TABLE 3.
Gene ID | Gene name | Enrichment factorb | DNA microarray ratioc | GntR1 binding motif (5′–3′) | Function |
---|---|---|---|---|---|
cgR_1513 | gnd | 5.66 | 3.65 | AAAGGTGTGACCATT | 6-Phosphogluconate dehydrogenase |
cgR_2397 | gntV | 5.19 | 60.60 | ATTGGTACTATCATA | Gluconate kinase |
cgR_1973 | pyk | 5.14 | 1.34 | ACAGGTACTACCATT | Pyruvate kinase |
cgR_0261 | iolT1 | 5.06 | 0.74 | ATTGGTAATACTTAG | Metabolite transport protein |
cgR_0402 | bglS | 5.01 | 10.72 | AAAGGGATTACCATT | Putative beta-glucosidase |
cgR_2751 | pckA | 4.91 | 0.42 | AAAGGGATTACCATT | Phosphoenolpyruvate carboxykinase |
cgR_2895 | maeB | 4.67 | 0.48 | AATGATATGACCATC | Malic enzyme |
cgR_2262 | mdh | 4.64 | 0.85 | GATGGTGTTACCTTT | Malate dehydrogenase |
cgR_1425 | ptsG | 4.54 | 0.29 | AAAAGTATTACCTTT | Phosphotransferase, glucose-specific enzyme II |
cgR_1624 | tkt | 4.46 | 1.82 | AAAGGTGTGACCAAT | Transketolase |
cgR_2806 | gntP | 4.32 | 2.79 | ATTAGTATGATCAAA | Gluconate permease |
cgR_2497 | dctA | 4.25 | 4.17 | ATTAATATTACCTTT | Na+/H+-dicarboxylate symporter |
cgR_1636 | gapA | 4.24 | 1.23 | ATTGGGATTACCATT | Glyceraldehyde-3-phosphate dehydrogenase |
cgR_2454 | 4.20 | 9.01 | TTAGGTGTGATCTTT | Sugar phosphate isomerase/epimerase | |
cgR_1038 | gapB | 4.14 | 0.31 | AAAGATGTGATCATT | Glyceraldehyde 3-phosphate dehydrogenase |
cgR_2451 | 3.91 | 2.40 | ATTAGTGTGACCAAA | Na+/H+-dicarboxylate symporter | |
cgR_2222 | dctP1 | 3.49 | 7.77 | AAAGGGATCACCATT | Putative C4-dicarboxylate-binding protein |
cgR_2896 | gntK | 3.18 | 1.83 | AAAGGTCTGACTAAT | Putative gluconate kinase |
cgR_2120 | aceE | 3.09 | 0.95 | TTAGGTACGACCAAA | Pyruvate dehydrogenase |
cgR_0784 | icd | 2.52 | 1.07 | CTTGGTGTGATCTTT | Isocitrate dehydrogenase |
cgR_2547 | ptsS | 2.29 | 1.69 | AATAGTGCCACCTTT | Enzyme II sucrose protein |
All ChIP-chip peaks were located upstream of the genes listed in the Gene ID column.
Relative peak height ratios of the array data in the ChIP DNA to input DNA are shown in the base 2 logarithm.
Relative ratios of the transcript levels in the gntR1-deleted cells to those in the wild-type strain were determined by DNA microarray analysis.