Search results for "biosynthesis"

showing 10 items of 523 documents

Heat shock proteins in three relatedDrosophila species belonging to theobscura group

1993

The effect of heat shock on protein synthesis in three related Drosophila species belonging to the obscura group was analyzed on SDS-acrylamide gels. Four major heat shock proteins (hsps) were found in these species, in which synthesis reaches a maximum at 34 degrees C. Although the higher molecular weight proteins are conserved, differences in size were found for the small hsps in these species. By means of in situ hybridization using D. melanogaster probes for the small hsp genes, it was inferred that the small hsp genes of the obscura group species are clustered at the 27A locus in all three species.

PharmacologyGeneticsGel electrophoresisHot TemperaturebiologyLocus (genetics)Cell Biologybiology.organism_classificationMolecular WeightCellular and Molecular NeuroscienceMolecular evolutionDrosophilidaeHeat shock proteinMelanogasterProtein biosynthesisAnimalsMolecular MedicineDrosophilaMolecular BiologyGeneHeat-Shock ProteinsIn Situ HybridizationExperientia
researchProduct

Ganodermycin, a novel inhibitor of CXCL10 expression from Ganoderma applanatum

2011

CXCL10 (inducible protein-10) is a highly inducible chemoattractant, which contributes to the recruitment of inflammatory cells, such as macrophages and T-lymphocytes, and thereby has important roles in chronic inflammatory conditions. In a search for new inhibitors of CXCL10 expression in MonoMac6 cells, a novel compound, designated as Ganodermycin, was isolated from fermentations of the basidiomycete Ganoderma applanatum. The structure was determined by a combination of spectroscopic techniques. Ganodermycin inhibited the lipopolysaccharide (LPS)/interferon (IFN)-γ-induced CXCL10 promoter activity in transiently transfected MonoMac6 cells in a dose-dependent manner with IC(50) values of 1…

PharmacologyLipopolysaccharidebiologyGanodermaChemotaxisTransfectionPharmacologybiology.organism_classificationMolecular biologychemistry.chemical_compoundGanoderma applanatumchemistryInterferonDrug DiscoveryProtein biosynthesismedicineCXCL10medicine.drugThe Journal of Antibiotics
researchProduct

The intermediate role of 18-hydroxycorticosteroids in aldosterone biosynthesis.

1968

Durch ihre Eigenschaft, bestimmte Stufen bei der Bildung radioaktiv markierten Aldosterons aus14C-Progesteron bzw.3H-11-Desoxycorticosteron zu hemmen, erwiesen sich 11-Desoxycorticosteron, Corticosteron und 18-Hydroxycorticosteron als wesentliche Zwischenstufen der Aldosteronbiosynthese. 18-Hydroxy-11-desoxycorticosteron hingegen scheint an der Bildung von Aldosteron nicht beteiligt zu sein.

PharmacologyMalemedicine.medical_specialtyCarbon IsotopesAldosteroneChemistry18-HydroxycorticosteroidsCell BiologyTritiumRatsCellular and Molecular Neurosciencechemistry.chemical_compoundEndocrinologyBiosynthesisCorticosteroneAdrenal Cortex HormonesInternal medicineAdrenal GlandsmedicineMolecular MedicineAnimalsMolecular BiologyAldosteroneProgesteroneExperientia
researchProduct

Nonsense codons suppression. An acute toxicity study of three optimized TRIDs in murine model, safety and tolerability evaluation.

2022

Stop mutations cause 11% of the genetic diseases, due to the introduction of a premature termination codon (PTC) in the mRNA, followed by the production of a truncated protein. A promising therapeutic approach is the suppression therapy by Translational Readthrough Inducing Drugs (TRIDs), restoring the expression of the protein. Recently, three new TRIDs (NV848, NV914, NV930) have been proposed, and validated by several in vitro assays, for the rescue of the CFTR protein, involved in Cystic Fibrosis disease. In this work, an acute toxicological study for the three TRIDs was conducted in vivo on mice, according to the OECD No.420 guidelines. Animals were divided into groups and treated with …

PharmacologyNonsense mutationCystic Fibrosis Transmembrane Conductance RegulatorGeneral MedicineOxadiazoleMiceDisease Models AnimalPremature termination codon (PTC)Pharmaceutical PreparationsCodon NonsenseProtein BiosynthesisAnimalsToxicity studyTranslational readthrough inducing drugs(TRIDs)Biomedicinepharmacotherapy = Biomedecinepharmacotherapie
researchProduct

Incorporation of phenylalanine-H3 in the fragments of the fertilized ascidian egg

1972

E'stata studiata l'incorporazione di fenilalanina-H3 nelle meta animali e vegetative delle uova fecondate di Ascidie tagliate subito dopo l'emissione del 1° e del 2° globulo polare, allo scopo di vedere se le potenzialita di sviluppo delle meta vegetative fossero legate con un diverso metabolismo proteico. I risultati hanno mostrato che entrambe le meta incorporano fenilalanina-H3.

PharmacologyPhenylalaninePhenylalanineCell BiologyBiologyTritiumCellular and Molecular NeuroscienceChordata NonvertebrateFertilizationProtein BiosynthesisBotanyAnimalsAutoradiographyMolecular MedicineFemaleMolecular BiologyCell DivisionOvumExperientia
researchProduct

Substrate Specificity of Vinorine Hydroxylase, a Novel Membrane-bound Key Enzyme of Rauwolfia Indole Alkaloid Biosynthesis

1995

Pharmacologychemistry.chemical_classificationEnzymeIndole alkaloid biosynthesischemistryBiochemistryStereochemistryMembrane boundOrganic ChemistrySubstrate specificityAnalytical ChemistryHETEROCYCLES
researchProduct

Enzymatic formation of the sarpagan-bridge: a key step in the biosynthesis of sarpagine- and ajmaline-type alkaloids.

1995

The glucoalkaloid strictosidine has been converted under cell-free conditions into 10-deoxysarpagine (= normacusine B) in the presence of a crude soluble enzyme extract and microsomal protein isolated from cell suspensions of Rauwolfia serpentina. The enzymatic formation of this alkaloid bearing the C-5/C-16 bond (sarpagan-bridge), which is characteristic for all sarpagine- and ajmaline-type alkaloids, is dependent on NADPH and oxygen. Inhibition studies indicate that for the synthesis of 10-deoxysarpagine a cytochrome P450 dependent monoxygenase is necessary.

Pharmacologychemistry.chemical_classificationbiologyApocynaceaeStereochemistryAlkaloidOrganic ChemistryPharmaceutical ScienceCytochrome P450biology.organism_classificationAnalytical ChemistryAjmalinechemistry.chemical_compoundEnzymeComplementary and alternative medicineBiochemistrychemistryBiosynthesisStrictosidineDrug DiscoverymedicineMicrosomebiology.proteinMolecular Medicinemedicine.drugPlanta medica
researchProduct

Editorial: Relevance of Steroid Biosynthesis, Metabolism and Transport in Pathophysiology and Drug Discovery

2019

Pharmacologysteroid hormonesOrganic anion transporter 1biologybusiness.industryDrug discoverySulfataselcsh:RM1-950intracrine actionCancerTransportertransportersMetabolismPharmacologySteroid biosynthesissulfatasemedicine.diseasePathophysiologylcsh:Therapeutics. PharmacologyEditorialbiology.proteincancerMedicinePharmacology (medical)businessFrontiers in Pharmacology
researchProduct

In vitro incorporation of amino acids into proteins stimulated by RNA from unfertilized sea urchin eggs.

1964

PhenylalanineBiophysicsIn Vitro TechniquesBiochemistrybiology.animalAnimalsRNA MessengerMolecular BiologySea urchinOvumchemistry.chemical_classificationAlaninebiologyLysineRNAValineCell BiologyIn vitroAmino acidRatsBiochemistrychemistryLiverFertilizationProtein BiosynthesisRNAFemaleEchinodermataBiochemical and biophysical research communications
researchProduct

Defense Responses of Fusarium oxysporum to 2,4-Diacetylphloroglucinol, a Broad-Spectrum Antibiotic Produced by Pseudomonas fluorescens

2004

A collection of 76 plant-pathogenic and 41 saprophytic Fusarium oxysporum strains was screened for sensitivity to 2,4-diacetylphloroglucinol (2,4-DAPG), a broad-spectrum antibiotic produced by multiple strains of antagonistic Pseudomonas fluorescens. Approximately 17% of the F. oxysporum strains were relatively tolerant to high 2,4-DAPG concentrations. Tolerance to 2,4-DAPG did not correlate with the geographic origin of the strains, formae speciales, intergenic spacer (IGS) group, or fusaric acid production levels. Biochemical analysis showed that 18 of 20 tolerant F. oxysporum strains were capable of metabolizing 2,4-DAPG. For two tolerant strains, analysis by mass spectrometry indicated…

PhysiologyPhloroglucinolPseudomonas fluorescensPhloroglucinoltomatoPseudomonas fluorescensMicrobiologyresistancestrainschemistry.chemical_compoundFusariumtake-allDrug Resistance BacterialFusarium oxysporum[SDV.BBM] Life Sciences [q-bio]/Biochemistry Molecular Biology[SDV.BBM]Life Sciences [q-bio]/Biochemistry Molecular BiologybiocontrolPhylogenyPlant DiseasesDose-Response Relationship DrugbiologyEPS-2food and beveragesgenetic diversityGeneral MedicineFungi imperfectiPlantspopulationssensitivitybiology.organism_classificationAnti-Bacterial AgentsLaboratorium voor PhytopathologiePRI BiosciencechemistryLaboratory of PhytopathologyPseudomonadales24-DiacetylphloroglucinolDNA Intergenicbiosynthesisabc transportersAgronomy and Crop ScienceFusaric acidPseudomonadaceaeMolecular Plant-Microbe Interactions®
researchProduct