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67 results for “Pestalotiopsis”
Figure 2 from: Hsu S-Y, Xu Y-C, Lin Y-C, Chuang W-Y, Lin S-R, Stadler M, Tangthirasunun N, Cheewangkoon R, AL-Shwaiman HA, Elgorban AM, Ariyawansa HA (2024) Hidden diversity of Pestalotiopsis and Neopestalotiopsis (Amphisphaeriales, Sporocadaceae) species allied with the stromata of entomopathogenic fungi in Taiwan. MycoKeys 101: 275-312. https://doi.org/10.3897/mycokeys.101.113090
Figure 2 ML phylogenetic tree of Pestalotiopsis obtained from the concatenated DNA sequence data of ITS, tub2 and tef1-α genes implemented in IQ-TREE. ML bootstrap values (MLB) ≥ 70%, Maximum Parsimony bootstrap (MPB) values ≥ 70% and Bayesian Posterior Probabilities (PP) ≥ 0.95 are given at the nodes. The scale-bar shows the number of estimated substitutions per site. Neopestalotiopsis protearum (CBS 114178) was used as an outgroup. The new isolates are in red and taxa representing ex-type cultures are in bold.
Figure 1 from: Hsu S-Y, Xu Y-C, Lin Y-C, Chuang W-Y, Lin S-R, Stadler M, Tangthirasunun N, Cheewangkoon R, AL-Shwaiman HA, Elgorban AM, Ariyawansa HA (2024) Hidden diversity of Pestalotiopsis and Neopestalotiopsis (Amphisphaeriales, Sporocadaceae) species allied with the stromata of entomopathogenic fungi in Taiwan. MycoKeys 101: 275-312. https://doi.org/10.3897/mycokeys.101.113090
Figure 1 The habitat of Pestalotiopsis and Neopestalotiopsis species, situated on the stromata of entomopathogenic fungi. Specimens AOphiocordyceps sp. NTUPPMH 18-160 BBeauveria sp. NTUPPMH 18-161 CTolypocladium sp. NTUPPMH 21-055 DOphiocordyceps sp. NTUPPMH 21-054 EOphiocordyceps sp. NTUPPMH 21-053 FOphiocordyceps sp. NTUPPMH 18-164 G, H the section of conidioma of Ophiocordyceps sp. showing the location of conidia of pestalotiopsis-like fungi (red arrow). Scale bars: 100 μm (G); 20 μm (H).
Figure 6 from: Hsu S-Y, Xu Y-C, Lin Y-C, Chuang W-Y, Lin S-R, Stadler M, Tangthirasunun N, Cheewangkoon R, AL-Shwaiman HA, Elgorban AM, Ariyawansa HA (2024) Hidden diversity of Pestalotiopsis and Neopestalotiopsis (Amphisphaeriales, Sporocadaceae) species allied with the stromata of entomopathogenic fungi in Taiwan. MycoKeys 101: 275-312. https://doi.org/10.3897/mycokeys.101.113090
Figure 6 The morphology of Pestalotiopsis manyueyuananiA the original habitat of conidia of Pestalotiopsis manyueyuanani; stroma of Ophiocordyceps sp. B top view (left) and bottom view (right) of the colony on potato dextrose agar (PDA) after incubation for seven days C formation of conidiomata on carnation leaf D, E conidiogenous cells and immature conidia F–K conidia L–N germinated conidia. Scale bars: 250 μm (C); 10 μm (D–K); 20 μm (L–N).
Figure 9 from: Hsu S-Y, Xu Y-C, Lin Y-C, Chuang W-Y, Lin S-R, Stadler M, Tangthirasunun N, Cheewangkoon R, AL-Shwaiman HA, Elgorban AM, Ariyawansa HA (2024) Hidden diversity of Pestalotiopsis and Neopestalotiopsis (Amphisphaeriales, Sporocadaceae) species allied with the stromata of entomopathogenic fungi in Taiwan. MycoKeys 101: 275-312. https://doi.org/10.3897/mycokeys.101.113090
Figure 9 Neopestalotiopsis haikouensis (NTUPPMCC 18-163 = CD04) A the original habitat of Neopestalotiopsis haikouensis; the stroma of Ophiocordyceps sp. B top view (left) and bottom view (right) of the colony on potato dextrose agar (PDA) after incubation for seven days C conidiomata on carnation leaf D, E conidiogenous cells and immature conidia F–I conidia. Scale bars: 250 μm (C); 20 μm (D–I).
Figure 11 from: Hsu S-Y, Xu Y-C, Lin Y-C, Chuang W-Y, Lin S-R, Stadler M, Tangthirasunun N, Cheewangkoon R, AL-Shwaiman HA, Elgorban AM, Ariyawansa HA (2024) Hidden diversity of Pestalotiopsis and Neopestalotiopsis (Amphisphaeriales, Sporocadaceae) species allied with the stromata of entomopathogenic fungi in Taiwan. MycoKeys 101: 275-312. https://doi.org/10.3897/mycokeys.101.113090
Figure 11 Temperature effect on mycelial growth according to the comparison of colonial growth (mm) of different species at each temperature, based on the mean values presented in Table S11. Colours represent different taxa: NTUPPMCC 18-160, Pestalotiopsis trachycarpicola; NTUPPMCC 18-161, Neopestalotiopsis sp.; NTUPPMCC 18-162, Pestalotiopsis hispanica; NTUPPMCC 18-163, Neopestalotiopsis haikouensis; NTUPPMCC 18-165, Pestalotiopsis manyueyuanani.; NTUPPMCC 18-166, Neopestalotiopsis camelliae-oleiferae; NTUPPMCC 21-054, Pestalotiopsis chamaeropis; NTUPPMCC 21-056, Pestalotiopsis formosana.
FIGURE 6 in Additions to pestalotioid fungi in Thailand: Neopestalotiopsis hydeana sp. nov. and Pestalotiopsis hydei sp. nov.
FIGURE 6. Pestalotiopsis hydei on leaf of Litsea petiolata.
Fig. 4 in Isolation, absolute configurations and bioactivities of pestaphilones A-I: Undescribed methylated side chain containing-azaphilones from Pestalotiopsis oxyanthi
Fig. 4. Rh2(OCOCF3)4-induced ECD spectrum of compounds 1–3.
Fig. 5 in Isolation, absolute configurations and bioactivities of pestaphilones A-I: Undescribed methylated side chain containing-azaphilones from Pestalotiopsis oxyanthi
Fig. 5. Experimental and calculated ECD spectra of compounds 1–9.
Fig. 2 in Isolation, absolute configurations and bioactivities of pestaphilones A-I: Undescribed methylated side chain containing-azaphilones from Pestalotiopsis oxyanthi
Fig. 2. Selective oxidation reaction of the double bond (Δ11,12) in compound 1.
Fig. 3 in Isolation, absolute configurations and bioactivities of pestaphilones A-I: Undescribed methylated side chain containing-azaphilones from Pestalotiopsis oxyanthi
Fig. 3. Stereochemical determination by acetonide formation of azaphilones.
Fig. 6. X in Isolation, absolute configurations and bioactivities of pestaphilones A-I: Undescribed methylated side chain containing-azaphilones from Pestalotiopsis oxyanthi
Fig. 6. X-ray ORTEP drawing of compounds 1–3.
Fig. 1 in Isolation, absolute configurations and bioactivities of pestaphilones A-I: Undescribed methylated side chain containing-azaphilones from Pestalotiopsis oxyanthi
Fig. 1. Structures of compounds 1–9.
Fig. 1 in Pestalopyrones A-D, four tricyclic pyrone derivatives from the endophytic fungus Pestalotiopsis neglecta S3
Fig. 1. Chemical structures of pestalopyrones A–D (1–4).
Fig. 4 in Pestalopyrones A-D, four tricyclic pyrone derivatives from the endophytic fungus Pestalotiopsis neglecta S3
Fig. 4. ΔδRS (δ- δ) values of (R)-MPA ester of 2 and (S)-MPA ester of 2.
Fig. 2 in Pestalopyrones A-D, four tricyclic pyrone derivatives from the endophytic fungus Pestalotiopsis neglecta S3
Fig. 2. Key COSY and HMBC correlations of pestalopyrones A–D (1–4).
Fig. 5. X in Caryophyllene sesquiterpenoids with various ring systems from the fungus Pestalotiopsis chamaeropis
Fig. 5. X-ray ORTEP drawing of compound 1.
Fig. 3. Key 1 H– 1 H in Caryophyllene sesquiterpenoids with various ring systems from the fungus Pestalotiopsis chamaeropis
Fig. 3. Key 1 H– 1 H COSY and HMBC correlations of compounds 1–6.
Fig. 1 in Caryophyllene sesquiterpenoids with various ring systems from the fungus Pestalotiopsis chamaeropis
Fig. 1. Representative examples of caryophyllene-type sesquiterpenoids.
Fig. 4 in Caryophyllene sesquiterpenoids with various ring systems from the fungus Pestalotiopsis chamaeropis
Fig. 4. Key NOESY correlations of compounds 1–6.
Fig. 6 in Caryophyllene sesquiterpenoids with various ring systems from the fungus Pestalotiopsis chamaeropis
Fig. 6. Derivatization reaction of compound 3.
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