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. 2008 Oct 6;76(12):5760–5767. doi: 10.1128/IAI.00618-08

TABLE 3.

Genes upregulated in the d-serine-treated sample at 30 mina

Function Gene name Product Fold change at 30 min (P value)
Carbon metabolism and energy generation aceE Pyruvate dehydrogenase 4.2 (P < 0.001)
aceF Pyruvate dehydrogenase 3.4 (P < 0.001)
dsdX d-Serine transporter 15 (P < 0.0005)
dsdA d-Serine deaminase 15 (P < 0.0005)
ndh NADH dehydrogenase II 3.9 (P < 0.005)
mqo (yojH) Malate quinone oxidoreductase 3.8 (P < 0.05)
ackA Acetate kinase 3.9 (P < 0.005)
pta Phosphotransacetylase 2.3 (P < 0.05)
garL Glucarate, galactarate, glycerate metabolism 3.6 (P < 0.001)
garR Glucarate, galactarate, glycerate metabolism 2.7 (P < 0.001
yfiD Pyruvate formate lyase accessory protein 3 (P < 0.005)
Methionine synthesis metE Tetrahydropteroyltriglutamate methyltransferase 2.8 (P < 0.001)
metB Cystathionine gamma-synthase 3.6 (P < 0.001)
metL Aspartokinase II and homoserine dehydrogenase II 2.1 (P < 0.001)
metF 5,10-Methylenetetrahydrofolate reductase 3.4 (P < 0.001)
sbp Periplasmic sulfate-binding protein 3.0 (P < 0.001)
Unknown c3104 Adjacent to yfiD 2.5 (P < 0.05)
c0143 Intergenic to aceE and aceF 3.6 (P < 0.005)
c4752 Adjacent to metE 3.2 (P < 0.001)
a

Fold changes of an ORF between strains were calculated as the following ratio: average d-serine-treated signal intensity/average water-treated CFT073 signal intensity. Only ORFs that had at least twofold changes, a P value of less than or equal to 0.05, and were called present on at least two biological replicate microarrays were considered significant.