Fig. 1From: Integrated analysis of gene expression from carbon metabolism, proteome and metabolome, reveals altered primary metabolism in Eucalyptus grandis bark, in response to seasonal variationSeasonal variation of transcripts involved in primary metabolism (a–d), in E. grandis bark, by RT-qPCR. Data are expressed as log fold change and winter values were used as a control. Expression was determined relative to α-tubulin and MDHc (Material and Methods). Asterisks indicates genes that are significantly expressed (P ≤ 0,05). Abbreviations: FBAcyt (fructose bisphosphate aldolase cytoplasmatic); GPI (glucose-6-phosphate isomerase); PGK (phosphoglycerate kinase); PK (pyruvate kinase); PEPC (phosphoenolpyruvate carboxylase); PFK (ATP-dependent phosphofructokinase); ENO (enolase); PGM (phosphoglucomutase); PGAM (phosphoglyceratemutase); PDH (pyruvate dehydrogenase); SuSy1 (sucrose synthase 1); SuSy3 (sucrose synthase 3); PFP (PPi-dependent phosphofructokinase); ADH2 (alcohol dehydrogenase 2); ADH3 (alcohol dehydrogenase 3); PDC (pyruvate decarboxylase); IDH (isocitrate dehyidrogenase); SCL (succinyl-coa ligase); NADP-ME (NADP malic enzyme); CA (carbonic anhydrase); RbcL (rubisco large subunit); RbcS (rubisco small subunit); FBAcl (fructose bisphosphate aldolase chloroplastidial) and RPI (ribose-5-phosphateisomerase). Three biological replicates, each with three technical replicates were analyzed per sample and error bars are standard errors of meanBack to article page