2021
DOI: 10.11646/phytotaxa.507.4.1
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New epiphytic sooty molds: Alloscorias syngonii (Readerielliopsidaceae) from Thailand

Abstract: A novel taxon was found as epiphytic sooty molds on Syngonium podophyllum from Thailand. A new genus, Alloscorias gen. nov. is established to accommodate a novel taxon, named A. syngonii. The morphological characters of the species are observed in culture. Phylogenetic analyses of a combined dataset of LSU, ITS, TEF-1α and RPB2 sequence data together with morphological support that Alloscorias is a distinct genus within Readerielliopsidaceae (Capnodiales). Detailed descriptions and illustrations are provided i… Show more

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Cited by 4 publications
(3 citation statements)
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“…The obtained genomic DNA was resuspended in 50 µL TE buffer and stored at −20 • C. Four loci sequences were amplified in an automated thermal cycler (Eppendorf AG, Germany). The primer pairs ITS5 and ITS4 were used for amplification of rDNA ITS regions [20], primers Bt2a (5 -GGT AAC CAA ATC GGT GCT TTC -3 ) and Bt2b (5 -ACC CTC AGT GTA GTG ACC CTT GGC -3 ) for the beta-tubulin gene (TUB) [21], primers 5F (5 -GAY MGW GAT CAY TTY GG -3 ) and 7CR (5 -CCC ATR GCT TGY TTR CCC AT -3 ) for the RNA polymerase II subunit B (RPB2) gene [22], and primers CMD5 (5 -CCG AGT ACA AGG ARG CCT TC -3 ) and CMD6 (5 -CCG ATR GAG GTC ATR ACG TGG -3 ) for the calmodulin gene [23]. The amplification was carried out in a 50 µL reaction volume containing 32.5 µL ddH 2 O, 5 µL 10 x PCR buffer, 4 µL of 2.5 mM dNTP, 2 µL of 10 µM of each primer, 4 µL template, and DNA 0.5 µL 5 U/µL Taq DNA polymerase (TaKaRa Bio Inc., Shiga, Japan).…”
Section: Phylogenetic Analysismentioning
confidence: 99%
“…The obtained genomic DNA was resuspended in 50 µL TE buffer and stored at −20 • C. Four loci sequences were amplified in an automated thermal cycler (Eppendorf AG, Germany). The primer pairs ITS5 and ITS4 were used for amplification of rDNA ITS regions [20], primers Bt2a (5 -GGT AAC CAA ATC GGT GCT TTC -3 ) and Bt2b (5 -ACC CTC AGT GTA GTG ACC CTT GGC -3 ) for the beta-tubulin gene (TUB) [21], primers 5F (5 -GAY MGW GAT CAY TTY GG -3 ) and 7CR (5 -CCC ATR GCT TGY TTR CCC AT -3 ) for the RNA polymerase II subunit B (RPB2) gene [22], and primers CMD5 (5 -CCG AGT ACA AGG ARG CCT TC -3 ) and CMD6 (5 -CCG ATR GAG GTC ATR ACG TGG -3 ) for the calmodulin gene [23]. The amplification was carried out in a 50 µL reaction volume containing 32.5 µL ddH 2 O, 5 µL 10 x PCR buffer, 4 µL of 2.5 mM dNTP, 2 µL of 10 µM of each primer, 4 µL template, and DNA 0.5 µL 5 U/µL Taq DNA polymerase (TaKaRa Bio Inc., Shiga, Japan).…”
Section: Phylogenetic Analysismentioning
confidence: 99%
“…The desired gene regions, partial large subunit nuclear rDNA (LSU) and internal transcribed spacer (ITS), were amplified using the primer pairs ITS5/ITS4 and LROR/LR5, respectively [21,22]. PCR was performed following the protocol described in Haituk et al [23]. The sequences were obtained from commercial sequence provider 1st BASE Company (Kembangan, Malaysia).…”
Section: Dna Extraction Amplification and Sequencingmentioning
confidence: 99%
“…The novel sequencing data generated in this work were analyzed using a nucleotide BLAST (BLASTn) search of the NCBI database (http://blast.ncbi.nlm.nih.gov/, accessed on 13 November 2021). The highly similar sequences were downloaded according to the BLASTn results and from recent publications [3,23,24]. The sequences were aligned using MAFFT v7 (RIMD, Osaka, Japan) [25].…”
Section: Phylogenetic Analysismentioning
confidence: 99%