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. 1999 May;181(9):2759–2764. doi: 10.1128/jb.181.9.2759-2764.1999

TABLE 2.

Gene expression during growth of wild-type bacteria in LB nutrient mediuma

Sampling time (h) OD600 Mean fluorescence signal ± SEM of PCR productb
oxyR katG dps gorA ahpCF sodA trxA
1.5 0.31 0.31 ± 0.07 (1.5) 0.79 ± 0.11 (1.0) 0.10 ± 0.02 (1.0) 1.92 ± 0.18 (1.3) 0.43 ± 0.07 (1.0) 0.18 ± 0.06 (2.0) 1.19 ± 0.12 (1.5)
2 0.58 0.21 ± 0.02 (1.0) 0.99 ± 0.08 (1.3) 0.18 ± 0.02 (1.8) 1.48 ± 0.28 (1.0) 0.47 ± 0.10 (1.1) 0.17 ± 0.06 (1.9) 0.82 ± 0.14 (1.0)
3 1.54 0.60 ± 0.15 (2.9) 3.42 ± 0.55 (4.3) 0.41 ± 0.02 (4.1) 2.48 ± 0.33 (1.7) 0.49 ± 0.08 (1.1) 0.09 ± 0.02 (1.0) 1.02 ± 0.13 (1.2)
5 3.17 0.66 ± 0.07 (3.1) 5.81 ± 0.21 (7.4) 6.22 ± 0.38 (62.2) 4.28 ± 0.43 (2.9) 0.65 ± 0.09 (1.5) 0.11 ± 0.02 (1.2) 1.72 ± 0.25 (2.1)
7 4.40 1.09 ± 0.30 (5.2) 4.07 ± 0.40 (5.2) 8.65 ± 1.50 (86.5) 6.24 ± 1.57 (4.2) 1.49 ± 0.14 (3.5) 0.50 ± 0.12 (5.6) 1.29 ± 0.30 (1.6)
12 4.86 1.18 ± 0.22 (5.6) 3.48 ± 0.43 (4.4) 7.55 ± 1.37 (75.5) 6.78 ± 0.91 (4.6) 2.72 ± 0.55 (6.3) 0.69 ± 0.13 (7.7) 1.45 ± 0.27 (1.8)
a

Cells from overnight cultures in LB broth were diluted in fresh medium and incubated at 37°C with shaking at 150 rpm. Samples were collected at regular time intervals and rapidly cooled to 0°C. Culture growth at the indicated times was monitored by measuring the OD600. RNA was purified and processed as specified in Materials and Methods. 

b

Based on eight MPCR amplifications. Data are relative to the fluorescence signal of the reference gene, gapA. Boldface type indicates statistically significant increments (P < 0.05).