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23 results for “Chaetomiaceae”
FIGURE 4 in Identification of a new species and three new records of Chaetomiaceae associated with commercial herbal teas in northern Thailand
FIGURE 4. Canariomyces arenarius (MFLUCC 24–0066, new host record). a Red goji berry tea sample. b, c Culture colony grown on PDA from the surface and reverse after one month. d Top view of white conidial colonies in culture. e Hyphae in culture. f–i Developing short conidiophores and conidiogenous cells with apical conidia. Scale bars: d = 500 µm, e–i = 10 µm.
FIGURE 2 in Identification of a new species and three new records of Chaetomiaceae associated with commercial herbal teas in northern Thailand
FIGURE 2. Arcopilus albae (MFLUCC 24–0064, ex-type culture). a Mulberry leaf tea sample. b, c Culture colony grown on PDA from the surface and reverse after one month. d Top view of ascomata covered by elongate red-brown hairs. e, f Ascomata with lateral hairs mounted in water. g Close-up of terminal hairs with red pigmented coarsely verrucose-walled and coiled at the apex. h Peridium. i Asci. j Ascospores with an apical germ pore. Scale bars: d = 200 µm, e, f = 100 µm, g, j = 10 µm, h = 5 µm, i = 20 µm.
FIGURE 1 in Identification of a new species and three new records of Chaetomiaceae associated with commercial herbal teas in northern Thailand
FIGURE 1. Phylogram generated from RAxML analysis based on combined ITS, LSU, RPB2, and TUB2 sequence data of Arcopilus taxa. Collariella bostrychodes (CBS 163.73) and Co. carteri (CBS 128.85T) are selected as the outgroup taxa Bootstrap support values. for ML values equal to or>70% and PP values equal to or>0.95 are shown as ML/PP above the nodes. The newly generated sequence in this study is in blue. Type strains are indicated in bold.
FIGURE 5 in Identification of a new species and three new records of Chaetomiaceae associated with commercial herbal teas in northern Thailand
FIGURE 5. Phylogram generated from RAxML analysis based on combined ITS, RPB2 and TUB2 sequence data of Chaetomium taxa. Xanthiomyces spinosus isolates CBS 789.71 and CBS 796.83 are selected as the outgroup taxa. Bootstrap support values for ML values equal to or>70% and PP values equal to or>0.95 are shown as ML/PP above the nodes. Newly generated sequences in this study are in blue. Type strains are indicated in bold.
FIGURE 3 in Identification of a new species and three new records of Chaetomiaceae associated with commercial herbal teas in northern Thailand
FIGURE 3. Phylogram generated from RAxML analysis based on combined ITS, LSU, RPB2 and TUB2 sequence data of Canariomyces taxa. Madurella pseudomycetomatis isolates CBS 129177T and CBS 217.55 are selected as the outgroup taxa. Bootstrap support values for ML values equal to or>70% and PP values equal to or>0.95 are shown as ML/PP above the nodes. Newly generated sequences in this study are in blue. Type strains are indicated in bold.
FIGURE 2 in New record of Chaetomium grande Asgari & Zare (Chaetomiaceae) for the Egyptian and African mycobiota
FIGURE 2: ITS sequence tree of Ch. grande (MF787599) made though NCBI blast based on neighbour joining method with max sequence difference of 0.75.
Fig. 3 in Bioactive metabolites from the desert plant-associated endophytic fungus Chaetomium globosum (Chaetomiaceae)
Fig. 3. Comparison of the 13C NMR chemical shift values of the left part of structure 1 with those of spiciferone A (3) in the same solvent (DMSO d).
Supplementary material 1 from: Wang H-Y, Li X, Dong C-B, Zhang Y-W, Chen W-H, Liang J-D, Han Y-F (2024) Two new species of Sordariomycetes (Chaetomiaceae and Nectriaceae) from China. MycoKeys 102: 301-315. https://doi.org/10.3897/mycokeys.102.114480
The alignments used in the phylogenetic analysis
Figure 2 from: Wang H-Y, Li X, Dong C-B, Zhang Y-W, Chen W-H, Liang J-D, Han Y-F (2024) Two new species of Sordariomycetes (Chaetomiaceae and Nectriaceae) from China. MycoKeys 102: 301-315. https://doi.org/10.3897/mycokeys.102.114480
Figure 2 Morphological characteristics of Bisifusarium keratinophilum sp. nov. a–c front and reverse of colony on MEA, OA and PDA after 7 days at 25 °C d, e conidiophores and macroconidia f phialidic pegs g hyphae h, i microconidia. Scale bars: 10 μm (d–i).
Figure 3 from: Wang H-Y, Li X, Dong C-B, Zhang Y-W, Chen W-H, Liang J-D, Han Y-F (2024) Two new species of Sordariomycetes (Chaetomiaceae and Nectriaceae) from China. MycoKeys 102: 301-315. https://doi.org/10.3897/mycokeys.102.114480
Figure 3 Phylogenetic tree of the genus Ovatospora constructed from ITS, LSU, tub2 and rpb2. Notes: Statistical support values (BI/ML) were shown at nodes. ML bootstrap values ≥ 75% and posterior probabilities ≥ 0.90 are shown above the internal branches. '–' indicates the absence of statistical support (< 75% for bootstrap proportions from ML analysis; < 0.90 for posterior probabilities from Bayesian analysis). Three new strains are shown in blue. CBS: CBS-KNAW Fungal Biodiversity Centre, Utrecht, The Netherlands; CGMCC: The China General Microbiological Culture Collection Centre; GZUIFR: The Institute of Fungus Resources, Guizhou University, China; LC: Lei Cai's personal culture collection, Beijing, China.
Figure 4 from: Wang H-Y, Li X, Dong C-B, Zhang Y-W, Chen W-H, Liang J-D, Han Y-F (2024) Two new species of Sordariomycetes (Chaetomiaceae and Nectriaceae) from China. MycoKeys 102: 301-315. https://doi.org/10.3897/mycokeys.102.114480
Figure 4 Morphological characteristics of Ovatospora sinensis sp. nov. a–c reverse and front of colony on MEA, OA and PDA after7 days at 45 °C d–h conidiophores and conidia i hyphae. Scale bars: 10 μm (d–i).
Figure 1 from: Wang H-Y, Li X, Dong C-B, Zhang Y-W, Chen W-H, Liang J-D, Han Y-F (2024) Two new species of Sordariomycetes (Chaetomiaceae and Nectriaceae) from China. MycoKeys 102: 301-315. https://doi.org/10.3897/mycokeys.102.114480
Figure 1 Phylogenetic tree of the genus Bisifusarium constructed from the dataset of ITS, LSU, tef1, cmdA, rpb2 and tub2. Notes: Statistical support values (BI/ML) were shown at nodes. ML bootstrap values ≥ 75% and posterior probabilities ≥ 0.90 are shown above the internal branches. '–' indicates the absence of statistical support (< 75% for bootstrap proportions from ML analysis; < 0.90 for posterior probabilities from Bayesian analysis). Three new strains are shown in blue font. BRIP: Queensland Plant Pathology Herbarium, Australia; CBS: CBS-KNAW Fungal Biodiversity Centre, Utrecht, The Netherlands; CGMCC: The China General Microbiological Culture Collection Centre; GZUIFR: The Institute of Fungus Resources, Guizhou University, China; LC: Lei Cai's personal culture collection, Beijing, China; MNHN: Museum National d'Histoire Naturelle culture collection, France; UBOCC: Universitée de Bretagne Occidentale Culture Collection, France; VTT: Culture Collection, Finland.
FIGURE 1 D in New record of Chaetomium grande Asgari & Zare (Chaetomiaceae) for the Egyptian and African mycobiota
FIGURE 1 D: Textura intricata mounted by deionized water under light microscope.
Fig. 6 in Bioactive metabolites from the desert plant-associated endophytic fungus Chaetomium globosum (Chaetomiaceae)
Fig. 6. Possible biosynthesis of 1.
Fig. 4 in Bioactive metabolites from the desert plant-associated endophytic fungus Chaetomium globosum (Chaetomiaceae)
Fig. 4. Experimental ECD spectra and the calculated ECD spectra of 1.
Fig. 1 in Bioactive metabolites from the desert plant-associated endophytic fungus Chaetomium globosum (Chaetomiaceae)
Fig. 1. Structures of compounds 1–12.
Fig. 5 in Bioactive metabolites from the desert plant-associated endophytic fungus Chaetomium globosum (Chaetomiaceae)
Fig. 5. CD Spectra of compounds 2 and 4.
Fig. 7. Compound 6 in Bioactive metabolites from the desert plant-associated endophytic fungus Chaetomium globosum (Chaetomiaceae)
Fig. 7. Compound 6 retarded seedling growth of A. thaliana.
Fig. 2. Key 2D in Bioactive metabolites from the desert plant-associated endophytic fungus Chaetomium globosum (Chaetomiaceae)
Fig. 2. Key 2D NMR correlations of 1 and 2.
FIGURE 7 in Identification of a new species and three new records of Chaetomiaceae associated with commercial herbal teas in northern Thailand
FIGURE 7. Chaetomium rectangulare (MFLUCC 24–0070, new host record and geographical distribution). a Black goji berry tea. b, c Culture colony on PDA after one month from surface and reverse. d, e Ascomata on top and side views surrounded by dark dense hairs. f Squash mouth of ascoma with basal hyphae in water. g Close-up of ascomatal hairs. h, i Ascospores. Scale bars: d, e = 500 µm, f = 50 µm, g–i = 10 µm.
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