Search results for "tuli"

showing 10 items of 223 documents

Mycotoxins and mycotoxigenic moulds in nuts and sunflower seeds for human consumption

1991

A survey was carried out to obtain data on the occurrence of mycotoxins and the mycotoxin-producing potential of fungi isolated from nuts (almonds, peanuts, hazelnuts, pistachio nuts) and sunflower seeds in Spain. Thin-layer chromatography was used to separate the toxins. Aflatoxins were detected in one sample of almonds (95 ppb aflatoxin B1 and 15 ppb aflaxtoxin B2) and in one sample of peanuts at a level below 10 ppb of aflatoxin B1. 100% of samples showed variable incidence of fungal contamination. The predominant fungi present in samples were Penicillium spp, Aspergillus niger, A. flavus, A. glaucus and Rhizopus spp. The results showed that isolates of different species were able to pro…

Ochratoxin AAflatoxinVeterinary (miscellaneous)Applied Microbiology and BiotechnologyMicrobiologyPatulinchemistry.chemical_compoundPenicillic acidBotanyHumansNutsFood scienceMycotoxinAnalysis of VariancebiologyFungitechnology industry and agriculturefood and beveragesMycotoxinsbiology.organism_classificationCitrininchemistrySeedsPenicilliumFood MicrobiologyHelianthusChromatography Thin LayerAgronomy and Crop ScienceSterigmatocystinMycopathologia
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Predominant mycotoxins, mycotoxigenic fungi and climate change related to wine

2017

Wine is a significant contributor to the economies of many countries. However, the commodity can become contaminated with mycotoxins produced by certain fungi. Most information on mycotoxins in wine is from Spain, Italy and France. Grapes can be infected by mycotoxigenic fungi, of which Aspergillus carbonarius producing ochratoxin A (OTA) is of highest concern. Climate is the most important factor in determining contamination once the fungi are established, with high temperatures being a major factor for OTA contamination: OTA in wine is at higher concentrations in warmer southern Europe than northern. Contamination by fumonisins is a particular concern, related to Aspergillus niger produci…

Ochratoxin AAflatoxinWineOchratoxin aBiologyFumonisinsRisk AssessmentPatulinToxicologychemistry.chemical_compound0404 agricultural biotechnologyAflatoxinsFumonisinBotanyAflatoxinHumansClimate changeVitisMycotoxin2. Zero hungerWineAspergillusScience & Technologydigestive oral and skin physiologyfungiFumonisin[ SDV.IDA ] Life Sciences [q-bio]/Food engineeringfood and beveragesOchratoxin A04 agricultural and veterinary sciencesMycotoxins15. Life on landbiology.organism_classificationAlternariaOchratoxins040401 food scienceAspergilluschemistryConsumer Product Safety13. Climate actionFruitFood MicrobiologyFood Science
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Detection and quantification of patulin and griseofulvin by high pressure liquid chromatography in different strains of Penicillium griseofulvum Dier…

1988

Patulin and griseofulvin production by twelve strains ofPenicillium griseofulvum Dierckx, eleven of which were isolated from pistachio (Pistacia vera) nuts and the other was supplied by the Spanish Collection of Type Culture, was investigated. Six strains of the eleven isolated had ability to produce patulin and griseofulvin in Yes medium. All the strains studied had no ability to produce patulin in Wickerham medium. Griseofulvin production was significant in both media but higher in Wickerham.These metabolites were separated and determined in the chloroform extracts of cultures by high performance liquid chromatography with ultraviolet detection. The best conditions were: acetonitrile - wa…

PatulinPenicillium griseofulvumchemistry.chemical_compoundChromatographyPistaciabiologyChemistryToxicologyGriseofulvinbiology.organism_classificationMicrobiologyHigh-performance liquid chromatographyBiotechnologyMycotoxin research
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Cytotoxic effects of individual and combined mycotoxins, patulin sterigmatocystin and beauvericin on CHO-K1 cells

2015

Patulinchemistry.chemical_compoundchemistryBiochemistryCytotoxic T cellGeneral MedicineToxicologyMycotoxinBeauvericinSterigmatocystinToxicology Letters
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In vitro cytotoxicity of patulin, deoxynivalenol, nivalenol and zearalenone on CHO-K1 cells

2006

Patulinchemistry.chemical_compoundchemistryIn vitro cytotoxicityGeneral MedicineToxicologyMolecular biologyZearalenoneToxicology Letters
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Comparison of different analytical processes for patulin determination in apple juice

2009

F. M. Valle-Algarra, R. Mateo, A. Medina, F. Mateo, E. M. Mateo, E. Sanchis Blanco, J.V. Gimeno-Adelantado, J. Peris-Vicente and M. Jimenez 1 Dpto. de Quimica Analitica, Facultad de Quimica, Universidad de Valencia, Dr. Moliner 50, E-46100 Burjassot, Valencia, Spain 2 Dpto. de Microbiologia y Ecologia, Facultad de Biologia, Universidad de Valencia, Dr. Moliner 50, E-46100 Burjassot, Valencia, Spain 3 Dpto. de Ingenieria Electronica, Universidad Politecnica de Valencia, Camino de Vera 14, E-46022, Valencia, Spain

Patulinchemistry.chemical_compoundchemistrymedia_common.quotation_subjectArtHumanitiesmedia_commonCurrent Research Topics in Applied Microbiology and Microbial Biotechnology
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Differentiation of Penicillium griseofulvum Dierckx isolates by enzyme assays and by patulin and griseofulvin analyses

1990

The production of patulin and griseofulvin by 49 different isolates of Penicillium griseofulvum Dierckx was analyzed by high-performance liquid chromatography. Eleven isolates were obtained from pistachio nuts, 37 were obtained from wheat seeds, and 1 was obtained from the American Type Culture Collection. Activities of 19 enzymes were also assayed by the API ZYM system. From these results it may be deduced that there are two different groups among the strains tested which cannot be distinguished by morphological and cultural characteristics. One group of isolates did not produce detectable amounts of patulin and griseofulvin when grown in sucrose-yeast extract and Wickerham media, while en…

Penicillium griseofulvumHydrolasesApplied Microbiology and BiotechnologyGriseofulvinPatulinLeucyl Aminopeptidasechemistry.chemical_compoundMycotoxinChromatography High Pressure LiquidEcologybiologybeta-GlucosidasePenicilliumPhosphoamidaseFungi imperfectibiology.organism_classificationGriseofulvinEnzyme assayCulture MediaPatulinchemistryBiochemistryPenicilliumbiology.proteinResearch ArticleFood ScienceBiotechnologyApplied and Environmental Microbiology
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De Vargas Llosa a Argullol

2007

PeriodistasDiversidadOPINIÓN PÚBLICASociedad mediáticaVidal-Beneyto JoséCOMUNICACIÓNBuenoVerdaderoEmpresariosArgullolOpinión publicadaOpinión de los públicosSondeosTertulianosTertuliasEl PaísTribunaPolíticosVargas LlosaBelloSindicatosDictaduraPublicaciones: Obra periodística: Cartas al director
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A review of natural and modified betulinic, ursolic and echinocystic acid derivatives as potential antitumor and anti-HIV agents.

2003

The aim of this review is to update current knowledge on the betulinic, ursolic and echinocystic acids and their natural and semisynthetic analogs, focussing on their cytotoxic and anti-HIV activities. Then, the last results of the authors' team on unusual semisynthetic derivatives of these triterpenoids will be presented in order to establish structure/activity relationships.

PharmacologyMolecular StructureAnti hivChemistryAnti-HIV AgentsTumor cellsAntineoplastic AgentsGeneral MedicinePharmacologyTriterpenesStructure-Activity RelationshipTriterpenoidDrug DiscoveryHIV-1Tumor Cells CulturedStructure–activity relationshipHumansEchinocystic acidOleanolic AcidBetulinic AcidPentacyclic TriterpenesHT29 CellsMini reviews in medicinal chemistry
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New ursolic and betulinic derivatives as potential cytotoxic agents.

2003

Fifteen new ursolic and betulinic triterpenoids, bearing various functionalities at C-3 and C-28 were synthesized as potential cytotoxic agents. All compounds were obtained by a hemisynthetic route via ursolic and betulinic acids. Preliminary screening of these compounds on human HT 29 colon cancer cells revealed inhibitory activity for three of them. Beta-D-Glucopyranosyl-3beta-hydroxyurs-12(13)-en-28-oate 1c, 3beta-3-(3-pyridyl)-prop-2-enoyloxyurs-12(13)-en-28-oic acid 1i and the potassium salt of 3beta-cinnamoyloxylup-20(29)-en-28-oic acid 2d demonstrated cytotoxic activity in the micromolar range: 8.0, 45.0 and 8.0 microM, respectively.

PharmacologyMolecular StructureStereochemistryCell SurvivalAntineoplastic AgentsGeneral MedicineTriterpeneschemistry.chemical_compoundInhibitory Concentration 50Structure-Activity RelationshipTriterpenoidUrsolic acidchemistryBetulinic acidDrug DiscoveryCytotoxic T cellHumansDrug Screening Assays AntitumorBetulinic AcidCytotoxicityPentacyclic TriterpenesHT29 CellsJournal of enzyme inhibition and medicinal chemistry
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