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145 results for “Basidiomycete”

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zenodo28/100

Figure 17 from: Petersen RH, Hughes KW (2016) Micromphale sect. Perforantia (Agaricales, Basidiomycetes); Expansion and phylogenetic placement. MycoKeys 18: 1-122. https://doi.org/10.3897/mycokeys.18.10007

Figure 17 - Gymnopus foliiphilus var. costaricensis. A Basidiomata and rhizomorphs B Pileus underside showing lamellar spacing C Pleurocystidia D Basidia E Pileipellis hyphae, showing encrustation and lobose side-branches F Basidiospores. Standard bars: A = 5 mm; B = not to scale; C–E = 20 µm; F = 5 µm. TFB 9750.

opencc-by-4.0Dec 2016View details →
zenodo28/100

Figure 13 from: Petersen RH, Hughes KW (2016) Micromphale sect. Perforantia (Agaricales, Basidiomycetes); Expansion and phylogenetic placement. MycoKeys 18: 1-122. https://doi.org/10.3897/mycokeys.18.10007

Figure 13 - Gymnopus foliiphilus. Pleurocystidia and basidia. A–D Pleurocystidia E–H Basidia. Standard bars = 10 µm. TFB 11555 (TENN-F-59441).

opencc-by-4.0Dec 2016View details →
zenodo28/100

Figure 16 from: Petersen RH, Hughes KW (2016) Micromphale sect. Perforantia (Agaricales, Basidiomycetes); Expansion and phylogenetic placement. MycoKeys 18: 1-122. https://doi.org/10.3897/mycokeys.18.10007

Figure 16 - Gymnopus foliiphilus. Caulocystidia from lower stipe. Standard bars = 10 µm. TFB 2800 (TENN-F-49363).

opencc-by-4.0Dec 2016View details →
zenodo28/100

Figure 12 from: Petersen RH, Hughes KW (2016) Micromphale sect. Perforantia (Agaricales, Basidiomycetes); Expansion and phylogenetic placement. MycoKeys 18: 1-122. https://doi.org/10.3897/mycokeys.18.10007

Figure 12 - Gymnopus foliiphilus. Pileipellis elements. A–C Encrusted hyphae D Hyphae showing secondary septa E Gelatinized hyphal walls F, G Lobate side branches. Standard bars = 10 µm. TFB 2800 (TENN-F-49363).

opencc-by-4.0Dec 2016View details →
zenodo28/100

Figure 15 from: Petersen RH, Hughes KW (2016) Micromphale sect. Perforantia (Agaricales, Basidiomycetes); Expansion and phylogenetic placement. MycoKeys 18: 1-122. https://doi.org/10.3897/mycokeys.18.10007

Figure 15 - Gymnopus foliiphilus. Caulocystidia from upper stipe. Standard bars = 10 µm. TFB 2800 (TENN-F-49363).

opencc-by-4.0Dec 2016View details →
zenodo28/100

Figure 14 from: Petersen RH, Hughes KW (2016) Micromphale sect. Perforantia (Agaricales, Basidiomycetes); Expansion and phylogenetic placement. MycoKeys 18: 1-122. https://doi.org/10.3897/mycokeys.18.10007

Figure 14 - Gymnopus foliiphilus. Basidiospores. Standard bar = 5 µm. A = TFB 11608 (TENN-F-59641); B = TFB 14322 (TENN-F-68183).

opencc-by-4.0Dec 2016View details →
zenodo28/100

Figure 1 from: Petersen RH, Hughes KW (2016) Micromphale sect. Perforantia (Agaricales, Basidiomycetes); Expansion and phylogenetic placement. MycoKeys 18: 1-122. https://doi.org/10.3897/mycokeys.18.10007

Figure 1 - Gymnopus bulliformis. A, B Basidiomata C, D Basidiospores. Standard bars: A, B = 20 mm; C, D = 5 µm. A, C WTU-F-9305; B, D WTU-F-51955.

opencc-by-4.0Dec 2016View details →
zenodo28/100

Figure 2 from: Qiao M, Li W, Huang Y, Xu J, Zhang L, Yu Z (2018) Classicula sinensis, a new species of basidiomycetous aquatic hyphomycetes from southwest China. MycoKeys 40: 1-12. https://doi.org/10.3897/mycokeys.40.23828

Figure 2 Microscopic features of Classiculasinensis (holotype YMF 1.04613). a, b Conidia c empty conidia d clamp connection on conidia e Haustorial branches with basal clamps on hyphae f Conidiogenous cells (black arrow) and clamp connection on hyphae (white arrow). Scale bar: 10 µm (a–f).

opencc-by-4.0Sep 2018View details →
zenodo28/100

Figure 1 from: Qiao M, Li W, Huang Y, Xu J, Zhang L, Yu Z (2018) Classicula sinensis, a new species of basidiomycetous aquatic hyphomycetes from southwest China. MycoKeys 40: 1-12. https://doi.org/10.3897/mycokeys.40.23828

Figure 1 Phylogenetic tree based on Bayesian analysis of the combined ITS, TEF1, 18S and 28S rDNA sequences. Auricularia sp. and Coprinuscomatus of Agaricomycotina are used as outgroups. Clades and taxa are labelled according to Schell et al. (2011). Bayesian posterior probabilities, greater than 0.95, are given above the nodes (out of 100). Maximum likelihood bootstrap values, greater than 75%, are given below the nodes (out of 100). The scale bar shows the expected changes per site.

opencc-by-4.0Sep 2018View details →
dryad28/100

Symbiotic nitrogen fixation in the reproductive structures of a basidiomycete fungus

<p><span>Nitrogen (N) fixation is a driving force for the formation of symbiotic associations between N</span><sub><span>2</span></sub><span>-fixing bacteria and eukaryotes.</span><sup><span>1</span></sup><span> Limited examples of these associations are known in fungi, and none with the sexual structures of species outside of lichens.</span><sup><span>2-6</span></sup><span>  The basidiomycete, </span><i><span>Guyanagaster necrorhizus</span></i><span>, is a sequestrate fungus endemic to the Guiana Shield.</span><sup><span>7</span></sup><span> Much like the root rot-causing species in its sister genera, </span><i><span>Armillaria</span></i><span> and </span><i><span>Desarmillaria</span></i><span>, </span><i><span>G. necrorhizus</span></i><span> sporocarps fruit from the roots of decaying trees (Figures 1A, 1B and 1C),</span><sup><span>8</span></sup><span> and genome sequencing is consistent with observations that </span><i><span>G. necrorhizus</span></i><span> is a white-rotting decomposer. This species also represents the first documented instance of an arthropod-dispersed sequestrate fungus. Numerous species of distantly related wood-feeding termites, which scavenge for N-rich food, </span><a><span>feed on </span></a><span>mature </span><i><span>G. necrorhizus</span></i><span> gleba, </span><span><span>the interior spore-bearing tissue</span></span><span>. During feeding, mature spores adhere to termites for subsequent dispersal.<sup>9</sup> Using chemical assays, isotope analysis and high-throughput sequencing, we show that the sporocarps harbor actively N</span><sub><span>2</span></sub><span>-fixing Enterobacteriaceae species and that the N content within fungal tissue increases with maturation. Untargeted proteomic profiling suggests that ATP generation in the gleba is accomplished via fermentation. The use of fermentation—an anaerobic process—indicates that the sporocarp environment is anoxic, likely an adaptation to protect the oxygen-sensitive nitrogenase enzyme. Sporocarps also have a thick outer covering, possibly to limit oxygen diffusion. The enriched N</span><sub><span>2</span></sub><span> content within mature sporocarps may offer a dietary inducement for termites in exchange for spore dispersal to woody substrates. These results show that the flexible metabolic capacity of fungi may facilitate N</span><sub><span>2</span></sub><span>-fixing associations, as well as higher-level organismal associations.</span></p>

opencc-zeroJul 2021View details →
zenodo28/100

Fig. 3. Key NOESY correlations for 1 and 4 in Lanostane triterpenoids from cultivated fruiting bodies of basidiomycete Ganoderma mbrekobenum

Fig. 3. Key NOESY correlations for 1 and 4 in acetone-d6.

opennotspecifiedApr 2022View details →
zenodo28/100

Fig. 2. COSY and HMBC correlations for 1, 4, 5 in Lanostane triterpenoids from cultivated fruiting bodies of basidiomycete Ganoderma mbrekobenum

Fig. 2. COSY and HMBC correlations for 1, 4, 5, and 9.

opennotspecifiedApr 2022View details →
zenodo28/100

Fig. 3 in Sesquiterpenes with diverse skeletons from histone deacetylase inhibitor modified cultures of the basidiomycete Cyathus stercoreus (Schwein.) De Toni HFG134

Fig. 3. ECD and NMR of 1 and 2.

opennotspecifiedMar 2022View details →
zenodo28/100

Fig. 2. Key 2D in Sesquiterpenes with diverse skeletons from histone deacetylase inhibitor modified cultures of the basidiomycete Cyathus stercoreus (Schwein.) De Toni HFG134

Fig. 2. Key 2D NMR correlations of compounds 1–9.

opennotspecifiedMar 2022View details →
zenodo28/100

Fig. 1 in Sesquiterpenes with diverse skeletons from histone deacetylase inhibitor modified cultures of the basidiomycete Cyathus stercoreus (Schwein.) De Toni HFG134

Fig. 1. The chemical structures of compounds 1–13.

opennotspecifiedMar 2022View details →
zenodo28/100

Fig. 1 in Lanostane triterpenoids from cultivated fruiting bodies of the wood-rot basidiomycete Ganoderma casuarinicola

Fig. 1. Structures of compounds 1–21.

opennotspecifiedFeb 2020View details →
zenodo28/100

Fig. 4 in Limonoids from fruiting bodies of the wood-rot basidiomycete Fulvifomes xylocarpicola associated with the mangrove tree Xylocarpus granatum

Fig. 4. Crystal structure of 1.

opennotspecifiedJan 2021View details →
zenodo28/100

Fig. 2. COSY and key HMBC correlations for 1 and 2 in Limonoids from fruiting bodies of the wood-rot basidiomycete Fulvifomes xylocarpicola associated with the mangrove tree Xylocarpus granatum

Fig. 2. COSY and key HMBC correlations for 1 and 2.

opennotspecifiedJan 2021View details →
zenodo28/100

Fig. 1 in Limonoids from fruiting bodies of the wood-rot basidiomycete Fulvifomes xylocarpicola associated with the mangrove tree Xylocarpus granatum

Fig. 1. Structures of compounds 1–5.

opennotspecifiedJan 2021View details →
zenodo28/100

Fig. 3. Key NOESY correlations for 1 in Limonoids from fruiting bodies of the wood-rot basidiomycete Fulvifomes xylocarpicola associated with the mangrove tree Xylocarpus granatum

Fig. 3. Key NOESY correlations for 1.

opennotspecifiedJan 2021View details →

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