Various methods for isolating DNA from fruiting bodies on the example of Pleurotus pulmonarius (higher basidiomycetes) of the Novosibirsk Region for barcoding of edible and medicinal mushrooms

. We conducted experiments to increase the concentration of extracted DNA from the fruiting bodies of this species using various lysis buffers and extraction time. In general, DNA isolation according to the protocol using SDS made it possible to obtain higher concentrations thereof, as in the case of increasing the extraction time from 1 to 24 hours and using additional purification with chloroform.

DNA barcoding is a potent approach for rapid identification of fungal specimens, it can be used to accurately identify edible and medicinal mushrooms.
In this study, experiments were conducted on the isolation of DNA from the fruit bodies of oyster mushrooms to obtain its highest concentration.

Materials and methods
Fruiting bodies of fungi were collected in the field studies in various habitats of the Novosibirsk Region. Dried specimens were preserved in the herbarium, they were used for molecular genetic studies.
An overview of taxa used for studies, shows the species names, herbarium voucher, habitats and substrates given in Table 1. DNA extraction and sequencing Specimens of P. pulmonarius was used for molecular analysis. A fragment of fungal fruiting bodies (20 mg) was homogenized in lysis buffer and extract the DNA with NucleoSpin® Plant II kit was used. The ITS1-5.8S-ITS2 region of the rDNA was amplified by PCR with the primers ITS1F and ITS4B (Table 2).
For PCR, HS Taq DNA Polymerase (Evrogen, Russia) was used. PCR reactions were performed in a C1000 Thermal Cycler (Bio-Rad, USA). PCR results were checked at Gel Doc XR+ Imager (Bio-Rad, USA). DNA amplicons sequencing performed in SB RAS Genomics Core Facilities (Novosibirsk, Russia).
Sequences were aligned using ClustalW methods. The ITS sequences were aligned in MEGA 7. Phylogeny reconstruction was inferred using the UPGMA method. The percentage of replicate trees in which the associated taxa clustered together in the bootstrap test (100 replicates) is shown to be next to the branches. The evolutionary distances were computed using the Maximum Composite Likelihood method and were in the units of the number of base substitutions per site. The differences in the composition bias among sequences were considered in evolutionary comparisons. All ambiguous positions were removed for each sequence pair (pairwise deletion option). There were a total of 609 positions in the final dataset. Evolutionary analyses were conducted in MEGA 7.

Results and Discussion
Lysis buffers PL-1 (CTAB method) and PL-2 (SDS-method) were used. Two types of extraction were used: 1 hour according to the manufacturer's protocol and 24 hours with additional purification with chloroform. The results of measurements of the concentration of extracted DNA are presented in Table 3. The results of PCR imaging are presented in Fig. 2. Phylogenetic analyses Additional 2 ITS sequences of other Pleurotus species based on BLAST results and 4 ITS sequences of other species were retrieved from GenBank (http://www.ncbi.nlm.nih.gov/Genbank/). We first generated a 2 new sequence for the ITS1-5.8S-ITS2 region for P. pulmonarius. The final dataset consisted of 7 ITS sequences. An overview of all taxa and on sequences used for tree reconstruction, shows the species names, herbarium vouchers/strain and Genbank accession numbers given in Table 4. The molecular phylogenetic analyses placed the specimens of Pleurotus genus from Novosibirsk Region close to P. pulmonarius (Fig. 3).

Conclusions
DNA isolation according to the protocol using SDS allows to obtain higher concentrations, as and in the case of increasing the extraction time from 1 to 24 hours and using additional purification with chloroform.