Archive for January, 2009

Coprinellus disseminatus

Thursday, January 22nd, 2009


The non-inky coprinus, Coprinellus disseminatus (Pers.) J.E. Lange.
Photo credit:
Dan Molter
Source: Mushroom Observer (CC-by-sa-3.0)

Synonyms

Agaricus disseminatus Pers.
 
  Syn. meth. fung. (Göttingen) 2: 403 (1801)
Agaricus disseminatus Pers.
 
  Syn. meth. fung. (Göttingen) 2: 403 (1801) var. disseminatus
Agaricus striatus sensu Sowerby [Col. Fig. Engl. Fung. Vol. 2, pl. 166 (1798)]

  fide Checklist of Basidiomycota of Great Britain and Ireland (2005)
Coprinarius disseminatus (Pers.) P. Kumm.

  Führ. Pilzk. (Zwickau): 68 (1871)
Coprinus disseminatus (Pers.) Gray

  Nat. Arr. Brit. Pl. (London) 1: 634 (1821)
Psathyrella disseminata (Pers.) Quél.

  Mém. Soc. Émul. Montbéliard, Sér. 2 5: 123 (1872)
Pseudocoprinus disseminatus (Pers.) Kühner

  Le Botaniste 20: 156 (1928)

Common names

Non-inky coprinus
Fairy bonnet
Little helmets
Crumble cap

Description

Cap: 0.5-2 cm diameter, conic to campanulate, yellow-brown to grey-brown, striate or with pleats over the margin; covered with minute glistening particles when young, but glabrous when mature. Flesh very soft, thin, pale buff.
Gills: adnate or free, distant, narrow, white when young, grey to black in age, not deliquescing to the same extent as other Coprinellus species.
Stem: 2-4 cm long, 0.1-0.2 cm thick, equal, curved, surface smooth to slightly scurfy, white, hollow.
Odor and taste: not distinctive.
Spore print: black.
Spores: elliptical, smooth, thick-walled, with an apical pore, nonamyloid, 7-10 x 4-6 µm.
Habitat: found growing gregariously in dense troops on well-rotted wood or buried wood, or at the base of standing dead trees. Fruiting in spring, summer and fall.
Edibility: edible (i.e., non-poisonous) but small and insubstantial.

Fruiting bodies are very fragile and likely to crumble on contact.

Medicinal properties

Antitumor effects

Extracts of the mycelial culture of Coprinellus disseminatus inhibits proliferation and induces apoptosis in human cervical carcinoma cells by activation of caspase, a key protein involved in the regulation of apoptosis (Han et al., 1999).

Polysaccharides extracted from the mycelial culture of C. disseminatus and administered intraperitoneally into white mice at a dosage of 300 mg/kg inhibited the growth of Sarcoma 180 and Ehrlich solid cancers by 100% and 90%, respectively (Ohtsuka et al., 1973).

Links

Mushroom Expert
California Fungi

References

Han BY, Toyomasu T, Shinozawa T.
Induction of apoptosis by Coprinus disseminatus mycelial culture broth extract in human cervical carcinoma cells.
Cell Structure and Function 24(4):209-15.

Ohtsuka S, Ueno S, Yoshikumi C, Hirose F, Ohmura Y, Wada T, Fujii T, Takahashi E.
Polysaccharides having an anticarcinogenic effect and a method of producing them from species of Basidiomycetes.
 UK Patent 1331513, 26 September 1973.

 

Last modified: 8-May-2009

Tricholomopsis rutilans

Thursday, January 15th, 2009

 

The medicinal mushroom Tricholomopsis rutilans

Top view of "plums and custard", Tricholomopsis rutilans (Schaeff.) Singer, displaying the characteristic red squamules.
Photo credit: Alan Rockefeller
Source: Mushroom Observer (CC-by-sa-3.0)

Synonyms

Agaricus rutilans Schaeff.

  Fung. Bavar. Palat. 4: 51 (1774)
Agaricus serratis Bolton

  Hist. fung. Halifax (Huddersfield) 1: pl. 14 (1788)
Agaricus variegatus Scop.

  Fl. carniol., Edn 2 (Wien) 2: 434 (1772)
Agaricus xerampelinus Sowerby

  Coloured figures of English Fungi or Mushrooms (London) 1: tab. 31 (1796)
Gymnopus rutilans (Schaeff.) Gray

  Nat. Arr. Brit. Pl. (London) 1: 605 (1821)
Tricholoma rutilans (Schaeff.) P. Kumm.

  Führ. Pilzk. (Zwickau): 133 (1871)
Tricholoma variegatum (Scop.) Fr.

  Syll. fung. (Abellini) 5: 96 (1887)
Tricholomopsis rutilans var. variegata (Scop.) Bon

  Encyclop. Mycol. 36: 291 (1984)
Tricholomopsis variegata (Scop.) Singer

  Annls mycol. 41(1/3): 67 (1943)

Common names

Plums and custard
Red-haired agaric
Tricholome rutilant (French)
Rötlicher Holzritterling Purpurfilziger (German)
Purpur væbnerhat (Danish)
Purppuravalmuska (Finnish)
Рядовка жёлто-красная Опёнок жёлто-красный (Russian)
Prickmusseron (Swedish)
Šafránka červenožlutá (Czech)
Rycerzyk czerwonozłoty (Polish)
Čírovec červenožltý (Slovakian)
Rdečkasta trhlenka (Slovenian)
 サマツモドキ (Japanese)
Tricoloma rutilante (Spanish)
Koningsmantel (Dutch)
Bársonyos pereszke (Hungarian)
Rød stubbemusserong (Norwegian)

Description

Cap: 3-8 cm in diameter, obtuse with an incurved often ribbed margin, expanding to campanulate and nearly flat in maturity, usually retaining a low obtuse umbo; surface dry and tomentose-squamulose, the squamules bright purplish red, at times appearing to be covered by a closely matted purplish-red tomentum and more granular-roughened than scaly; scales developing in age as the tomentose layer becomes pulled apart; a strong yellow cast finally showing beneath the fibrillose layer, or this region often yellowish where bruised; flesh thick, up to 2 cm in the umbo, about 5 mm half way to the margin, pale yellow, the odor none, the taste slightly of radish.
Gills: adnate becoming adnexed, narrow (5 mm), crowded (3-4 tiers of lamellulae), straw yellow or a deeper shade, edges crenulate.

Note the characteristic red fibrils on the stem with a pale zone at the apex, and the yellow gills.
Photo credit & source: Alan Rockefeller, as above.

Stem: 5-10 cm long x 8-15 mm diameter at apex (up to 25 mm at the slightly enlarged base) stuffed becoming hollow, yellowish within, the surface covered with appressed "Corinthian red" fibrils with a paler zone at apex, staining yellow where handled.
Spore print: white.
Spores: ellipsoid to drop-shaped, smooth, nonamyloid, 5-6 x 3.5-4.5 um.
Taste:
Odor: farinaceous. An in-depth analysis of the various volatile and semivolatile compounds responsible for the aroma of this species is presented in De Pinho et al., (2008).
Edibility: edible, or inedible depending on your taste and who you listen to.  Not recommended by several authors.
Habitat: found fruiting solitry or clustered on conifer stumps, logs, and wood chips.
Distribution: T. rutilans has a widespread distribution, especially in Northern temperate regions.

Description largely adapted from Smith (1960), who also gives details on microscopic features, and mentions the variant T. rutilans var. albofimbriata, characterized by elongated cheilocystidia.

Biochemistry

Amino acid composition

Various unusual amino acids have been isolated and identified from T. rutilans, namely l-3-(3-carboxy-4-furyl)alanine (Hatanaka and Niimura, 1975), l-2-aminohex-4-ynoic acid (Hatanaka et al., 1972) and 2-amino-3-hydroxyhex-4-ynoic acid as a mixture of threo- and erythro-2-amino-3-hydroxyhex-4-ynoic acid forms (Niimura and Hatanaka, 1974). An extensive compositional amino acid analysis was recently undertaken, and this species had the lowest total amino acid composition (>5 g/kg dry matter) of all eight edible species tested; glutamine (1.46 mg/kg) and alanine (0.94 mg/mg) were present in the greatest abundance (Ribeiro et al., 2008).

Organic acids & phenolics

The sum of the carboxylic acids assayed in T. rutilans (specifically: oxalic, aconitric, citric, ketoglutaric, malic and quinic, ascorbic, succinic, shikimic and fumaric acids) was approximately 40 g/kg dried mushroom. This species contains malic and quinic acids as the major compounds (approximately 52% of nonaromatic acids), followed by citric acid (19% of nonaromatic compounds). Variations in geographical location and maturity of the collected specimens resulted in some variability in results (Ribeiro et al., 2006).

Bioactive compounds

The highly oxygenated phenol fomecin B (shown below) has been isolated from T. rutilans. Fomecin B is cytotoxic against HeLa, MDCK, and FL cells with IC50 values of 20, 14, and 17 μg/mL, respectively (Liberra et al., 1995).
 
Fomecin B.

Sterols

The novel sterols 3β,5α-dihydroxy-(22E,24R)-ergosta-7,22-dien-6β-yl oleate and 3β,5α-dihydroxy-(22E,24R)-ergosta-22-en-7-one-6β-yl oleate has been isolated from the ethanol extract, as well as the previously known (22E,24R)-5α,8α-epidioxyergosta-6,22-dien-3β-ol, 3β-hydroxy-(22E,24R)-ergosta-5,8,22-trien-7-one, and (22E,24R)-5α,6α-epoxyergosta-8(14),22-dien-3β,7α-diol (Wang and Lui, 2004).

Medicinal properties
Antioxidant effects

Measured with the DPPH• radical scavenging assay, the antioxidative capacity of T. rutilans although relatively low, was the highest of several edible mushroom species tested (Ribeiro et al., 2006). The extract showed a concentration-dependent DPPH• radical scavenging ability; at a concentration of 600 μg/ml, radical scavenging was over 90%.

Antitumor effects

Polysaccharides extracted from the mycelial culture of T. rutilans and administered intraperitoneally into white mice at a dosage of 300 mg/kg inhibited the growth of both Sarcoma 180 and Ehrlich solid cancers by 60% (Ohtsuka et al., 1973).

Antiinflammatory effects

T. rutilans has been studied for its influence on the binding of lipopolysaccharides to CD14+ cells and on the release of inflammatory mediators (Koch et al., 1998, 2002). Ethanol extracts were shown to reduce the binding of LPS and the release of mediators, as well as decrease the LPS-induced release of IL-1 and TNF-αin a concentration dependent manner.

Links

References

De Pinho PG, Ribeiro B, Goncalves RF, Baptista P, Valentao P, Seabra RM, Andrade PB.
Correlation between the pattern volatiles and the overall aroma of wild edible mushrooms.
J Agric Food Chem 2008 56(5):1704-12.
Pubmed

Hatanaka S-I, Niimura Y.
l-3-(3-carboxy-4-furyl)alanine from Tricholomopsis rutilans.
Phytochemistry 1975

Hatanaka SI, Niimura Y, Taniguchi K.
l-2-Aminohex-4-ynoic acid: a new amino acid from Tricholomopsis rutilans.
Phytochemistry 1972 11(11):3327-9.

Koch J, Witt S, Liberra K, Lindequist U.
The influence of extracts of Tricholomopsis rutilans (schff.ex fr.) sing. on the binding of LPS to CD14+- cells and on the release of inflammatory mediators.
Phytother. Res. 1998 12:27-29.

Koch J, Witt S, Lindequist U.
The influence of selected higher Basidiomycetes on the binding of lipopolysaccharide to CD14+ cells and on the release of cytokines.
Int J Medicin Mushr. 2002 4(3):229-235.

Liberra K, Jansen R, Wegner U, Lindequist U.
Tricholomopsis rutilans Formecin B as a cytotoxic metabolite from the basidiomycete (Schaeff. ex Fr.) Sing.
Pharmazie 1995 50(5):370-371.
Pubmed

Niimura Y, Hatanaka SI.
l-threo- and l-erythro-2-amino-3-hydroxyhex-4-ynoic acids: new amino acids from Tricholomopsis rutilans.
Phytochemistry 1974 13:175-178.

Ohtsuka S, Ueno S, Yoshikumi C, Hirose F, Ohmura Y, Wada T, Fujii T, Takahashi E.

Polysaccharides having an anticarcinogenic effect and a method of producing them from species of Basidiomycetes.

UK Patent 1331513, 26 September 1973.

Ribeiro B, Rangel J, Valentao P, Baptista P, Seabra RM, Andrade PB.

Contents of carboxylic acids and two phenolics and antioxidant activity of dried Portuguese wild edible mushrooms.

J Agric Food Chem. 2006 54(22):8530-7.

Pubmed

Ribeiro B, Andrade PB, Silva BM, Baptista P, Seabra RM, Valentao P.
Comparative study on free amino acid composition of wild edible mushroom species.
J Agric Food Chem 56(22):10973-9.
Pubmed

Smith AH.
Tricholomopsis (Agaricales) in the Western Hemisphere.
Brittonia 1960 12(1):41-70.

Wang F, Liu JK.
Two new steryl esters from the basidiomycete Tricholomopsis rutilans.
Steroids 2005 70(2):127-130.
Pubmed

 

Last modified: 15-Jan-2009

Cyathus stercoreus

Saturday, January 3rd, 2009

The "dung-loving bird's nest", Cyathus stercoreus (Schwein.) de Toni. These specimens were found in Japan.
Photo credit: user:forestwander
Source: Mushroom Observer (CC-by-sa-3.0)

Synonyms

Cyathia stercorea (Schwein.) V.S. White

  Bull. Torrey bot. Club 29: 266 (1902)

Nidularia stercorea Schwein.

  Trans. Am. phil. Soc. 4(2): 253 (1832)

Common name

Dung loving bird's nest

Description

Fruiting bodies: up to 1.5 cm tall x 4-8 mm wide, goblet-shaped (obconic) "nests". The inner surface is nongrooved and nonfurrowed, which helps distinguish it from the related bird's nest fungi Cyathus striatus. The outer surface is tomentose (more so when young) and yellow-brown in color, becoming smoother and darker in color in maturity. Periodioles are attached to the fruiting bodies by a thin cord called a funiculus. Peridioles are dark grey to black in color, 1-2 mm in diameter.
Spores: variable in size and shape, but typically globose or oval, smooth, thick-walled, and 18-40 x 18-30 µm. Further details about spore morphology may be found in Brodie and Dietrich (1977).
Habitat: this saprobic species is found growing on dung of herbivores, on soil containing manure, or on wood chips. Grows gregariously or in dense clusters.

The ultrastructure of this species has been described in detail (Flegler and Hooper, 1978).

Medicinal properties

Antioxidant effects

The polyketide antioxidative compounds, cyathusals A, B, and C as well as the previously known compound pulvinatal have been isolated from C. stercoreus (Kang et al., 2007). The cyathusals have antioxidant activity (measured by DPPH and ABTS radical scavenging assays) roughly comparable to reference antioxidants Trolox and BHA.

Antioxidant polyketides from C. stercoreus: from left to right, cyathusals A, B, C.

Further investigations led to the discovery of of cyathuscavins A, B, and C along with the known compound 4-hydroxy-6-propenyl-pyran-2-one (Kang et al., 2008). The former 3 compounds showed good antioxidative activity, as measured by radical scavenging activity in the DPPH assay, and the ABTS+ assay. Cyathuscavins A and B (but not C) also scavenged superoxide (O2-) radicals more effectively than the control compound BHA. All three cyathuscavins also protected supercoiled DNA from Fenton reaction-mediated DNA breakage.


Cyathuscavin A.

Cyathuscavin B.

Cyathuscavin C.

4-hydroxy-6-propenyl-pyran-2-one.

Links

References

Brodie HJ, Dietrich HF.
Spore morphology in the Nidulariaceae fungi as revealed by the scanning electron microscope.
Can J Bot 1977 55(24):3042-3045.

Flegler SL, Hooper GR.
Ultrastructure of Cyathus stercoreus.
Mycologia 1978 70(6):1181-1190.

Kang H-S, Jun E-M, Park S-H, Heo S-J, Lee T-S, Yoo I-D, Kim J-P.
Cyathusals A, B, and C, antioxidants from the fermented mushroom Cyathus stercoreus.
J Nat Prod 2007 70(6):1043-1045.

Kang H-S, Kim K-R, Jun E-M, Park S-H, Lee T-S, Suh J-W, Kim J-P.
Cyathuscavins A, B, and C, new free radical scavengers with DNA protection activity from the Basidiomycete Cyathus stercoreus.
Bioorganic & Medicinal Chemistry Letters. 2008 18(14):4047-4050.

 

 

Last modified: 03-Jan-2008

Clavaria vermicularis

Thursday, January 1st, 2009


The coral fungus Clavaria vermicularis, commonly known as fairy fingers.
Photo credit: Dr. Robert Thomas and Dorothy B. Orr © 2001 California Academy of Sciences
Source:  Calphotos

Synonyms

This species is also known as Clavaria fragilis Holmsk.

Description

Sporocarp: the fruiting body, typically between 2-8 cm tall x 2-3 mm thick, is white in color (yellowish towards the tips), smooth, and fragile. Sporocarps are occasionally forked once, and often curved.
Spore print: white.
Spores: elliptical in shape, smooth, thin-walled, and 4.5-7 x 2.5-4.0 µm.
Edibility: edible but watery and insubstantial.
Habitat: this species usually found clustered in tufts growing on the ground in mixed woods or in grassy places; late-fall to mid-winter.

C. vermicularis is the type species of the genus Clavaria.

Common name

Fairy fingers
White spindles
White worm coral
Valkonuijakas (Finnish)
Clavaire vermiclée (French)
Weisse Keule (German)
Maskfingersvamp (Swedish) 

Medicinal properties
Antitumor effects

An extract of the fruit bodies of C. vermicularis inhibited the growth of Sarcoma 180 and Ehrlich solid cancers in mice by 90% and 80%, respectively (Ohtsukaet al., 1973).

Links

References

Ohtsuka S, Ueno S, Yoshikumi C, Hirose F, Ohmura Y, Wada T, Fujii T, Takahashi E.
Polysaccharides having an anticarcinogenic effect and a method of producing them from species of Basidiomycetes.
UK Patent 1331513, 26 September 1973.

 

Last modified: 01-Jan-2009