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. 2004 Oct;186(20):6714–6720. doi: 10.1128/JB.186.20.6714-6720.2004

TABLE 3.

Phenotypic analysis

Substrate Plate Testa Well Log2 ratio WT ODb FB23401 OD
Tween 80 PM5 Supplement H12 −4.8 1.0 ± 0.5 0.0
2′-Deoxycytidine PM5 Supplement D12 −4.7 1.2 ± 0.2 0.0
α-Methyl-d-glucoside PM2 C source C6 −3.6 1.0 ± 0.7 0.1
2′-Deoxylnosine PM5 Supplement C12 −3.6 1.1 ± 0.4 0.1
d-Lysine PM3 N source C7 −3.0 0.9 ± 0.4 0.1
m-Inositol PM5 Supplement G12 −2.6 1.0 ± 0.3 0.2
Thiophosphate PM4 P source B1 −2.4 1.5 ± 0.9 0.3
N-Phthaloyl-l-glutamate PM3 N source D2 −2.2 0.5 ± 0.1 0.1
Agmatine PM3 N source D12 −2.2 0.7 ± 0.6 0.1
α-Keto valeric acid PM2 C source E10 −2.0 0.5 ± 0.3 0.1
a

Different BIOLOG plates were designed to test for carbon, nitrogen, or phosphorous sources or the effects of a growth supplement.

b

Cells were inoculated into BIOLOG plates as per the manufacturer's instructions, grown overnight at 37°C, and then the OD595 was measured in a plate reader. Data are shown from five replicates of WT (± SD) and one of FB23401 (disrupted at frmB).