sonntag, Denise ; Zellnig, Günther ; Daum, Günther ; Graf, Alexandra B. ; Altmann, Friedrich ; Koellensperger, Gunda ; Hann, Stephan ; Sauer, Michael ; Mattanovich, Diethard ; Gasser, Brigitte
Erschienen in
BMC Biology, 2015, Jg. 13,
ErschienenBioMed Central (BMC), 2015
DokumenttypAufsatz in einer Zeitschrift
Schlagwörter (EN)Metabolome / Methanol / Peroxisome / Pichia pastoris / Proteome / Transcriptome / Xylulose-monophosphate cycle
URNurn:nbn:at:at-ubbw:3-1265 Persistent Identifier (URN)
 Das Werk ist frei verfügbar
Systems-level organization of yeast methylotrophic lifestyle [3.08 mb]
Zusammenfassung (Englisch)


Some yeasts have evolved a methylotrophic lifestyle enabling them to utilize the single carbon compound methanol as a carbon and energy source. Among them, Pichia pastoris (syn. Komagataella sp.) is frequently used for the production of heterologous proteins and also serves as a model organism for organelle research. Our current knowledge of methylotrophic lifestyle mainly derives from sophisticated biochemical studies which identified many key methanol utilization enzymes such as alcohol oxidase and dihydroxyacetone synthase and their localization to the peroxisomes. C1 assimilation is supposed to involve the pentose phosphate pathway, but details of these reactions are not known to date.


In this work we analyzed the regulation patterns of 5,354 genes, 575 proteins, 141 metabolites, and fluxes through 39 reactions of P. pastoris comparing growth on glucose and on a methanol/glycerol mixed medium, respectively. Contrary to previous assumptions, we found that the entire methanol assimilation pathway is localized to peroxisomes rather than employing part of the cytosolic pentose phosphate pathway for xylulose-5-phosphate regeneration. For this purpose, P. pastoris (and presumably also other methylotrophic yeasts) have evolved a duplicated methanol inducible enzyme set targeted to peroxisomes. This compartmentalized cyclic C1 assimilation process termed xylose-monophosphate cycle resembles the principle of the Calvin cycle and uses sedoheptulose-1,7-bisphosphate as intermediate. The strong induction of alcohol oxidase, dihydroxyacetone synthase, formaldehyde and formate dehydrogenase, and catalase leads to high demand of their cofactors riboflavin, thiamine, nicotinamide, and heme, respectively, which is reflected in strong up-regulation of the respective synthesis pathways on methanol. Methanol-grown cells have a higher protein but lower free amino acid content, which can be attributed to the high drain towards methanol metabolic enzymes and their cofactors. In context with up-regulation of many amino acid biosynthesis genes or proteins, this visualizes an increased flux towards amino acid and protein synthesis which is reflected also in increased levels of transcripts and/or proteins related to ribosome biogenesis and translation.


Taken together, our work illustrates how concerted interpretation of multiple levels of systems biology data can contribute to elucidation of yet unknown cellular pathways and revolutionize our understanding of cellular biology.