Table 1. Effects of cell density and conditioned medium on localization of Y-EI in E. coli BL21-DE3-ΔEI harboring the plasmid pRSETB-Y-EI.
OD420
|
Punctate cells after incubation at 37°C, %
|
||||||
---|---|---|---|---|---|---|---|
Exp. | Cells | Supernatant | Mixture | 0 min | 30 min | 60 min | 150 min |
I | 1 | 1 | 1.0 | 5 | — | — | — |
II | 1 | 1 | 4.5 | 5 | 40 | 50 | 70 |
III | 1 | 4.5 | 1.0 | 5 | — | — | 15-20 (4 h) |
IV | 1 | 4.5 | 4.5 | 5 | — | 70 | — |
V-VIII | 4.5 | 1 or 4.5 | 1.0 or 4.5 | 70-80 | — | — | — |
E. coli BL21-DE3-ΔEI harboring pRSETB-Y-EI was grown overnight in Neidhardt medium containing 20 mM ribose and inoculated at a dilution of 1:100 into two 25-ml culture flasks. One contained 4 ml of the same medium with 1.89 mM ribose (culture 1); the second contained 20 mM ribose (culture 2). Growth was followed as described in the text. At stationary phase, culture 1 exhibited an OD420 of 1.0, and culture 2 was at OD420 of 4.5. After 7 h in stationary phase, 4-ml samples of the cultures were centrifuged, and the cells were separated from the supernatants. This gave four fractions: cells 1 and supernatant 1 from culture 1 and cells 4.5 and supernatant 4.5 from culture 2. Microscopic examination showed that the fluorescence in cells 1 was 95% diffuse and ≈5% punctate; cells 4.5 were ≈70-80% punctate and ≈20% diffuse. The cells were not washed but were resuspended to an OD420 of 1.0 or 4.5 in supernatants 1 or 4.5 as specified. The suspension were shaken at 37°C, and aliquots were examined microscopically at the indicated times.
—, no change.