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Fig. 1 | BMC Plant Biology

Fig. 1

From: Integrated analysis of gene expression from carbon metabolism, proteome and metabolome, reveals altered primary metabolism in Eucalyptus grandis bark, in response to seasonal variation

Fig. 1

Seasonal variation of transcripts involved in primary metabolism (ad), 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 mean

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