Search results for "Isoenzyme"

showing 10 items of 247 documents

Glutamine synthetase from roots of Brassica napus. Nucleotide sequence of a cytosolic isoform.

1994

chemistry.chemical_classificationGene isoformDNA ComplementarybiologyBase SequencePhysiologyMolecular Sequence DataBrassicaNucleic acid sequencePlant ScienceBrassicabiology.organism_classificationGenes PlantIsoenzymesCytosolEnzymeCytosolchemistryBiochemistryGlutamate-Ammonia LigaseComplementary DNAGlutamine synthetaseGeneticsCarbon-Nitrogen LigasesResearch ArticlePlant physiology
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Biochemical characterization of two functional human liver acyl-CoA oxidase isoforms 1a and 1b encoded by a single gene

2007

Abstract Human acyl-CoA oxidase 1 (ACOX1) is a rate-limiting enzyme in peroxisomal fatty acids β-oxidation and its deficiency is associated with a lethal, autosomal recessive disease, called pseudoneonatal-adrenoleukodystrophy. Two mRNA variants, transcribed from a single gene encode ACOX1a or ACOX1b isoforms, respectively. Recently, a mutation in a splice site has been reported [H. Rosewich, H.R. Waterham, R.J. Wanders, S. Ferdinandusse, M. Henneke, D. Hunneman, J. Gartner, Pitfall in metabolic screening in a patient with fatal peroxisomal β-oxidation defect, Neuropediatrics 37 (2006) 95–98.], which results in the defective peroxisomal fatty acids β-oxidation. Here, we show that these mRNA…

chemistry.chemical_classificationGene isoformOxidase testBiophysicsCell BiologyBiologyPeroxisomeBiochemistryIsozymeMolecular biologyArticleEnzyme ActivationIsoenzymesMolecular WeightEnzymechemistryBiochemistryLiverEnzyme StabilityAcyl-CoA oxidaseACOX1HumansHeterologous expressionAcyl-CoA OxidaseMolecular Biology
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Differential function of the phosphoglucomutase isozymes PGM1 and PGM2

1979

A total of 13 metabolites thought to be possibly inhibitory were tested for their influence on PGM isozyme activities, each at several different concentrations. The analysis of statistical significance was based on enzyme activities obtained by densitometric measurements of starch gels. Five of the substances were found to inhibit PGM activity, three of which definitely and a further one probably led to a significantly stronger inhibition of the isozymes of the PGM2 locus than of PGM1 isozymes. They are (1) fructose-1,6-diphosphate, (2) adenosine triphosphate, (3) citrate, and (4) possibly 2,3-diphosphoglycerate. Thus, PGM1 isozymes proved to function better in hard or perhaps marginal meta…

chemistry.chemical_classificationStarchChromosome MappingLocus (genetics)BiologyDiphosphoglyceric AcidsMolecular biologyIsozymeIsoenzymeschemistry.chemical_compoundAdenosine TriphosphateEnzymeGenesPhosphoglucomutasechemistryBiochemistryPGM1FructosediphosphatesGeneticsHumansPhosphoglucomutaseCitratesAdenosine triphosphateGeneGenetics (clinical)Human Genetics
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On the biochemical classification of yeast trehalases: Candida albicans contains two enzymes with mixed features of neutral and acid trehalase activi…

2009

Abstract Two enzymes endowed with trehalase activity are present in Candida albicans . The cytosolic trehalase (Ntc1p), displayed high activity in exponential phase regardless of the carbon source (glucose, trehalose or glycerol). Ntc1p activity was similar in neutral (pH 7.1) or acid (pH 4.5) conditions, strongly inhibited by ATP, weakly stimulated by divalent cations (Ca 2+ or Mn 2+ ) and unaffected in the presence of cyclic AMP. The Ntc1p activity decreased in stationary phase, except in glycerol-grown cultures, but the catalytic properties did not change. In turn, the cell wall-linked trehalase (Atc1p) showed elevated activity in resting cells or in cultures growing on trehalose or glyc…

chemistry.chemical_classificationbiologyBiophysicsTrehalase activityCell BiologyHydrogen-Ion Concentrationbiology.organism_classificationBiochemistryTrehaloseYeastDivalentFungal ProteinsIsoenzymesCytosolchemistry.chemical_compoundAdenosine TriphosphateEnzymechemistryBiochemistryCandida albicansCyclic AMPTrehalaseTrehalaseCandida albicansMolecular BiologyBiochemical and Biophysical Research Communications
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Differential behaviour of Pseudomonas sp. 42A2 LipC, a lipase showing greater versatility than its counterpart LipA

2009

Abstract Growth of Pseudomonas sp. 42A2 on oleic acid releases polymerized hydroxy-fatty acids as a result of several enzymatic conversions that could involve one or more lipases. To test this hypothesis, the lipolytic system of strain Pseudomonas sp. 42A2 was analyzed, revealing the presence of at least an intracellular carboxylesterase and a secreted lipase. Consensus primers derived from a conserved region of bacterial lipase subfamilies I.1 and I.2 allowed isolation of two secreted lipase genes, lipA and lipC, highly homologous to those of Pseudomonas aeruginosa PAO1. Homologous cloning of the isolated lipA and lipC genes was performed in Pseudomonas sp. 42A2 for LipA and LipC over-expr…

chemistry.chemical_classificationbiologyStrain (chemistry)PseudomonasFatty acidLipaseGeneral Medicinebiology.organism_classificationBiochemistrySubstrate SpecificityIsoenzymesCarboxylesteraseOleic acidchemistry.chemical_compoundEnzymeBacterial ProteinschemistryBiochemistryPseudomonasEnzyme Stabilitybiology.proteinEnzyme kineticsLipaseBiochimie
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Population structure of a parasitic plant and its perennial host

2002

Characterization of host and parasite population genetic structure and estimation of gene flow among populations are essential for the understanding of parasite local adaptation and coevolutionary interactions between hosts and parasites. We examined two aspects of population structure in a parasitic plant, the greater dodder (Cuscuta europaea) and its host plant, the stinging nettle (Urtica dioica), using allozyme data from 12 host and eight parasite populations. First, we examined whether hosts exposed to parasitism in the past contain higher levels of genetic variation. Second, we examined whether host and parasite populations differ in terms of population structure and if their populati…

education.field_of_studyGeographyEcologyParasitic plantHost (biology)PopulationGenetic VariationUrtica dioicaParasitismZoologyCuscuta europaeaBiologybiology.organism_classificationHost-Parasite InteractionsIsoenzymesGene FrequencyGenetic variationGeneticsParasite hostingeducationAllelesFinlandSolanaceaeGenetics (clinical)Local adaptationHeredity
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Genetic differentiation and structure of Hippocrepis valentina (Leguminosae) populations

2000

We present an analysis of isozyme variability in natural populations of the plant species Hippocrepis valentina (Leguminosae), which is endemic to the eastern Mediterranean coast of Spain and currently has endangered species status. Our results, obtained by starch-gel electrophoresis of 15 loci, show normal levels of variability for species with similar biology. The comparison with the patterns of genetic variability of two closely related species, H. balearica and H. grosii, confirms the taxonomic status of H. valentina as a proper species, independent of H. balearica, as previously suggested. The analysis of population subdivision shows that substantial variation among populations is pres…

education.field_of_studyHippocrepisPlants MedicinalGenotypebiologyEcologyElectrophoresis Starch GelPopulationEndangered speciesZoologyPopulation geneticsFabaceaebiology.organism_classificationGene flowIsoenzymesBalearicaGene FrequencyGenetic variationGeneticsGenetic variabilityeducationMolecular BiologyGenetics (clinical)BiotechnologyJournal of Heredity
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Absence of the endo-beta-1,4-glucanases Cel1 and Cel2 reduces susceptibility to Botrytis cinerea in tomato.

2007

Cel1 and Cel2 are members of the tomato (Solanum lycopersicum Mill) endo-beta-1,4-glucanase (EGase) family that may play a role in fruit ripening and organ abscission. This work demonstrates that Cel1 protein is present in other vegetative tissues and accumulates during leaf development. We recently reported the downregulation of both the Cel1 mRNA and protein upon fungal infection, suggesting the involvement of EGases in plant-pathogen interactions. This hypothesis was confirmed by assessing the resistance to Botrytis cinerea infection of transgenic plants expressing both genes in an antisense orientation (Anti-Cel1, Anti-Cel2 and Anti-Cel1-Cel2). The Anti-Cel1-Cel2 plants showed enhanced …

food.ingredientPseudomonas syringaePlant ScienceDeoxyglucoseGene Expression Regulation EnzymologicMicrobiologychemistry.chemical_compoundfoodAbscissionSolanum lycopersicumGene Expression Regulation PlantGeneticsPseudomonas syringaeCellulose 14-beta-CellobiosidaseGlucansBotrytis cinereaBotrytisPlant DiseasesbiologyReverse Transcriptase Polymerase Chain ReactionfungiCallosefood and beveragesCell BiologyGlucanasebiology.organism_classificationPlants Genetically ModifiedIsoenzymesPlant LeavesAntisense Elements (Genetics)BiochemistrychemistryFruitBotrytisSolanumSolanaceaeThe Plant journal : for cell and molecular biology
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Seminar 2_Clinical Enzimology

2022

Este documento ha sido revisado por el Servicio de política Linguística. Su labor ha sido muy importante para la correción del documento. Este documento contiene un pdf con las diapositivas utilizadas para el seminario 2, dentro de la asignatura de Integración de Bioquímica y Biología Molecular, para los alumnos de 2º curso del grado de Medicina. El seminario habla de los ensayos clínicos realizados en sangre, del valor diagnóstico de determinadas activades enzimáticas, y como realizar correctamente un análisis de sangre. Una segunda parte de este seminario trata sobre las isoenzimas. This document contains a pdf with the slides used for the seminar 2, within the subject of Integration of B…

half life of an enzymeisoenzymesUNESCO::CIENCIAS MÉDICASclinical enzymologyblood test
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The Myristoylated Alanine-Rich C-Kinase Substrate (MARCKS) is Sequentially Phosphorylated by Conventional, Novel and Atypical Isotypes of Protein Kin…

1995

The myristoylated alanine-rich C-kinase substrate (MARCKS) is the major protein kinase C (PKC) substrate in many cell types including fibroblasts and brain cells. Here we describe the phosphorylation of MARCKS and the site specificity for different PKC isotypes. Conventional (c)PKC beta 1, novel (n)PKC delta and nPKC epsilon efficiently phosphorylated the MARCKS protein in vitro. The Km values were extremely low, reflecting a high affinity between kinases and substrate. The apparent affinity of nPKC delta (Km = 0.06 microM) was higher than that of nPKC epsilon and cPKC beta 1 (Km = 0.32 microM). The rate of substrate phosphorylation was inversely correlated with affinity and decreased in th…

inorganic chemicalsKinaseChemistryIntracellular Signaling Peptides and ProteinsMembrane ProteinsProteinsContext (language use)macromolecular substancesenvironment and public healthBiochemistryMolecular biologyCell biologyIsoenzymesSerineKineticsenzymes and coenzymes (carbohydrates)Substrate-level phosphorylationbacteriaPhosphorylationPhosphorylationMARCKSMyristoylated Alanine-Rich C Kinase SubstrateProtein Kinase CProtein kinase CMyristoylationEuropean Journal of Biochemistry
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