Table 2.
Characterization of the transformants of the wild-type strain with integrative plasmid YIplac204-LPG carrying either undamaged or MDS-1-containing oligonucleotide
| Transformation with YIplac204-LPG carrying oligonucleotide | Undamaged | MDS-containing | Controla | |
|---|---|---|---|---|
| Frequency of Trp+Leu+ clones observed in two experimentsb | I | 6.1 × 10−6 | 7.2 × 10−6 | 2.6 × 10−6 |
| II | 10 × 10−6 | 7.6 × 10−6 | 3.8 × 10−6 | |
| Total clones analyzed | 26 | 39 | ||
| Total integrations into trp1 locus | 8 (31%) | 16 (41%) | ||
| Integrations into trp1 locus those that contain oligonucleotide | 8 (100%)c | 16 (100%)c | ||
| Total integrations outside of trp1 locus | 18 (69%)d | 23 (59%)e | ||
| Integrations outside of trp1 locus those that contain oligonucleotide | 14 (78%) | 18 (78%) | ||
| Total clones carrying oligonucleotide | 22 (85%) | 34 (87%) | NAf |
aTransformation with NheI/XhoI/BsgI-digested YIplac204-LPG (see Materials and methods section).
bThe mean RTE (see footnote to Table 1) from the two experiments is 0.98.
cAll samples yielded PCR product with either ES3/trp-R primers or gal-P/trp-R primers.
dThree samples yielded PCR product neither with ES3/trp-P primers, nor with gal-P/trp-P primers. One sample yielded PCR product with gal-P/trp-P primers, but not with ES3/trp-P primers.
eFour samples yielded PCR product neither with ES3/trp-P primers, nor with gal-P/trp-P primers. One sample yielded PCR product with gal-P/trp-P primers, but not with ES3/trp-P primers.
fTransformants were not analyzed by PCR.