Table 3.
l-Tyrosine production of the various strains constructed in the studya
| Strain | Plasmids | Titer (mg/liter) | mgTyr/gCDWb | % Yt |
|---|---|---|---|---|
| A | pS0 and pY0 | 746 ± 18 | 921 ± 22 | 27 |
| B | pS0 and pY1 | 897 ± 28 | 944 ± 29 | 33 |
| C | pS4 and pY1 | 1,150 ± 28 | 1,307 ± 32 | 42 |
| D | pS5 and pY1 | 1,219 ± 24 | 1,451 ± 29 | 44 |
| E | pS4 and pY2 | 908 ± 5 | 987 ± 5 | 33 |
| F | pS4 and pY3 | 2,169 ± 382 | 2,645 ± 466 | 79 |
| G | pS5 and pY3 | 1,310 ± 75 | 1,617 ± 93 | 48 |
The basal strain was E. coli MG1655, which was transformed with the various shikimate and l-tyrosine plasmids (Table 2). The l-tyrosine titer (in mg/liter) reported was the final production obtained within 24 h when glucose had been completely consumed, with the exception of strain F (which was 48 h), in a 50-ml MOPS-M9 minimal medium shake flask culture containing 5 g/liter glucose, shaken at 200 rpm and 37°C. For strain F, the l-tyrosine titer at 24 h was 1,512 ± 27 mg/liter. All cultures were induced with 50 μM IPTG, except for that of strain A. For strain A, the production was maximized at 1 mM IPTG.
The average cell dry weight for all of the strains was 0.38 g/liter per optical-density (OD) unit of culture; it is consistent with the value reported previously (6).