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. 2005 Feb;187(3):1135–1160. doi: 10.1128/JB.187.3.1135-1160.2005

TABLE 1.

Functional gene groups

Functional groupa No. of genes wt N2:wt O2b
Δfnr N2fnr O2b
Δfnr N2:wt N2b
Up Down Up Down Up Down
Energy metabolism, carbon 61c 29 21 18 12 13 15
Central intermediary metabolism 12 3 5 3 1 7 2
Fatty acid and phosphatidic acid biosynthesis 2 1 1 1
Global regulatory functions 3 1 1 1
Macromolecule synthesis; modification: polysaccharides (cytoplasmic) 1 1
Ribosomal proteins: synthesis, modification 1 1
Purine ribonucleotide biosynthesis 1 1 1
Protein, peptide secretion 2 2
Cell division 1 1
Amino acid biosynthesis 3 1 1 1
Biosynthesis of cofactors; carriers: thiamine 1 1
2′-Deoxyribonucleotide metabolism 3 1 2
Degradation of proteins, peptides, glyco 1 1 1
Degradation of small molecules, carbon compounds 4 2 1 1
Detoxification 3 2 1 1
Drug and/or analog sensitivity 2 2 2
Outer membrane constituents 3 1 2 1 1
Osmotic adaptation 4 1 1 4
Chemotaxis and mobility 10 4 10
Surface structures 37 5 16 2 32
Transport of small molecules 22 7 9 2 7 4 6
Unknown 119 32 27 39 12 47 24
Total 297 78 69 75 55 90 92
a

Functional group assignments are those described by Serres et al. (77). wt, wild type.

b

The change (n-fold) between two experimental conditions was calculated by taking the ratio of the signal intensity (difference of the log2 value) between two experimental conditions. Genes that showed at least a threefold increase in mRNA abundance relative to the control and had an average log2 signal intensity greater than 8 were considered upregulated. Conversely, genes whose transcript abundance decreased more than threefold and had an average log2 signal intensity greater than 8 in the control were considered downregulated.

c

The same genes could appear in more than one comparison using this classification system.