Either 1 μl of crude colony lysate or 1 μl of DNA extracted using the YeaStar Genomic DNA Kit was added into the reaction. Amplification was performed in a Rapid Cycler

2 apparatus (Idaho Technology Inc., Salt Lake City, Utah, USA) applying an empirically optimized protocol of initial denaturation at 95°C, 5 min, followed by 45 cycles of denaturation at 95°C for 5 s, annealing at 48°C for 10 s, and extension at 72°C for 40 s, with ramping 1°C/s, followed by final extension at 72°C for 5 min. Analysis of McRAPD data RAPD amplicons were subjected to melting analysis on a high-resolution melting instrument HR-1 (Idaho Technology Inc., Salt Lake City, Utah, USA). The samples C646 purchase were heated at ramping rate of 0.3°C/s with acquisition of fluorescence data ranging from 75 to 95°C. Results were analysed using the HR-1 melt analysis software. Relative fluorescence was first plotted versus temperature and fluorescence intensity values were normalized as recommended by the manufacturer. For this purpose, temperature ranges preceding and following the

melting domain were optimized empirically to result in reproducible normalized melting curves in all of the yeast species examined. The optimized intervals for normalization were 75.5-77.5°C and 91.5-93.5°C, respectively. A simple procedure phosphatase inhibitor library for comparison of normalized melting profiles was developed by us. Briefly, differences in McRAPD data of selleck compound a pair of isolates were calculated by subtracting their normalized fluorescence values measured at each temperature point during melting analysis. Then, the sum of these subtracted values represented absolute numerical distance between the pair of isolates, i.e.: where AD 1,2 was absolute distance between isolates No. 1 and 2 f 1(t) was normalized fluorescence of isolate No. 1 measured at temperature t f 2(t)was normalized fluorescence of isolate No. 2 measured at temperature

t After the absolute distance was established in all pairs (combinations) of isolates, the relative distance 1.0 was assigned to the highest absolute value obtained in the most dissimilar (numerically distant) pair of isolates, abbreviated as AD max. Relative distance values for the remaining pairs of isolates were calculated as a fraction of the highest absolute value, i.e.: A matrix of relative distances was assembled for the isolates included into each comparison. Then, the matrix of relative distances was used to calculate tree data for a cladogram using the UPGMA method and Phylip software [28, 29]. PhyloDraw 0.8 software [30, 31] was used for cladogram construction. For additional analysis, plots of the first negative derivation of fluorescence depending on temperature were also prepared based on melting data normalized previously. To delineate the melting peaks better, smoothing of data was performed using the HR-1 analysis software as recommended by the manufacturer.