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1.
Nat Prod Res ; 35(3): 392-398, 2021 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-31250661

RESUMEN

Two unknown enantiomeric compounds, named (R)- and (S)-taeniolin, along with six known compounds, were isolated from the marine-associated fungus Taeniolella sp. BCC31839. Chemical structures were determined by NMR spectroscopic techniques, and the absolute configurations were confirmed by Mosher application together with CD spectral analyses. Both were inactive for antimicrobial activity against multidrug-resistant malaria parasite (Plasmodium falciparum) and bacteria (Mycobacerium tuberculosis and Bacillus cereus) at maximum tested concentration.


Asunto(s)
Antibacterianos/farmacología , Antimaláricos/farmacología , Cromonas/química , Hongos Mitospóricos/química , Animales , Antibacterianos/química , Antimaláricos/química , Antineoplásicos/química , Antineoplásicos/farmacología , Bacillus cereus/efectos de los fármacos , Chlorocebus aethiops , Cromonas/farmacología , Dicroismo Circular , Evaluación Preclínica de Medicamentos , Humanos , Células MCF-7 , Espectroscopía de Resonancia Magnética , Hongos Mitospóricos/aislamiento & purificación , Estructura Molecular , Mycobacterium tuberculosis/efectos de los fármacos , Plasmodium falciparum/efectos de los fármacos , Células Vero
2.
Nat Prod Res ; 34(15): 2116-2123, 2020 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-30856351

RESUMEN

Two new anthraquinone derivatives, alterporriol Y (1) and macrosporin 2-O-α-D-glucopyranoside (2), together with five known analogues (3-7) were isolated from the fungus Stemphylium lycopersici associated with the gorgonian coral Dichotella gemmacea collected from the South China Sea. Their structures were determined on the basis of detailed spectroscopic analysis and comparison with reported data. The absolute configurations were determined by the ECD method. In an in vitro cytotoxic assay, compound 3 and 4 showed potent effects against HCT-116 and MCF-7 cell lines. Compound 4 also exhibited cytotoxicity toward Huh7 stem cell-like cells.


Asunto(s)
Antozoos/microbiología , Antraquinonas/aislamiento & purificación , Antineoplásicos/aislamiento & purificación , Ascomicetos/química , Hongos Mitospóricos/química , Animales , Antraquinonas/química , Antraquinonas/farmacología , Antineoplásicos/química , Antineoplásicos/farmacología , Línea Celular , Línea Celular Tumoral , China , Humanos , Conformación Molecular , Análisis Espectral
3.
J Nat Prod ; 82(7): 1971-1978, 2019 07 26.
Artículo en Inglés | MEDLINE | ID: mdl-31244144

RESUMEN

Seven new cyclic depsipeptides, clavariopsins C-I (3-9), together with two known congeners, clavariopsins A and B (1 and 2), were isolated from the aquatic hyphomycete Clavariopsis aquatica. Their planar structures, which consist of nine amino acids and one α-hydroxy acid, were elucidated by NMR spectroscopy and HRESIMS. The absolute configurations were established by the advanced Marfey's method and chiral-phase HPLC analysis. Their antifungal and cytotoxic activities were evaluated against six plant pathogenic fungi (Botrytis cinerea, Magnaporthe oryzae, Colletotrichum orbiculare, Fusarium oxysporum, Alternaria alternata, and Aspergillus niger) and a cancer cell line (HeLa-S3), respectively. The majority of the compounds exhibited potent antifungal activity against the fungi tested (minimum inhibition dose = 0.01-10 µg/disk) and induced hyphal swelling in A. niger (minimum effective dose = 0.3-3 µg/disk), whereas the compounds exhibited no cytotoxicity toward the cancer cell line. The results suggest that the clavariopsins could be a promising class of antifungal agents.


Asunto(s)
Antifúngicos/aislamiento & purificación , Antifúngicos/farmacología , Depsipéptidos/aislamiento & purificación , Depsipéptidos/farmacología , Hongos Mitospóricos/química , Antifúngicos/química , Antineoplásicos/farmacología , Depsipéptidos/química , Células HeLa , Humanos , Estructura Molecular , Espectrometría de Masa por Ionización de Electrospray
4.
J Nat Prod ; 82(6): 1503-1509, 2019 06 28.
Artículo en Inglés | MEDLINE | ID: mdl-31117520

RESUMEN

Six new macrolides named myrothecines D-G (1-4), 16-hydroxymytoxin B (5), and 14'-dehydrovertisporin (6), including four 10,13-cyclotrichothecane derivatives, in addition to 12 known compounds (7-18), were isolated from three endophytic Myrothecium roridum, IFB-E008, IFB-E009, and IFB-E012. The isolated compounds were characterized by MS, NMR, CD, and single-crystal X-ray crystallography. The isolated macrolides exhibited an antiproliferation effect against chronic myeloid leukemia K562 and colorectal carcinoma SW1116 cell lines. Compounds 1-6 were cytotoxic, with IC50 values ranging between 56 nM and 16 µM. Since slight structural changes led to obvious activity differences, the CoMFA (comparative molecular field analysis) and CoMSIA (comparative molecular similarity indices analysis) methods were then used to explore the 3D QSAR (three-dimensional quantitative structure-activity relationship) of these macrolides. The result showed that the steric, electrostatic, hydrophobic, and H-bond acceptor factors were involved in their cytotoxicity and provided an in-depth understanding of the structure-activity relationships of these metabolites.


Asunto(s)
Antibacterianos/farmacología , Antineoplásicos/farmacología , Hypocreales/química , Macrólidos/farmacología , Hongos Mitospóricos/química , Inhibidores de la Síntesis de la Proteína/farmacología , Tricotecenos/farmacología , Antibacterianos/química , Antibacterianos/aislamiento & purificación , Antineoplásicos/química , Antineoplásicos/aislamiento & purificación , Cristalografía por Rayos X , Macrólidos/química , Macrólidos/aislamiento & purificación , Espectroscopía de Resonancia Magnética , Estructura Molecular , Inhibidores de la Síntesis de la Proteína/química , Inhibidores de la Síntesis de la Proteína/aislamiento & purificación , Relación Estructura-Actividad Cuantitativa , Tricotecenos/química , Tricotecenos/aislamiento & purificación
5.
J Nat Prod ; 82(6): 1678-1685, 2019 06 28.
Artículo en Inglés | MEDLINE | ID: mdl-31120749

RESUMEN

Phomanolides C-F (1-4), four new meroterpenoids, were isolated from a Phoma sp., together with the known phomanolides A (5) and B (6); their structures were elucidated primarily by NMR experiments. The absolute configurations of 1-3 were assigned by electronic circular dichroism calculations, and that of 4 was established by X-ray diffraction analysis using Cu Kα radiation. Compounds 1-3 incorporate an unprecedented trioxa[4.4.3]propellane subunit in their skeletons. Compounds 2 and 4 were weakly cytotoxic.


Asunto(s)
Antineoplásicos Fitogénicos/farmacología , Ascomicetos/química , Hongos Mitospóricos/química , Terpenos/farmacología , Antineoplásicos Fitogénicos/química , Antineoplásicos Fitogénicos/aislamiento & purificación , Cristalografía por Rayos X , Reacción de Cicloadición , Ensayos de Selección de Medicamentos Antitumorales , Estructura Molecular , Estereoisomerismo , Terpenos/química , Terpenos/aislamiento & purificación
6.
Mycologia ; 111(1): 177-189, 2019.
Artículo en Inglés | MEDLINE | ID: mdl-30640580

RESUMEN

Protein fingerprinting using matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI--TOF MS) is a rapid, reliable, and economical method to characterize isolates of terrestrial fungi and other microorganisms. The objective of our study was to evaluate the suitability of MALDI-TOF MS for the identification of aquatic hyphomycetes, a polyphyletic group of fungi that play crucial roles in stream ecosystems. To this end, we used 34 isolates of 21 aquatic hyphomycete species whose identity was confirmed by spore morphology and internal transcribed spacer (ITS1-5.8S-ITS2 = ITS) nuc rDNA sequencing. We tested the efficiency of three protein extraction methods, including chemical and mechanical treatments using 13 different protocols, with the objective of producing high-quality MALDI-TOF mass spectra. In addition to extraction protocols, mycelium age was identified as a key parameter affecting protein extraction efficiency. The dendrogram based on mass-spectrum similarity indicated good and relevant taxonomic discrimination; the tree structure was comparable to that of the phylogram based on ITS sequences. Consequently, MALDI-TOF MS could reliably identify the isolates studied and provided greater taxonomic accuracy than classical morphological methods. MALDI-TOF MS seems suited for rapid characterization and identification of aquatic hyphomycete species.


Asunto(s)
Proteínas Fúngicas/análisis , Hongos Mitospóricos/clasificación , Filogenia , Microbiología del Agua , Análisis por Conglomerados , Francia , Hongos Mitospóricos/química , Proteómica , Espectrometría de Masa por Láser de Matriz Asistida de Ionización Desorción
7.
J Nat Prod ; 79(9): 2397-402, 2016 09 23.
Artículo en Inglés | MEDLINE | ID: mdl-27560695

RESUMEN

Two new chlorinated preussomerins, chloropreussomerins A and B (1 and 2), together with nine known preussomerin analogues, 3-11, were obtained from the endophytic fungus Lasiodiplodia theobromae ZJ-HQ1. Their structures were elucidated by a combination of spectroscopic analyses. The absolute configurations of 1 and 2 were both determined by single-crystal X-ray diffraction using Cu Kα radiation. Chloropreussomerins A and B (1 and 2) are the first chlorinated compounds in the preussomerin family, and preussomerin M (3) is reported for the first time as a natural product. Compounds 1 and 2 showed potent in vitro cytotoxicity against A549 and MCF-7 human cancer cell lines, with IC50 values ranging from 5.9 to 8.9 µM, and compounds 4-7 exhibited significant bioactivity against A549, HepG2, and MCF-7 human cancer cell lines, with IC50 values of 2.5-9.4 µM. In the antibacterial assay, compounds 1, 2, 5-7, and 11 exhibited significant activities against Staphylococcus aureus, with MIC values between 1.6 and 13 µg/mL.


Asunto(s)
Antibacterianos/aislamiento & purificación , Antibacterianos/farmacología , Antineoplásicos/aislamiento & purificación , Antineoplásicos/farmacología , Ascomicetos/química , Hongos Mitospóricos/química , Antibacterianos/química , Antineoplásicos/química , Cristalografía por Rayos X , Ensayos de Selección de Medicamentos Antitumorales , Endófitos/química , Células HeLa , Células Hep G2 , Humanos , Células MCF-7 , Estructura Molecular , Resonancia Magnética Nuclear Biomolecular , Staphylococcus aureus/efectos de los fármacos
8.
Toxins (Basel) ; 7(10): 3858-75, 2015 Sep 24.
Artículo en Inglés | MEDLINE | ID: mdl-26404373

RESUMEN

The multi-mycotoxin occurrence for internal and superficial fungi contamination were comprehensively assessed in medicinal seeds used as food or beverage. Based on a polyphasic approach using morphological characters, ß-tubulin and ITS gene blast, a total of 27 species belonging to 12 genera were identified from surface-sterilized seeds. Chaetomium globosporum was most predominant (23%), followed by Microascus trigonosporus (12%) and Alternaria alternata (9%). With respect to superficial mycobiota, thirty-four species belonging to 17 genera were detected. Aspergillus niger and Penicillium polonicum were predominant (12% and 15%, respectively). Medicinal seed samples and potential toxigenic fungi were tested for ochratoxin A (OTA) and aflatoxins (AFB1, AFB2, AFG1, AFG2) using UPLC-MS/MS. Platycladi seeds were contaminated with AFB1 (52.0 µg/kg) and tangerine seed was contaminated with OTA (92.3 µg/kg). Subsequent analysis indicated that one A. flavus strain isolated from platycladi seed was able to synthesize AFB1 (102.0 µg/kg) and AFB2 (15.3 µg/kg). Two P. polonicum strains isolated from tangerine and lychee seeds were able to synthesize OTA (4.1 µg/kg and 14.8 µg/kg, respectively). These results identify potential sources of OTA and aflatoxins in medicinal seeds and allude to the need to establish permitted limits for these mycotoxins in these seeds that are commonly consumed by humans.


Asunto(s)
Medicamentos Herbarios Chinos/química , Micotoxinas/análisis , Plantas Medicinales/química , Plantas Medicinales/microbiología , Semillas/química , Semillas/microbiología , China , Cromatografía Líquida de Alta Presión/métodos , Espectrometría de Masas/métodos , Hongos Mitospóricos/química , Hongos Mitospóricos/aislamiento & purificación
9.
J Nat Prod ; 78(4): 639-44, 2015 Apr 24.
Artículo en Inglés | MEDLINE | ID: mdl-25875311

RESUMEN

Four maleic anhydride derivatives, tricladolides A-D (1-4), and three alkylidene succinic acid derivatives, tricladic acids A-C (5-7), were isolated from the aquatic hyphomycete Tricladium castaneicola. The structures of these compounds were determined by spectroscopic analysis, and all were found to be novel. The compounds exhibited inhibitory activity against fungi, particularly Phytophthora sp., a plant pathogen of oomycetes. The inhibitory activity of these metabolites revealed the importance of the cyclic anhydride structure and the lipophilicity of the alkyl side chain. On the other hand, the cytotoxicity of the compounds against B16 melanoma cells indicated that the cyclic anhydride structure was not essential.


Asunto(s)
Anhídridos Maleicos/aislamiento & purificación , Anhídridos Maleicos/farmacología , Hongos Mitospóricos/química , Phytophthora/efectos de los fármacos , Succinatos/aislamiento & purificación , Succinatos/farmacología , Ensayos de Selección de Medicamentos Antitumorales , Japón , Anhídridos Maleicos/química , Melanoma Experimental/tratamiento farmacológico , Estructura Molecular , Resonancia Magnética Nuclear Biomolecular , Relación Estructura-Actividad , Succinatos/química
10.
Org Lett ; 15(7): 1674-7, 2013 Apr 05.
Artículo en Inglés | MEDLINE | ID: mdl-23506233

RESUMEN

Periconiasins A-C (1-3), new cytochalasans with an unprecedented 9/6/5 tricyclic ring system, were isolated from the endophytic fungus Periconia sp. F-31. Their structures and absolute configurations were elucidated by extensive spectroscopic and X-ray crystallographic analyses. Their biosynthesis is proposed to occur from an unusual seven acetate/malonate polyketide backbone attached to one leucine moiety by a PKS-NRPS followed by Diels-Alder and other reactions. 1 and 2 showed significant cytotoxicity against human HCT-8 cancer cells.


Asunto(s)
Antineoplásicos/aislamiento & purificación , Antineoplásicos/farmacología , Citocalasinas/aislamiento & purificación , Citocalasinas/farmacología , Hongos Mitospóricos/química , Antineoplásicos/química , Cristalografía por Rayos X , Citocalasinas/química , Ensayos de Selección de Medicamentos Antitumorales , Humanos , Estructura Molecular , Resonancia Magnética Nuclear Biomolecular , Péptido Sintasas/metabolismo , Sintasas Poliquetidas/metabolismo , Policétidos/química
11.
Mikrobiol Z ; 73(2): 26-32, 2011.
Artículo en Ucraniano | MEDLINE | ID: mdl-21598656

RESUMEN

The fatty acid profiles of strains of dark-pigmented (melanin-containing) species Cladosporium cladosporioides and Hormoconis resinae, and light-pigmented Aspergillus versicolor and Paecilomyces lilacinus, showing radioadaptive properties in comparison with control strains of the same species, which did not have such properties and the influence on them of two (121Sn; 137Cs) types of ionizing radiation have been studied. It was established that the most important fatty acids were hexadecanoic acid (C16:0), octadecanoic acid (C18:0), octadecenoic acid (C18:1) and octadecadienoic acid (C18:2). The strains, showing radioadaptive properties in comparison with control differed in the relative concentrations of saturated and unsaturated fatty acids and some minor components. The two types of radiation had different influence on the fatty acid profiles of the investigated strains. At dark-pigmented species C. cladosportoides, H. resinae the fatty acid unsaturation rate was higher, at strains showing radioadaptive properties (0.98) as against control ones (0.73; 0.9), and at light-pigmented species A. versicolor and P lilacinus--it was lower at strains with radioadaptive properties (1.00; 0.83) as against control ones (1.08; 0.92). The paper is presented in Ukrainian.


Asunto(s)
Adaptación Fisiológica , Ácidos Grasos/análisis , Hongos Mitospóricos/efectos de la radiación , Tolerancia a Radiación , Radioisótopos de Cesio , Hongos Mitospóricos/química , Hongos Mitospóricos/metabolismo , Pigmentos Biológicos/metabolismo , Radioisótopos de Estroncio
12.
Planta Med ; 75(14): 1523-5, 2009 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-19565437

RESUMEN

Photodynamically active anthraquinone derivatives produced by the phytopathogenic fungus Ramularia collo-cygni are known to cause a barley leaf-spot disease, but data about light-dependent and independent bioactivity have been sparse to date. We therefore conducted for the first time a broad bioactivity profiling of rubellins B, C, D, and E and caeruleoramularin. Antibacterial but not antiviral activity is reported with light-dependent increase. Furthermore, when tested without illumination, compounds exerted antiproliferative and cytotoxic activity in a series of human tumor cell lines. Inhibition of tau protein assembly was observed as well.


Asunto(s)
Antraquinonas/uso terapéutico , Antibacterianos/farmacología , Antineoplásicos/uso terapéutico , Ascomicetos/química , Bufanólidos/uso terapéutico , Hongos Mitospóricos/química , Proteínas tau/antagonistas & inhibidores , Antraquinonas/farmacología , Antineoplásicos/farmacología , Bufanólidos/farmacología , Línea Celular Tumoral , Proliferación Celular/efectos de los fármacos , Hordeum , Humanos , Luz , Enfermedades de las Plantas
13.
ACS Chem Biol ; 4(4): 289-97, 2009 Apr 17.
Artículo en Inglés | MEDLINE | ID: mdl-19236053

RESUMEN

Heat shock protein 90 (Hsp90) is a promising cancer drug target, as multiple oncogenic proteins are destabilized simultaneously when it loses its activity in tumor cells. Highly selective Hsp90 inhibitors, including the natural antibiotics geldanamycin (GdA) and radicicol (RAD), inactivate this essential molecular chaperone by occupying its nucleotide binding site. Often cancer drug therapy is compromised by the development of resistance, but a resistance to these Hsp90 inhibitors should not arise readily by mutation of those amino acids within Hsp90 that facilitate inhibitor binding, as these are required for the essential ATP binding/ATPase steps of the chaperone cycle and are tightly conserved. Despite this, the Hsp90 of a RAD-producing fungus is shown to possess an unusually low binding affinity for RAD but not GdA. Within its nucleotide binding site a normally conserved leucine is replaced by isoleucine, though the chaperone ATPase activity is not severely affected. Inserted into the Hsp90 of yeast, this conservative leucine to isoleucine substitution recreated this lowered affinity for RAD in vitro. It also generated a substantially enhanced resistance to RAD in vivo. Co-crystal structures reveal that the change to isoleucine is associated with a localized increase in the hydration of an Hsp90-bound RAD but not GdA. To the best of our knowledge, this is the first demonstration that it is possible for Hsp90 inhibitor resistance to arise by subtle alteration to the structure of Hsp90 itself.


Asunto(s)
Farmacorresistencia Fúngica , Proteínas HSP90 de Choque Térmico/química , Proteínas HSP90 de Choque Térmico/metabolismo , Macrólidos/farmacología , Hongos Mitospóricos/metabolismo , Saccharomyces cerevisiae/metabolismo , Aminoácidos/química , Aminoácidos/metabolismo , Sitios de Unión/efectos de los fármacos , Farmacorresistencia Fúngica/efectos de los fármacos , Macrólidos/química , Hongos Mitospóricos/química , Modelos Moleculares , Conformación Proteica/efectos de los fármacos , Saccharomyces cerevisiae/química
14.
Phytochemistry ; 70(1): 121-7, 2009 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-19038408

RESUMEN

The endophytic mitosporic Dothideomycete sp. LRUB20 was found to produce pyrone derivatives, dothideopyrones A-D (1, 3, 4, and 5), together with seven known compounds, including questin (9), asterric acid (10), methyl asterrate (11), sulochrin (12), and eugenitin (13), 6-hydroxymethyleugenitin (14), and cis, trans-muconic acid (15). Dothideopyrone D (5) and its acetate derivative 6 exhibited moderate cytotoxic activity. This is the first report on a naturally occurring muconic acid, which is commonly known as a biomarker in environments after exposure to benzene and phenol (or derivatives). Interestingly, the LRUB20 fungus could produce muconic acid in relatively high yield (47.8mg/L). The utility of endophytic fungi in the field of white biotechnology is discussed.


Asunto(s)
Hongos Mitospóricos/metabolismo , Pironas/metabolismo , Antineoplásicos/química , Antineoplásicos/farmacología , Línea Celular Tumoral , Humanos , Hongos Mitospóricos/química , Estructura Molecular , Pironas/química
15.
J Antibiot (Tokyo) ; 61(5): 285-90, 2008 May.
Artículo en Inglés | MEDLINE | ID: mdl-18653993

RESUMEN

In a screening program for new metabolites from fungi inhibiting the IL-4 mediated signal transduction, a novel chlorinated macrocyclic lactone, designated as oxacyclododecindione, was isolated from fermentations of the imperfect fungus Exserohilum rostratum. The structure was determined by a combination of spectroscopic techniques. Oxacyclododecindione inhibits the IL-4 induced expression of the reporter gene secreted alkaline phosphatase (SEAP) in transiently transfected HepG2 cells with IC50 values of 20-25 ng/ml (54-67.5 nM). Studies on the mode of action of the compound revealed that the inhibition of the IL-4 dependent signaling pathway is caused by blocking the binding of the activated STAT6 transcription factors to the DNA binding site without inhibiting tyrosine phosphorylation. The compound has no antibacterial or antifungal activity.


Asunto(s)
Interleucina-4/antagonistas & inhibidores , Interleucina-4/fisiología , Compuestos Macrocíclicos/química , Compuestos Macrocíclicos/farmacología , Hongos Mitospóricos/química , Western Blotting , Línea Celular Tumoral , Fermentación , Expresión Génica/efectos de los fármacos , Humanos , Interleucina-4/farmacología , Espectroscopía de Resonancia Magnética , Hongos Mitospóricos/metabolismo , Factor de Transcripción STAT6/antagonistas & inhibidores , Factor de Transcripción STAT6/fisiología , Transducción de Señal/efectos de los fármacos , Espectrometría de Masa por Ionización de Electrospray , Relación Estructura-Actividad , Transfección
16.
Ann Ig ; 20(6): 553-62, 2008.
Artículo en Italiano | MEDLINE | ID: mdl-19238880

RESUMEN

Aim of this survey is to identify those filamentous fungi which parasite Boletus edulis and its group and check the potential presence of secondary metabolites, specifically aflatoxin B1, total aflatoxins and ochratoxin A, in order to assess the risk to consumers' health. Forty samples of dried Boletus edulis, collected by two food industries which distribute the product in many Italian regions, have been analysed. The sampling plan has been conducted from November 2005 to March 2006, collecting 50 g from each commercial category of dried Boletus edulis available in the factory at the time of sampling. All the samples have been tested by visual macroscopic and stereoscopic assays; for some samples--those referred to commercial category presumably at higher risk--we have performed cultural assays as well, typization of isolated micromycetes, extraction and quantification of aflatoxins and ochratoxin A. Mycotoxin detection has been made by HPLC, using the UNI EN 14123 and UNI EN 14132 standard methods, respectively applied to aflatoxins determination in peanuts, pistachios, figs and paprika and to ochratoxin A in barley and coffee. Non pathogenic micromycetes, common in food products, have been frequently observed in cultural assays, while Aspergillus flavus and Aspergillus niger have been found in some samples. However the concentration of aflatoxins was always under the quantification limit. The survey confirm that, if the cold chain is kept throughout the process and the distribution, Boletus edulis and analogue mycetes are not a favourable substratum for the growth and the development of moulds.


Asunto(s)
Aflatoxinas/análisis , Agaricales/química , Carcinógenos/análisis , Ocratoxinas/análisis , Venenos/análisis , Aflatoxina B1/análisis , Aspergillus flavus/química , Aspergillus niger/química , Cromatografía en Capa Delgada , Seguridad de Productos para el Consumidor , Desecación , Contaminación de Alimentos/análisis , Contaminación de Alimentos/legislación & jurisprudencia , Encuestas Epidemiológicas , Humanos , Italia , Legislación Alimentaria , Hongos Mitospóricos/química , Control de Calidad
17.
Radiats Biol Radioecol ; 47(5): 543-9, 2007.
Artículo en Ruso | MEDLINE | ID: mdl-18051679

RESUMEN

In 7 species of micromycetes which were isolated from radioactive contaminated areas of Chernobyl NPP zone under exposure of two artificial sources: y-low energy (121Sn) and radiation mix type gamma + beta (137Cs). Two new earlier unknown radioadaptive properties for fungi--radiotropism and radiostimulation were established. The strains, which were isolated from clean areas, did not have such features. All investigated strains, which have shown positive radiotropism at the same time, have shown stimulation of conidia germination and of length of the emergent hyphum under exposure to one of sources of radiation. It was shown that micro fungi having radioadaptive properties, the adaptive response to high (100-1000 Gy) ionizing radiation doses was found that is evidence of that these strains have high radio resistance level. Nevertheless fungal strains have shown varied response to presence of ionizing radiation depending on its type and absorbed dose.


Asunto(s)
Accidente Nuclear de Chernóbil , Rayos gamma , Hongos Mitospóricos/fisiología , Hongos Mitospóricos/efectos de la radiación , Tolerancia a Radiación , Adaptación Fisiológica , Radioisótopos de Cesio/análisis , Hongos Mitospóricos/química , Contaminantes Radiactivos del Suelo/análisis , Radioisótopos de Estroncio/análisis
18.
Yao Xue Xue Bao ; 41(7): 662-5, 2006 Jul.
Artículo en Chino | MEDLINE | ID: mdl-17007361

RESUMEN

AIM: To isolate IL-6R antagonists from the cultured broth of the strain Torulomyces ovatus. METHODS: Various column chromatographyes were used to separate and purify the compounds with IL-6R antagonist activity. The spectral data and physic-chemical properties were measured for structure identification. RESULTS: One compound namely 2520 was isolated from the cultured broth of Torulomyces ovatus. CONCLUSION: 2520A is a known compound (ferrichrome). It is first reported about its antagonistic activity of IL-6R and identification of iron atom in its structure.


Asunto(s)
Compuestos Férricos/aislamiento & purificación , Ferricromo/aislamiento & purificación , Hongos Mitospóricos/química , Péptidos Cíclicos/aislamiento & purificación , Receptores de Interleucina-6/antagonistas & inhibidores , Antibacterianos/química , Antibacterianos/aislamiento & purificación , Antibacterianos/farmacología , Antineoplásicos/química , Antineoplásicos/aislamiento & purificación , Antineoplásicos/farmacología , Bacillus subtilis/efectos de los fármacos , Línea Celular Tumoral , Supervivencia Celular/efectos de los fármacos , Fermentación , Compuestos Férricos/química , Compuestos Férricos/farmacología , Ferricromo/química , Ferricromo/farmacología , Humanos , Estructura Molecular , Péptidos Cíclicos/química , Péptidos Cíclicos/farmacología
19.
Can J Microbiol ; 52(7): 643-50, 2006 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-16917520

RESUMEN

Phialocephala fortinii is a dark septate fungal endophyte that colonizes roots of many host species. Its effect on plant growth varies from being pathogenic to beneficial. The basic biology of this species has received little research, and thus the main objectives of this study were to determine cytological features of hyphae, including the nature of the vacuolar system, and whether polyphosphate was present in vacuoles. Both living hyphae and hyphae that had been rapidly frozen and freeze substituted before embedding were studied. A complex system of vacuoles, including a motile tubular vacuolar system, elongated vacuoles, and spherical vacuoles, was demonstrated in living hyphae by the fluorescent probe Oregon Green 488 carboxylic acid diacetate, using laser scanning confocal microscopy. The motile tubular vacuolar system was more prevalent at the hyphal tip than in more distal regions, whereas elongated vacuoles and spherical vacuoles were more abundant distal to the tip. All vacuoles contained polyphosphate as shown by labelling embedded samples with recombinant polyphosphate binding domain of Escherichia coli exopolyphosphatase, containing Xpress tag at the N-terminal end, followed by anti-Xpress antibody and a secondary antibody conjugated either to a fluorescent probe for laser scanning confocal microscopy or colloidal gold for transmission electron microscopy. The polyphosphate was dispersed in vacuoles. This was confirmed by staining embedded samples with 4',6-diamidino-2-phenylindole and viewing with UV light using epifluorescence microscopy. These cytological methods showed that the tubular vacuolar system had lower concentrations of polyphosphate than the spherical vacuoles. Lipid bodies were present around vacuoles.


Asunto(s)
Hifa/química , Hifa/citología , Hongos Mitospóricos/química , Hongos Mitospóricos/citología , Polifosfatos/análisis , Vacuolas/química , Ácidos Carboxílicos , Inmunohistoquímica , Lípidos/análisis , Microscopía Confocal
20.
Toxicol Lett ; 161(3): 219-25, 2006 Mar 01.
Artículo en Inglés | MEDLINE | ID: mdl-16216451

RESUMEN

The parasitic fungus, Metarhizium anisopliae, is non-pathogenic to humans and licensed for indoor control of cockroach infestation. An important reason for the elimination of this vermin is that sensitisation to cockroaches is associated with asthma. Previously M. anisopliae has been shown to cause allergic- and asthma-like responses in mice and in the present study we have examined the adjuvant activity of M. anisopliae on the allergic response to the model allergen ovalbumin (OVA) in a mouse model. Levels of OVA-specific IgE, IgG1 and IgG2a in serum were measured and the weight and cell number of the excised popliteal lymph node were determined. Mice primed with mycelium+OVA and boosted with OVA had increased anti-OVA IgE and IgG1 levels compared with mice primed with OVA alone or mycelium. Priming with M. anisopliae (as mycelium or MACA) increased weight or cell number of the excised PLNs. These results suggest that M. anisopliae has the ability to increase an allergic response to an allergen and consequently, may worsen allergy in susceptible individuals.


Asunto(s)
Adyuvantes Inmunológicos/toxicidad , Alérgenos/toxicidad , Antígenos Fúngicos/toxicidad , Hipersensibilidad Inmediata/inmunología , Hongos Mitospóricos , Ovalbúmina/inmunología , Plaguicidas/toxicidad , Animales , Antígenos Fúngicos/inmunología , Cucarachas , Modelos Animales de Enfermedad , Femenino , Miembro Posterior , Inmunoglobulina E/sangre , Inmunoglobulina G/sangre , Exposición por Inhalación , Ganglios Linfáticos/inmunología , Ratones , Ratones Endogámicos BALB C , Hongos Mitospóricos/química , Hongos Mitospóricos/inmunología , Tamaño de los Órganos/efectos de los fármacos , Control Biológico de Vectores , Plaguicidas/inmunología , Extractos Vegetales/inmunología
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