Fig. 2From: Transcriptome analysis of Zymomonas mobilis ZM4 reveals mechanisms of tolerance and detoxification of phenolic aldehyde inhibitors from lignocellulose pretreatmentComparison of gene expression levels of Z. mobilis ZM4 between the DNA microarray and qRT-PCR. The gene expression ratios of both microarray data and qRT-PCR data for 20 genes were log transformed in base 2 (log2, treatment/control), and the microarray log2 ratio values were plotted against the qRT-PCR log2 values. The 20 selected genes included ZMO0152 (pyruvate kinase), ZMO0177 (16S rRNA), ZMO0179 (fructose-bisphosphate aldolase), ZMO0367 (glucose-6-phosphate 1-dehydrogenase), ZMO0368 (6-phosphogluconate dehydrogenase), ZMO0369 (glucokinase), ZMO0387 (hpcH/hpaI aldolase), ZMO0543 (aconitate hydratase), ZMO0544 (isocitrate dehydrogenase), ZMO0567 (succinyl-CoA synthetase), ZMO0569 (succinate dehydrogenase), ZMO0997 (KDPG aldolase), ZMO1237 (d-isomer specific 2-hydroxyacid dehydrogenase), ZMO1307 (fumarase), ZMO1360 (pyruvate decarboxylase), ZMO1478 (6-phosphogluconolactonase), ZMO1496 (phosphoenolpyruvate carboxylase), ZMO1596 (Fe-containing alcohol dehydrogenase), ZMO1608 (phosphopyruvate hydratase), and ZMO1963 (citrate synthase). The primers for qRT-PCR of the genes are listed in Additional file 1 Back to article page