TABLE 4.
Genotype
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Line | Strain | MOT1 | SNF1 | ADR1a | ADH2 | ADHII activity (R)b | AtRc |
1 | SSH35 | WT | WT | 220 | WT | 29 | − |
2 | S54 | adr7-1 | WT | 220 | WT | 195 | +++ |
3 | S54 | adr7-1 | WT | Δ | WT | 50 | −+ |
4 | S54ΔS | adr7-1 | Δ | 220 | WT | 20 | − |
5 | S54ΔS | adr7-1 | Δ | Δ | WT | 22 | − |
6 | LK13 | WT | WT | 220 | ADH2-10 | 240 | +++ |
7 | LV14 | adr7-1 | WT | 220 | ADH2-10 | 500 | +++ |
8 | LK13ΔS | WT | Δ | 220 | ADH2-10 | 18 | − |
9 | LV14ΔS | adr7-1 | Δ | 220 | ADH2-10 | 75 | −+ |
10 | LK13ΔS | WT | Δ | Δ | ADH2-10 | 15 | − |
11 | LV14ΔS | adr7-1 | Δ | Δ | ADH2-10 | 50 | −+ |
Cells were grown in synthetic medium containing 5% glucose and crude cell extracts were assayed for ADH activity as described in materials and methods.
The ADR1-220 allele was present on a CEN4-TRP1 plasmid (Karnitz et al. 1992). In strains denoted Δ in the ADR1 column the pRS314 vector was present.
The ADH activity is the average of triplicate measurements that had a standard deviation of ∼10%.
Growth in the presence of the respiratory inhibitor Antimycin A (AtR) is indicative of constitutive ADH2 expression (Karnitz et al. 1992). Growth was scored as good growth (+++), very poor growth (−+), or no growth (−) after replica plating patches from a plate containing synthetic Trp− medium supplemented with 5% glucose.