TABLE 2.
Prosequence | Internal site | Primary site | Doubling time
|
|
---|---|---|---|---|
Actual (h)b | Relative | |||
Krp1[KR82][KR102][R102*] | Lys-Arg | Lys-Arg | 4.12 | 1.00 |
Krp1[KA82][KR102][R102*] | Lys-Ala | Lys-Arg | 5.55 | 1.35 |
Krp1[KR82][Y100*] | Lys-Arg | Absent | 4.21 | 1.02 |
Krp1[KA82][Y100*] | Lys-Ala | Absent | 4.13 | 1.00 |
Plasmids containing the indicated Krp1 prosequence constructs under the transcriptional control of the nmt1 promoter were transformed into S. pombe cells expressing wild-type Krp1 from its chromosomal allele. Transformants were cultured at 29°C in the absence of thiamine to induce expression from the nmt1 promoter.
Data are averages of five separate determinations.