Search results for "Bulos"

showing 10 items of 48 documents

Life span, dispersal and age of nesting Great Grey Owls (Strix nebulosa lapponica) in Sweden.

2016

3,073 Great Grey Owls were banded in Sweden in 1955–2012. 416 were controlled at least once (54.6%) or recovered dead (45.4%). Three birds banded as nestlings were recovered in their 17th calendar year. Most birds were recovered during first year of life. Only 4 females were controlled breeding as 2CY birds. 91.3% of birds controlled as first time breeders were at least 4CY. Birds banded as nestlings and recovered dead between September and July moved 100.8 km (mean) with a median distance of 64 km. Juveniles controlled alive moved 45.9 km (mean) with a median distance of 23 km during first year of life. Maximum natal dispersal was 650 km. Median natal dispersal for females was 40 km, betwe…

NestStrix nebulosa lapponicaLife spanHatchingZoologyBiological dispersalAnimal Science and ZoologyBird ringingFirst year of lifeBiologyPopulation ecology
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C172S Substitution in the Chloroplast-encoded Large Subunit Affects Stability and Stress-induced Turnover of Ribulose-1,5-bisphosphate Carboxylase/Ox…

1999

Previous work has indicated that the turnover of chloroplast ribulose-1,5-bisphosphate carboxylase/oxygenase (Rubisco; EC 4.1.1. 39) may be controlled by the redox state of certain cysteine residues. To test this hypothesis, directed mutagenesis and chloroplast transformation were employed to create a C172S substitution in the Rubisco large subunit of the green alga Chlamydomonas reinhardtii. The C172S mutant strain was not substantially different from the wild type with respect to growth rate, and the purified mutant enzyme had a normal circular dichroism spectrum. However, the mutant enzyme was inactivated faster than the wild-type enzyme at 40 and 50 degrees C. In contrast, C172S mutant …

OxygenaseChloroplastsProtein ConformationRibulose-Bisphosphate CarboxylaseMutantChlamydomonas reinhardtiiBiochemistrychemistry.chemical_compoundEnzyme StabilitySerineAnimalsCysteineMolecular BiologyCysteine metabolismRibulose 15-bisphosphatebiologyCircular DichroismRuBisCOWild typeCell Biologybiology.organism_classificationChloroplastPhenotypeAmino Acid SubstitutionchemistryBiochemistryMutagenesis Site-Directedbiology.proteinSpectrophotometry UltravioletOxidation-ReductionChlamydomonas reinhardtiiJournal of Biological Chemistry
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Cysteines 449 and 459 modulate the reduction-oxidation conformational changes of ribulose 1.5-bisphosphate carboxylase/oxygenase and the translocatio…

2006

The role of cysteines 449 (Cys449) and 459 (Cys459) from the large subunit (LS) of ribulose 1-5-bisphosphate carboxylase/oxygenase (Rubisco) in the reduction-oxidation (redox) regulation of the enzyme was assessed by site-directed mutagenesis of these residues and chloroplast transformation of Chlamydomonas reinhardtii. In vitro studies indicated that mutations C449S, C459S or C449S/ C459S do not affect the activity and proteolytic susceptibility of the enzyme in the reduced state. However, when oxidized, the mutant enzymes differed from the wild type (WT), showing an increased resistance to inactivation and, in the case of the double mutant (DM), an altered structural conformation as refle…

OxygenaseProtein ConformationPhysiologyRibulose-Bisphosphate CarboxylaseBlotting WesternChlamydomonas reinhardtiiPlant ScienceBiologychemistry.chemical_compoundCysteinechemistry.chemical_classificationRibulose 15-bisphosphateRibuloseCell MembraneRuBisCOWild typebiology.organism_classificationPyruvate carboxylaseProtein TransportEnzymeBiochemistrychemistryMutagenesis Site-Directedbiology.proteinElectrophoresis Polyacrylamide GelOxidation-ReductionPlant, Cell and Environment
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Modification of the proteolytic fragmentation pattern upon oxidation of cysteines from ribulose 1,5-bisphosphate carboxylase/oxygenase.

2003

The proteolytic susceptibility of the native CO 2 -fixing photosynthetic enzyme ribulose 1,5-bisphosphate carboxylase/oxygenase (EC 4.1.1.39, Rubisco) has been shown to increase in vitro after oxidative treatments that affect cysteine thiols. A limited incubation of oxidized (pretreated with the disulfide cystamine) Rubisco from Chlamydomonas reinhardtii with subtilisin or proteinase K generated fragments of molecular mass about 53 kDa (band I in SDS-PAGE) and 47 kDa (band II) derived from the large subunit (55 kDa) of the enzyme. In contrast, proteolysis of the reduced Rubisco (pretreated with the free thiol cysteamine) produced only the 53 kDa band. The same fragmentation pattern was repr…

OxygenaseProtein subunitRibulose-Bisphosphate CarboxylaseMolecular Sequence DataBiochemistrychemistry.chemical_compoundEndopeptidasesAnimalsEuglena gracilisAmino Acid SequenceCysteineConserved SequenceRibulose 15-bisphosphatebiologyRibuloseHydrolysisfungiRuBisCOSubtilisinPeptide FragmentsKineticsProtein SubunitschemistryBiochemistryModels Chemicalbiology.proteinProtein quaternary structureHoloenzymesOxidation-ReductionProtein Processing Post-TranslationalChlamydomonas reinhardtiiCysteineBiochemistry
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Oxidative modification and breakdown of ribulose-1,5-bisphosphate carboxylase/oxygenase induced in Euglena gracitis by nitrogen starvation

1994

When photoheterotrophic Euglena gracilis Z Pringsheim was subjected to nitrogen (N)-deprivation, the abundant photosynthetic enzyme ribulose-1,5-bis-phosphate carboxylase/oxygenase (Rubisco; EC 4.1.1.39) was rapidly and selectively degraded. The breakdown began after a 4-h lag period and continued for a further 8 h at a steady rate. After 12 h of starvation, when the amount of Rubisco was reduced to 40%, the proteolysis of this enzyme slowed down while degradation of other proteins started at a similar pace. This resulted in a decline of culture growth, chloroplast disassembly — as witnessed by chlorophyll (Chl) loss — and cell bleaching. Experiments with spectinomycin, an inhibitor of chlo…

OxygenaseRibulose 15-bisphosphateEuglena gracilisbiologyved/biologyved/biology.organism_classification_rank.speciesRuBisCOfood and beveragesPlant Sciencebiology.organism_classificationPhotosynthesisEuglenaChloroplastchemistry.chemical_compoundBiochemistrychemistryChloroplast disassemblyGeneticsbiology.proteinPlanta
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Increased susceptibility of ribulose-1,5-bisphosphate carboxylase/oxygenase to proteolytic degradation caused by oxidative treatments

1990

The susceptibility of the chloroplastic enzyme ribulose-1,5-bisphosphate carboxylase/oxygenase to proteolysis by trypsin, chymotrypsin, proteinase K, and papain is enhanced by oxidative treatments including spontaneous oxidation of cysteines. Proteinases exhibit a high specificity for the oxidized inactive form of the carboxylase, cleaving its large subunit. Treatment of the inactive enzyme with dithiothreitol results in partial recovery of both carboxylase activity and resistance to proteolysis. This behavior may explain the specific degradation of ribulose-1,5-bisphosphate carboxylase/oxygenase that occurs in vivo during leaf senescence.

OxygenaseTime FactorsRibulose-Bisphosphate CarboxylaseProteolysisBiophysicsBiochemistryDithiothreitolchemistry.chemical_compoundEnzyme StabilitymedicineCysteineMolecular Biologychemistry.chemical_classificationChymotrypsinRibulose 15-bisphosphatebiologymedicine.diagnostic_testHydrolysisPlantsTrypsinPyruvate carboxylaseEnzymechemistryBiochemistrybiology.proteinOxidation-ReductionPeptide Hydrolasesmedicine.drugArchives of Biochemistry and Biophysics
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Expression of a vegetative-storage-protein gene from Arabidopsis is regulated by copper, senescence and ozone

2001

Emerging data suggest that the mechanisms regulating plant copper homeostasis could be implicated in stress and senescence signal transduction pathways. To gain insight into copper-modulated patterns of gene expression, copper-treated Arabidopsis thaliana (L.) Heynh. plants were analysed by mRNA differential display. The experimental conditions were selected using aggregation of ribulose-1,5-bisphosphate carboxylase-oxygenase (Rubisco) as a molecular sensor to monitor copper-induced oxidative stress. Two copper-induced messengers encoding a vegetative storage protein (VSP2) were isolated by this technique. Both clones differed in the length of their 3'-untranslated region according to the p…

ParaquatSenescenceCopper SulfateRibulose-Bisphosphate CarboxylaseMolecular Sequence DataArabidopsisPlant Sciencemedicine.disease_causeOzoneGene Expression Regulation PlantArabidopsisGene expressionGeneticsmedicineStorage proteinArabidopsis thalianaRNA MessengerCloning Molecularchemistry.chemical_classificationBase SequencebiologyArabidopsis ProteinsRuBisCOGene Expression Regulation DevelopmentalHydrogen Peroxidebiology.organism_classificationOxidative StresschemistryBiochemistrybiology.proteinSignal transductionSequence AnalysisCopperOxidative stressPlanta
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Humoral responses during wound healing in Holothuria tubulosa (Gmelin, 1788)

2021

Abstract Wounds in living organisms trigger tissue-repair mechanisms. The sea cucumber (Holoturia tubulosa) is an excellent model species for achieving a better understanding of the humoral and cellular aspects involved in such healing processes. Consequently, this study assesses data on its morphometric, physiological and humoral responses 1, 2, 6, 24 and 48h after wound induction. In particular, morphometric data on the weight, width, length and coelomic-fluid volume of the species were estimated at different times during our experiments. In addition, the humoral aspects related to the enzymatic activity of esterase, alkaline phosphatase and peroxidase, as well as the cytotoxic activity o…

PhysiologySettore BIO/05 - ZoologiaBiochemistryEsteraseCytotoxic activity Echinoderm Enzyme activity Regeneration mechanism Immunity sea cucumber03 medical and health sciencesSea cucumberAnimalsHolothuriaCytotoxic T cellSettore BIO/06 - Anatomia Comparata E CitologiaMolecular Biology030304 developmental biologyWound Healing0303 health sciencesSheepbiologyBody WeightHolothuria tubulosa04 agricultural and veterinary sciencesbiology.organism_classificationEnzyme assayFISIOLOGIABiochemistry040102 fisheriesbiology.protein0401 agriculture forestry and fisheriesAlkaline phosphataseRabbitssense organsWound healingPeroxidaseComparative Biochemistry and Physiology Part B: Biochemistry and Molecular Biology
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Changes in enzymes involved in photosynthesis and other metabolic processes in the fruit of Opuntia ficus-indica during growth and ripening

2011

The aim of this study was to investigate changes in the abundance of a number of enzymes in the peel, core and seeds of fruits of Opuntia ficus-indica (L.) Miller during development. The enzymes studied were phosphoenolpyruvate carboxylase (PEPC; EC: 4.1.1.31), ribulose-1,5-bisphosphate carboxylase/oxygenase (RUBISCO; EC: 4.1.1.39), aldolase (EC: 4.1.2.13), pyruvate, orthophosphate dikinase (PPDK; EC: 2.7.9.1), phosphoenolpyruvate carboxykinase (PEPCK; EC: 4.1.1.49) and aspartate aminotransferase (AspAT; EC: 2.6.1.1). To detect these enzymes, antibodies specific for each enzyme were used to probe Western blots of sodium dodecyl sulphate polyacrylamide gels. Fruit weight increased throughout…

PyruvateOxygenaseOpuntia ficus-indica (L) Miller; Fruit metabolism; Phosphoenolpyruvate carboxylase; Phosphoenolpyruvate carboxykinase; Pyruvate orthophosphate dikinase; Aspartate aminotransferase; Aldolase; Ribulose-15-bisphosphate carboxylase/oxygenaseHorticultureAspartate aminotransferasePhosphoenolpyruvate carboxylaseAldolaseOpuntia ficus-indica (L.) Miller Fruit metabolism Phosphoenolpyruvate carboxylase Phosphoenolpyruvate carboxykinase Pyruvate orthophosphatedikinase Aspartate aminotransferase Aldolase Ribulose-15-bisphosphatecarboxylase/oxygenaseorthophosphate dikinasebiologyRuBisCOAldolase Afood and beveragesRipeningFruit metabolismPyruvate carboxylaseRibulose-1Settore AGR/03 - Arboricoltura Generale E Coltivazioni ArboreeOpuntia ficus-indica (L) MillerPhosphoenolpyruvate carboxykinaseBiochemistrybiology.protein5-bisphosphate carboxylase/oxygenaseCrassulacean acid metabolismPhosphoenolpyruvate carboxykinasePhosphoenolpyruvate carboxylaseScientia Horticulturae
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Ribulose-1,5-bisphosphate Carboxylase-Oxygenase: New Aspects Respective the pH-Dependance of the Carboxylation Reaction

1983

The investigation was directed towards the effects of reaction conditions, substrates and pH on the carboxylation reaction of ribulose-1 ,5-bisphosphate carboxylase-oxygenase in the crude enzyme extracts from several plants. Optimal substrate concentrations (HCO3 - and RubP) were determined. The highest carboxylase activity was attained with Tris/HCl buffer. The pH activity profile was quite sharp with an optimum at pH 7.8. Purified and crystallized carboxylase yielded a broad optimum curve under the same reaction conditions

Reaction conditionschemistry.chemical_compoundOxygenaseRibulose 15-bisphosphateCarboxylationchemistryBiochemistryGeneral Biochemistry Genetics and Molecular BiologyPyruvate carboxylaseZeitschrift für Naturforschung C
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