Table 3.
Effects of RIM15 deletion
|  | RIM15/RIM15a | rim15Δ/rim15Δa | ||
|---|---|---|---|---|
| log | stat | log | stat | |
| Enzymes and metabolites | ||||
| Tre6P synthase (μmole/sec per gram protein) | 0.33 | 1.32 | 0.37 | 1.17 | 
| trehalase (μmole/sec per gram protein) | 0.09 | 0.17 | 0.05 | 0.16 | 
| invertase (μmole/sec per gram protein) | 2.00 | 12.93 | 1.93 | 12.06 | 
| SSA3–lacZ inductionb (Miller units) | 4.30 | 105.20 | 2.40 | 16.30 | 
| trehalose (gram/gram protein) | <0.001 | 0.199 | <0.001 | 0.009 | 
| glycogen (mg/gram protein) | 1.63 | 38.53 | 0.93 | 11.36 | 
| Thermotolerancec (% survival) | 0.13 | 35.60 | 0.07 | 0.03 | 
| Stationary phase survivald (%) | 100.00 | 20.20 | ||
| Budded cellse (%) | 65.70 | 0.90 | 65.70 | 24.30 | 
Wild-type and rim15Δ/rim15Δ strains were YEF473 and AR2, respectively. All experiments were carried out on YPD (2% glucose) medium using either log phase (log) or 4-day-old stationary phase (stat) cells, except where otherwise stated. Values represent means of at least three independent experiments; s.d.s were, in each case, <10% of the corresponding means.
β-Galactosidase activities were measured to monitor the induction of an SSA3–lacZ fusion gene (from plasmid pWB204Δ–236).
Thermotolerance was measured as the percent survival following a heat shock for 8 min at 50°C (log-phase cells) or 20 min at 53°C (stationary-phase cells).
The percentage of viable cells was determined by the colony-forming efficiency on YPD agar of 10-day-old stationary-phase cultures.
The percentage of budded cells was determined by microscopic examination of at least 200 cells.