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Ganoderma applanatum

Fig. (3). Hydroxylation of myrcene by Diplodia gossypina (after[24]> and by Ganoderma applanatum and Pleurotus sp. (after [25])... Fig. (3). Hydroxylation of myrcene by Diplodia gossypina (after[24]> and by Ganoderma applanatum and Pleurotus sp. (after [25])...
One of the most recent publications dealing with the bioconversion of myrcene [25] described its transformation to a variety of oxygenated metabolites, with Ganoderma applanatum, Pleurotus flabellatus and Pleurotus sajor-caju possessing the highest transformation activity. The extracted metabolites represented a complex mixture of numerous acyclic and monocyclic metabolites of which myrcenol (12) (2-methyl-6-... [Pg.131]

Vijay HM, Comtois P, Sharma R, Lemieux R Allergenic components of Ganoderma applanatum. Grana 1991 30 167-170. [Pg.47]

WG Campbell. The Chemistry of wood. III. The effect on wood substance of Ganoderma applanatum (Pers.) Pat., Pomes fomentarius (Linn.) Fr., Polyporus adustus (Willd.) Fr., Pleurotus ostreatus (Jacq.) Fr., Armillaria mellea (Vahl.) Fr., Trametes pini (Brot.) Fr., and Polystictus abietinus (Dicks.) Fr. Biochem J. 26 1829-1838, 1932. [Pg.513]

I Dill, G Kraepelin. Palo Podrido Model for extensive delignification of wood by Ganoderma applanatum. Appl Environ Microbiol 52 1305-1312, 1986. [Pg.514]

Ganoderma applanatum (Pers. ex Wallr.) Pat. = Elfvingia applanatum (Pers. ex Wallr.) Karst. [Pg.11]

Chart 10. Bitter triterpenes from Ganoderma applanatum... [Pg.13]

Ganoderma applanatum in addition to some other ergosterol-related steroids (22, 37). [Pg.13]

Nishitoba, T, S. Goto, H. Sato, and S. Sakamura Bitter triterpenoids from the fungus Ganoderma applanatum. Phytochem. 28, 193 (1988). [Pg.19]

Reviews Microbiology 4,102-112. Moncalvo, J.M., Buchanan, P.K. (2008). Molecular evidence for long distance dispersal across the southern hemisphere in the Ganoderma applanatum-australe species complex (Basidiomycota). Mycological Research 112, 425-436. [Pg.189]

Wang F, Dong Z-J, Liu J-K (2007) Benzopyran-4-one Derivatives from the Fungus Ganoderma applanatum. Z Naturforsch 62b 1329... [Pg.265]

Metabolic pathways of myrcene (302) and citronellene (309) by microorganisms and insects are summarized in Figure 14.205. i-Myrcene (302) was metabolized with Diplodia gossypina ATCC 10936 (Abragam et al., 1985) to the diol (303) and a side-product (304). P-Myrcene (302) was metabolized with Ganoderma applanatum, Pleurotus flabellatus, and Pleurotus sajor-caju to myrcenol (305) (2-methyl-6-methylene-7-octen-2-ol) and 306 (Busmann and Berger, 1994). [Pg.720]

Ma J-Q, Liu C-M, Qin Z-H, Jiang J-H, Sun Y-Z (2011) Ganoderma applanatum terpenes protect mouse liver against benzo(a)pyren-induced oxidative stress and inflammation. Enviom Toxicol Pharmacol 31 460-468... [Pg.2689]

Ganoderma lucidum, G. japonicum, G. capense, and G. applanatum are used as fungal sources for the fermentative production of lingzhi biomass (wang). [Pg.301]

See other pages where Ganoderma applanatum is mentioned: [Pg.267]    [Pg.461]    [Pg.498]    [Pg.19]    [Pg.749]    [Pg.587]    [Pg.2679]    [Pg.203]    [Pg.301]    [Pg.267]    [Pg.461]    [Pg.498]    [Pg.19]    [Pg.749]    [Pg.587]    [Pg.2679]    [Pg.203]    [Pg.301]    [Pg.37]    [Pg.241]   
See also in sourсe #XX -- [ Pg.11 , Pg.12 , Pg.14 ]

See also in sourсe #XX -- [ Pg.587 , Pg.720 ]



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