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. 2001 Feb 1;29(3):683–692. doi: 10.1093/nar/29.3.683

Table 2. The glucose-repressive genes detected through microarray analysis.

Genea
Functiona
Ratio (wt)b
Ratio (ccpA1)b
glmS l-glutamine-d-fructose-6-phosphate amidotransferase 7.2 3.5
ybcM similar to d-glucosamine-d-fructose-6-phosphate aminotransferase 5.4 <2
glpQ glycerophosphoryl diester phosphodiesterase 5.5 <2
ycnKc similar to transcriptional regulator (DeoR family) 6.4 <2
yerA similar to adenine deaminase >100 <2
yesL similar to unknown proteins from B.subtilis 14.0 <2
yesM similar to two-component sensor histidine kinase 8.2 <2
yfmQ unknown function 12.5 <2
acoAc,d acetoin dehydrogenase E1 component (TPP-dependent α subunit) >100 12.9
acoCc acetoin dehydrogenase E2 component (dihydrolipoamide acetyltransferase) 58.0 5.3
glpF glycerol uptake facilitator 5.3 <2
yisS similar to myo-inositol 2-dehydrogenase 20.6 4.7
ykuL unknown function 6.7 <2
ctaC cytochrome caa3 oxidase (subunit II) 31.3 <2
ctaDd cytochrome caa3 oxidase (subunit I) 37.3 <2
ctaE cytochrome caa3 oxidase (subunit I) 22.6 <2
ctaG function unknown 7.8 <2
sucC succinyl-CoA synthetase (β subunit) 5.2 <2
sucD succinyl-CoA synthetase (α subunit) 5.1 <2
tdh threonine 3-dehydrogenase 10.6 <2
yocH similar to cell wall-binding protein 6.3 <2
qcrB menaquinol:cytochrome c oxidoreductase (cytochrome b subunit) 5.7 <2
qcrA menaquinol:cytochrome c oxidoreductase (iron-sulfur subunit) 16.0 <2
resE two-component sensor histidine kinase involved in aerobic and anaerobic respiration 6.7 <2
sacC levanase 14.4 <2
cstAd carbon starvation-induced protein 6.2 <2
araA l-arabinose isomerase 7.5 <2
speD (ytcF) unknown function 13.2 2.0
gapB glyceraldehyde-3-phosphate dehydrogenase >100 25.2
pckA phosphoenolpyruvate carboxykinase 26.8 3.7
ytkA unknown function 6.1 <2
dhbC isochorismate synthase 5.5 <2
yvfL similar to maltodextrin transport system permease 5.6 <2
yvfK similar to maltose/maltodextrin-binding protein 8.3 <2
yvdR similar to molecular chaperone 26.4 7.1
gerBC germination response to the combination of glucose, fructose, l-asparagine and KCl 23.0 <2
ywtD similar to murein hydrolase 5.8 <2
rbsRd transcriptional repressor of the ribose operon >100 <2
rbsK ribokinase >100 <2
rbsD ribose ABC transporter (membrane protein) >100 <2
rbsAd ribose ABC transporter (ATP-binding protein) >100 <2
rbsB ribose ABC transporter (ribose-binding protein) >100 <2
ywsB similar to unknown proteins from B.subtilis 32.2 <2
ywsA unknown function 23.2 <2
ywqM similar to transcriptional regulator (LysR family) 16.0 <2
rocA pyrroline-5 carboxylate dehydrogenase 5.6 <2
rocG (yweB) glutamate dehydrogenase (major) 48.6 <2
licA PTS lichenan-specific enzyme IIA component 5.2 <2
msmXc,d similar to multiple sugar-binding transport ATP-binding protein 9.2 <2
yxeF unknown function >100 22.3
iolJc aldolase in myo-inositol catabolism 28.4 4.5
iolIc unknown function in myo-inositol catabolism >100 9.2
iolHc unknown function in myo-inositol catabolism >100 22.3
iolGc myo-inositol 2-dehydrogenase >100 9.2
iolFc myo-inositol permease >100 6.5
iolEc 2-inosose dehydratase >100 8.3
iolDc 2,3-diketo-4-deoxy-epi-inositol hydrolase >100 14.4
iolCc kinase in myo-inositol catabolism >100 7.0
iolBc,d unknown function in myo-inositol catabolism 91.5 7.5
iolAc oxidative decarboxylase in myo-inositol catabolism 87.8 6.0
iolR transcriptional repressor of the inositol operon 6.7 4.2
iolS unknown function in myo-inositol catabolism 5.0 2.0
yxbF unknown function 15.3 3.6
rocF arginase 5.5 <2
rocE amino acid permease 7.5 <2
rocD ornithine aminotransferase 8.3 <2

aThe gene names and functions are basically as in the literature (13) and SubtiList (http://genolist.pasteur.fr/SubtiList). The functions of some iol genes were deduced from unpublished results (K.Yoshida and Y.Fujita).

bThe repression ratios [wild-type (wt) and ccpA1] were calculated by dividing the spot intensities obtained for cells grown without glucose by those with glucose after subtraction of their backgrounds and subsequent normalization.

cGlucose repression of the expression of these genes were confirmed on first level analysis of pMUTIN integrants, the results of which are obtainable from JAFAN (http://bacillus.genome.ad.jp).

dPutative catabolite responsible elements (cres) are associated with these genes (9).