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. 2004 May;24(10):4083–4091. doi: 10.1128/MCB.24.10.4083-4091.2004

TABLE 3.

Carbon source regulation of transactivation properties of serine mutant alleles of Kl-Cat8p and ScCat8p fusion proteinsa

Allele 2% glucose 0.05% glucose 2% galactose-1% raffinose 3% glycerol 3% ethanol
Gal4 0.03 (0.0) 0.06 (0.01) 0.08 (0.01) 0.0 (0.0) 0.0 (0.0)
Gal4 KlCat8 0.06 (0.03) 0.14 (0.06) 0.95 (0.4) 2.6 (0.8) 36 (7.9)
Gal4 KlCat8S661A 0.01 (0.0) 0.0 (0.0) 0.03 (0.05) 0.66 (0.4) 13 (1.1)
Gal4 KlCat8S661E 0.54 (0.16) 10 (0.67) 14 (4.1) 23 (0.6) 25 (0.44)
Gal4 KlCat8S871A 0.08 (0.03) 0.29 (0.14) 1.2 (0.03) 2.5 (0.25) 49.1 (2.8)
Gal4 KlCat8S871E 0.07 (0.02) 0.38 (0.11) 2.2 (0.15) 5.0 (2.5) 36 (7.9)
Gal4 ScCat8 0.25 (0.04) 0.25 (0.02) 1.4 (0.07) 10.5 (0.4) 43.14 (2.9)
Gal4 ScCat8S562A 0.22 (0.2) 0.2 (0.02) 0.48 (0.12) 3.92 (1.0) 26.8 (0.82)
Gal4 ScCat8S562E 1.02 (0.04) 9.6 (0.7) 6.8 (0.54) 26 (2.2) 44 (9.7)
Gal4 ScCat8S802-4A 0.21 (0.24) 0.28 (0.04) NDb ND 51.2 (5.6)
a

Strain MAV103 was transformed with pGBT9-based plasmids expressing different alleles of Gal4-KlCat8p and Gal4-ScCat8p fusions from a truncated ScADH1 promoter. Transformants were grown on selective culture medium supplemented with the indicated carbon sources and assayed for β-galactosidase activity as described in Materials and Methods. β-Galactosidase activities (Miller units) are means of three independent measurements, with standard deviations in parentheses.

b

ND, not determined.