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1.
Chembiochem ; 21(11): 1613-1620, 2020 06 02.
Artigo em Inglês | MEDLINE | ID: mdl-31972067

RESUMO

Mycenarubin C, a previously unknown red pyrroloquinoline alkaloid, was isolated from fruiting bodies of the mushroom Mycena rosea and its structure was elucidated mainly by NMR spectroscopy and mass spectrometry. Unlike mycenarubin A, the major pyrroloquinoline alkaloid in fruiting bodies of M. rosea, mycenarubin C, contains an eight-membered ring with an additional C1 unit that is hitherto unprecedented for pyrroloquinoline alkaloids known in nature. Incubation of mycenarubin A with an excess of formaldehyde revealed that mycenarubin C was generated nearly quantitatively from mycenarubin A. An investigation into the formaldehyde content of fresh fruiting bodies of M. rosea showed the presence of considerable amounts of formaldehyde, with values of 5 µg per gram of fresh weight in fresh fruiting bodies. Although mycenarubin C did not show bioactivity against selected bacteria and fungi, formaldehyde inhibits the growth of the mycoparasite Spinellus fusiger at concentrations present in fruiting bodies of M. rosea. Therefore, formaldehyde might play an ecological role in the chemical defence of M. rosea against S. fusiger. In turn, S. fusiger produces gallic acid-presumably to detoxify formaldehyde by reaction of this aldehyde with amino acids and gallic acid to Mannich adducts.


Assuntos
Agaricales/química , Alcaloides/farmacologia , Formaldeído/farmacologia , Carpóforos/química , Mucorales/efeitos dos fármacos , Pirróis/farmacologia , Quinolinas/farmacologia , Agaricales/imunologia , Agaricales/metabolismo , Alcaloides/biossíntese , Aminoácidos/metabolismo , Antibiose , Formaldeído/metabolismo , Carpóforos/imunologia , Carpóforos/metabolismo , Ácido Gálico/metabolismo , Inativação Metabólica/fisiologia , Espectroscopia de Ressonância Magnética , Estrutura Molecular , Mucorales/metabolismo , Pirróis/metabolismo , Quinolinas/metabolismo
2.
J Microbiol Biotechnol ; 19(6): 566-72, 2009 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-19597314

RESUMO

Lentinus edodes is a well-known edible and medicinal mushroom used in Oriental cultures. Recently, L. edodes has attracted a lot of attention owing to its antifungal activity, antibacterial activity, antiviral activity, hepatoprotective effect, antitumor activities, and immunomodulatory and cytotoxic effects. In this study, the water-soluble crude polysaccharides, CPF and CPB, which were obtained from the fruiting body and culture cell-free broth of L. edodes by hot-water extraction and ethanol precipitation, were fractionated by DEAE cellulose and Sepharose CL-6B column chromatography, resulting in six polysaccharide fractions, CPFN-G-I, CPFN-G-II, CPFN-G-III, CPFA-G, CPBN-G, and CPBA-G. Among these fractions, CPFN-GI, CPBN-G, and CPBA-G were shown to stimulate the functional activation of macrophages including NO production cytokine expression and phagocytosis.


Assuntos
Carpóforos/imunologia , Imunização , Macrófagos/efeitos dos fármacos , Polissacarídeos/farmacologia , Cogumelos Shiitake/imunologia , Animais , Linhagem Celular , Sobrevivência Celular , Cromatografia em Gel , Cromatografia por Troca Iônica , Carpóforos/química , Macrófagos/imunologia , Macrófagos/metabolismo , Camundongos , Óxido Nítrico/biossíntese , Polissacarídeos/imunologia , Polissacarídeos/isolamento & purificação , Cogumelos Shiitake/química , Fator de Necrose Tumoral alfa/biossíntese
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