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8 results for “Ganoderma sichuanense”
Figure 2 from: Thawthong A, Hapuarachchi KK, Wen T-C, Raspé O, Thongklang N, Kang J-C, Hyde KD (2017) Ganoderma sichuanense (Ganodermataceae, Polyporales) new to Thailand. MycoKeys 22: 27-43. https://doi.org/10.3897/mycokeys.22.13083
Figure 2 - Ganoderma sichuanense (MFU 16-2668). A upper surface B lower surface C cut side of pileus D pore surface E–H spore I generative hyphae J binding hyphae K skeleton hyphae. Scale bars: 10 µm.
Figure 3 from: Thawthong A, Hapuarachchi KK, Wen T-C, Raspé O, Thongklang N, Kang J-C, Hyde KD (2017) Ganoderma sichuanense (Ganodermataceae, Polyporales) new to Thailand. MycoKeys 22: 27-43. https://doi.org/10.3897/mycokeys.22.13083
Figure 3 - Microscopic structures of Ganoderma sichuanense (MFU 16-2668) A basidiospores B hyphae from trama C hyphae from context. Scale bars: 5 μm.
Figure 1 from: Thawthong A, Hapuarachchi KK, Wen T-C, Raspé O, Thongklang N, Kang J-C, Hyde KD (2017) Ganoderma sichuanense (Ganodermataceae, Polyporales) new to Thailand. MycoKeys 22: 27-43. https://doi.org/10.3897/mycokeys.22.13083
Figure 1 - Phylogram generated by maximum likelihood analysis of 5.8S-ITS rDNA sequences. Bootstrap support values for maximum likelihood (in black) greater than 70% and Posterior Probabilities (PP) from Bayesian Inference (in blue) ≥0.95 are given above branches. The tree was rooted with Tomophagus colossus. The strain numbers are mentioned after the species names. Specimens of the newly recorded species are indicated in red and type specimens are indicated in black bold. (Treebase ID 20740)
Fig. 3. Key NOESY correlations for compound 1 in Lanostane triterpenoids from cultivated fruiting bodies of Ganoderma sichuanense: Determination of the C-25 absolute configuration of ganoderic acid A and its derivatives using the phenylglycine methyl ester (PGME) method
Fig. 3. Key NOESY correlations for compound 1.
Fig. 2. COSY and HMBC correlations for compounds 1–3 in Lanostane triterpenoids from cultivated fruiting bodies of Ganoderma sichuanense: Determination of the C-25 absolute configuration of ganoderic acid A and its derivatives using the phenylglycine methyl ester (PGME) method
Fig. 2. COSY and HMBC correlations for compounds 1–3.
Fig. 4 in Lanostane triterpenoids from cultivated fruiting bodies of Ganoderma sichuanense: Determination of the C-25 absolute configuration of ganoderic acid A and its derivatives using the phenylglycine methyl ester (PGME) method
Fig. 4. Δδ-Values (δ(S) – δ(R)) of the PGME amides 25a/25b, 26a/26b, and 27a/27b.
Fig. 1 in Lanostane triterpenoids from cultivated fruiting bodies of Ganoderma sichuanense: Determination of the C-25 absolute configuration of ganoderic acid A and its derivatives using the phenylglycine methyl ester (PGME) method
Fig. 1. Structures of compounds 1–15.
Fig. 5 in Lanostane triterpenoids from cultivated fruiting bodies of Ganoderma sichuanense: Determination of the C-25 absolute configuration of ganoderic acid A and its derivatives using the phenylglycine methyl ester (PGME) method
Fig. 5. Δδ-Values (δ(S) – δ(R)) of the bis-MTPA esters 28a/28b.
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