2015
DOI: 10.11646/phytotaxa.226.3.1
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Hyphomycetes from aquatic habitats in Southern China: Species of Curvularia (Pleosporaceae) and Phragmocephala (Melannomataceae)

Abstract: Aquatic hyphomycetes are a diverse, polyphyletic group of asexually reproducing fungi involved in the decomposition of litter in freshwater ecosystems. Curvularia eragrostidis, C. verruculosa and Phragmocephala atra were identified from submerged wood collected from freshwater streams in Yunnan Province, Southwestern China. They were characterised based on morphology and LSU, ITS and SSU sequence data. Phylogenetic analysis of LSU sequences placed the isolates within the order Pleosporales. Curvularia eragrost… Show more

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Cited by 47 publications
(18 citation statements)
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“…The final volume of the PCR reaction was 25 μL and contained 12.5 μL of 2×Power Taq PCR MasterMix (a premix and ready to use solution, including 0.1 Units/μl Taq DNA Polymerase, 500 μm dNTP Mixture each (dATP, dCTP, dGTP, dTTP), 20 mM Tris-HCl pH 8.3, 100MmKCl, 3 mMMgCl 2 , stabilizer and enhancer), 1 μL of each primer (10 μM), 1 μL genomic DNA extract and 9.5 μL deionised water. The PCR thermal cycles for the amplification of the gene regions were as described in Su et al (2015). PCR products were purified using minicolumns, purification resin and buffer according to the manufacturer's protocols (Amershamproduct code: 27-9602-01).…”
Section: Dna Extraction Pcr Amplification and Sequencingmentioning
confidence: 99%
“…The final volume of the PCR reaction was 25 μL and contained 12.5 μL of 2×Power Taq PCR MasterMix (a premix and ready to use solution, including 0.1 Units/μl Taq DNA Polymerase, 500 μm dNTP Mixture each (dATP, dCTP, dGTP, dTTP), 20 mM Tris-HCl pH 8.3, 100MmKCl, 3 mMMgCl 2 , stabilizer and enhancer), 1 μL of each primer (10 μM), 1 μL genomic DNA extract and 9.5 μL deionised water. The PCR thermal cycles for the amplification of the gene regions were as described in Su et al (2015). PCR products were purified using minicolumns, purification resin and buffer according to the manufacturer's protocols (Amershamproduct code: 27-9602-01).…”
Section: Dna Extraction Pcr Amplification and Sequencingmentioning
confidence: 99%
“…the production of sympodial conidiophores with tretic, terminal and intercalary conidiogenous cells and elongate, transversely septate conidia with a dark basal scar (Boedijn 1933). Phylogenetic analyses compared the DNA sequence from four phylogenetic markers with related species in the trifolii -clade: Curvularia akaii , C. borreriae , C. gladioli , C. gaudauskasii , C. heteropogonis , C. pallescens and C. trifolii (Figure 1, Manamgoda et al 2012, 2015, Madrid et al 2014, Jeong et al 2015, Su et al 2015). These taxa are morphologically similar in producing a strongly protruding hilum (Madrid et al 2014).…”
Section: Discussionmentioning
confidence: 99%
“…The amplifications were carried out in a 25 µL reaction volume containing 9.5 µL ddH 2 O, 12.5 µL 2 × PCR Master Mix, 1 µL DNA template, 1 µL each primer (10 µM). The PCR thermal cycles for the amplification of the gene regions followed the methods in Jeewon et al (2004); Réblová et al (2011), andSu et al (2015). PCR products were checked on 1% agarose electrophoresis gels stained with Gel Red.…”
Section: Dna Extraction Pcr Amplification and Sequencingmentioning
confidence: 99%