2008
DOI: 10.1134/s0026261708040140
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Characterization of yeast groupings in the phyllosphere of Sphagnum mosses

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Cited by 37 publications
(15 citation statements)
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“…In the present study, R. mucilaginosa was the most frequently isolated yeast (21 strains, 32.3 % of all strains) in peat. Among the ten species detected in this study, only R. mucilaginosa and P. laurentii are known to have been isolated from peatland in Russia and Canada (Kachalkin and Yurkov 2012;Kachalkin et al 2008;Thormann et al 2007). R. mucilaginosa is one of the most, or perhaps the most, ubiquitous basidiomycetous yeast, found in a wide range of habitats (Sampaio 2011).…”
Section: Discussionmentioning
confidence: 94%
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“…In the present study, R. mucilaginosa was the most frequently isolated yeast (21 strains, 32.3 % of all strains) in peat. Among the ten species detected in this study, only R. mucilaginosa and P. laurentii are known to have been isolated from peatland in Russia and Canada (Kachalkin and Yurkov 2012;Kachalkin et al 2008;Thormann et al 2007). R. mucilaginosa is one of the most, or perhaps the most, ubiquitous basidiomycetous yeast, found in a wide range of habitats (Sampaio 2011).…”
Section: Discussionmentioning
confidence: 94%
“…Cryptococcus (ten species), Candida (eight species), Pichia (five species) and Rhodotorula (four species) were reported as the most prevalent genera, accounting for 58 % of known species. Kachalkin et al (2008) investigated the epiphytic yeast communities formed on Sphagnum mosses on peat in Moscow, Russia, and reported that among various known yeast species R. mucilaginosa was included. Kachalkin and Yurkov (2012) studied the yeast communities in Sphagnum mosses phyllosphere in boreal forest and swamp biotopes in the Tver region, Russia and found a significantly higher relative abundance of ascomycetous yeasts on swamp moss.…”
Section: Discussionmentioning
confidence: 99%
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“…Mini-and microsatellite-specific PCR fingerprints and Restriction Fragments Length Polymorphism analysis were performed as described before (Yurkov and Chernov 2005;Kachalkin et al 2008). For sequencing of the D1/D2 region of the 26S ribosomal gene and the internal transcribed spacers (ITS), DNA fragments were amplified with the ITS1f (5 0 -CTT GGT CAT TTA GAG GAA GTA) and NL4 (5 0 -GGT CCG TGT TTC AAG ACG G) primer pair using a program consisting of an initial denaturation step of 2 min at 96°C, followed by 35 cycles of 20 s at 96°C, 50 s 52°C and 1.5 min at 72°C and a final extension step of 7 min at 72°C.…”
Section: Methodsmentioning
confidence: 99%