Search results for " decarboxylase"

showing 10 items of 88 documents

The anaerobic metabolism of malate of Saccharomyces bailii and the partial purification and characterization of malic enzyme.

1982

1. The main pathway of the anaerobic metabolism of l-malate in Saccharomyces bailii is catalyzed by a l-malic enzyme. 2. The enzyme was purified more than 300-fold. During the purification procedure fumarase and pyruvate decarboxylase were removed completely, and malate dehydrogenase and oxalacetate decarboxylase were removed to a very large extent. 3. Manganese ions are not required for the reaction of malic enzyme of Saccharomyces bailii, but the activity of the enzyme is increased by manganese. 4. The reaction of l-malic enzyme proceeds with the coenzymes NAD and (to a lesser extent) NADP. 5. The Km-values of the malic enzyme of Saccharomyces bailii were 10 mM for l-malate and 0.1 mM for…

Malic enzymeMalatesSaccharomyces cerevisiaeBiochemistryMicrobiologyMalate dehydrogenasechemistry.chemical_compoundSaccharomycesSpecies SpecificityMalate DehydrogenaseGeneticsAnaerobiosisMolecular Biologychemistry.chemical_classificationfungifood and beveragesSubstrate (chemistry)General MedicineKineticsEnzymechemistryBiochemistryFumaraseMalic acidNAD+ kinasePyruvate decarboxylaseArchives of microbiology
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Inhibition of the dimorphic transition of Candida albicans by the ornithine decarboxylase inhibitor 1,4-diaminobutanone: alterations in the glycoprot…

1990

Hyphal development in Candida albicans was selectively blocked by the ornithine decarboxylase competitive inhibitor 1,4-diaminobutanone (DAB). Inhibition of hyphal development required DAB during both yeast inoculum growth and subsequent incubation at 37 degrees C to induce mycelial growth. This effect was not due to general growth inhibition since DAB did not inhibit yeast growth, and reduced protein synthesis by 30% at most. Moreover, protein synthesis was unaffected by DAB when cells were pre-grown in drug-containing media. Since DAB inhibited dimorphic transition at 37 degrees C, morphology- and temperature-dependent protein synthesis could be distinguished. DAB stimulated the synthesis…

Membrane GlycoproteinsOrnithine Decarboxylase InhibitorsBiologybiology.organism_classificationMicrobiologyMolecular biologyYeastOrnithine decarboxylaseFungal Proteinschemistry.chemical_compoundchemistryBiochemistryOrnithine Decarboxylase InhibitorCell WallEnzyme inhibitorCandida albicansPutrescinebiology.proteinProtein biosynthesisGrowth inhibitionCandida albicansPolyamineJournal of General Microbiology
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Estimation of ambient GABA levels in layer I of the mouse neonatal cortex in brain slices

2010

GABAergic synapses on Cajal–Retzius neurons in layer I of the murine neocortex experience GABAB receptor (GABABR)-mediated tonic inhibition. Extracellular GABA concentration ([GABA]o) that determines the strength of GABABR-mediated inhibition is controlled by GABA transporters (GATs). In this study, we hypothesized that the strength ofpresynaptic GABABR activation reflects [GABA]o in the vicinity of synaptic contacts. Slices obtained from two age groups were used, namely postnatal days (P)2–3 and P5–7. GABAergic postsynaptic currents (IPSCs) were recorded using the whole-cell patch-clamp technique. Minimal electrical stimulation in layer I was applied to elicit evoked IPSCs (eIPSCs) using a…

NeocortexPhysiologyGlutamate decarboxylaseStimulationBiologyGABAB receptormedicine.anatomical_structurenervous systemmedicineExcitatory postsynaptic potentialBiophysicsGABAergicGABA Uptake InhibitorsPatch clampNeuroscienceThe Journal of Physiology
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Neurofilament light chain levels reflect outcome in a patient with glutamic acid decarboxylase 65 antibody–positive autoimmune encephalitis under imm…

2020

Neurological immune-mediated side effects are rare but often severe complications of immune checkpoint inhibitor (ICI) treatment. This report describes a severe case of nivolumab/ipilimumab-associated glutamic acid decarboxylase 65-positive autoimmune encephalitis. It proposes neurofilament light chain levels, a biomarker indicating axonal damage, in the cerebrospinal fluid and serum as a putative novel biomarker for this diagnostically and therapeutically challenging entity with an often unfavorable outcome. Additionally, we provide an overview of previous reports of patients developing autoimmune encephalitis under ICI treatment.

NeurofilamentGlutamate decarboxylaseIntermediate Filaments610 MedizinHashimoto Disease03 medical and health sciences0302 clinical medicineCerebrospinal fluid610 Medical sciencesHumansMedicine030212 general & internal medicineImmune Checkpoint InhibitorsAutoimmune encephalitisbiologyGlutamate Decarboxylasebusiness.industrymedicine.diseaseIpilimumabNivolumabNeurologyImmunologybiology.proteinEncephalitisBiomarker (medicine)Neurology (clinical)AntibodyNivolumabbusiness030217 neurology & neurosurgeryEncephalitisEuropean Journal of Neurology
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Brain histamine and oleoylethanolamide restore behavioral deficits induced by chronic social defeat stress in mice.

2021

The physiological mechanisms underlying the complex interplay between life stressors and metabolic factors is receiving growing interest and is being analyzed as one of the many factors contributing to depressive illness. The brain histaminergic system modulates neuronal activity extensively and we demonstrated that its integrity is necessary for peripheral signals such as the bioactive lipid mediator oleoylethanolamide (OEA) to exert its central actions. Here, we investigated the role of brain histamine and its interaction with OEA in response to chronic social defeat stress (CSDS), a preclinical protocol widely used to study physio-pathological mechanisms underlying symptoms observed in d…

Neurophysiology and neuropsychologyPhysiologyHistidine decarboxylaseNeurosciences. Biological psychiatry. NeuropsychiatryT-pattern analysis OxytocinT-pattern analysisOxytocinSettore BIO/09 - FisiologiaBiochemistrySocial interactionSocial defeatRecognition memory03 medical and health sciencesCellular and Molecular Neurosciencechemistry.chemical_compoundOleoylethanolamide0302 clinical medicineEndocrinologyMedicineChronic stressOriginal Research ArticleNeurotransmitterRC346-429Molecular BiologySocial stressEndocrine and Autonomic Systemsbusiness.industryHistidine decarboxylase; Oxytocin; Recognition memory; Social interaction; T-pattern analysisQP351-495HistaminergicHistidine decarboxylase030227 psychiatrychemistryNeurology. Diseases of the nervous systembusinessNeuroscience030217 neurology & neurosurgeryHistamineRC321-571Neurobiology of stress
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Post-weaning social isolation rearing influences the expression of molecules related to inhibitory neurotransmission and structural plasticity in the…

2012

Several lines of evidence indicate that alterations in the structure of neural circuits and inhibitory neurotransmission underlie the physiopathogenesis of schizophrenia. Most of the studies on these parameters have been focused on cortical regions and, despite the crucial role of the amygdala in this psychiatric disorder, there is less information on this region. In order to expand this knowledge, we have studied the expression of molecules related to inhibitory neurotransmission and structural plasticity in rats subjected to post-weaning isolation rearing, an animal model that reproduces several core symptoms of schizophrenia. We have analyzed, using qRT-PCR and immunohistochemistry, the …

NeuropilInterneuronGlutamate decarboxylaseSynaptophysinNeural Cell Adhesion Molecule L1NeurotransmissionInhibitory postsynaptic potentialReal-Time Polymerase Chain ReactionAmygdalaSynaptic TransmissionInterneuronsPregnancymedicineAnimalsRNA MessengerMolecular BiologyNeural Cell Adhesion MoleculesNeuronal PlasticitybiologyGlutamate DecarboxylaseGeneral Neurosciencemedicine.diseaseAmygdalaImmunohistochemistryRatsmedicine.anatomical_structurenervous systemSocial IsolationSchizophreniaSynaptophysinbiology.proteinSialic AcidsNeural cell adhesion moleculeFemaleNeurology (clinical)PsychologyNeuroscienceDevelopmental BiologyDensitometryBrain research
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Gliadin activates arginase pathway in RAW264.7 cells and in human monocytes

2014

AbstractCeliac disease (CD) is an autoimmune enteropathy triggered in susceptible individuals by the ingestion of gliadin-containing grains. Recent studies have demonstrated that macrophages play a key role in the pathogenesis of CD through the release of inflammatory mediators such as cytokines and nitric oxide (NO). Since arginine is the obliged substrate of iNOS (inducible nitric oxide synthase), the enzyme that produces large amount of NO, the aim of this work is to investigate arginine metabolic pathways in RAW264.7 murine macrophages after treatment with PT-gliadin (PTG) in the absence and in the presence of IFNγ. Our results demonstrate that, besides strengthening the IFNγ-dependent …

OrnithineArginineBlotting WesternNitric Oxide Synthase Type IIOrnithine DecarboxylaseReal-Time Polymerase Chain ReactionArginineMonocytesGliadinOrnithine decarboxylaseInterferon-gammaMicechemistry.chemical_compoundmedicineAnimalsHumansCeliac diseaseMacrophageRNA MessengerMolecular BiologyCells CulturedArginasebiologyReverse Transcriptase Polymerase Chain ReactionMacrophagesMonocytenutritional and metabolic diseasesNitric oxideOrnithineMolecular biologyPeptide FragmentsNitric oxide synthaseArginasemedicine.anatomical_structureBiochemistrychemistrybiology.proteinMolecular MedicineInterferon-γGliadinBiochimica et Biophysica Acta (BBA) - Molecular Basis of Disease
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Mutation of the oxaloacetate decarboxylase gene of Lactococcus lactis subsp. lactis impairs the growth during citrate metabolism

2007

 ; Aims: Citrate metabolism generates metabolic energy through the generation of a membrane potential and a pH gradient. The purpose of this work was to study the influence of oxaloacetate decarboxylase in citrate metabolism and intracellular pH maintenance in relation to acidic conditions. Methods and Results: A Lactococcus lactis oxaloacetate decarboxylase mutant [ILCitM (pFL3)] was constructed by double homologous recombination. During culture with citrate, and whatever the initial pH, the growth rate of the mutant was lower. In addition, the production of diacetyl and acetoin was altered in the mutant strain. However, our results indicated no relationship with a change in the maintenanc…

Oxaloacetic AcidATP citrate lyaseCarboxy-LyasesCITRATE METABOLISMIntracellular pHMolecular Sequence DataDiacetylACIDE LACTIQUEApplied Microbiology and BiotechnologyCitric Acidchemistry.chemical_compoundLACTIC ACID BACTERIAOxaloacetic acidCitrate synthaseBacteriological TechniquesBase SequencebiologyOXALOACETATE DECARBOXYLASEAcetoinLactococcus lactisGeneral MedicineHydrogen-Ion Concentrationbiology.organism_classificationLactococcus lactis[SDV.MP]Life Sciences [q-bio]/Microbiology and ParasitologyOxaloacetate decarboxylaseBiochemistrychemistryGenes BacterialFermentationMutationINTRACELLULAR PHFood Microbiologybiology.proteinGenetic EngineeringCitric acidPhosphoenolpyruvate carboxykinaseBiotechnologyJournal of Applied Microbiology
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Tyramine and phenylethylamine production among lactic acid bacteria isolated from wine.

2007

The ability of wine lactic acid bacteria to produce tyramine and phenylethylamine was investigated by biochemical and genetic methods. An easy and accurate plate medium was developed to detect tyramine-producer strains, and a specific PCR assay that detects the presence of tdc gene was employed. All strains possessing the tdc gene were shown to produce tyramine and phenylethylamine. Wines containing high quantities of tyramine and phenylethylamine were found to contain Lactobacillus brevis or Lactobacillus hilgardii. The main tyramine producer was L. brevis. The ability to produce tyramine was absent or infrequent in the rest of the analysed wine species.

Pcr assayved/biology.organism_classification_rank.speciesColony Count MicrobialTyramineWineLactobacillus hilgardiiMicrobiologychemistry.chemical_compoundPhenethylaminesFood microbiologyWinebiologyLactobacillus brevisved/biologyfood and beveragesGeneral MedicineTyramineTyrosine Decarboxylasebiology.organism_classificationLactic acidCulture MediaLactobacilluschemistryBiochemistryFood MicrobiologyBacteriaFood ScienceInternational journal of food microbiology
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Zur Wirkung von Butazolidin im Intermedi�rstoffwechsel

1956

Butazolidin (Phenylbutazone) inhibits the oxidative decarboxylation of pyruvate and α-ketoglutarate in a final concentration of 10 mg-% (3,24 · 10−4 m). Data are presented suggesting that the β-ketothiolase is inhibited. The following enzymes or enzyme systems are not inhibited: The enzymes of the respiratory chain, the enzymes of the citric acid cycle with exception of α-ketoglutaric oxidase, the glycolysis of hexosediphosphate (slight inhibition), acetate thiokinase, sulfanilamid transacetylase, pyruvic decarboxylase from yeast, arginase, xanthine oxidase, and D-amino acid oxidase.

Pharmacologychemistry.chemical_classificationOxidase testRespiratory chainGeneral MedicineCitric acid cyclechemistry.chemical_compoundEnzymechemistryBiochemistryAcetate thiokinaseXanthine oxidaseOxidative decarboxylationPyruvate decarboxylaseNaunyn-Schmiedebergs Archiv f�r Experimentelle Pathologie und Pharmakologie
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