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. 2009 Jan 27;37(6):1767–1777. doi: 10.1093/nar/gkp010

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.