Samples were collected in sterile plastic bags, transported on ice and processed in the same day by diluting in sterile saline to 3×10-4,

and 0.1 mL of this dilution was plated onto MRS medium [21] containing cycloheximide at 0.1% to inhibit yeast growth. Plates were incubated at 37°C in anaerobic jars for 4 days. Twenty Apoptosis inhibitor representative bacterial colony morphotypes were selected for further taxonomic identification. Isolates are maintained in glycerol 30% at -80°C. In total 7 samples (days 1, 30, 60, 90, 120, 150, and 180) were used to estimate bacterial CFU numbers in the four distilleries. Each sample was analyzed in duplicate. Ethanol tolerance test was performed with representative LAB isolates grown in MRS broth supplemented with Ethanol (100 g/L) at 37°C and pH 6.5. Cell growth was estimated by www.selleckchem.com/products/XAV-939.html means of optical density measurement at 600 nm using a Biophotometer (Eppendorf). Diluted samples (0.1 mL) were also plated onto Wallerstein laboratory nutrient agar (WLN) medium

containing 0.1% bromocresol green for the determinations of yeast abundance and presumptive identification [22]. ARDRA fingerprinting The fragment of the 16S-23S spacer was amplified with the primers 16-1A (5′-GAATCGCTAGTAATCG-3′) that anneals to nucleotides 1361 to 1380 of 16S rRNA gene (using L. casei genome location) and 23-1B (5′-GGGTTCCCCCATTCGGA-3′) this website that anneals to nucleotides 123 to 113 of 23S rRNA gene (using L. casei genome location) [23]. The amplification reaction contained 0.5 μM of each primer, 0.2 mM dNTP mix, 1.5 mM MgCl2 and 5 U Taq DNA polymerase (Invitrogen) in 50 μL final volume. The PCR amplification used a standard thermal program (two minutes at 94°C, followed by 35 cycles of 94°C for 30

seconds, 55°C for one minute and 72°C for one minute, with a final extension step at 72°C for 10 minutes). ARDRA analysis was performed using the 12 restriction enzymes SphI, NcoI, NheI, SspI, SfuI, EcoRV, DraI, VspI, HincII, EcoRI, HindIII and AvrII as described previously [23]. The restriction profiles of the isolates obtained from the bioethanol process were compared to the ARDRA database reported by Moreira et al. [24]. The ARDRA profiles of the isolates were compared tuclazepam with the ARDRA database. An isolate having an ARDRA profile matching an ARDRA profile of known LAB species was identified into this species. pheS and 16S rRNA sequencing The 16S rRNA was amplified by PCR using the primers 27F (5′-AGAGTTTGATCCTGGCTCAG-3′) and 1492R (5′-GGTTACCTTGTTACGACTT-3′) [25], while the pheS was amplified with the primers 21-F (5′-CAYCCNGCHCGYGAYATGC-3′) and 22-R (5′-CCWARVCCRAARGCAAARCC-3′) or 23-R (5′-GGRTGRACCATVCCNGCHCC-3′) [26]. The reactions contained 0.5 μM each primer, 0.2 mM dNTP mix, 1.5 mM MgCl2 and 1 U Taq DNA polymerase (Invitrogen) in a final volume of 50 μL. Amplification and sequencing was performed as described previously [27]. Gene sequences were analyzed using the software BioEdit v7.0.